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Journal Abstract Search

270 related items for PubMed ID: 5317551

  • 1. Glycogen storage disease in Israel. A clinical, biochemical and genetic study.
    Levin S, Moses SW, Chayoth R, Jagoda N, Steinitz K.
    Isr J Med Sci; 1967; 3(3):397-410. PubMed ID: 5317551
    [No Abstract] [Full Text] [Related]

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  • 4. Disorders of glycogen and lipid metabolism.
    DiMauro S, Eastwood AB.
    Adv Neurol; 1977; 17():123-42. PubMed ID: 142420
    [No Abstract] [Full Text] [Related]

  • 5. Diet and growth of children with glycogen storage disease Types I and III.
    Daeschel IE, Janick LS, Kramish MJ, Coleman RA.
    J Am Diet Assoc; 1983 Aug; 83(2):135-41. PubMed ID: 6409953
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  • 6. [Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
    Popovich IuG, Chibisov IV, Potapova-Vinogradova IN, Chistova LV.
    Pediatriia; 1988 Aug; (1):35-9. PubMed ID: 3163143
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  • 7. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM.
    Ann Clin Lab Sci; 1982 Aug; 12(6):431-8. PubMed ID: 6817693
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  • 8. Liver glycogenosis. A biochemical and ultrastructural study.
    De Bruijn WC, Fernandes J, Huber J, Koster JF.
    Pathol Eur; 1975 Aug; 10(1):3-15. PubMed ID: 170575
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  • 9. [Chemical study of the conformation of hepatic glycogen in two cases of glycogenosis].
    Benkoël L, Gulian JM, Chamlian A.
    Cell Mol Biol; 1984 Aug; 30(2):145-52. PubMed ID: 6585274
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  • 12. [Glycogen storage disease by amylo 1,6-glucosidase deficiency (author's transl)].
    Méndez Aparicio FM.
    An Esp Pediatr; 1980 Oct; 13(10):901-8. PubMed ID: 6937153
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  • 13. Parental genetic contribution to mode of presentation in Pompe disease.
    Cottrill CM, Johnson GL, Noonan JA.
    Pediatrics; 1987 Mar; 79(3):379-81. PubMed ID: 3469615
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  • 14. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Mar; 42(12):61-71. PubMed ID: 7011274
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  • 15. Glycogen metabolism and glycogen-storage diseases.
    Huijing F.
    Physiol Rev; 1975 Oct; 55(4):609-58. PubMed ID: 1103168
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  • 16. A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients.
    Parvari R, Moses S, Shen J, Hershkovitz E, Lerner A, Chen YT.
    Eur J Hum Genet; 1997 Oct; 5(5):266-70. PubMed ID: 9412782
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  • 17. Glycogen storage disease. (Report of three cases).
    Devi T, Mathew O.
    Indian Pediatr; 1971 Jan; 8(1):43-5. PubMed ID: 5284580
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  • 18. [2 cases of glycogen storage disease in twins].
    Nizankowska-Błaz T.
    Pediatr Pol; 1975 Aug; 50(8):1049-51. PubMed ID: 1057760
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  • 19. [Hereditary storage diseases of the liver (author's transl)].
    Schaub J.
    Leber Magen Darm; 1979 Sep; 9(5):227-34. PubMed ID: 392211
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  • 20. A family with Pompe's disease (glycogenesis type II).
    Lamabadusuriya SP, Canagarayar UT, Vijeyaratnam G.
    Ceylon Med J; 1979 Sep; 24(1-2):42-4. PubMed ID: 299071
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