Molecular diagnosis of glycogen storage disease type I : a review

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Molecular diagnosis of glycogen storage disease type I ; Vol. 18 2019
EXCLI journal ; Vol. 18 2019

Classification: Medizin, Gesundheit

Creator: Beyzaei, Zahra
Geramizadeh, Bita

Handle: 2003/38065

URN: urn:nbn:de:101:1-2019052403441412371398

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

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Beyzaei, Zahra
Geramizadeh, Bita

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Molecular diagnosis of glycogen storage disease type I : a review

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Other Objects (12)

Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome

Liver transplantation in glycogen storage disease type I

A glycogen storage disease type 1a patient with type 2 diabetes

Next-generation glycogen storage diseases

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French recommendations for the management of glycogen storage disease type III

Estimation of Health Utility Scores for Glycogen Storage Disease Type Ia

Successful pregnancy in a woman with glycogen storage disease type 6

Glycogen Storage Disease Type I and Bone: Clinical and Cellular Characterization

A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0

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A glycogen storage disease type 1a patient with type 2 diabetes

Next-generation glycogen storage diseases

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The phenotypic and genetic spectrum of glycogen storage disease type VI

Intestinal microbiota composition of children with glycogen storage Type I patients

French recommendations for the management of glycogen storage disease type III

Estimation of Health Utility Scores for Glycogen Storage Disease Type Ia

Successful pregnancy in a woman with glycogen storage disease type 6

Glycogen Storage Disease Type I and Bone: Clinical and Cellular Characterization

A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0

Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome

Liver transplantation in glycogen storage disease type I

A glycogen storage disease type 1a patient with type 2 diabetes

Next-generation glycogen storage diseases

Glycogen storage disease type III: modified Atkins diet improves myopathy

The phenotypic and genetic spectrum of glycogen storage disease type VI

Intestinal microbiota composition of children with glycogen storage Type I patients

French recommendations for the management of glycogen storage disease type III

Estimation of Health Utility Scores for Glycogen Storage Disease Type Ia

Successful pregnancy in a woman with glycogen storage disease type 6

Glycogen Storage Disease Type I and Bone: Clinical and Cellular Characterization

A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0

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