Hepatocellular failure in glycogen storage disorder type 3.

Ingle, S A; Moulick, N D; Ranadive, N U; Khedekar, K.
Artículo en Inglés | IMSEAR | ID: sea-91287

Documentos relacionados

  1. The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type III.
  2. Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations.
  3. [Analysis of two cases of glycogen storage disease type III due to compound heterozygous variants of AGL gene].
  4. Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.
  5. Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China.
  6. [Characteristics of lipid metabolism and the cardiovascular system in glycogenosis types I and III].
  7. In vivo characterization of glycogen storage disease type III in a mouse model using glycoNOE MRI.
  8. Liver transplantation in patients with type IIIa glycogen storage disease, cirrhosis and hepatocellular carcinoma.
  9. First report of glycogen storage disease type 111a in a Nigerian child.
  10. Dietary management in glycogen storage disease type III: what is the evidence?