These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 6758769

  • 21. The effect of age on biochemical and morphological changes in the semitendinosus muscle of cattle with generalized glycogenosis type II.
    Howell JM, Dorling PR, Cook RD.
    Neuropathol Appl Neurobiol; 1984; 10(4):255-66. PubMed ID: 6435005
    [Abstract] [Full Text] [Related]

  • 22. Generalized glycogenosis in Brahman-derived breeds: diagnosis and prevalence in Argentina.
    Caffaro ME, Raschia MA, Amadio AF, Poli MA.
    Trop Anim Health Prod; 2020 Mar; 52(2):483-488. PubMed ID: 31377960
    [Abstract] [Full Text] [Related]

  • 23. An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type II.
    Van der Ploeg AT, Kroos MA, Swallow DM, Reuser AJ.
    Ann Hum Genet; 1989 May; 53(2):185-92. PubMed ID: 2688540
    [Abstract] [Full Text] [Related]

  • 24. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T, Sandig KR.
    Kinderarztl Prax; 1984 Aug; 52(8):377-82. PubMed ID: 6384623
    [No Abstract] [Full Text] [Related]

  • 25. Cell-free translation of human lysosomal alpha-glucosidase: evidence for reduced precursor synthesis in an adult patient with glycogenosis type II.
    van der Horst GT, Hoefsloot EH, Kroos MA, Reuser AJ.
    Biochim Biophys Acta; 1987 Nov 20; 910(2):123-9. PubMed ID: 3315002
    [Abstract] [Full Text] [Related]

  • 26. A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies.
    Loonen MC, Busch HF, Koster JF, Martin JJ, Niermeijer MF, Schram AW, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM.
    Neurology; 1981 Oct 20; 31(10):1209-16. PubMed ID: 6810200
    [Abstract] [Full Text] [Related]

  • 27. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls].
    Matsuoka Y, Hirayama M, Senda Y, Matsui T.
    Rinsho Shinkeigaku; 1985 Jan 20; 25(1):39-45. PubMed ID: 3922655
    [No Abstract] [Full Text] [Related]

  • 28. [Molecular pathology and gene diagnosis of muscle glycogenosis].
    Suzuki Y.
    Nihon Rinsho; 1997 Dec 20; 55(12):3302-6. PubMed ID: 9436455
    [Abstract] [Full Text] [Related]

  • 29. Haemopoietic chimaerism: a complication in heterozygote detection tests for inherited defects in cattle.
    Healy PJ, Dennis JA, Nicholls PJ, Reichmann KG.
    Anim Genet; 1994 Feb 20; 25(1):1-6. PubMed ID: 8161014
    [Abstract] [Full Text] [Related]

  • 30. Genotyping glycogen storage disease type II and type V in cattle reared in the Czech Republic.
    Cítek J, Rehout V, Vecerek L, Hájková J.
    J Vet Med A Physiol Pathol Clin Med; 2007 Jun 20; 54(5):257-9. PubMed ID: 17523960
    [Abstract] [Full Text] [Related]

  • 31. Glycogen storage diseases in animals and their potential value as models of human disease.
    Walvoort HC.
    J Inherit Metab Dis; 1983 Jun 20; 6(1):3-16. PubMed ID: 6408305
    [Abstract] [Full Text] [Related]

  • 32. Changes in nervous tissue in bovine generalized glycogenosis type II.
    Cook RD, Howell JM, Dorling PR, Richards RB.
    Neuropathol Appl Neurobiol; 1982 Jun 20; 8(2):95-107. PubMed ID: 6954372
    [Abstract] [Full Text] [Related]

  • 33. A sensitive semi-automated kinetic assay of alpha-D-glucosidase for the prenatal diagnosis of type 2 glycogenosis (Pompe's disease).
    Blau K.
    J Inherit Metab Dis; 1978 Jun 20; 1(3):85-8. PubMed ID: 116083
    [Abstract] [Full Text] [Related]

  • 34. Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation.
    Ausems MG, Wokke JH, Reuser AJ, van Diggelen OP.
    Neurology; 2001 Nov 27; 57(10):1938. PubMed ID: 11723305
    [No Abstract] [Full Text] [Related]

  • 35. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H, Goebel HH, Stefan H, Seidel D, Kohlschütter A.
    J Clin Chem Clin Biochem; 1977 Dec 27; 15(12):705-8. PubMed ID: 342670
    [No Abstract] [Full Text] [Related]

  • 36. Genotyping Brahman cattle for generalised glycogenosis.
    Dennis JA, Healy PJ, Reichmann KG.
    Aust Vet J; 2002 May 27; 80(5):286-91. PubMed ID: 12074310
    [Abstract] [Full Text] [Related]

  • 37. Glycogen-storage diseases of muscle: genetic problems.
    Rowland LP, DiMauro S.
    Res Publ Assoc Res Nerv Ment Dis; 1983 May 27; 60():239-54. PubMed ID: 6337394
    [No Abstract] [Full Text] [Related]

  • 38. A family with pseudodeficiency of acid alpha-glucosidase.
    Nishimoto J, Inui K, Okada S, Ishigami W, Hirota S, Yamano T, Yabuuchi H.
    Clin Genet; 1988 Apr 27; 33(4):254-61. PubMed ID: 3282727
    [Abstract] [Full Text] [Related]

  • 39. Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease).
    Blom W, Luteyn JC, Kelholt-Dijkman HH, Huijmans JG, Loonen MC.
    Clin Chim Acta; 1983 Oct 31; 134(1-2):221-7. PubMed ID: 6418415
    [No Abstract] [Full Text] [Related]

  • 40. A new mutant of Japanese quail (Coturnix coturnix japonica) characterized by generalized glycogenosis.
    Nunoya T, Tajima M, Mizutani M.
    Lab Anim; 1983 Apr 31; 17(2):138-42. PubMed ID: 6575219
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.