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Items: 3

1.

Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry.

Valles-Ayoub Y, Esfandiarifard S, No D, Sinai P, Khokher Z, Kohan M, Kahen T, Darvish D.

Genet Test Mol Biomarkers. 2011 Jun;15(6):395-8. doi: 10.1089/gtmb.2010.0203. Epub 2011 Feb 3.

PMID:
21291321
2.

Prevalence of fatty liver in children and adolescents.

Schwimmer JB, Deutsch R, Kahen T, Lavine JE, Stanley C, Behling C.

Pediatrics. 2006 Oct;118(4):1388-93.

PMID:
17015527
3.

Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations.

Fischel-Ghodsian N, Bykhovskaya Y, Taylor K, Kahen T, Cantor R, Ehrenman K, Smith R, Keithley E.

Hear Res. 1997 Aug;110(1-2):147-54.

PMID:
9282897

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