Author:
Weinreb Neal J.,Finegold David N.,Feingold Eleanor,Zeng Zhen,Rosenbloom Barry E.,Shankar Suma P.,Amato Dominick
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Reference46 articles.
1. Grabowski G, Kolodny E, Weinreb N, Rosenbloom B, Prakash-Cheng A, Kaplan P, et al. Gaucher disease: Phenotypic and genetic variation. In: Scriver C, Beaudet A, Valle D, Slye W, editors. The Online Metabolic and Molecular Basis of Inherited Metabolic Disease. New York: McGraw-Hill Publishers; 2010. http://genetics.accessmedicine.com/server-java/Arknoid/amed/mmbid/co_chapters/ch146.1/146.1_p01.hhtml Access Date: 1 Sept 2011.
2. Rosenbloom BE, Weinreb NJ. Gaucher disease: a comprehensive review. Crit Rev Oncog. 2013;18:163–75.
3. Sidransky E. Heterozygosity for a Mendelian disorder as a risk factor for complex disease. Clin Genet. 2006;70:275–82.
4. Lo SM, Choi M, Liu J, Jain D, Boot RG, Kallemeijn WW, et al. Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis. Blood. 2012;119:4731–40.
5. Weinreb NJ, Taylor J, Cox T, Yee J, Vom DS. A benchmark analysis of the achievement of therapeutic goals for type 1 Gaucher disease patients treated with imiglucerase. Am J Hematol. 2008;83:890–5.
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