Anikster Y - Search Results

1

Prenatal detection of Canavan disease (aspartoacylase deficiency) by DNA analysis.

Elpeleg ON, Shaag A, Anikster Y, Jakobs C. Elpeleg ON, et al. Among authors: anikster y. J Inherit Metab Dis. 1994;17(6):664-6. doi: 10.1007/BF00712008. J Inherit Metab Dis. 1994. PMID: 7707689

2

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: anikster y. Am J Hum Genet. 1995 Sep;57(3):572-80. Am J Hum Genet. 1995. PMID: 7668285 Free PMC article.

3

The frequency of the C854 mutation in the aspartoacylase gene in Ashkenazi Jews in Israel.

Elpeleg ON, Anikster Y, Barash V, Branski D, Shaag A. Elpeleg ON, et al. Among authors: anikster y. Am J Hum Genet. 1994 Aug;55(2):287-8. Am J Hum Genet. 1994. PMID: 8037206 Free PMC article.

4

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

5

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: anikster y. 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.

6

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: anikster y. Mol Genet Metab. 2001 May;73(1):107-10. doi: 10.1006/mgme.2001.3166. Mol Genet Metab. 2001. PMID: 11350191

7

Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews.

Anikster Y, Kleta R, Shaag A, Gahl WA, Elpeleg O. Anikster Y, et al. Am J Hum Genet. 2001 Dec;69(6):1218-24. doi: 10.1086/324651. Epub 2001 Oct 19. Am J Hum Genet. 2001. PMID: 11668429 Free PMC article.

8

Glyceryl triacetate for Canavan disease: a low-dose trial in infants and evaluation of a higher dose for toxicity in the tremor rat model.

Madhavarao CN, Arun P, Anikster Y, Mog SR, Staretz-Chacham O, Moffett JR, Grunberg NE, Gahl WA, Namboodiri AMA. Madhavarao CN, et al. Among authors: anikster y. J Inherit Metab Dis. 2009 Oct;32(5):640. doi: 10.1007/s10545-009-1155-3. Epub 2009 Aug 15. J Inherit Metab Dis. 2009. PMID: 19685155 Clinical Trial.

9

Metabolic acetate therapy improves phenotype in the tremor rat model of Canavan disease.

Arun P, Madhavarao CN, Moffett JR, Hamilton K, Grunberg NE, Ariyannur PS, Gahl WA, Anikster Y, Mog S, Hallows WC, Denu JM, Namboodiri AM. Arun P, et al. Among authors: anikster y. J Inherit Metab Dis. 2010 Jun;33(3):195-210. doi: 10.1007/s10545-010-9100-z. Epub 2010 May 13. J Inherit Metab Dis. 2010. PMID: 20464498 Free PMC article.

10

A safety trial of high dose glyceryl triacetate for Canavan disease.

Segel R, Anikster Y, Zevin S, Steinberg A, Gahl WA, Fisher D, Staretz-Chacham O, Zimran A, Altarescu G. Segel R, et al. Among authors: anikster y. Mol Genet Metab. 2011 Jul;103(3):203-6. doi: 10.1016/j.ymgme.2011.03.012. Epub 2011 Mar 15. Mol Genet Metab. 2011. PMID: 21474353 Clinical Trial.

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