Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy-Reference-Cited by-同舟云学术

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Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy

Published:2007-02 Issue:2 Volume:150 Page:202-206
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Burrow T. Andrew,Cohen Mitchell B.,Bokulic Ronald,Deutsch Gail,Choudhary Arabinda,Falcone Richard A.,Grabowski Gregory A.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference8 articles.

1. Gaucher Disease;Beutler,2001

2. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry;Weinreb;Am J Med,2002

3. Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypes;Zhao;Am J Med Genet A,2003

4. Loss of inhibitors of the blood coagulation system in protein-losing enteropathy;Muntean;Klin Padiatr,1979

5. The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease;Altarescu;J Pediatr,2001

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1. Therapies for lysosomal storage diseases: Principles, practice, and prospects for refinements based on evolving science;Molecular Genetics and Metabolism;2022-09

2. The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?;Molecular Genetics and Metabolism;2022-05

3. Abdominal lymphadenopathy in children with Gaucher disease: Relation to disease severity and glucosylsphingosine;Pediatric Hematology and Oncology;2021-10-20

4. Case report of mesenteric lymphadenopathy in Gaucher disease: rare and benign complication;Pediatric Hematology/Oncology and Immunopathology;2021-04-21

5. Gaucher disease: Basic and translational science needs for more complete therapy and management;Molecular Genetics and Metabolism;2021-02

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