Joseph A - Search Results

1

Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews.

Shaag A, Saada A, Berger I, Mandel H, Joseph A, Feigenbaum A, Elpeleg ON. Shaag A, et al. Among authors: joseph a. Am J Med Genet. 1999 Jan 15;82(2):177-82. Am J Med Genet. 1999. PMID: 9934985

2

Glutaric aciduria type I in the Arab and Jewish communities in Israel.

Anikster Y, Shaag A, Joseph A, Mandel H, Ben-Zeev B, Christensen E, Elpeleg ON. Anikster Y, et al. Among authors: joseph a. Am J Hum Genet. 1996 Nov;59(5):1012-8. Am J Hum Genet. 1996. PMID: 8900228 Free PMC article.

3

Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence.

Elpeleg ON, Shaag A, Glustein JZ, Anikster Y, Joseph A, Saada A. Elpeleg ON, et al. Among authors: joseph a. Hum Mutat. 1997;10(3):256-7. doi: 10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z. Hum Mutat. 1997. PMID: 9298831 No abstract available.

4

Mutation analysis of the MCM gene in Israeli patients with mut(0) disease.

Berger I, Shaag A, Anikster Y, Baumgartner ER, Bar-Meir M, Joseph A, Elpeleg ON. Berger I, et al. Among authors: joseph a. Mol Genet Metab. 2001 May;73(1):107-10. doi: 10.1006/mgme.2001.3166. Mol Genet Metab. 2001. PMID: 11350191

5

3-Methylglutaconic aciduria in the Iraqi-Jewish 'optic atrophy plus' (Costeff) syndrome.

Elpeleg ON, Costeff H, Joseph A, Shental Y, Weitz R, Gibson KM. Elpeleg ON, et al. Among authors: joseph a. Dev Med Child Neurol. 1994 Feb;36(2):167-72. doi: 10.1111/j.1469-8749.1994.tb11825.x. Dev Med Child Neurol. 1994. PMID: 7510656

6

Recurrent metabolic decompensation in profound carnitine palmitoyltransferase II deficiency.

Elpeleg ON, Joseph A, Branski D, Christensen E, Holme E, Demaugre F, Saudubray JM, Gutman A. Elpeleg ON, et al. Among authors: joseph a. J Pediatr. 1993 Jun;122(6):917-9. doi: 10.1016/s0022-3476(09)90019-1. J Pediatr. 1993. PMID: 8501570

7

Anaesthetic management of a patient with Leigh's syndrome.

Shenkman Z, Krichevski I, Elpeleg ON, Joseph A, Kadari A. Shenkman Z, et al. Among authors: joseph a. Can J Anaesth. 1997 Oct;44(10):1091-5. doi: 10.1007/BF03019232. Can J Anaesth. 1997. PMID: 9350370

8

Familial microcephaly with severe neurological deficits: a description of five affected siblings.

Gross-Tsur V, Joseph A, Blinder G, Amir N. Gross-Tsur V, et al. Among authors: joseph a. Clin Genet. 1995 Jan;47(1):33-7. doi: 10.1111/j.1399-0004.1995.tb03918.x. Clin Genet. 1995. PMID: 7774041

9

Epilepsy and attention deficit hyperactivity disorder: is methylphenidate safe and effective?

Gross-Tsur V, Manor O, van der Meere J, Joseph A, Shalev RS. Gross-Tsur V, et al. Among authors: joseph a. J Pediatr. 1997 Apr;130(4):670-4. doi: 10.1016/s0022-3476(97)70258-0. J Pediatr. 1997. PMID: 9432523 Clinical Trial.

10

Epilepsy and attention deficit hyperactivity disorder: is methylphenidate safe and effective?

Gross-Tsur V, Manor O, van der Meere J, Joseph A, Shalev RS. Gross-Tsur V, et al. Among authors: joseph a. J Pediatr. 1997 Jan;130(1):40-4. doi: 10.1016/s0022-3476(97)70308-1. J Pediatr. 1997. Corrected and republished in: J Pediatr. 1997 Apr;130(4):670-4. doi: 10.1016/s0022-3476(97)70258-0 PMID: 9003849 Corrected and republished. Clinical Trial.

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

2,410 results

Search Page

Filters