Literature DB >> 20723115

Case of glycogen storage disease type VI (phosphorylase deficiency) complicated by focal nodular hyperplasia.

Atsushi Ogawa1, Emi Ogawa, Shigenori Yamamoto, Tokiko Fukuda, Hideo Sugie, Yoichi Kohno.   

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Year:  2010        PMID： 20723115     DOI： 10.1111/j.1442-200X.2010.03073.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  4 in total

Review 1.  The Phenotypic and Genetic Spectrum of Glycogen Storage Disease Type VI.

Authors:  Sarah Catharina Grünert; Luciana Hannibal; Ute Spiekerkoetter
Journal:  Genes (Basel)       Date:  2021-08-03       Impact factor: 4.096

Review 2.  Liver glucose metabolism in humans.

Authors:  María M Adeva-Andany; Noemi Pérez-Felpete; Carlos Fernández-Fernández; Cristóbal Donapetry-García; Cristina Pazos-García
Journal:  Biosci Rep       Date:  2016-11-29       Impact factor: 3.840

3.  Liver Glycogen Phosphorylase Deficiency Leads to Profibrogenic Phenotype in a Murine Model of Glycogen Storage Disease Type VI.

Authors:  Lane H Wilson; Jun-Ho Cho; Ana Estrella; Joan A Smyth; Rong Wu; Tayoot Chengsupanimit; Laurie M Brown; David A Weinstein; Young Mok Lee
Journal:  Hepatol Commun       Date:  2019-09-24

Review 4.  Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI.

Authors:  Miriam Massese; Francesco Tagliaferri; Carlo Dionisi-Vici; Arianna Maiorana
Journal:  Orphanet J Rare Dis       Date:  2022-06-20       Impact factor: 4.303
  4 in total

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