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Susan Blaser

TitleNeuroradiologist
InstitutionThe Hospital for Sick Children
DepartmentDiagnostic Imaging
Address555 University Avenue
Toronto ON M5G 1X8
Phone416-813-1500
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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Propst EJ, Wolter NE, Morency AM, Amin R, Blaser S, Moore AM, Windrim R, Ryan G. Fetoscopic Balloon Dilation and Cricotracheal Resection for Laryngeal Atresia in CHAOS. Laryngoscope. 2020 Jun 23. PMID: 32574407.
      View in: PubMed
    2. Alkhunaizi E, Unger S, Shannon P, Nishimura G, Blaser S, Chitayat D. Maternal SLE and brachytelephalangic chondrodysplasia punctata in a patient with unrelated de novo RAF1 and SIX2 variants. Am J Med Genet A. 2020 Jul; 182(7):1807-1811. PMID: 32506814.
      View in: PubMed
    3. Shinar S, Blaser S, Chitayat D, Selvanathan T, Chau V, Shannon P, Agrawal S, Ryan G, Pruthi V, Miller SP, Krishnan P, Van Mieghem T. Long-term postnatal outcomes of fetuses with prenatally suspected septo-optic dysplasia. Ultrasound Obstet Gynecol. 2020 Mar 20. PMID: 32196785.
      View in: PubMed
    4. Chao BK, Claessens NHP, Lim JM, Gorodetsky C, Au-Young SH, Guerguerian AM, Marini D, Blaser S, Shroff M, Saini AK, Seed M, Chau V, Miller SP. Decreased Brain Volumes and Infants With Congenital Heart Disease Undergoing Venoarterial Extracorporeal Membrane Oxygenation. Pediatr Crit Care Med. 2020 Mar 13. PMID: 32195905.
      View in: PubMed
    5. Grass B, El Shahed A, Ly LG, Chau V, Branson HM, Blaser S, Runeckles K, Wilson D, Whyte H. Therapeutic hypothermia for hypoxic-ischemic encephalopathy after perinatal sentinel events: less brain injury on MRI and improved neurodevelopmental outcome at 18-36 months. J Perinatol. 2020 Apr; 40(4):633-639. PMID: 32051541.
      View in: PubMed
    6. Al Balushi A, Matviychuk D, Jobling R, Salomons GS, Blaser S, Mercimek-Andrews S. Phenotypes and genotypes of mitochondrial aminoacyl-tRNA synthetase deficiencies from a single neurometabolic clinic. JIMD Rep. 2020 Jan; 51(1):3-10. PMID: 32071833.
      View in: PubMed
    7. Watts GD, Antonarakis GS, Blaser SI, Phillips JH, Forrest CR. Cranioorbital Morphology Caused by Coronal Ring Suture Synostosis. Plast Reconstr Surg. 2019 12; 144(6):1403-1411. PMID: 31764659.
      View in: PubMed
    8. Mitani T, Punetha J, Akalin I, Pehlivan D, Dawidziuk M, Coban Akdemir Z, Yilmaz S, Aslan E, Hunter JV, Hijazi H, Grochowski CM, Jhangiani SN, Karaca E, Fatih JM, Iwanowski P, Gambin T, Wlasienko P, Goszczanska-Ciuchta A, Bekiesinska-Figatowska M, Hosseini M, Arzhangi S, Najmabadi H, Rosenfeld JA, Du H, Marafi D, Blaser S, Teitelbaum R, Silver R, Posey JE, Ropers HH, Gibbs RA, Wiszniewski W, Lupski JR, Chitayat D, Kahrizi K, Gawlinski P. Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders. Am J Hum Genet. 2019 11 07; 105(5):1005-1015. PMID: 31630790.
      View in: PubMed
    9. Jilani A, Matviychuk D, Blaser S, Dyack S, Mathieu J, Prasad AN, Prasad C, Kyriakopoulou L, Mercimek-Andrews S. High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses. JIMD Rep. 2019 Nov; 50(1):20-30. PMID: 31741823.
      View in: PubMed
    10. Purcell PL, Marquez Garcia J, Zawawi F, Propst EJ, Papsin BC, Blaser SI, Wolter NE. Ectopic cervical thymus in children: Clinical and radiographic features. Laryngoscope. 2020 Jun; 130(6):1577-1582. PMID: 31461169.
      View in: PubMed
    11. Niles KM, Blaser S, Shannon P, Chitayat D. Fetal arthrogryposis multiplex congenita/fetal akinesia deformation sequence (FADS)-Aetiology, diagnosis, and management. Prenat Diagn. 2019 08; 39(9):720-731. PMID: 31218730.
      View in: PubMed
    12. Leijser LM, Chau V, Seed M, Poskitt KJ, Synnes A, Blaser S, Au-Young SH, Hickey EJ, Campbell A, McQuillen PS, Miller SP. Anticoagulation therapy and the risk of perioperative brain injury in neonates with congenital heart disease. J Thorac Cardiovasc Surg. 2019 06; 157(6):2406-2413.e2. PMID: 30981520.
      View in: PubMed
    13. Nimmo GAM, Venkatesh S, Pandey AK, Marshall CR, Hazrati LN, Blaser S, Ahmed S, Cameron J, Singh K, Ray PN, Suzuki CK, Yoon G. Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy. Hum Mol Genet. 2019 01 15; 28(2):290-306. PMID: 30304514.
      View in: PubMed
    14. Siu JM, Blaser SI, Gordon KA, Papsin BC, Cushing SL. Efficacy of a selective imaging paradigm prior to pediatric cochlear implantation. Laryngoscope. 2019 Nov; 129(11):2627-2633. PMID: 30613974.
      View in: PubMed
    15. Hannah-Shmouni F, MacNeil L, Potter M, Jobling R, Yoon G, Laughlin S, Blaser S, Inbar-Feigenberg M. Severe cystic degeneration and intractable seizures in a newborn with molybdenum cofactor deficiency type B. Mol Genet Metab Rep. 2019 Mar; 18:11-13. PMID: 30619713.
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    16. AlRefai A, Drake J, Kulkarni AV, Connor KL, Shannon P, Toi A, Chitayat D, Blaser S, Church PT, Abbasi N, Ryan G, Van Mieghem T. Fetal myelomeningocele surgery: Only treating the tip of the iceberg. Prenat Diagn. 2019 01; 39(1):10-15. PMID: 30536580.
      View in: PubMed
    17. Van Ommeren RH, Gao AF, Blaser SI, Chitayat DA, Hazrati LN. BRAT1 Mutation: The First Reported Case of Chinese Origin and Review of the Literature. J Neuropathol Exp Neurol. 2018 12 01; 77(12):1071-1078. PMID: 30346566.
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    18. Vilchez-Madrigal LD, Blaser SI, Wolter NE, James AL, Papsin BC, Gordon KA, Cushing SL, Propst EJ. Children with unilateral cochlear nerve canal stenosis have bilateral cochleovestibular anomalies. Laryngoscope. 2019 10; 129(10):2403-2408. PMID: 30353559.
      View in: PubMed
    19. Costain G, Callewaert B, Gabriel H, Tan TY, Walker S, Christodoulou J, Lazar T, Menten B, Orkin J, Sadedin S, Snell M, Vanlander A, Vergult S, White SM, Scherer SW, Hayeems RZ, Blaser S, Wodak SJ, Chitayat D, Marshall CR, Meyn MS. De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome. Genet Med. 2019 04; 21(4):1021-1026. PMID: 30293988.
      View in: PubMed
    20. Alkhunaizi E, Shaheen R, Bharti SK, Joseph-George AM, Chong K, Abdel-Salam GMH, Alowain M, Blaser SI, Papsin BC, Butt M, Hashem M, Martin N, Godoy R, Brosh RM, Alkuraya FS, Chitayat D. Warsaw breakage syndrome: Further clinical and genetic delineation. Am J Med Genet A. 2018 11; 176(11):2404-2418. PMID: 30216658.
      View in: PubMed
    21. Parkes WJ, Cushing SL, Blaser SI, Papsin BC. Transmastoid access in branchio-oto-renal syndrome: A reappraisal of computed tomography imaging. Int J Pediatr Otorhinolaryngol. 2018 Nov; 114:92-96. PMID: 30262375.
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    22. Sokolov M, Gordon KA, Polonenko M, Blaser SI, Papsin BC, Cushing SL. Vestibular and balance function is often impaired in children with profound unilateral sensorineural hearing loss. Hear Res. 2019 02; 372:52-61. PMID: 29655975.
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    23. Inbar-Feigenberg M, Blaser S, Hawkins C, Shannon P, Hewson S, Chitayat D. Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrest. Metab Brain Dis. 2018 08; 33(4):1369-1373. PMID: 29574624.
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    24. Khalid R, Krishnan P, Andres K, Blaser S, Miller S, Moharir M, Dlamini N. COL4A1 and fetal vascular origins of schizencephaly. Neurology. 2018 01 30; 90(5):232-234. PMID: 29282339.
      View in: PubMed
    25. Hamilton EMC, Bertini E, Kalaydjieva L, Morar B, Dojcáková D, Liu J, Vanderver A, Curiel J, Persoon CM, Diodato D, Pinelli L, van der Meij NL, Plecko B, Blaser S, Wolf NI, Waisfisz Q, Abbink TEM, van der Knaap MS. UFM1 founder mutation in the Roma population causes recessive variant of H-ABC. Neurology. 2017 Oct 24; 89(17):1821-1828. PMID: 28931644.
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    26. Ejaz R, Lionel AC, Blaser S, Walker S, Scherer SW, Babul-Hirji R, Marshall CR, Stavropoulos DJ, Chitayat D. De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay. Am J Med Genet A. 2017 Oct; 173(10):2725-2730. PMID: 28840640.
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    27. Barmherzig R, Bullivant G, Cordeiro D, Sinasac DS, Blaser S, Mercimek-Mahmutoglu S. A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla Disease. Pediatr Neurol. 2017 Sep; 74:87-91.e2. PMID: 28662915.
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    28. O'Brien A, Marshall CR, Blaser S, Ray PN, Yoon G. Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTB. Eur J Hum Genet. 2017 06; 25(6):775-778. PMID: 28378817.
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    29. Tran C, Patel J, Stacy H, Mamak EG, Faghfoury H, Raiman J, Clarke JTR, Blaser S, Mercimek-Mahmutoglu S. Long-term outcome of patients with X-linked adrenoleukodystrophy: A retrospective cohort study. Eur J Paediatr Neurol. 2017 Jul; 21(4):600-609. PMID: 28274546.
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    30. Lardelli RM, Schaffer AE, Eggens VR, Zaki MS, Grainger S, Sathe S, Van Nostrand EL, Schlachetzki Z, Rosti B, Akizu N, Scott E, Silhavy JL, Heckman LD, Rosti RO, Dikoglu E, Gregor A, Guemez-Gamboa A, Musaev D, Mande R, Widjaja A, Shaw TL, Markmiller S, Marin-Valencia I, Davies JH, de Meirleir L, Kayserili H, Altunoglu U, Freckmann ML, Warwick L, Chitayat D, Blaser S, Çaglayan AO, Bilguvar K, Per H, Fagerberg C, Christesen HT, Kibaek M, Aldinger KA, Manchester D, Matsumoto N, Muramatsu K, Saitsu H, Shiina M, Ogata K, Foulds N, Dobyns WB, Chi NC, Traver D, Spaccini L, Bova SM, Gabriel SB, Gunel M, Valente EM, Nassogne MC, Bennett EJ, Yeo GW, Baas F, Lykke-Andersen J, Gleeson JG. Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing. Nat Genet. 2017 Mar; 49(3):457-464. PMID: 28092684.
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    31. Miscevic F, Foong J, Schmitt B, Blaser S, Brudno M, Schulze A. An MRspec database query and visualization engine with applications as a clinical diagnostic and research tool. Mol Genet Metab. 2016 12; 119(4):300-306. PMID: 27847299.
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    32. Birca A, Vakorin VA, Porayette P, Madathil S, Chau V, Seed M, Doesburg SM, Blaser S, Nita DA, Sharma R, Duerden EG, Hickey EJ, Miller SP, Hahn CD. Interplay of brain structure and function in neonatal congenital heart disease. Ann Clin Transl Neurol. 2016 09; 3(9):708-22. PMID: 27648460.
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    33. Al-Maawali A, Yoon G, Feigenbaum AS, Halliday WC, Clarke JT, Branson HM, Banwell BL, Chitayat D, Blaser SI. Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis. Neuroradiology. 2016 Oct; 58(10):1035-1042. PMID: 27516098.
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    34. Parkes WJ, Cushing SL, Papsin BC, Blaser SI, James AL. Assessment of Mastoid Function with Magnetic Resonance Imaging after Canal Wall Up Cholesteatoma Surgery. J Int Adv Otol. 2016 Aug; 12(2):132-136. PMID: 27716596.
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    35. Blaser SI, Steinlin M, Al-Maawali A, Yoon G. The Pediatric Cerebellum in Inherited Neurodegenerative Disorders: A Pattern-recognition Approach. Neuroimaging Clin N Am. 2016 Aug; 26(3):373-416. PMID: 27423800.
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    36. Propst EJ, Amin R, Talwar N, Zaman M, Zweerink A, Blaser S, Zaarour C, Luginbuehl I, Karsli C, Aziza A, Forrest C, Drake J, Narang I. Midline posterior glossectomy and lingual tonsillectomy in obese and nonobese children with down syndrome: Biomarkers for success. Laryngoscope. 2017 03; 127(3):757-763. PMID: 27345007.
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    37. Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT. Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. Am J Med Genet A. 2016 Apr; 170A(4):1070-5. PMID: 26754023.
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    38. Al-Hashim AH, Blaser S, Raybaud C, MacGregor D. Corpus callosum abnormalities: neuroradiological and clinical correlations. Dev Med Child Neurol. 2016 05; 58(5):475-84. PMID: 26661037.
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    39. Patay Z, Blaser SI, Poretti A, Huisman TA. Neurometabolic diseases of childhood. Pediatr Radiol. 2015 Sep; 45 Suppl 3:S473-84. PMID: 26346153.
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    40. Blaser SI, Padfield N, Chitayat D, Forrest CR. Skull base development and craniosynostosis. Pediatr Radiol. 2015 Sep; 45 Suppl 3:S485-96. PMID: 26346154.
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    41. Cameron JM, MacKay N, Feigenbaum A, Tarnopolsky M, Blaser S, Robinson BH, Schulze A. Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome. Eur J Paediatr Neurol. 2015 Sep; 19(5):525-32. PMID: 26008862.
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    42. Sharma A, Liu ES, Le TD, Adatia FA, Buncic JR, Blaser S, Richardson S. Pediatric orbital cellulitis in the Haemophilus influenzae vaccine era. J AAPOS. 2015 Jun; 19(3):206-10. PMID: 25900771.
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    43. Jobling RK, Assoum M, Gakh O, Blaser S, Raiman JA, Mignot C, Roze E, Dürr A, Brice A, Lévy N, Prasad C, Paton T, Paterson AD, Roslin NM, Marshall CR, Desvignes JP, Roëckel-Trevisiol N, Scherer SW, Rouleau GA, Mégarbané A, Isaya G, Delague V, Yoon G. PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia. Brain. 2015 Jun; 138(Pt 6):1505-17. PMID: 25808372.
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    44. Guo A, Chitayat D, Blaser S, Keating S, Shannon P. Fetal syringomyelia. Acta Neuropathol Commun. 2014 Aug 06; 2:91. PMID: 25092126.
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    45. Al-Maawali A, Dupuis L, Blaser S, Heon E, Tarnopolsky M, Al-Murshedi F, Marshall CR, Paton T, Scherer SW, Roelofsen J, van Kuilenburg AB, Mendoza-Londono R. Prenatal growth restriction, retinal dystrophy, diabetes insipidus and white matter disease: expanding the spectrum of PRPS1-related disorders. Eur J Hum Genet. 2015 Mar; 23(3):310-6. PMID: 24961627.
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    46. Le TD, Liu ES, Adatia FA, Buncic JR, Blaser S. The effect of adding orbital computed tomography findings to the Chandler criteria for classifying pediatric orbital cellulitis in predicting which patients will require surgical intervention. J AAPOS. 2014 Jun; 18(3):271-7. PMID: 24924283.
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    47. Chung BH, Bradley T, Grosse-Wortmann L, Blaser S, Dirks P, Hinek A, Chitayat D. Hand and fibrillin-1 deposition abnormalities in Loeys-Dietz syndrome--expanding the clinical spectrum. Am J Med Genet A. 2014 Feb; 164A(2):461-6. PMID: 24194458.
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    48. Kava M, Chitayat D, Blaser S, Ray PN, Vajsar J. Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutations. Pediatr Neurol. 2013 Nov; 49(5):374-8. PMID: 24139536.
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    49. Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB. Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 2013 Oct 16; 80(2):429-41. PMID: 24139043.
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    50. Rachmiel M, Blaser S, Widjaja E, Rovet J. Children with congenital hypothyroidism have similar neuroradiological abnormal findings as healthy ones. ScientificWorldJournal. 2013; 2013:194918. PMID: 24222727.
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    51. Al-Maawali A, Blaser S, Zhao XY, Yoon G. Prospective study of activities of daily living outcomes in children with cerebellar atrophy. Dev Med Child Neurol. 2014 May; 56(5):460-7. PMID: 24116951.
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    52. Al-Maawali AA, Miller E, Schulze A, Yoon G, Blaser SI. Subcutaneous fat pads on body MRI--an early sign of congenital disorder of glycosylation PMM2-CDG (CDG1a). Pediatr Radiol. 2014 Feb; 44(2):222-5. PMID: 24037084.
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    53. Mignone Philpott C, Shannon P, Chitayat D, Ryan G, Raybaud CA, Blaser SI. Diffusion-weighted imaging of the cerebellum in the fetus with Chiari II malformation. AJNR Am J Neuroradiol. 2013 Aug; 34(8):1656-60. PMID: 23721901.
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    54. Siriwardena K, Al-Maawali A, Guerin A, Blaser S, Chitayat D. XY sex reversal, pontocerebellar hypoplasia and intellectual disability: confirmation of a new syndrome. Am J Med Genet A. 2013 Jul; 161A(7):1714-7. PMID: 23686794.
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    55. Philpott CM, Widjaja E, Raybaud C, Branson HM, Kannu P, Blaser S. Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation. Pediatr Radiol. 2013 Sep; 43(9):1190-5. PMID: 23649205.
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    56. Kevelam SH, Bugiani M, Salomons GS, Feigenbaum A, Blaser S, Prasad C, Häberle J, Baric I, Bakker IM, Postma NL, Kanhai WA, Wolf NI, Abbink TE, Waisfisz Q, Heutink P, van der Knaap MS. Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy. Brain. 2013 May; 136(Pt 5):1534-43. PMID: 23482991.
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    57. Buysse K, Riemersma M, Powell G, van Reeuwijk J, Chitayat D, Roscioli T, Kamsteeg EJ, van den Elzen C, van Beusekom E, Blaser S, Babul-Hirji R, Halliday W, Wright GJ, Stemple DL, Lin YY, Lefeber DJ, van Bokhoven H. Missense mutations in ß-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome. Hum Mol Genet. 2013 May 01; 22(9):1746-54. PMID: 23359570.
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    58. Jain-Ghai S, Cameron JM, Al Maawali A, Blaser S, MacKay N, Robinson B, Raiman J. Complex II deficiency--a case report and review of the literature. Am J Med Genet A. 2013 Feb; 161A(2):285-94. PMID: 23322652.
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    59. Siriwardena K, Mackay N, Levandovskiy V, Blaser S, Raiman J, Kantor PF, Ackerley C, Robinson BH, Schulze A, Cameron JM. Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations. Mol Genet Metab. 2013 Jan; 108(1):40-50. PMID: 23266196.
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    60. Chung B, Hinek A, Keating S, Weksberg R, Shah V, Blaser S, Hawkins C, Chitayat D. Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome? Am J Med Genet A. 2012 Oct; 158A(10):2373-81. PMID: 22965799.
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    61. Propst EJ, Ngan BY, Mount RJ, Martin-Munoz D, Blaser S, Harrison RV, Cushing SL, Papsin BC. Ossicular fusion and cholesteatoma in auriculo-condylar syndrome: in vivo evidence of arrest of embryogenesis. Laryngoscope. 2013 Feb; 123(2):528-32. PMID: 22865651.
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    62. Al-Maawali A, Blaser S, Yoon G. Diagnostic approach to childhood-onset cerebellar atrophy: a 10-year retrospective study of 300 patients. J Child Neurol. 2012 Sep; 27(9):1121-32. PMID: 22764178.
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    63. Carter MT, Blaser S, Papsin B, Meschino W, Reardon W, Klatt R, Babul-Hirji R, Milunsky J, Chitayat D. Middle and inner ear malformations in mutation-proven branchio-oculo-facial (BOF) syndrome: case series and review of the literature. Am J Med Genet A. 2012 Aug; 158A(8):1977-81. PMID: 22711382.
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    64. Gardiner K, Chitayat D, Choufani S, Shuman C, Blaser S, Terespolsky D, Farrell S, Reiss R, Wodak S, Pu S, Ray PN, Baskin B, Weksberg R. Brain abnormalities in patients with Beckwith-Wiedemann syndrome. Am J Med Genet A. 2012 Jun; 158A(6):1388-94. PMID: 22585446.
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    65. Mendoza-Londono R, Chitayat D, Kahr WH, Hinek A, Blaser S, Dupuis L, Goh E, Badilla-Porras R, Howard A, Mittaz L, Superti-Furga A, Unger S, Nishimura G, Bonafe L. Extracellular matrix and platelet function in patients with musculocontractural Ehlers-Danlos syndrome caused by mutations in the CHST14 gene. Am J Med Genet A. 2012 Jun; 158A(6):1344-54. PMID: 22581468.
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    66. Poretti A, Blaser SI, Lequin MH, Fatemi A, Meoded A, Northington FJ, Boltshauser E, Huisman TA. Neonatal neuroimaging findings in inborn errors of metabolism. J Magn Reson Imaging. 2013 Feb; 37(2):294-312. PMID: 22566357.
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    67. Miller E, Daneman A, Doria AS, Blaser S, Traubici J, Jarrin J, Moineddin R, Moore A, Shroff M. Color Doppler US of normal cerebral venous sinuses in neonates: a comparison with MR venography. Pediatr Radiol. 2012 Sep; 42(9):1070-9. PMID: 22532234.
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    68. Cushing SL, Daly MJ, Treaba CG, Chan H, Irish JC, Blaser S, Gordon KA, Papsin BC. High-resolution cone-beam computed tomography: a potential tool to improve atraumatic electrode design and position. Acta Otolaryngol. 2012 Apr; 132(4):361-8. PMID: 22235960.
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    69. Valero J, Blaser S, Papsin BC, James AL, Gordon KA. Electrophysiologic and behavioral outcomes of cochlear implantation in children with auditory nerve hypoplasia. Ear Hear. 2012 Jan-Feb; 33(1):3-18. PMID: 21750462.
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    70. Osborn AJ, Blaser S, Papsin BC. Decisions regarding intracranial complications from acute mastoiditis in children. Curr Opin Otolaryngol Head Neck Surg. 2011 Dec; 19(6):478-85. PMID: 21926622.
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    71. Gillis J, Burashnikov E, Antzelevitch C, Blaser S, Gross G, Turner L, Babul-Hirji R, Chitayat D. Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndrome. Am J Med Genet A. 2012 Jan; 158A(1):182-7. PMID: 22106044.
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    72. Epelman M, Daneman A, Halliday W, Whyte H, Blaser SI. Abnormal corpus callosum in neonates after hypoxic-ischemic injury. Pediatr Radiol. 2012 Mar; 42(3):321-30. PMID: 21935701.
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    73. Jain-Ghai S, Nagamani SC, Blaser S, Siriwardena K, Feigenbaum A. Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported? Mol Genet Metab. 2011 Sep-Oct; 104(1-2):107-11. PMID: 21802329.
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    74. Skidmore DL, Chitayat D, Morgan T, Hinek A, Fischer B, Dimopoulou A, Somers G, Halliday W, Blaser S, Diambomba Y, Lemire EG, Kornak U, Robertson SP. Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding ?¹-pyrroline-5-carboxylate synthase (P5CS). Am J Med Genet A. 2011 Aug; 155A(8):1848-56. PMID: 21739576.
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    75. Fong K, Chong K, Toi A, Uster T, Blaser S, Chitayat D. Fetal ventriculomegaly secondary to isolated large choroid plexus cysts: prenatal findings and postnatal outcome. Prenat Diagn. 2011 Apr; 31(4):395-400. PMID: 21328578.
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    76. Prisman E, Ramsden JD, Blaser S, Papsin B. Traumatic perilymphatic fistula with pneumolabyrinth: diagnosis and management. Laryngoscope. 2011 Apr; 121(4):856-9. PMID: 21305555.
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    77. Yinon Y, Chitayat D, Blaser S, Seed M, Amsalem H, Yoo SJ, Jaeggi ET. Fetal cardiac tumors: a single-center experience of 40 cases. Prenat Diagn. 2010 Oct; 30(10):941-9. PMID: 20721876.
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    78. Steenweg ME, Vanderver A, Blaser S, Bizzi A, de Koning TJ, Mancini GM, van Wieringen WN, Barkhof F, Wolf NI, van der Knaap MS. Magnetic resonance imaging pattern recognition in hypomyelinating disorders. Brain. 2010 Oct; 133(10):2971-82. PMID: 20881161.
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    79. Koifman A, Feigenbaum A, Bi W, Shaffer LG, Rosenfeld J, Blaser S, Chitayat D. A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features. Am J Med Genet A. 2010 May; 152A(5):1268-72. PMID: 20425834.
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    80. Epelman M, Daneman A, Kellenberger CJ, Aziz A, Konen O, Moineddin R, Whyte H, Blaser S. Neonatal encephalopathy: a prospective comparison of head US and MRI. Pediatr Radiol. 2010 Oct; 40(10):1640-50. PMID: 20411255.
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    81. Miller E, Widjaja E, Nilsson D, Yoon G, Banwell B, Blaser S. Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher disease. Am J Med Genet A. 2010 Mar; 152A(3):748-52. PMID: 20186781.
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    82. Chadha NK, James AL, Gordon KA, Blaser S, Papsin BC. Bilateral cochlear implantation in children with anomalous cochleovestibular anatomy. Arch Otolaryngol Head Neck Surg. 2009 Sep; 135(9):903-9. PMID: 19770423.
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    83. Trakadis Y, Blaser S, Hahn CD, Yoon G. A case report of prenatal exposure to rosuvastatin and telmisartan. Paediatr Child Health. 2009 Sep; 14(7):450-2. PMID: 20808473.
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    84. de Almeida JR, James AL, Papsin BC, Weksburg R, Clark H, Blaser S. Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes. Laryngoscope. 2009 Aug; 119(8):1495-500. PMID: 19507237.
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    85. Gillis J, Blaser S, Miller S, Li C. Phalangeal hypoplasia, mental retardation, agenesis of the corpus callosum, brainstem abnormalities and ectopic grey matter: unique case or newly recognized syndrome? Clin Dysmorphol. 2009 Jul; 18(3):160-3. PMID: 19451812.
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    86. Werner KG, Morel CF, Kirton A, Benseler SM, Shoffner JM, Addis JB, Robinson BH, Burrowes DM, Blaser SI, Epstein LG, Feigenbaum AS. Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations. Pediatr Neurol. 2009 Jul; 41(1):27-33. PMID: 19520270.
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    87. Widjaja E, Geibprasert S, Blaser S, Rayner T, Shannon P. Abnormal fetal cerebral laminar organization in cobblestone complex as seen on post-mortem MRI and DTI. Pediatr Radiol. 2009 Aug; 39(8):860-4. PMID: 19415260.
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    88. Toi A, Chitayat D, Blaser S. Abnormalities of the foetal cerebral cortex. Prenat Diagn. 2009 Apr; 29(4):355-71. PMID: 19235759.
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    89. Brenner C, Ashwin M, Smith D, Blaser S. Sub-Tenon's space abscess after strabismus surgery. J AAPOS. 2009 Apr; 13(2):198-9. PMID: 19157934.
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    90. Miller E, Blaser S, Shannon P, Widjaja E. Brain and bone abnormalities of thanatophoric dwarfism. AJR Am J Roentgenol. 2009 Jan; 192(1):48-51. PMID: 19098178.
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    91. McInnes M, Fong K, Grin A, ter Brugge K, Blaser S, Halliday W, Shannon P. Malformations of the fetal dural sinuses. Can J Neurol Sci. 2009 Jan; 36(1):72-7. PMID: 19294892.
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    92. Vachhrajani S, Jea A, Rutka JA, Blaser S, Cusimano M, Rutka JT. Meningioma with dural venous sinus invasion and jugular vein extension. J Neurosurg Pediatr. 2008 Dec; 2(6):391-6. PMID: 19035683.
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    93. Tam EW, Widjaja E, Blaser SI, Macgregor DL, Satodia P, Moore AM. Occipital lobe injury and cortical visual outcomes after neonatal hypoglycemia. Pediatrics. 2008 Sep; 122(3):507-12. PMID: 18762519.
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    94. Miller E, Blaser S, Miller S, Keating S, Thompson M, Unger S, Toi A, Berger H, Chong K. Fetal MR imaging of atelosteogenesis type II (AO-II). Pediatr Radiol. 2008 Dec; 38(12):1345-9. PMID: 18716767.
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    95. Robinson AJ, Blaser S, Toi A, Chitayat D, Pantazi S, Keating S, Viero S, Ryan G. MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlation. Pediatr Radiol. 2008 Sep; 38(9):971-81. PMID: 18633608.
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    96. Blaser SI. Abnormal skull shape. Pediatr Radiol. 2008 Jun; 38 Suppl 3:S488-96. PMID: 18470460.
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    97. Konen O, Armstrong D, Clarke H, Padfield N, Weksberg R, Blaser S. C1-2 vertebral anomalies in 22q11.2 microdeletion syndrome. Pediatr Radiol. 2008 Jul; 38(7):766-71. PMID: 18516601.
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    98. Villani A, Bouffet E, Blaser S, Millar BA, Hawkins C, Bartels U. Inherent diagnostic and treatment challenges in germinoma of the basal ganglia: a case report and review of the literature. J Neurooncol. 2008 Jul; 88(3):309-14. PMID: 18365143.
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    99. Propst EJ, Blaser S, Trimble K, James A, Friedberg J, Papsin BC. Cochleovestibular anomalies in children with cholesteatoma. Laryngoscope. 2008 Mar; 118(3):517-21. PMID: 18091330.
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    100. Hawkes M, Kitai I, Blaser S, Cohen E, Bitnun A, Fluss J, Tran D. Neuroimaging findings in isoniazid central nervous system toxicity, presumed intramyelinic edema. Eur J Paediatr Neurol. 2008 Nov; 12(6):512-5. PMID: 18243740.
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    101. Chitayat D, Shannon P, Keating S, Toi A, Blaser S, Friedberg T, Superti-Furga A, Chong K, Unger S. Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings. Am J Med Genet A. 2007 Dec 15; 143A(24):3280-5. PMID: 18000911.
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    102. Yoon G, Rosenberg J, Blaser S, Rauen KA. Neurological complications of cardio-facio-cutaneous syndrome. Dev Med Child Neurol. 2007 Dec; 49(12):894-9. PMID: 18039235.
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    103. Miller E, Widjaja E, Blaser S, Dennis M, Raybaud C. The old and the new: supratentorial MR findings in Chiari II malformation. Childs Nerv Syst. 2008 May; 24(5):563-75. PMID: 18026960.
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    104. Robinson AJ, Blaser S, Toi A, Chitayat D, Halliday W, Pantazi S, Gundogan M, Laughlin S, Ryan G. The fetal cerebellar vermis: assessment for abnormal development by ultrasonography and magnetic resonance imaging. Ultrasound Q. 2007 Sep; 23(3):211-23. PMID: 17805192.
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    105. Nofech-Mozes Y, Blaser SI, Kobayashi J, Grunebaum E, Roifman CM. Neurologic abnormalities in patients with adenosine deaminase deficiency. Pediatr Neurol. 2007 Sep; 37(3):218-21. PMID: 17765813.
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    106. Propst EJ, Blaser S, Holowka S, Lewin PK, Armstrong D, Papsin BC. Dilated endolymphatic fossae in a 2800-year-old Egyptian mummy. J Otolaryngol. 2007 Aug; 36(4):E45-7. PMID: 18684345.
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    107. Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Bénéjean O, Manouvrier-Hanu S, Mortier G, Loeys B, Rauch A, Bitoun P. The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance. Am J Med Genet A. 2007 Jun 15; 143A(12):1268-81. PMID: 17506106.
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    108. Parmar HA, Hawkins C, Ozelame R, Chuang S, Rutka J, Blaser S. Fluid-attenuated inversion recovery ring sign as a marker of dysembryoplastic neuroepithelial tumors. J Comput Assist Tomogr. 2007 May-Jun; 31(3):348-53. PMID: 17538277.
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    109. Ben-Omran TI, Wong H, Blaser S, Feigenbaum A. Late-onset cobalamin-C disorder: a challenging diagnosis. Am J Med Genet A. 2007 May 01; 143A(9):979-84. PMID: 17431913.
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    110. Widjaja E, Blaser S, Miller E, Kassner A, Shannon P, Chuang SH, Snead OC, Raybaud CR. Evaluation of subcortical white matter and deep white matter tracts in malformations of cortical development. Epilepsia. 2007 Aug; 48(8):1460-9. PMID: 17441991.
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    111. Castagna AE, Addis J, McInnes RR, Clarke JT, Ashby P, Blaser S, Robinson BH. Late onset Leigh syndrome and ataxia due to a T to C mutation at bp 9,185 of mitochondrial DNA. Am J Med Genet A. 2007 Apr 15; 143A(8):808-16. PMID: 17352390.
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    112. Trimble K, Blaser S, James AL, Papsin BC. Computed tomography and/or magnetic resonance imaging before pediatric cochlear implantation? Developing an investigative strategy. Otol Neurotol. 2007 Apr; 28(3):317-24. PMID: 17414036.
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    113. Levine DS, Navarro OM, Chaudry G, Doyle JJ, Blaser SI. Imaging the complications of bone marrow transplantation in children. Radiographics. 2007 Mar-Apr; 27(2):307-24. PMID: 17374855.
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    114. Bell JW, Osborn AG, Salzman KL, Blaser SI, Jones BV, Chin SS. Neuroradiologic characteristics of astroblastoma. Neuroradiology. 2007 Mar; 49(3):203-9. PMID: 17216265.
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    115. Blaser S, Propst EJ, Martin D, Feigenbaum A, James AL, Shannon P, Papsin BC. Inner ear dysplasia is common in children with Down syndrome (trisomy 21). Laryngoscope. 2006 Dec; 116(12):2113-9. PMID: 17146381.
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    116. Abla O, Sandlund JT, Sung L, Brock P, Corbett R, Kirov I, Griffin TC, Blaser S, Weitzman S. A case series of pediatric primary central nervous system lymphoma: favorable outcome without cranial irradiation. Pediatr Blood Cancer. 2006 Dec; 47(7):880-5. PMID: 16365864.
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    117. Propst EJ, Blaser S, Stockley TL, Harrison RV, Gordon KA, Papsin BC. Temporal bone imaging in GJB2 deafness. Laryngoscope. 2006 Dec; 116(12):2178-86. PMID: 17146393.
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    118. Maegawa GH, Stockley T, Tropak M, Banwell B, Blaser S, Kok F, Giugliani R, Mahuran D, Clarke JT. The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported. Pediatrics. 2006 Nov; 118(5):e1550-62. PMID: 17015493.
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    119. Maegawa GH, Chitayat D, Blaser S, Whyte H, Thomas M, Kim P, Kim J, Taylor G, McNamara PJ. Duodenal and biliary atresia associated with facial, thyroid and auditory apparatus abnormalities: a new mandibulofacial dysostosis syndrome? Clin Dysmorphol. 2006 Oct; 15(4):191-6. PMID: 16957470.
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    120. Daneman A, Epelman M, Blaser S, Jarrin JR. Imaging of the brain in full-term neonates: does sonography still play a role? Pediatr Radiol. 2006 Jul; 36(7):636-46. PMID: 16770668.
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    121. Milic A, Blaser S, Robinson A, Viero S, Halliday W, Winsor E, Toi A, Thomas M, Chitayat D. Prenatal detection of microtia by MRI in a fetus with trisomy 22. Pediatr Radiol. 2006 Jul; 36(7):706-10. PMID: 16770674.
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    122. Widjaja E, Blaser S, Raybaud C. Diffusion tensor imaging of midline posterior fossa malformations. Pediatr Radiol. 2006 Jun; 36(6):510-7. PMID: 16708205.
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    123. Fluss J, Blaser S, Chitayat D, Akoury H, Glanc P, Skidmore M, Raybaud C. Molar tooth sign in fetal brain magnetic resonance imaging leading to the prenatal diagnosis of Joubert syndrome and related disorders. J Child Neurol. 2006 Apr; 21(4):320-4. PMID: 16900929.
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    124. Ghai S, Fong KW, Toi A, Chitayat D, Pantazi S, Blaser S. Prenatal US and MR imaging findings of lissencephaly: review of fetal cerebral sulcal development. Radiographics. 2006 Mar-Apr; 26(2):389-405. PMID: 16549605.
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    125. Ozelame RV, Shroff M, Wood B, Bouffet E, Bartels U, Drake JM, Hawkins C, Blaser S. Basal ganglia germinoma in children with associated ipsilateral cerebral and brain stem hemiatrophy. Pediatr Radiol. 2006 Apr; 36(4):325-30. PMID: 16463029.
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    126. Ahmet A, Blaser S, Stephens D, Guger S, Rutkas JT, Hamilton J. Weight gain in craniopharyngioma--a model for hypothalamic obesity. J Pediatr Endocrinol Metab. 2006 Feb; 19(2):121-7. PMID: 16562584.
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    127. Epelman M, Daneman A, Blaser SI, Ortiz-Neira C, Konen O, Jarrín J, Navarro OM. Differential diagnosis of intracranial cystic lesions at head US: correlation with CT and MR imaging. Radiographics. 2006 Jan-Feb; 26(1):173-96. PMID: 16418251.
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    128. Parmar H, Blaser S, Unger S, Yoo SJ, Papsin B. Petrified ears in a patient with Keutel syndrome: temporal bone CT findings. Pediatr Radiol. 2006 Mar; 36(3):241-3. PMID: 16328322.
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    129. Propst EJ, Blaser S, Gordon KA, Harrison RV, Papsin BC. Temporal bone findings on computed tomography imaging in branchio-oto-renal syndrome. Laryngoscope. 2005 Oct; 115(10):1855-62. PMID: 16222209.
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    130. AlOtaibi SF, Blaser S, MacGregor DL. Neurological complications of kernicterus. Can J Neurol Sci. 2005 Aug; 32(3):311-5. PMID: 16225171.
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    131. Shah PS, Blaser S, Toi A, Fong K, Glanc P, Babul-Hirji R, Rutka J, Chitayat D. Cavum veli interpositi: prenatal diagnosis and postnatal outcome. Prenat Diagn. 2005 Jul; 25(7):539-42. PMID: 16034837.
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    132. Daya H, Lo S, Papsin BC, Zachariasova A, Murray H, Pirie J, Laughlin S, Blaser S. Retropharyngeal and parapharyngeal infections in children: the Toronto experience. Int J Pediatr Otorhinolaryngol. 2005 Jan; 69(1):81-6. PMID: 15627452.
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    133. Haidar S, Ortiz-Neira C, Shroff M, Gilday D, Blaser S. Intracranial involvement in extramedullary hematopoiesis: case report and review of the literature. Pediatr Radiol. 2005 Jun; 35(6):630-4. PMID: 15580341.
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    134. Blaser S, Feigenbaum A. A neuroimaging approach to inborn errors of metabolism. Neuroimaging Clin N Am. 2004 May; 14(2):307-29, ix. PMID: 15182821.
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    135. Hahn CD, Shroff MM, Blaser SI, Banwell BL. MRI criteria for multiple sclerosis: Evaluation in a pediatric cohort. Neurology. 2004 Mar 09; 62(5):806-8. PMID: 15007138.
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    136. Hahn CD, Miles BS, MacGregor DL, Blaser SI, Banwell BL, Hetherington CR. Neurocognitive outcome after acute disseminated encephalomyelitis. Pediatr Neurol. 2003 Aug; 29(2):117-23. PMID: 14580654.
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    137. Nabi NU, Mezer E, Blaser SI, Levin AA, Buncic JR. Ocular findings in lissencephaly. J AAPOS. 2003 Jun; 7(3):178-84. PMID: 12825057.
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    138. Shroff M, Blaser S, Jay V, Chitayat D, Armstrong D. Basilar artery duplication associated with pituitary duplication: a new finding. AJNR Am J Neuroradiol. 2003 May; 24(5):956-61. PMID: 12748101.
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    139. Bitnun A, Ford-Jones E, Blaser S, Richardson S. Mycoplasma pneumoniae ecephalitis. Semin Pediatr Infect Dis. 2003 Apr; 14(2):96-107. PMID: 12881797.
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    140. Salman MS, Blaser S, Buncic JR, Westall CA, Héon E, Becker L. Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosis. J Child Neurol. 2003 Mar; 18(3):220-5. PMID: 12731647.
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    141. van der Knaap MS, van der Voorn P, Barkhof F, Van Coster R, Krägeloh-Mann I, Feigenbaum A, Blaser S, Vles JS, Rieckmann P, Pouwels PJ. A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate. Ann Neurol. 2003 Feb; 53(2):252-8. PMID: 12557294.
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    142. Unger S, Mornet E, Mundlos S, Blaser S, Cole DE. Severe cleidocranial dysplasia can mimic hypophosphatasia. Eur J Pediatr. 2002 Nov; 161(11):623-6. PMID: 12424591.
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    143. Miller DL, Blaser S, Laxer RM. Clinical images: Epidural lipomatosis in a 14-year-old boy with systemic lupus erythematosus. Arthritis Rheum. 2002 May; 46(5):1291. PMID: 12115235.
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    144. Pandya J, Valverde K, Heon E, Blaser S, Gallie BL, Chan HS. Predilection of retinoblastoma metastases for the mandible. Med Pediatr Oncol. 2002 Apr; 38(4):271-3. PMID: 11920795.
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    145. Blaser SI, Jay V. Disorders of cortical formation: radiologic-pathologic correlation. Neurosurg Clin N Am. 2002 Jan; 13(1):41-62, viii. PMID: 11754316.
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    146. McAdam LC, Blaser SI, Banwell BL. Pediatric tumefactive demyelination: case series and review of the literature. Pediatr Neurol. 2002 Jan; 26(1):18-25. PMID: 11814730.
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    147. Al-Rasheed AK, Blaser SI, Minassian BA, Benson L, Weiss SK. Cyclosporine A neurotoxicity in a patient with idiopathic renal magnesium wasting. Pediatr Neurol. 2000 Oct; 23(4):353-6. PMID: 11068171.
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    148. Blaser SI, Jay V. Disorders of cortical formation: radiologic-pathologic correlation. Neuroimaging Clin N Am. 1999 Feb; 9(1):53-72. PMID: 9974499.
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    149. Boerkoel CF, Nowaczyk MJ, Blaser SI, Meschino WS, Weksberg R. Schimke immunoosseous dysplasia complicated by moyamoya phenomenon. Am J Med Genet. 1998 Jun 30; 78(2):118-22. PMID: 9674900.
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    150. Carcao M, Blaser SI, Grant RM, Weksberg R, Siegel-Bartelt J. MRI findings in macrocephaly-cutis marmorata telangiectatica congenita. Am J Med Genet. 1998 Mar 05; 76(2):165-7. PMID: 9511980.
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    151. Nowaczyk MJ, Blaser SI, Clarke JT. Central nervous system malformations in ethylmalonic encephalopathy. Am J Med Genet. 1998 Jan 23; 75(3):292-6. PMID: 9475600.
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    152. Nowaczyk MJ, Saunders EF, Tein I, Blaser SI, Clarke JT. Immunoablation does not delay the neurologic progression of X-linked adrenoleukodystrophy. J Pediatr. 1997 Sep; 131(3):453-5. PMID: 9329427.
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    153. Balslev T, Cortez MA, Blaser SI, Haslam RH. Recurrent seizures in metachromatic leukodystrophy. Pediatr Neurol. 1997 Sep; 17(2):150-4. PMID: 9367296.
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    154. Connolly B, Blaser SI, Humphreys RP, Becker L. Long-term survival of an infant with 'anaplastic' astrocytoma. Pediatr Neurosurg. 1997 Feb; 26(2):97-102. PMID: 9419039.
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    155. Blaser SI, Harwood-Nash DC. Neuroradiology of pediatric posterior fossa medulloblastoma. J Neurooncol. 1996 Jul; 29(1):23-34. PMID: 8817413.
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    156. Terespolsky D, Clarke JT, Blaser SI. Evolution of the neuroimaging changes in fucosidosis type II. J Inherit Metab Dis. 1996; 19(6):775-81. PMID: 8982951.
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    157. Steinlin MI, Blaser SI, Gilday DL, Eddy AA, Logan WJ, Laxer RM, Silverman ED. Neurologic manifestations of pediatric systemic lupus erythematosus. Pediatr Neurol. 1995 Oct; 13(3):191-7. PMID: 8554655.
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    158. Dautenhahn L, Blaser SI, Weitzman S, Crysdale WS. Infantile myofibromatosis: a cause of vertebra plana. AJNR Am J Neuroradiol. 1995 Apr; 16(4 Suppl):828-30. PMID: 7611050.
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    159. Steinlin MI, Blaser SI, MacGregor DL, Buncic JR. Eye problems in children with multiple sclerosis. Pediatr Neurol. 1995 Apr; 12(3):207-12. PMID: 7619186.
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    160. Blaser SI, Clarke JT, Becker LE. Neuroradiology of lysosomal disorders. Neuroimaging Clin N Am. 1994 May; 4(2):283-98. PMID: 8081629.
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    161. Blaser SI, Harwood-Nash DC. Radiology of the developing central nervous system. Curr Opin Neurol Neurosurg. 1992 Dec; 5(6):843-8. PMID: 1467576.
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    162. Hoffman HJ, De Silva M, Humphreys RP, Drake JM, Smith ML, Blaser SI. Aggressive surgical management of craniopharyngiomas in children. J Neurosurg. 1992 Jan; 76(1):47-52. PMID: 1727168.
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    163. Taylor DB, Blaser SI, Burrows PE, Stringer DA, Clarke JT, Thorner P. Arteriopathy and coarctation of the abdominal aorta in children with mucopolysaccharidosis: imaging findings. AJR Am J Roentgenol. 1991 Oct; 157(4):819-23. PMID: 1909834.
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    164. Mirich DR, Blaser SI, Harwood-Nash DC, Armstrong DC, Becker LE, Posnick JC. Melanotic neuroectodermal tumor of infancy: clinical, radiologic, and pathologic findings in five cases. AJNR Am J Neuroradiol. 1991 Jul-Aug; 12(4):689-97. PMID: 1652883.
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    165. May PL, Blaser SI, Hoffman HJ, Humphreys RP, Harwood-Nash DC. Benign intrinsic tectal "tumors" in children. J Neurosurg. 1991 Jun; 74(6):867-71. PMID: 2033445.
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    166. St Clair SK, Humphreys RP, Pillay PK, Hoffman HJ, Blaser SI, Becker LE. Current management of choroid plexus carcinoma in children. Pediatr Neurosurg. 1991-1992; 17(5):225-33. PMID: 1822687.
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    167. Peled N, Blaser SI, Moore A, Harwood-Nash D. Computerized tomography appearance of accidental infusion of air into the venous sinuses. Pediatr Neurosurg. 1991-1992; 17(5):251-3. PMID: 1822690.
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