Results 161 to 170 of about 5,278 (187)
Some of the next articles are maybe not open access.

The RETRIEVE Study: A natural history study of type 2 Gaucher disease, and GM1 and GM2 gangliosidoses with early onset, in preparation of a clinical trial

, 2021
B. Héron‐Longe   +10 more
semanticscholar   +1 more source

Motor function limitations and impacts among patients with GM1 AND GM2 gangliosidoses in the United States: A qualitative study

Molecular Genetics and Metabolism
Daisy Ng-Mak   +7 more
semanticscholar   +1 more source

Use of wearable sensor technology to identify digital biomarkers for monitoring gait parameters in children and adolescents with GM1 and GM2 gangliosidoses

Molecular Genetics and Metabolism
R. M. Quintela   +5 more
semanticscholar   +1 more source

OP-104 Utilizing lactate dehydrogenase and aspartate transaminase as diagnostic biomarkers in GM2 gangliosidoses

Oral Presentation
Muhammet Terzioğlu   +9 more
semanticscholar   +1 more source

A natural history study of late-infantile and juvenile GM1 and GM2 gangliosidoses (PRONTO): Patients' and caregivers' assessments

Molecular Genetics and Metabolism
Roberto Giugliani   +18 more
semanticscholar   +1 more source

Biomedical genetics of the inherited metabolic diseases: the GM2-gangliosidoses.

American journal of mental deficiency, 1984
Many of the known gene defects result in inborn errors of metabolism that produce irreversible damage to the central nervous system. A variety of new clinical, morphologic, biochemical, and genetic techniques are being used to characterize these disorders more precisely.
openaire   +1 more source

A natural history study of late-infantile and juvenile GM1 and GM2 gangliosidoses (PRONTO): Baseline clinical data

Molecular Genetics and Metabolism
Roberto Giugliani   +18 more
semanticscholar   +1 more source

AB-Variant of GM2-Gangliosidoses

2009
Hubert Scharnagl   +199 more
openaire   +1 more source

Maladie de tay-sachs: Gangliosidose à gm2

Archives de Pédiatrie, 1997
D. Guerin   +3 more
openaire   +1 more source

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