Tein I - Search Results

1

Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy.

Tein I, Haslam RH, Rhead WJ, Bennett MJ, Becker LE, Vockley J. Tein I, et al. Neurology. 1999 Jan 15;52(2):366-72. doi: 10.1212/wnl.52.2.366. Neurology. 1999. PMID: 9932958

2

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations.

Koo B, Becker LE, Chuang S, Merante F, Robinson BH, MacGregor D, Tein I, Ho VB, McGreal DA, Wherrett JR, et al. Koo B, et al. Among authors: tein i. Ann Neurol. 1993 Jul;34(1):25-32. doi: 10.1002/ana.410340107. Ann Neurol. 1993. PMID: 8517676

3

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

4

CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency.

Isackson PJ, Bennett MJ, Lichter-Konecki U, Willis M, Nyhan WL, Sutton VR, Tein I, Vladutiu GD. Isackson PJ, et al. Among authors: tein i. Mol Genet Metab. 2008 Aug;94(4):422-427. doi: 10.1016/j.ymgme.2008.05.002. Epub 2008 Jun 11. Mol Genet Metab. 2008. PMID: 18550408

5

Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone.

Tein I, Donner EJ, Hale DE, Murphy EG. Tein I, et al. Pediatr Neurol. 1995 Jan;12(1):68-76. doi: 10.1016/0887-8994(94)00109-f. Pediatr Neurol. 1995. PMID: 7748366

6

Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oil.

Tein I, Vajsar J, MacMillan L, Sherwood WG. Tein I, et al. Neurology. 1999 Feb;52(3):640-3. doi: 10.1212/wnl.52.3.640. Neurology. 1999. PMID: 10025805

7

Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation.

Ibdah JA, Tein I, Dionisi-Vici C, Bennett MJ, IJlst L, Gibson B, Wanders RJ, Strauss AW. Ibdah JA, et al. Among authors: tein i. J Clin Invest. 1998 Sep 15;102(6):1193-9. doi: 10.1172/JCI2091. J Clin Invest. 1998. PMID: 9739053 Free PMC article.

8

Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: primary or secondary defect(s)?

Tein I, Sloane AE, Donner EJ, Lehotay DC, Millington DS, Kelley RI. Tein I, et al. Pediatr Neurol. 1995 Jan;12(1):21-30. doi: 10.1016/0887-8994(94)00100-g. Pediatr Neurol. 1995. PMID: 7748356

9

Metabolic myopathies.

Tein I. Tein I. Semin Pediatr Neurol. 1996 Jun;3(2):59-98. doi: 10.1016/s1071-9091(96)80038-6. Semin Pediatr Neurol. 1996. PMID: 8795843 Review.

10

Deficient muscle carnitine transport in primary carnitine deficiency.

Pons R, Carrozzo R, Tein I, Walker WF, Addonizio LJ, Rhead W, Miranda AF, Dimauro S, De Vivo DC. Pons R, et al. Among authors: tein i. Pediatr Res. 1997 Nov;42(5):583-7. doi: 10.1203/00006450-199711000-00005. Pediatr Res. 1997. PMID: 9357927

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

91 results

Search Page

Filters