Tein I - Search Results

1

Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria.

Elpeleg ON, Saada AB, Shaag A, Glustein JZ, Ruitenbeek W, Tein I, Halevy J. Elpeleg ON, et al. Among authors: tein i. Muscle Nerve. 1997 Feb;20(2):238-40. doi: 10.1002/(sici)1097-4598(199702)20:2<238::aid-mus18>3.0.co;2-z. Muscle Nerve. 1997. PMID: 9040667 Free article. No abstract available.

2

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.

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. Tein I, et al. Mol Genet Metab. 2008 Feb;93(2):179-89. doi: 10.1016/j.ymgme.2007.09.021. Epub 2007 Dec 3. Mol Genet Metab. 2008. PMID: 18054510

3

Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein.

Spiekerkoetter U, Bennett MJ, Ben-Zeev B, Strauss AW, Tein I. Spiekerkoetter U, et al. Among authors: tein i. Muscle Nerve. 2004 Jan;29(1):66-72. doi: 10.1002/mus.10500. Muscle Nerve. 2004. PMID: 14694500

4

Recurrent childhood myoglobinuria.

Tein I, DiMauro S, DeVivo DC. Tein I, et al. Adv Pediatr. 1990;37:77-117. Adv Pediatr. 1990. PMID: 2264536 Review.

5

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

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. Tein I, et al. Mol Genet Metab. 2007 Jan 17. doi: 10.1016/j.ymgme.2006.11.011. Online ahead of print. Mol Genet Metab. 2007. PMID: 17234443

6

Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.

Tein I, De Vivo DC, Hale DE, Clarke JT, Zinman H, Laxer R, Shore A, DiMauro S. Tein I, et al. Ann Neurol. 1991 Sep;30(3):415-9. doi: 10.1002/ana.410300315. Ann Neurol. 1991. PMID: 1835339

7

The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophy.

Zolkipli Z, Mai L, Lamhonwah AM, Tein I. Zolkipli Z, et al. Among authors: tein i. Muscle Nerve. 2012 Nov;46(5):767-72. doi: 10.1002/mus.23368. Muscle Nerve. 2012. PMID: 23055315

8

Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis.

Tein I, Christodoulou J, Donner E, McInnes RR. Tein I, et al. J Pediatr. 1994 Jun;124(6):938-40. doi: 10.1016/s0022-3476(05)83187-7. J Pediatr. 1994. PMID: 8201482

9

Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants.

Zolkipli Z, Pedersen CB, Lamhonwah AM, Gregersen N, Tein I. Zolkipli Z, et al. Among authors: tein i. PLoS One. 2011 Apr 1;6(4):e17534. doi: 10.1371/journal.pone.0017534. PLoS One. 2011. PMID: 21483766 Free PMC article.

10

Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.

Verbeeten KC, Lamhonwah AM, Bulman D, Faghfoury H, Chakraborty P, Tein I, Geraghty MT. Verbeeten KC, et al. Among authors: tein i. Mol Genet Metab. 2020 Mar;129(3):213-218. doi: 10.1016/j.ymgme.2019.12.006. Epub 2019 Dec 10. Mol Genet Metab. 2020. PMID: 31864849

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