Christensen E - Search Results

1

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: christensen e. Am J Hum Genet. 1996 Nov;59(5):1012-8. Am J Hum Genet. 1996. PMID: 8900228 Free PMC article.

2

Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds.

Amir N, Elpeleg ON, Shalev RS, Christensen E. Amir N, et al. Among authors: christensen e. J Pediatr. 1989 Jun;114(6):983-9. doi: 10.1016/s0022-3476(89)80442-1. J Pediatr. 1989. PMID: 2723913

3

The molecular basis of canavan (aspartoacylase deficiency) disease in European non-Jewish patients.

Shaag A, Anikster Y, Christensen E, Glustein JZ, Fois A, Michelakakis H, Nigro F, Pronicka E, Ribes A, Zabot MT, et al. Shaag A, et al. Among authors: christensen e. Am J Hum Genet. 1995 Sep;57(3):572-80. Am J Hum Genet. 1995. PMID: 7668285 Free PMC article.

4

Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features.

Amir N, el-Peleg O, Shalev RS, Christensen E. Amir N, et al. Among authors: christensen e. Neurology. 1987 Oct;37(10):1654-7. doi: 10.1212/wnl.37.10.1654. Neurology. 1987. PMID: 3658174

5

Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations.

Goodman SI, Stein DE, Schlesinger S, Christensen E, Schwartz M, Greenberg CR, Elpeleg ON. Goodman SI, et al. Among authors: christensen e. Hum Mutat. 1998;12(3):141-4. doi: 10.1002/(SICI)1098-1004(1998)12:3<141::AID-HUMU1>3.0.CO;2-K. Hum Mutat. 1998. PMID: 9711871 Review.

6

Variability of clinical presentation in fumarate hydratase deficiency.

Elpeleg ON, Amir N, Christensen E. Elpeleg ON, et al. Among authors: christensen e. J Pediatr. 1992 Nov;121(5 Pt 1):752-4. doi: 10.1016/s0022-3476(05)81910-9. J Pediatr. 1992. PMID: 1432428

7

Glutaric aciduria type I. Brain CT features and a diagnostic pitfall.

Mandel H, Braun J, el-Peleg O, Christensen E, Berant M. Mandel H, et al. Among authors: christensen e. Neuroradiology. 1991;33(1):75-8. doi: 10.1007/BF00593342. Neuroradiology. 1991. PMID: 2027453

8

Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria.

Elpeleg ON, Christensen E, Hurvitz H, Branski D. Elpeleg ON, et al. Among authors: christensen e. Eur J Pediatr. 1990 Jul;149(10):709-12. doi: 10.1007/BF01959528. Eur J Pediatr. 1990. PMID: 2120061

9

3-Methylglutaconic aciduria type III in a non-Iraqi-Jewish kindred: clinical and molecular findings.

Kleta R, Skovby F, Christensen E, Rosenberg T, Gahl WA, Anikster Y. Kleta R, et al. Among authors: christensen e. Mol Genet Metab. 2002 Jul;76(3):201-6. doi: 10.1016/s1096-7192(02)00047-1. Mol Genet Metab. 2002. PMID: 12126933

10

[Results of screening for organic aciduria in Israel].

Elpeleg O, Amir N, Hurvitz H, Navon P, Christensen E. Elpeleg O, et al. Among authors: christensen e. Harefuah. 1988 Dec 15;115(12):377-9. Harefuah. 1988. PMID: 3240901 Hebrew. No abstract available.

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