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228 related items for PubMed ID: 26437929

  • 1. Muscle Ultrasound in Patients with Glycogen Storage Disease Types I and III.
    Verbeek RJ, Sentner CP, Smit GP, Maurits NM, Derks TG, van der Hoeven JH, Sival DA.
    Ultrasound Med Biol; 2016 Jan; 42(1):133-42. PubMed ID: 26437929
    [Abstract] [Full Text] [Related]

  • 2. Hepatic ultrasound findings in the glycogen storage diseases.
    Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C.
    Br J Radiol; 1994 Nov; 67(803):1062-6. PubMed ID: 7820397
    [Abstract] [Full Text] [Related]

  • 3. Skeletal and cardiac muscle involvement in children with glycogen storage disease type III.
    Mogahed EA, Girgis MY, Sobhy R, Elhabashy H, Abdelaziz OM, El-Karaksy H.
    Eur J Pediatr; 2015 Nov; 174(11):1545-8. PubMed ID: 25948107
    [Abstract] [Full Text] [Related]

  • 4. Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literature.
    Paschall A, Khan AA, Enam SF, Boggs T, Hijazi G, Bowling M, Austin S, Case LE, Kishnani P.
    Mol Genet Metab; 2021 Nov; 134(3):223-234. PubMed ID: 34649782
    [Abstract] [Full Text] [Related]

  • 5. The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinism.
    Lee PJ, Patel A, Hindmarsh PC, Mowat AP, Leonard JV.
    Clin Endocrinol (Oxf); 1995 Jun; 42(6):601-6. PubMed ID: 7634500
    [Abstract] [Full Text] [Related]

  • 6. Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?
    Preisler N, Pradel A, Husu E, Madsen KL, Becquemin MH, Mollet A, Labrune P, Petit F, Hogrel JY, Jardel C, Maillot F, Vissing J, Laforêt P.
    Mol Genet Metab; 2013 May; 109(1):14-20. PubMed ID: 23507172
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Glomerular and tubular function in glycogen storage disease.
    Lee PJ, Dalton RN, Shah V, Hindmarsh PC, Leonard JV.
    Pediatr Nephrol; 1995 Dec; 9(6):705-10. PubMed ID: 8747109
    [Abstract] [Full Text] [Related]

  • 9. Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa.
    Horvath JJ, Austin SL, Jones HN, Drake EJ, Case LE, Soher BJ, Bashir MR, Kishnani PS.
    Mol Genet Metab; 2012 Nov; 107(3):496-500. PubMed ID: 23062577
    [Abstract] [Full Text] [Related]

  • 10. [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 Nov; (7-8):78-84. PubMed ID: 25563007
    [Abstract] [Full Text] [Related]

  • 11. A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III.
    Hijazi G, Paschall A, Young SP, Smith B, Case LE, Boggs T, Amarasekara S, Austin SL, Pendyal S, El-Gharbawy A, Deak KL, Muir AJ, Kishnani PS.
    Mol Genet Metab Rep; 2021 Dec; 29():100821. PubMed ID: 34820282
    [Abstract] [Full Text] [Related]

  • 12. Long-term results of living donor liver transplantation for glycogen storage disorders in children.
    Iyer SG, Chen CL, Wang CC, Wang SH, Concejero AM, Liu YW, Yang CH, Yong CC, Jawan B, Cheng YF, Eng HL.
    Liver Transpl; 2007 Jun; 13(6):848-52. PubMed ID: 17539004
    [Abstract] [Full Text] [Related]

  • 13. 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 Jun; 27(1):1-9. PubMed ID: 14970741
    [Abstract] [Full Text] [Related]

  • 14. Prediction of premature atherosclerosis by endothelial dysfunction and increased intima-media thickness in glycogen storage disease types Ia and III.
    Yekeler E, Dursun M, Emeksiz E, Akkoyunlu M, Akyol Y, Demir F, Gökcay G, Demirkol M.
    Turk J Pediatr; 2007 Jun; 49(2):115-9. PubMed ID: 17907509
    [Abstract] [Full Text] [Related]

  • 15. [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; 47(8):608-12. PubMed ID: 19951495
    [Abstract] [Full Text] [Related]

  • 16. Neuromuscular involvement in glycogen storage disease type III.
    Moses SW, Gadoth N, Bashan N, Ben-David E, Slonim A, Wanderman KL.
    Acta Paediatr Scand; 1986 Mar; 75(2):289-96. PubMed ID: 3457519
    [Abstract] [Full Text] [Related]

  • 17. [Natural history of hepatic glycogen storage diseases].
    Labrune P, Eberschweiler PT, Boudjemline AM, Hubert-Buron A, Petit F, Gajdos V.
    Presse Med; 2008 Mar; 37(7-8):1172-7. PubMed ID: 18313893
    [Abstract] [Full Text] [Related]

  • 18. A monocentric pilot study of an antioxidative defense and hsCRP in pediatric patients with glycogen storage disease type IA and III.
    Kalkan Ucar S, Coker M, Sözmen E, Goksen Simsek D, Darcan S.
    Nutr Metab Cardiovasc Dis; 2009 Jul; 19(6):383-90. PubMed ID: 19073362
    [Abstract] [Full Text] [Related]

  • 19. Radiography of glycogen storage diseases.
    Miller JH, Stanley P, Gates GF.
    AJR Am J Roentgenol; 1979 Mar; 132(3):379-87. PubMed ID: 106640
    [Abstract] [Full Text] [Related]

  • 20. Peripheral neuropathy in glycogen storage disease type III: Fact or myth?
    Herlin B, Laforět P, Labrune P, Fournier E, Stojkovic T.
    Muscle Nerve; 2016 Feb; 53(2):310-2. PubMed ID: 26575860
    [Abstract] [Full Text] [Related]

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