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MEDICAL-NUTRITIONAL INTERVENTION IN A JORDANIAN CHILD WITH GLYCOGEN STORAGE DISEASE TYPE IIIA: CASE REPORT.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China.
- Published in:
- BMC Medical Genetics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12881-018-0560-6
- By:
- Publication type:
- Article
Glycogen Storage Disease Type IIIa Presenting with Hyperglycemia: A Novel Mutation.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
Liver Transplantation in a Myopathic Patient with Glycogen Storage Disease Type IIIa and Decompensated Cirrhosis.
- Published in:
- International Journal of Organ Transplantation Medicine, 2017, v. 8, n. 4, p. 217
- By:
- Publication type:
- Article
A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series.
- Published in:
- Canadian Medical Association Journal (CMAJ), 2015, v. 187, n. 2, p. 108, doi. 10.1503/cmaj.140840
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- Publication type:
- Article