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PUBMED FOR HANDHELDS

Journal Abstract Search


373 related items for PubMed ID: 25266922

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  • 3. Liver histology in children with glycogen storage disorders type VI and IX.
    Degrassi I, Deheragoda M, Creegen D, Mundy H, Mustafa A, Vara R, Hadzic N.
    Dig Liver Dis; 2021 Jan; 53(1):86-93. PubMed ID: 32505569
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  • 9. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
    Kishnani PS, Goldstein J, Austin SL, Arn P, Bachrach B, Bali DS, Chung WK, El-Gharbawy A, Brown LM, Kahler S, Pendyal S, Ross KM, Tsilianidis L, Weinstein DA, Watson MS, ACMG Work Group on Diagnosis and Management of Glycogen Storage Diseases Type VI and IX.
    Genet Med; 2019 Apr; 21(4):772-789. PubMed ID: 30659246
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  • 10. Glycogen storage disease type IX: High variability in clinical phenotype.
    Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho KL, Raiman J, Walter J, Treacy E, Tanner S, Sharrard M.
    Mol Genet Metab; 2007 Apr; 92(1-2):88-99. PubMed ID: 17689125
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  • 11. Molecular diagnosis of glycogen storage disease type IX using a glycogen storage disease gene panel.
    Kim TH, Kim KY, Kim MJ, Seong MW, Park SS, Moon JS, Ko JS.
    Eur J Med Genet; 2020 Jun; 63(6):103921. PubMed ID: 32244026
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  • 13. Diagnosis and follow-up of glycogen storage disease (GSD) type VI from the largest GSD center in China.
    Luo X, Duan Y, Fang D, Sun Y, Xiao B, Zhang H, Han L, Liang L, Gong Z, Gu X, Yu Y, Qiu W.
    Hum Mutat; 2022 May; 43(5):557-567. PubMed ID: 35143115
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  • 15. Glycogen storage diseases.
    Hug G.
    Birth Defects Orig Artic Ser; 1976 May; 12(6):145-75. PubMed ID: 788807
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  • 16. Characterization of liver GSD IX γ2 pathophysiology in a novel Phkg2-/- mouse model.
    Gibson RA, Lim JA, Choi SJ, Flores L, Clinton L, Bali D, Young S, Asokan A, Sun B, Kishnani PS.
    Mol Genet Metab; 2021 Jul; 133(3):269-276. PubMed ID: 34083142
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  • 17. Glycogen storage disease type VI can progress to cirrhosis: ten Chinese patients with GSD VI and a literature review.
    Lu SQ, Feng JY, Liu J, Xie XB, Lu Y, Abuduxikuer K.
    J Pediatr Endocrinol Metab; 2020 Sep 07; 33(10):1321-1333. PubMed ID: 32892177
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