International audienceThis is the first report of a viable animal model of the hepatic pathology of GSD1a, including the late development of hepatocellular adenomas
Glycogen storage disease type 1a (GSD1a) is a rare metabolic disorder due to an absence of glucose‐...
Patients with Glycogen Storage Disease type Ia (GSD Ia), a rare inherited disease affecting glucose ...
Background and aims: Glycogen storage disease type Ib (GSD1b) is a rare metabolic and immune disorde...
International audienceThis is the first report of a viable animal model of the hepatic pathology of ...
Glycogen storage disease type 1a (GSD-1a) is caused by a deficiency in glucose-6-phosphatase-α (G6Pa...
International audiencePatients with glycogen storage diseases type 1 (GSD1) suffer from life-threate...
International audienceGlycogen storage disease type Ia (GSD Ia) is caused by mutations in the glucos...
Background and Aims Patients with glycogen storage disease type 1a (GSD-1a) primarily present with l...
Background and Aims: Patients with glycogen storage disease type 1a (GSD-1a) primarily present with ...
La glycogénose de type 1a (GSD1a) est une maladie métabolique rare liée à une absence d’activité glu...
Glycogen storage disease type 1a (GSD-1a) is a rare genetic disease caused by mutations in the catal...
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive metabolic disorder caused by a d...
Glycogen storage disease type Ia (GSD-Ia), characterized by impaired glucose homeostasis and chronic...
International audienceGlycogen storage disease type 1a (GSD1a) is a rare disease due to the deficien...
Abstract Glycogen storage disease type 1 (GSD1) is an inherited disorder caused by impaired glucose ...
Glycogen storage disease type 1a (GSD1a) is a rare metabolic disorder due to an absence of glucose‐...
Patients with Glycogen Storage Disease type Ia (GSD Ia), a rare inherited disease affecting glucose ...
Background and aims: Glycogen storage disease type Ib (GSD1b) is a rare metabolic and immune disorde...
International audienceThis is the first report of a viable animal model of the hepatic pathology of ...
Glycogen storage disease type 1a (GSD-1a) is caused by a deficiency in glucose-6-phosphatase-α (G6Pa...
International audiencePatients with glycogen storage diseases type 1 (GSD1) suffer from life-threate...
International audienceGlycogen storage disease type Ia (GSD Ia) is caused by mutations in the glucos...
Background and Aims Patients with glycogen storage disease type 1a (GSD-1a) primarily present with l...
Background and Aims: Patients with glycogen storage disease type 1a (GSD-1a) primarily present with ...
La glycogénose de type 1a (GSD1a) est une maladie métabolique rare liée à une absence d’activité glu...
Glycogen storage disease type 1a (GSD-1a) is a rare genetic disease caused by mutations in the catal...
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive metabolic disorder caused by a d...
Glycogen storage disease type Ia (GSD-Ia), characterized by impaired glucose homeostasis and chronic...
International audienceGlycogen storage disease type 1a (GSD1a) is a rare disease due to the deficien...
Abstract Glycogen storage disease type 1 (GSD1) is an inherited disorder caused by impaired glucose ...
Glycogen storage disease type 1a (GSD1a) is a rare metabolic disorder due to an absence of glucose‐...
Patients with Glycogen Storage Disease type Ia (GSD Ia), a rare inherited disease affecting glucose ...
Background and aims: Glycogen storage disease type Ib (GSD1b) is a rare metabolic and immune disorde...