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Ingrid Tein

TitleStaff Neurologist
InstitutionThe Hospital for Sick Children
DepartmentNeurology
Address555 University Avenue
Toronto ON M5G 1X8
Phone416-813-1500
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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. Pipo-Deveza J, Fehlings D, Chitayat D, Yoon G, Sroka H, Tein I. Rationale for dopa-responsive CTNNB1/ß-catenin deficient dystonia. Mov Disord. 2018 04; 33(4):656-657. PMID: 29436745.
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    2. Lamhonwah AM, Baric I, Lamhonwah J, Grubic M, Tein I. Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449). Clin Case Rep. 2018 04; 6(4):585-591. PMID: 29636919.
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    3. Nabavi Nouri M, Lamhonwah AM, Tein I. Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intolerance. Clin Case Rep. 2018 03; 6(3):499-501. PMID: 29531726.
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    4. Karaa A, Rahman S, Lombès A, Yu-Wai-Man P, Sheikh MK, Alai-Hansen S, Cohen BH, Dimmock D, Emrick L, Falk MJ, McCormack S, Mirsky D, Moore T, Parikh S, Shoffner J, Taivassalo T, Tarnopolsky M, Tein I, Odenkirchen JC, Goldstein A. Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project. J Inherit Metab Dis. 2018 01; 41(1):151. PMID: 28980269.
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    5. Karaa A, Rahman S, Lombès A, Yu-Wai-Man P, Sheikh MK, Alai-Hansen S, Cohen BH, Dimmock D, Emrick L, Falk MJ, McCormack S, Mirsky D, Moore T, Parikh S, Shoffner J, Taivassalo T, Tarnopolsky M, Tein I, Odenkirchen JC, Goldstein A. Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project. J Inherit Metab Dis. 2017 05; 40(3):403-414. PMID: 28303425.
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    6. Tkachyova I, Fan X, LamHonWah AM, Fedyshyn B, Tein I, Mahuran DJ, Schulze A. NDST1 Preferred Promoter Confirmation and Identification of Corresponding Transcriptional Inhibitors as Substrate Reduction Agents for Multiple Mucopolysaccharidosis Disorders. PLoS One. 2016; 11(9):e0162145. PMID: 27657498.
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    7. Tein I. Mitochondrial diseases: need for international collaborations? Dev Med Child Neurol. 2016 05; 58(5):425. PMID: 27103187.
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    8. Siddiq I, Widjaja E, Tein I. Clinical and radiologic reversal of stroke-like episodes in MELAS with high-dose L-arginine. Neurology. 2015 Jul 14; 85(2):197-8. PMID: 26070336.
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    9. Rodan LH, Wells GD, Banks L, Thompson S, Schneiderman JE, Tein I. L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome. PLoS One. 2015; 10(5):e0127066. PMID: 25993630.
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    10. Tein I. Impact of fatty acid oxidation disorders in child neurology: from Reye syndrome to Pandora's box. Dev Med Child Neurol. 2015 Apr; 57(4):304-6. PMID: 25761966.
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    11. Rodan LH, Poublanc J, Fisher JA, Sobczyk O, Wong T, Hlasny E, Mikulis D, Tein I. Cerebral hyperperfusion and decreased cerebrovascular reactivity correlate with neurologic disease severity in MELAS. Mitochondrion. 2015 May; 22:66-74. PMID: 25801712.
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    12. Rodan LH, Tein I, Buncic R. Clinical reasoning: a case of abnormal eye movements in an infant: more than meets the eye. Neurology. 2013 Oct 08; 81(15):e112-5. PMID: 24101752.
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    13. Rodan LH, Mishra N, Tein I. MR spectroscopy in pediatric Wernicke encephalopathy. Neurology. 2013 Mar 05; 80(10):969. PMID: 23460620.
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    14. Rodan LH, Mishra N, Yau I, Andrade A, Siriwardena K, Tein I. Expanding the Spectrum of Methylmalonic Acid-Induced Pallidal Stroke: First Reported Case of Metabolic Globus Pallidus Stroke in Transcobalamin II Deficiency. JIMD Rep. 2013; 11:7-11. PMID: 23430814.
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    15. Tein I. Disorders of fatty acid oxidation. Handb Clin Neurol. 2013; 113:1675-88. PMID: 23622388.
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    16. Zolkipli Z, Mai L, Lamhonwah AM, Tein I. The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophy. Muscle Nerve. 2012 Nov; 46(5):767-72. PMID: 23055315.
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    17. Rodan L, Tein I. Clinical reasoning: encephalopathy in a 10-year-old boy. Neurology. 2012 Jul 17; 79(3):e12-8. PMID: 22802596.
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    18. Zolkipli Z, Sherlock M, Biggar WD, Taylor G, Hutchison JS, Peliowski A, Alman BA, Ling SC, Tein I. Abnormal fatty acid metabolism in spinal muscular atrophy may predispose to perioperative risks. Eur J Paediatr Neurol. 2012 Sep; 16(5):549-53. PMID: 22264649.
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    19. Stockler S, Plecko B, Gospe SM, Coulter-Mackie M, Connolly M, van Karnebeek C, Mercimek-Mahmutoglu S, Hartmann H, Scharer G, Struijs E, Tein I, Jakobs C, Clayton P, Van Hove JL. Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up. Mol Genet Metab. 2011 Sep-Oct; 104(1-2):48-60. PMID: 21704546.
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    20. Zolkipli Z, Pedersen CB, Lamhonwah AM, Gregersen N, Tein I. Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants. PLoS One. 2011 Apr 01; 6(4):e17534. PMID: 21483766.
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    21. Wells GD, Wilkes DL, Schneiderman JE, Rayner T, Elmi M, Selvadurai H, Dell SD, Noseworthy MD, Ratjen F, Tein I, Coates AL. Skeletal muscle metabolism in cystic fibrosis and primary ciliary dyskinesia. Pediatr Res. 2011 Jan; 69(1):40-5. PMID: 20938370.
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    22. Lamhonwah AM, Mai L, Chung C, Lamhonwah D, Ackerley C, Tein I. Upregulation of mammary gland OCTNs maintains carnitine homeostasis in suckling infants. Biochem Biophys Res Commun. 2011 Jan 28; 404(4):1010-5. PMID: 21187065.
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    23. Lamhonwah AM, Bear CE, Huan LJ, Kim Chiaw P, Ackerley CA, Tein I. Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise. Ann Neurol. 2010 Jun; 67(6):802-8. PMID: 20517942.
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    24. Pedersen CB, Zolkipli Z, Vang S, Palmfeldt J, Kjeldsen M, Stenbroen V, Schmidt SP, Wanders RJ, Ruiter JP, Wibrand F, Tein I, Gregersen N. Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria. J Inherit Metab Dis. 2010 Jun; 33(3):211-22. PMID: 20443061.
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    25. Wells GD, Selvadurai H, Tein I. Bioenergetic provision of energy for muscular activity. Paediatr Respir Rev. 2009 Sep; 10(3):83-90. PMID: 19651377.
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    26. Lamhonwah AM, Wong J, Tam C, Mai L, Tein I. Organic cation/carnitine transporter family expression patterns in adult murine heart. Pathol Res Pract. 2009; 205(6):395-402. PMID: 19233567.
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    27. Isackson PJ, Bennett MJ, Lichter-Konecki U, Willis M, Nyhan WL, Sutton VR, Tein I, Vladutiu GD. CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency. Mol Genet Metab. 2008 Aug; 94(4):422-7. PMID: 18550408.
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    28. Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, Tein I, Matern D, Rinaldo P, Vianey-Saban C, Ribes A, Lehnert W, Christensen E, Corydon TJ, Andresen BS, Vang S, Bolund L, Vockley J, Bross P, Gregersen N. The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level. Hum Genet. 2008 Aug; 124(1):43-56. PMID: 18523805.
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    29. Wells GD, Noseworthy MD, Hamilton J, Tarnopolski M, Tein I. Skeletal muscle metabolic dysfunction in obesity and metabolic syndrome. Can J Neurol Sci. 2008 Mar; 35(1):31-40. PMID: 18380275.
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    30. Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Vockley J, Berry GT, Lamhonwah AM, Matern D, Roe CR, Gregersen N. Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin. Mol Genet Metab. 2008 Feb; 93(2):179-89. PMID: 18054510.
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    31. Lamhonwah AM, Hawkins CE, Tam C, Wong J, Mai L, Tein I. Expression patterns of the organic cation/carnitine transporter family in adult murine brain. Brain Dev. 2008 Jan; 30(1):31-42. PMID: 17576045.
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    32. Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, Lerman-Sagie T, Vockley G, Berry GT, Lamhownah AM, Matern D, Roe CR, Gregersen N. REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population. Mol Genet Metab. 2007 Jan 17. PMID: 17234443.
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    33. Lamhonwah AM, Tein I. Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria. Biochem Biophys Res Commun. 2006 Jul 14; 345(4):1315-25. PMID: 16729965.
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    34. Lamhonwah AM, Ackerley CA, Tilups A, Edwards VD, Wanders RJ, Tein I. OCTN3 is a mammalian peroxisomal membrane carnitine transporter. Biochem Biophys Res Commun. 2005 Dec 30; 338(4):1966-72. PMID: 16288981.
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    35. Lamhonwah AM, Ackerley C, Onizuka R, Tilups A, Lamhonwah D, Chung C, Tao KS, Tellier R, Tein I. Epitope shared by functional variant of organic cation/carnitine transporter, OCTN1, Campylobacter jejuni and Mycobacterium paratuberculosis may underlie susceptibility to Crohn's disease at 5q31. Biochem Biophys Res Commun. 2005 Dec 02; 337(4):1165-75. PMID: 16246312.
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    36. Rafay MF, Murphy EG, McGarry JD, Kaufmann P, DiMauro S, Tein I. Clinical and biochemical heterogeneity in an Italian family with CPT II deficiency due to Ser 113 Leu mutation. Can J Neurol Sci. 2005 Aug; 32(3):316-20. PMID: 16225172.
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    37. Cameron JM, Levandovskiy V, Mackay N, Tein I, Robinson BH. Deficiency of pyruvate dehydrogenase caused by novel and known mutations in the E1alpha subunit. Am J Med Genet A. 2004 Nov 15; 131(1):59-66. PMID: 15384102.
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    38. Spiekerkoetter U, Bennett MJ, Ben-Zeev B, Strauss AW, Tein I. Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein. Muscle Nerve. 2004 Jan; 29(1):66-72. PMID: 14694500.
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    39. Kinali M, Olpin SE, Clayton PT, Daubeney PE, Mercuri E, Manzur AY, Tein I, Leonard J, Muntoni F. Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy. Eur J Paediatr Neurol. 2004; 8(4):217-9. PMID: 15261886.
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    40. Lamhonwah AM, Onizuka R, Olpin SE, Muntoni F, Tein I. OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation? J Inherit Metab Dis. 2004; 27(4):473-6. PMID: 15303004.
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    41. Xuan W, Lamhonwah AM, Librach C, Jarvi K, Tein I. Characterization of organic cation/carnitine transporter family in human sperm. Biochem Biophys Res Commun. 2003 Jun 20; 306(1):121-8. PMID: 12788076.
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    42. Chace DH, Pons R, Chiriboga CA, McMahon DJ, Tein I, Naylor EW, De Vivo DC. Neonatal blood carnitine concentrations: normative data by electrospray tandem mass spectometry. Pediatr Res. 2003 May; 53(5):823-9. PMID: 12612202.
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    43. Lamhonwah AM, Skaug J, Scherer SW, Tein I. A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5). Biochem Biophys Res Commun. 2003 Jan 31; 301(1):98-101. PMID: 12535646.
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    44. Al-Ruwaishid A, Vajsar J, Tein I, Benson L, Jay V. Centronuclear myopathy and cardiomyopathy requiring heart transplant. Brain Dev. 2003 Jan; 25(1):62-6. PMID: 12536036.
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    45. Tein I. Carnitine transport: pathophysiology and metabolism of known molecular defects. J Inherit Metab Dis. 2003; 26(2-3):147-69. PMID: 12889657.
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    46. Tein I. Role of carnitine and fatty acid oxidation and its defects in infantile epilepsy. J Child Neurol. 2002 Dec; 17 Suppl 3:3S57-82; discussion 3S82-3. PMID: 12597056.
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    47. Cederbaum SD, Koo-McCoy S, Tein I, Hsu BY, Ganguly A, Vilain E, Dipple K, Cvitanovic-Sojat L, Stanley C. Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency. Mol Genet Metab. 2002 Nov; 77(3):195-201. PMID: 12409266.
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    48. Renaud DL, Edwards V, Wilson GJ, Tein I. Glucose-free medium exacerbates microvesicular steatosis in cultured skin fibroblasts of genetic defects of fatty acid oxidation. A novel screening test. J Inherit Metab Dis. 2002 Nov; 25(7):547-55. PMID: 12638938.
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    49. Lamhonwah AM, Olpin SE, Pollitt RJ, Vianey-Saban C, Divry P, Guffon N, Besley GT, Onizuka R, De Meirleir LJ, Cvitanovic-Sojat L, Baric I, Dionisi-Vici C, Fumic K, Maradin M, Tein I. Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy. Am J Med Genet. 2002 Aug 15; 111(3):271-84. PMID: 12210323.
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    50. Dipchand AI, Tein I, Robinson B, Benson LN. Maternally inherited hypertrophic cardiomyopathy: a manifestation of mitochondrial DNA mutations--clinical course in two families. Pediatr Cardiol. 2001 Jan-Feb; 22(1):14-22. PMID: 11123121.
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    51. Tein I. Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancy. Pediatr Res. 2000 Jan; 47(1):6-8. PMID: 10625076.
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    52. Lamhonwah AM, Tein I. GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defect. Biochem Biophys Res Commun. 1999 Nov 02; 264(3):909-14. PMID: 10544029.
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    53. Tein I. Neonatal metabolic myopathies. Semin Perinatol. 1999 Apr; 23(2):125-51. PMID: 10331465.
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    54. Tein I, Vajsar J, MacMillan L, Sherwood WG. Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oil. Neurology. 1999 Feb; 52(3):640-3. PMID: 10025805.
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    55. Tein I, Haslam RH, Rhead WJ, Bennett MJ, Becker LE, Vockley J. Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy. Neurology. 1999 Jan 15; 52(2):366-72. PMID: 9932958.
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    56. Raha S, Merante F, Shoubridge E, Myint AT, Tein I, Benson L, Johns T, Robinson BH. Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction. Hum Mutat. 1999; 13(3):245-54. PMID: 10090480.
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    57. Lamhonwah AM, Tein I. Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter gene. Biochem Biophys Res Commun. 1998 Nov 18; 252(2):396-401. PMID: 9826541.
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    58. De Vivo DC, Bohan TP, Coulter DL, Dreifuss FE, Greenwood RS, Nordli DR, Shields WD, Stafstrom CE, Tein I. L-carnitine supplementation in childhood epilepsy: current perspectives. Epilepsia. 1998 Nov; 39(11):1216-25. PMID: 9821988.
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    59. Ibdah JA, Tein I, Dionisi-Vici C, Bennett MJ, IJlst L, Gibson B, Wanders RJ, Strauss AW. Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation. J Clin Invest. 1998 Sep 15; 102(6):1193-9. PMID: 9739053.
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    60. Pons R, Carrozzo R, Tein I, Walker WF, Addonizio LJ, Rhead W, Miranda AF, Dimauro S, De Vivo DC. Deficient muscle carnitine transport in primary carnitine deficiency. Pediatr Res. 1997 Nov; 42(5):583-7. PMID: 9357927.
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    61. 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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    62. Elpeleg ON, Saada AB, Shaag A, Glustein JZ, Ruitenbeek W, Tein I, Halevy J. Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria. Muscle Nerve. 1997 Feb; 20(2):238-40. PMID: 9040667.
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    63. Tein I, Xie ZW. The human plasmalemmal carnitine transporter defect is expressed in cultured lymphoblasts: a new non-invasive method for diagnosis. Clin Chim Acta. 1996 Aug 30; 252(2):201-4. PMID: 8853567.
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    64. Tein I. Metabolic myopathies. Semin Pediatr Neurol. 1996 Jun; 3(2):59-98. PMID: 8795843.
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    65. Tein I, Bukovac SW, Xie ZW. Characterization of the human plasmalemmal carnitine transporter in cultured skin fibroblasts. Arch Biochem Biophys. 1996 May 15; 329(2):145-55. PMID: 8638946.
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    66. Geenen C, Tein I, Ehrlich RM. Addison's disease presenting with cerebral edema. Can J Neurol Sci. 1996 May; 23(2):141-4. PMID: 8738929.
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    67. Merante F, Myint T, Tein I, Benson L, Robinson BH. An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy. Hum Mutat. 1996; 8(3):216-22. PMID: 8889580.
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    68. Tein I, DiMauro S, Xie ZW, De Vivo DC. Heterozygotes for plasmalemmal carnitine transporter defect are at increased risk for valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts. J Inherit Metab Dis. 1995; 18(3):313-22. PMID: 7474898.
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    69. Tein I, Sloane AE, Donner EJ, Lehotay DC, Millington DS, Kelley RI. Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: primary or secondary defect(s)? Pediatr Neurol. 1995 Jan; 12(1):21-30. PMID: 7748356.
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    70. Tein I, Donner EJ, Hale DE, Murphy EG. Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone. Pediatr Neurol. 1995 Jan; 12(1):68-76. PMID: 7748366.
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    71. Tein I, Xie ZW. Reversal of valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts. Biochem Biophys Res Commun. 1994 Oct 28; 204(2):753-8. PMID: 7980539.
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    72. Merante F, Tein I, Benson L, Robinson BH. Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene. Am J Hum Genet. 1994 Sep; 55(3):437-46. PMID: 8079988.
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    73. Tein I, Christodoulou J, Donner E, McInnes RR. Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis. J Pediatr. 1994 Jun; 124(6):938-40. PMID: 8201482.
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    74. Tein I, DiMauro S, Xie ZW, De Vivo DC. Valproic acid impairs carnitine uptake in cultured human skin fibroblasts. An in vitro model for the pathogenesis of valproic acid-associated carnitine deficiency. Pediatr Res. 1993 Sep; 34(3):281-7. PMID: 8134167.
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    75. Koo B, Becker LE, Chuang S, Merante F, Robinson BH, MacGregor D, Tein I, Ho VB, McGreal DA, Wherrett JR, et al. Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations. Ann Neurol. 1993 Jul; 34(1):25-32. PMID: 8517676.
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    76. Tein I, De Vivo DC, Ranucci D, DiMauro S. Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders. J Inherit Metab Dis. 1993; 16(1):135-46. PMID: 8387612.
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    77. Tein I, De Vivo DC, Hale DE, Clarke JT, Zinman H, Laxer R, Shore A, DiMauro S. Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy. Ann Neurol. 1991 Sep; 30(3):415-9. PMID: 1835339.
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    78. Tein I, De Vivo DC, Bierman F, Pulver P, De Meirleir LJ, Cvitanovic-Sojat L, Pagon RA, Bertini E, Dionisi-Vici C, Servidei S, et al. Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy. Pediatr Res. 1990 Sep; 28(3):247-55. PMID: 2235122.
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    79. Tein I, DiMauro S, DeVivo DC. Recurrent childhood myoglobinuria. Adv Pediatr. 1990; 37:77-117. PMID: 2264536.
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    80. Bonnefont JP, Tein I, Saudubray JM, Demaugre F. Hepatic and muscular forms of palmitoyl carnitine transferase deficiency. Prog Clin Biol Res. 1990; 321:451-6. PMID: 2326305.
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    81. Tein I, Demaugre F, Bonnefont JP, Saudubray JM. Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1? J Neurol Sci. 1989 Sep; 92(2-3):229-45. PMID: 2809620.
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    82. Tein I, MacGregor DL. Possible valproate teratogenicity. Arch Neurol. 1985 Mar; 42(3):291-3. PMID: 3919693.
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    83. Venturelli J, Tein I, Hollenberg R. Increased intracranial pressure associated with N-acetylcysteine inhalation therapy. Crit Care Med. 1984 Oct; 12(10):926-7. PMID: 6488843.
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