Case of Glycogen Storage Disease Type VI (phosphorylase Deficiency) Complicated by Focal Nodular Hyperplasia
Overview
Affiliations
Glycogen storage diseases: An update.
Gumus E, Ozen H World J Gastroenterol. 2023; 29(25):3932-3963.
PMID: 37476587 PMC: 10354582. DOI: 10.3748/wjg.v29.i25.3932.
Clinical and genetic spectrum of GSD type 6 in Korea.
Hahn J, Lee H, Seong M, Kang G, Moon J, Ko J Orphanet J Rare Dis. 2023; 18(1):132.
PMID: 37264426 PMC: 10233917. DOI: 10.1186/s13023-023-02750-1.
Massese M, Tagliaferri F, Dionisi-Vici C, Maiorana A Orphanet J Rare Dis. 2022; 17(1):241.
PMID: 35725468 PMC: 9208159. DOI: 10.1186/s13023-022-02387-6.
The Phenotypic and Genetic Spectrum of Glycogen Storage Disease Type VI.
Grunert S, Hannibal L, Spiekerkoetter U Genes (Basel). 2021; 12(8).
PMID: 34440378 PMC: 8391619. DOI: 10.3390/genes12081205.
Glycogen storage disease type VI: clinical course and molecular background.
Aeppli T, Rymen D, Allegri G, Bode P, Haberle J Eur J Pediatr. 2019; 179(3):405-413.
PMID: 31768638 DOI: 10.1007/s00431-019-03499-1.