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Journal Abstract Search


196 related items for PubMed ID: 25563007

  • 1. [Mitochondrial dysfunction in children with hepatic forms of glycogen storage disease].
    Kurbatova OV, Izmaĭlova TD, Surkov AN, Namazova-Baranova LS, Poliakova SI, Miroshkina LV, Semenova GF, Samokhina IV, Kapustina EIu, Dukhova ZN, Potapov AS, Petrichuk SV.
    Vestn Ross Akad Med Nauk; 2014; (7-8):78-84. PubMed ID: 25563007
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  • 2. Hepatic glycogen storage disorders: what have we learned in recent years?
    Burda P, Hochuli M.
    Curr Opin Clin Nutr Metab Care; 2015 Jul; 18(4):415-21. PubMed ID: 26001652
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  • 5. Elevated serum biotinidase activity in hepatic glycogen storage disorders--a convenient biomarker.
    Paesold-Burda P, Baumgartner MR, Santer R, Bosshard NU, Steinmann B.
    J Inherit Metab Dis; 2007 Nov; 30(6):896-902. PubMed ID: 17994282
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  • 6. Liver transplantation in glycogen storage disease: a single-center experience.
    Beyzaei Z, Shamsaeefar A, Kazemi K, Nikeghbalian S, Bahador A, Dehghani M, Malekhosseini SA, Geramizadeh B.
    Orphanet J Rare Dis; 2022 Mar 21; 17(1):127. PubMed ID: 35313948
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  • 7. Hepatic ultrasound findings in the glycogen storage diseases.
    Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C.
    Br J Radiol; 1994 Nov 21; 67(803):1062-6. PubMed ID: 7820397
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  • 9. An association among iron, copper, zinc, and selenium, and antioxidative status in dyslipidemic pediatric patients with glycogen storage disease types IA and III.
    Kalkan Ucar S, Coker M, Sözmen E, Goksen Simsek D, Darcan S.
    J Trace Elem Med Biol; 2010 Jan 21; 24(1):42-5. PubMed ID: 20122579
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  • 10. Glomerular and tubular function in glycogen storage disease.
    Lee PJ, Dalton RN, Shah V, Hindmarsh PC, Leonard JV.
    Pediatr Nephrol; 1995 Dec 21; 9(6):705-10. PubMed ID: 8747109
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  • 12. Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring.
    Halaby CA, Young SP, Austin S, Stefanescu E, Bali D, Clinton LK, Smith B, Pendyal S, Upadia J, Schooler GR, Mavis AM, Kishnani PS.
    Genet Med; 2019 Dec 21; 21(12):2686-2694. PubMed ID: 31263214
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  • 14. Bone mineral density and markers of bone turnover in patients with glycogen storage disease types I, III and IX.
    Cabrera-Abreu J, Crabtree NJ, Elias E, Fraser W, Cramb R, Alger S.
    J Inherit Metab Dis; 2004 Dec 21; 27(1):1-9. PubMed ID: 14970741
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  • 17. The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.
    Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S.
    Mol Genet Metab; 2014 Nov 21; 113(3):171-6. PubMed ID: 25266922
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  • 19. [Diagnosis of glycogen storage disease type IIIA by detecting glycogen debranching enzyme activity, glycogen content and structure in muscle].
    Wang W, We M, Song HM, Qiu ZQ, Zhang WM, Wu XY, Lu CX, Qi JM, Jing H, Li F.
    Zhonghua Er Ke Za Zhi; 2009 Aug 21; 47(8):608-12. PubMed ID: 19951495
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  • 20. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Aug 21; 42(12):61-71. PubMed ID: 7011274
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