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Journal Abstract Search

215 related items for PubMed ID: 34836082

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  • 4. Glucose-6-phosphatase deficiency.
    Froissart R, Piraud M, Boudjemline AM, Vianey-Saban C, Petit F, Hubert-Buron A, Eberschweiler PT, Gajdos V, Labrune P.
    Orphanet J Rare Dis; 2011 May 20; 6():27. PubMed ID: 21599942
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  • 5. A triple-blinded crossover study to evaluate the short-term safety of sweet manioc starch for the treatment of glycogen storage disease type Ia.
    Monteiro VCL, de Oliveira BM, Dos Santos BB, Sperb-Ludwig F, Refosco LF, Nalin T, Derks TGJ, Moura de Souza CF, Schwartz IVD.
    Orphanet J Rare Dis; 2021 Jun 03; 16(1):254. PubMed ID: 34082801
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  • 7. Effect of continuous glucose therapy begun in infancy on the long-term clinical course of patients with type I glycogen storage disease.
    Wolfsdorf JI, Crigler JF.
    J Pediatr Gastroenterol Nutr; 1999 Aug 03; 29(2):136-43. PubMed ID: 10435649
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  • 9. Cornstarch requirements of the adult glycogen storage disease Ia population: A retrospective review.
    Dahlberg KR, Ferrecchia IA, Dambska-Williams M, Resler TE, Ross KM, Butler GL, Kuo CL, Ryan PT, Weinstein DA.
    J Inherit Metab Dis; 2020 Mar 03; 43(2):269-278. PubMed ID: 31415093
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  • 11. Uncooked cornstarch--efficacy in type I glycogenosis.
    Lee PJ, Dixon MA, Leonard JV.
    Arch Dis Child; 1996 Jun 03; 74(6):546-7. PubMed ID: 8758135
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  • 13. Utilization of cornstarch in glycogen storage disease type Ia.
    Bodamer OA, Feillet F, Lane RE, Lee PJ, Dixon MA, Halliday D, Leonard JV.
    Eur J Gastroenterol Hepatol; 2002 Nov 03; 14(11):1251-6. PubMed ID: 12439121
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  • 14. Dietary exacerbation of metabolic stress leads to accelerated hepatic carcinogenesis in glycogen storage disease type Ia.
    Gjorgjieva M, Calderaro J, Monteillet L, Silva M, Raffin M, Brevet M, Romestaing C, Roussel D, Zucman-Rossi J, Mithieux G, Rajas F.
    J Hepatol; 2018 Nov 03; 69(5):1074-1087. PubMed ID: 30193922
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  • 15. Potential use of other starch sources in the treatment of glycogen storage disease type Ia - an in vitro study.
    Monteiro V, Colonetti K, Pagno CH, Schmidt HO, Sperb-Ludwig F, Oliveira BM, Poloni S, Rios AO, de Souza CFM, Schwartz IVD.
    Orphanet J Rare Dis; 2024 Jul 30; 19(1):283. PubMed ID: 39080776
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  • 16. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec 30; 93(12):1423-30. PubMed ID: 8245377
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  • 17. Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.
    Weinstein DA, Wolfsdorf JI.
    Eur J Pediatr; 2002 Oct 30; 161 Suppl 1():S35-9. PubMed ID: 12373568
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  • 18. Liver and liver cell transplantation for glycogen storage disease type IA.
    Muraca M, Burlina AB.
    Acta Gastroenterol Belg; 2005 Oct 30; 68(4):469-72. PubMed ID: 16433006
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  • 19. Endogenous Glucose Production in Patients With Glycogen Storage Disease Type Ia Estimated by Oral D-[6,6-2H2]-glucose.
    Rossi A, Oosterveer MH, van Dijk TH, Bleeker A, Koehorst M, Weinstein DA, Bakker BM, Derks TGJ.
    J Clin Endocrinol Metab; 2024 Jan 18; 109(2):389-401. PubMed ID: 37690115
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