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Journal Abstract Search

106 related items for PubMed ID: 7049057

  • 1. Reversal of debrancher deficiency myopathy by the use of high-protein nutrition.
    Slonim AE, Weisberg C, Benke P, Evans OB, Burr IM.
    Ann Neurol; 1982 Apr; 11(4):420-2. PubMed ID: 7049057
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  • 2. Diet therapy in severe clinical expression of debrancher deficiency.
    Azael Meza A, Ayub M, Cantú JM, Flores J.
    Arch Invest Med (Mex); 1991 Apr; 22(3-4):285-8. PubMed ID: 1844114
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  • 3. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec; 93(12):1423-30. PubMed ID: 8245377
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  • 4. [Continuous nocturnal intragastric feeding in glycogenosis type I and III].
    de Parscau L, Guibaud P, Hermier M, François R.
    Pediatrie; 1986 Dec; 41(3):197-203. PubMed ID: 3095784
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  • 11. Nocturnal intragastric therapy in type I glycogen storage disease: effect on hormonal and amino acid metabolism.
    Slonim AE, Lacy WW, Terry A, Greene HL, Burr IM.
    Metabolism; 1979 Jul; 28(7):707-15. PubMed ID: 286865
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  • 12. Low level of fasting plasma mannose in a child with glycogen storage disease type 0 (liver glycogen synthase deficiency).
    Miwa I, Taguchi T, Asano H, Murata T, Yorifuji T, Nagasaka H, Takatani T.
    Clin Chim Acta; 2010 Jul 04; 411(13-14):998-9. PubMed ID: 20331987
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  • 13. [Treatment of glycogenosis type III with total parenteral nutrition, continuous intragastric infusion and D-thyroxine].
    Böhles H, Dick W, Scharf J.
    Infusionsther Klin Ernahr; 1982 Aug 04; 9(4):160-1. PubMed ID: 6813261
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  • 14. [Metabolic adaptation in the fasting test in children with glycogenoses types III and IV].
    Bührdel P, Böhme HJ, Hubald J.
    Kinderarztl Prax; 1987 Nov 04; 55(11):543-8. PubMed ID: 3481641
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  • 15. 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 04; 70(6):638-41. PubMed ID: 21857385
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  • 18. Glycogen storage disease type I and III and pyruvate carboxylase deficiency: results of long-term treatment with uncooked cornstarch.
    Ullrich K, Schmidt H, van Teeffelen-Heithoff A.
    Acta Paediatr Scand; 1988 Jul 04; 77(4):531-6. PubMed ID: 3134793
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  • 19. [Forbes-Cori disease: reversible worsening in a case with non-evolutive neuromuscular disorder].
    Martínez Matos JA, Vila Duplá MJ, Montero J, Ferrer I, Baguñá J, Peres Serra J.
    Neurologia; 1987 Jul 04; 2(2):75-80. PubMed ID: 3078946
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