Type I Gaucher Disease
Overview
Overview
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Authors
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Citing Articles
An Unexpected Finding of Hepatosplenomegaly in a Pediatric Patient.
Barootes H, Prasad C, Rupar C, Ashok D Clin Pediatr (Phila). 2021; 61(1):81-85.
PMID: 34789027 PMC: 8679167. DOI: 10.1177/00099228211059668.
Altarescu G, Beeri R, Eiges R, Epsztejn-Litman S, Eldar-Geva T, Elstein D Mol Biol Int. 2013; 2012:797342.
PMID: 23320174 PMC: 3540816. DOI: 10.1155/2012/797342.
References
1.
Goldblatt J, Beighton P
. Cutaneous manifestations of Gaucher disease. Br J Dermatol. 1984; 111(3):331-4.
DOI: 10.1111/j.1365-2133.1984.tb04731.x.
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2.
BAR-MAOR J
. Partial splenectomy in children with Gaucher's disease. Pediatrics. 1985; 76(3):398-401.
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3.
Sorge J, KUHL W, West C, Beutler E
. Gaucher disease: retrovirus-mediated correction of the enzymatic defect in cultured cells. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 2:1041-6.
DOI: 10.1101/sqb.1986.051.01.120.
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4.
Goldblatt J, Sacks S, Beighton P
. The orthopedic aspects of Gaucher disease. Clin Orthop Relat Res. 1978; (137):208-14.
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5.
Brady R, Kanfer J, Shapiro D
. METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE. Biochem Biophys Res Commun. 1965; 18:221-5.
DOI: 10.1016/0006-291x(65)90743-6.
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