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Journal Abstract Search

373 related items for PubMed ID: 25266922

  • 21. Benign or not benign? Deep phenotyping of liver Glycogen Storage Disease IX.
    Fernandes SA, Cooper GE, Gibson RA, Kishnani PS.
    Mol Genet Metab; 2020 Nov; 131(3):299-305. PubMed ID: 33317799
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  • 25. Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.
    Beyzaei Z, Ezgu F, Geramizadeh B, Alborzi A, Shojazadeh A.
    BMC Pediatr; 2021 Apr 15; 21(1):175. PubMed ID: 33858366
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  • 26. Clinical and genetic characteristics of 17 Chinese patients with glycogen storage disease type IXa.
    Zhang J, Yuan Y, Ma M, Liu Y, Zhang W, Yao F, Qiu Z.
    Gene; 2017 Sep 05; 627():149-156. PubMed ID: 28627441
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  • 27. Neurological Characteristics of Pediatric Glycogen Storage Disease.
    Muzetti JH, do Valle DA, Santos MLSF, Telles BA, Cordeiro ML.
    Front Endocrinol (Lausanne); 2021 Sep 05; 12():685272. PubMed ID: 34093448
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  • 31. Novel mutations in PHKA2 gene in glycogen storage disease type IX patients from Hong Kong, China.
    Lau CK, Hui J, Fong FN, To KF, Fok TF, Tang NL, Tsui SK.
    Mol Genet Metab; 2011 Feb 05; 102(2):222-5. PubMed ID: 21131218
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  • 37. Clinical, Biochemical, and Genetic Characterization of Glycogen Storage Type IX in a Child with Asymptomatic Hepatomegaly.
    Kim JA, Kim JH, Lee BH, Kim GH, Shin YS, Yoo HW, Kim KM.
    Pediatr Gastroenterol Hepatol Nutr; 2015 Jun 05; 18(2):138-43. PubMed ID: 26157701
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  • 38. Clinical, pathological and molecular spectrum of patients with glycogen storage diseases in Pakistan.
    Ahmed S, Akbar F, Ali AJ, Afroze B.
    J Pediatr Endocrinol Metab; 2022 Mar 28; 35(3):373-385. PubMed ID: 34989216
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