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PUBMED FOR HANDHELDS

Journal Abstract Search


187 related items for PubMed ID: 25097048

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  • 3. First report of glycogen storage disease type 111a in a Nigerian child.
    Senbanjo IO, Lamina MO, Kumolu-Johnson T, El-Said H, El-Guindi MAS.
    Niger Postgrad Med J; 2019; 26(2):138-141. PubMed ID: 31187755
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  • 5. Successful treatment of severe cardiomyopathy in glycogen storage disease type III With D,L-3-hydroxybutyrate, ketogenic and high-protein diet.
    Valayannopoulos V, Bajolle F, Arnoux JB, Dubois S, Sannier N, Baussan C, Petit F, Labrune P, Rabier D, Ottolenghi C, Vassault A, Broissand C, Bonnet D, de Lonlay P.
    Pediatr Res; 2011 Dec; 70(6):638-41. PubMed ID: 21857385
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  • 6. [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
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  • 9. Chanarin-Dorfman syndrome: A case report and review of the literature.
    Mogahed EA, El-Hennawy A, El-Sayed R, El-Karaksy H.
    Arab J Gastroenterol; 2015 Aug; 16(3-4):142-4. PubMed ID: 26520282
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  • 10. Hepatic Glycogenosis In Children: Spectrum Of Presentation And Diagnostic Modalities.
    Bilal H, Cheema HA, Fayyaz Z, Saeed A, Batool Hamdani SS.
    J Ayub Med Coll Abbottabad; 2019 Aug; 31(3):368-371. PubMed ID: 31535508
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  • 12. 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 Aug; 49(2):115-9. PubMed ID: 17907509
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  • 14. Lens opacities in glycogenoses type I and III.
    Allegrini D, Autelitano A, Fogagnolo P, De Cillà S, Piozzi E, Mazza M, Paci S, Montanari C, Riva E, Rossetti L.
    Can J Ophthalmol; 2015 Dec; 50(6):480-4. PubMed ID: 26651310
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  • 18. 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(12):2686-2694. PubMed ID: 31263214
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