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Journal Abstract Search

162 related items for PubMed ID: 1057811

  • 1. Incidence of glycogen storage disease in the German Federal Republic.
    Schaub J, Bayerl P.
    Z Kinderheilkd; 1975 Aug 11; 120(2):79-85. PubMed ID: 1057811
    [Abstract] [Full Text] [Related]

  • 2. Radiography of glycogen storage diseases.
    Miller JH, Stanley P, Gates GF.
    AJR Am J Roentgenol; 1979 Mar 11; 132(3):379-87. PubMed ID: 106640
    [Abstract] [Full Text] [Related]

  • 3. Disorders of glycogen metabolism.
    Mahler RF.
    Clin Endocrinol Metab; 1976 Nov 11; 5(3):579-98. PubMed ID: 797481
    [No Abstract] [Full Text] [Related]

  • 4. [Hyperlipoproteinemia in glycogenosis and its treatment].
    Chibisov IV, Karmanskiĭ IM.
    Pediatriia; 1982 Feb 11; (2):6-9. PubMed ID: 6951139
    [No Abstract] [Full Text] [Related]

  • 5. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec 11; 93(12):1423-30. PubMed ID: 8245377
    [Abstract] [Full Text] [Related]

  • 6. Elevated serum biotinidase activity in hepatic glycogen storage disorders--a convenient biomarker.
    Paesold-Burda P, Baumgartner MR, Santer R, Bosshard NU, Steinmann B.
    J Inherit Metab Dis; 2007 Nov 11; 30(6):896-902. PubMed ID: 17994282
    [Abstract] [Full Text] [Related]

  • 7. Proceedings: Morphology of liver glycogenosis.
    de Bruijn WC, Fernandes J, Huber J, Koster JF.
    Arch Dis Child; 1975 Aug 11; 50(8):663-4. PubMed ID: 1060439
    [No Abstract] [Full Text] [Related]

  • 8. Liver-spleen scintigraphy in glycogen storage disease (glycogenoses).
    Heyman S.
    Clin Nucl Med; 1985 Dec 11; 10(12):839-43. PubMed ID: 3865755
    [Abstract] [Full Text] [Related]

  • 9. Glycogen metabolism and glycogen-storage diseases.
    Huijing F.
    Physiol Rev; 1975 Oct 11; 55(4):609-58. PubMed ID: 1103168
    [No Abstract] [Full Text] [Related]

  • 10. Hepatic ultrasound findings in the glycogen storage diseases.
    Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C.
    Br J Radiol; 1994 Nov 11; 67(803):1062-6. PubMed ID: 7820397
    [Abstract] [Full Text] [Related]

  • 11. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Nov 11; 42(12):61-71. PubMed ID: 7011274
    [Abstract] [Full Text] [Related]

  • 12. [Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
    Popovich IuG, Chibisov IV, Potapova-Vinogradova IN, Chistova LV.
    Pediatriia; 1988 Nov 11; (1):35-9. PubMed ID: 3163143
    [No Abstract] [Full Text] [Related]

  • 13.
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    [No Abstract] [Full Text] [Related]

  • 14. Diagnosis of hepatic glycogen storage disease patients with overlapping clinical symptoms by massively parallel sequencing: a systematic review of literature.
    Beyzaei Z, Geramizadeh B, Karimzadeh S.
    Orphanet J Rare Dis; 2020 Oct 14; 15(1):286. PubMed ID: 33054851
    [Abstract] [Full Text] [Related]

  • 15. [Hereditary storage diseases of the liver (author's transl)].
    Schaub J.
    Leber Magen Darm; 1979 Sep 14; 9(5):227-34. PubMed ID: 392211
    [Abstract] [Full Text] [Related]

  • 16. Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis.
    Slonim AE, Coleman RA, Moses S, Bashan N, Shipp E, Mushlin P.
    Metabolism; 1983 Jan 14; 32(1):70-4. PubMed ID: 6336817
    [Abstract] [Full Text] [Related]

  • 17. [A case of glycogenosis of type VI with associated de Toni-Debré-Fanconi syndromei1].
    Rossi LN, Bianchi GP.
    Minerva Pediatr; 1975 Jun 23; 27(22):1242-6. PubMed ID: 1056501
    [No Abstract] [Full Text] [Related]

  • 18. 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 23; 42(6):601-6. PubMed ID: 7634500
    [Abstract] [Full Text] [Related]

  • 19. [Chinese experts consensus on diagnosis and treatment of glycogen storage disease type Ⅱ in children].
    Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, the Society of Pediatrics, Chinese Medical Association, Society of Medical Genetics, Chinese Medical Association, Subspecialty Group of Rare Diseases, the Society of Pediatrics, Chinese Medical Association, Medical Genetics Branch of Beijing Medical Association, Beijing Rare Disease Diagnosis and Protection Association, China Alliance of Rare Diseases.
    Zhonghua Er Ke Za Zhi; 2021 Jun 02; 59(6):439-445. PubMed ID: 34102815
    [Abstract] [Full Text] [Related]

  • 20. The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.
    Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S.
    Mol Genet Metab; 2014 Nov 02; 113(3):171-6. PubMed ID: 25266922
    [Abstract] [Full Text] [Related]

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