Systematic approach to the diagnosis of lysosomal storage disorders-Reference-Cited by-同舟云学术

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Systematic approach to the diagnosis of lysosomal storage disorders

Published:2001 Issue:3 Volume:7 Page:190-199
ISSN:1080-4013
Container-title:Mental Retardation and Developmental Disabilities Research Reviews
language:en
Short-container-title:Ment. Retard. Dev. Disabil. Res. Rev.

Author:

Weibel Tha�s D.,Brady Roscoe O.

Publisher

Wiley

Subject

Genetics (clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology and Child Health

Reference30 articles.

1. Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation

2. 2001. Disorders of free sialic acid storage. In editors. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill. p 5109-5120.

3. 9 Gaucher's disease: studies of gene transfer to haematopoietic cells

4. Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease

5. Gaucher disease as a paradigm of current issues regarding single gene mutations of humans.

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal Diagnosis of Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;2021-04-20

2. Lysosomale Speicherkrankheiten, Diagnostik;Springer Reference Medizin;2019

3. Lysosomale Speicherkrankheiten, Diagnostik;Lexikon der Medizinischen Laboratoriumsdiagnostik;2018

4. Prenatal Diagnosis of Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;2015-11-23

5. Lysosomal Storage Disorders;Encyclopedia of the Neurological Sciences;2014

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