Prenatal sonographic findings in a case of Wolman's disease-Reference-Cited by-同舟云学术

Prenatal sonographic findings in a case of Wolman's disease

Published:2017-04-04 Issue:1 Volume:46 Page:66-68
ISSN:0091-2751
Container-title:Journal of Clinical Ultrasound
language:en
Short-container-title:J. Clin. Ultrasound

Author:

Blitz Matthew J.¹^ORCID,Rochelson Burton¹,Sood Monica²,Bialer Martin G.³,Vohra Nidhi¹

Affiliation:

1. Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Hofstra Northwell School of Medicine; North Shore University Hospital; Manhasset NY

2. Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology; Kaiser Permanente, Walnut Creek Medical Center; Walnut CA

3. Division of Medical Genetics, Department of Pediatrics; Hofstra Northwell School of Medicine, Cohen Children's Medical Center of New York; New Hyde Park NY

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

Reference15 articles.

1. Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman disease;Anderson;Proc Natl Acad Sci USA,1994

2. Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry;Valles-Ayoub;Genet Test Mol Biomarkers,2011

3. Deficiency of an acid lipase in Wolman's disease;Patrick;Nature,1969

4. Primary familial xanthomatosis with involvement and calcification of the adrenals. Report of two more cases in siblings of a previously described infant;Wolman;Pediatrics,1961

5. Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity;Aslanidis;Genomics,1996

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