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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 125955)

  • 21. [Hepatic forms of glycogenosis - clinical and biochemical findings in 15 cases].
    Pronicka E; Pieniazek D; Miłoszewska E; Gruszczyńska B; Moszczyńska A
    Pediatr Pol; 1983 May; 58(5):437-45. PubMed ID: 6579490
    [No Abstract]   [Full Text] [Related]  

  • 22. [Results of clinical, biochemical, light-microscopical and ultrastructural studies of childhood glycogenosis in two brothers and their sister (author's transl)].
    Ketelsen UP; Beckmann R; Nolte J; Menzel K
    Z Kinderheilkd; 1973 Dec; 116(1):23-41. PubMed ID: 4272442
    [No Abstract]   [Full Text] [Related]  

  • 23. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-1986. A 29-year-old woman with slowly progressive proximal-muscle weakness.
    N Engl J Med; 1986 Sep; 315(11):694-701. PubMed ID: 3092049
    [No Abstract]   [Full Text] [Related]  

  • 24. Acid maltase deficiency in childhood. Early diagnosis and clinical follow-up of late-onset glycogen storage disease type II.
    di Fiore MT; Manfredi R; Marri L; Zucchini A; Azzaroli L; Manfredi G
    Acta Neurol (Napoli); 1993 Aug; 15(4):258-67. PubMed ID: 8249669
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Infantile acid maltase deficiency. III. Ultrastructure of metachromatic material and glycogen in muscle fibers.
    Griffin JL
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984; 45(1):51-61. PubMed ID: 6199887
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease).
    Pokorny KS; Ritch R; Friedman AH; Desnick RJ
    Invest Ophthalmol Vis Sci; 1982 Jan; 22(1):25-31. PubMed ID: 6948796
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Immunochemical study of acid alpha-1,4-glucosidase in 7 patients with type II glycogenosis].
    Bienvenu J; Mathieu M; Collombel C; Baltassat P; Divry P; Dorche C; Cotte J
    Pediatrie; 1979 Sep; 34(6):659-76. PubMed ID: 388338
    [No Abstract]   [Full Text] [Related]  

  • 28. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A; Massin M; Lombet J; Grattagliano B; Soyeur D; Rigo J; Koulischer L; Van Hoof F
    Am J Med Genet; 1997 Oct; 72(2):135-42. PubMed ID: 9382133
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Generalized glycogenosis in beef shorthorn cattle--heterozygote detection.
    Jolly RD; Van-de-Water NS; Richards RB; Dorling PR
    Aust J Exp Biol Med Sci; 1977 Apr; 55(2):14U-50. PubMed ID: 20072
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
    Meola G; Scarpini E; Manfredi L; Velicogna M; Pellegrini G; Redi CA; Scarlato G
    Basic Appl Histochem; 1984; 28(3):245-55. PubMed ID: 6440527
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid alpha-glucosidase deficiency).
    Walvoort HC; Slee RG; Sluis KJ; Koster JF; Reuser AJ
    Am J Med Genet; 1984 Nov; 19(3):589-98. PubMed ID: 6391168
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Cardiomuscular lysosomal glycogenosis in adults without known enzyme deficiency. A cause of familial myocardiopathy and lysosomal glycogen overload with normal acid maltase].
    Bru P; Pellissier JF; Gatau-Pelanchon J; Faugère G; de Barsy T; Levy S; Gérard R
    Arch Mal Coeur Vaiss; 1988 Jan; 81(1):109-14. PubMed ID: 3130016
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Severe form of juvenile type II glycogenosis in a compound-heterozygous boy (Tyr-292--> Cys/Arg-854-->Stop)].
    Castro-Gago M; Eirís-Puñal J; Rodríguez-Núñez A; Pintos-Martínez E; Benlloch-Marín T; Barros-Angueira F
    Rev Neurol; 1999 Jul 1-15; 29(1):46-9. PubMed ID: 10528311
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Acid maltase deficiency myopathy infantile and adult forms (author's transl)].
    Saenz Lope E; Cocero Oviedo E; Ricoy Campo JR; Benlloch T
    Arch Neurobiol (Madr); 1981; 44(1):49-62. PubMed ID: 6784694
    [No Abstract]   [Full Text] [Related]  

  • 35. Acid maltase deficiency (type II glycogenosis). Morphological and biochemical study of a childhood phenotype.
    Martin JJ; De Barsy T; De Schrijver ; Leroy JG; Palladini G
    J Neurol Sci; 1976 Nov; 30(1):155-66. PubMed ID: 1068222
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].
    Nakagawa M; Nakazato O; Osame M; Nakashima H; Igata A
    Rinsho Shinkeigaku; 1982 Jan; 22(1):57-65. PubMed ID: 6807597
    [No Abstract]   [Full Text] [Related]  

  • 37. Electromyography in type II glycogenosis.
    Lenard HG; Schaub J; Keutel J; Osang M
    Neuropadiatrie; 1974 Nov; 5(4):410-24. PubMed ID: 4534311
    [No Abstract]   [Full Text] [Related]  

  • 38. The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult.
    Schlenska GK; Heene R; Spalke G; Seiler D
    J Neurol; 1976 Jun; 212(3):237-52. PubMed ID: 58976
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. alpha-Glucosidase in Pompe's disease.
    Broadhead DM; Butterworth J
    J Inherit Metab Dis; 1978; 1(4):153-4. PubMed ID: 41974
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.