Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
about
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disordersGlucocerebrosidase 1 deficient Danio rerio mirror key pathological aspects of human Gaucher disease and provide evidence of early microglial activation preceding alpha-synuclein-independent neuronal cell deathParkinson disease in Gaucher disease.Genes associated with Parkinson's disease: regulation of autophagy and beyond.A Next Generation Multiscale View of Inborn Errors of Metabolism.The Underexploited Role of Non-Coding RNAs in Lysosomal Storage Diseases.Are There Neurological Symptoms in Type 1 of Gaucher Disease?Parkinsonism in Inherited Metabolic Disorders: Key Considerations and Major Features
P2860
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P2860
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
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2014年學術文章
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name
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
@en
type
label
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
@en
prefLabel
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
@en
P2860
P1476
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.
@en
P2093
Hagit N Baris
Pramod K Mistry
P2860
P478
12 Suppl 1
P50
P577
2014-09-01T00:00:00Z