BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 17540597)

  • 1. Muscular glycogen storage diseases without increased glycogen content on histopathological examination.
    Hoeksma M; den Dunnen WF; Niezen-Koning KE; van Diggelen OP; van Spronsen FJ
    Mol Genet Metab; 2007 Aug; 91(4):370-3. PubMed ID: 17540597
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An unusual pathologic feature associated with dermatomyositis.
    Sampson JB; Chin SS; Clayton FC; Pestronk A; Swoboda KJ; Flanigan KM
    Neuromuscul Disord; 2006 Jun; 16(6):391-3. PubMed ID: 16697198
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.
    Iwamasa T; Ninomiya N; Fukuda S; Hamada T; Hirashima M; Osame M
    Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polyglucosan body disease myopathy: an unusual presentation.
    Vucic S; Pamphlett R; Wills EJ; Yiannikas C
    Muscle Nerve; 2007 Apr; 35(4):536-9. PubMed ID: 17221878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Study of human muscle biopsies with muscle glycogen storage diseases using 1H nuclear magnetic resonance spectroscopy (NMRS)--analysis of perchloric acid extracts of muscles].
    Sugie H; Sugie Y; Ito M; Tsurui S
    Rinsho Shinkeigaku; 1991 Jun; 31(6):616-8. PubMed ID: 1657479
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparative skeletal muscle histopathologic and ultrastructural features in two forms of polysaccharide storage myopathy in horses.
    McCue ME; Armién AG; Lucio M; Mickelson JR; Valberg SJ
    Vet Pathol; 2009 Nov; 46(6):1281-91. PubMed ID: 19605906
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disorders of glycogen metabolism of muscle.
    DiMauro S; Bresolin N; Hays AP
    CRC Crit Rev Clin Neurobiol; 1984; 1(2):83-116. PubMed ID: 6242726
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Electron microscopic study of liver and muscles in two cases of type 3 glycogenosis].
    Leung TK; Feroldi J
    Pathol Eur; 1972; 7(2):112-25. PubMed ID: 4508390
    [No Abstract]   [Full Text] [Related]  

  • 9. Ubiquitin expression in muscle from horses with polysaccharide storage myopathy.
    Valentine BA; Flint TH; Fischer KA
    Vet Pathol; 2006 May; 43(3):270-5. PubMed ID: 16672573
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Skin biopsy findings in glycogenosis III: clinical, biochemical, and electrophysiological correlations.
    Sancho S; Navarro C; Fernández JM; Domínguez C; Ortega A; Roig M; Cervera C
    Ann Neurol; 1990 May; 27(5):480-6. PubMed ID: 2360788
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polysaccharide storage myopathy in Cob Normand draft horses.
    Larcher T; Herszberg B; Molon-Noblot S; Guigand L; Chaffaux S; Guerin G; Cherel Y
    Vet Pathol; 2008 Mar; 45(2):154-8. PubMed ID: 18424827
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Development of polyglucosan inclusions in skeletal muscle.
    Valentine BA; Cooper BJ
    Neuromuscul Disord; 2006 Oct; 16(9-10):603-7. PubMed ID: 16919952
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Study of skeletal muscle glycogenolysis and glycolysis in chronic steroid myopathy, non-steroid histochemical type-2 fiber atrophy, and denervation.
    Danon MJ; Schliselfeld LH
    Clin Biochem; 2007 Jan; 40(1-2):46-51. PubMed ID: 17054931
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited.
    Schoser BG; Müller-Höcker J; Horvath R; Gempel K; Pongratz D; Lochmüller H; Müller-Felber W
    Neuropathol Appl Neurobiol; 2007 Oct; 33(5):544-59. PubMed ID: 17573812
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neonatal neuromuscular variant of glycogen storage disease type IV: histopathological findings leading to the diagnosis.
    Konstantinidou AE; Anninos H; Gyftodimou Y; Petersen MB; Karadimas C; Fotopoulos S; Paraskevakou H; Akman HO; Dimauro S; Patsouris E
    Histopathology; 2006 Jun; 48(7):878-80. PubMed ID: 16722943
    [No Abstract]   [Full Text] [Related]  

  • 16. Asymptomatic or minimally symptomatic hyperCKemia: histopathologic correlates.
    Dabby R; Sadeh M; Herman O; Berger E; Watemberg N; Hayek S; Jossiphov J; Nevo Y
    Isr Med Assoc J; 2006 Feb; 8(2):110-3. PubMed ID: 16544734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pseudoscleroderma concomitant with a muscular glycogenosis of unknown enzymatic defect.
    Jablonska S; Stachow A
    Acta Derm Venereol; 1972; 52(5):379-85. PubMed ID: 4117086
    [No Abstract]   [Full Text] [Related]  

  • 18. Glycogen storage myopathy with abnormal lactate dehydrogenase.
    Nagata N; Miike T; Matsuda I; Shikama H; Tokumitsu Y; Ui M
    Neuropediatrics; 1982 May; 13(2):103-7. PubMed ID: 6957732
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Delayed or late-onset type II glycogenosis with globular inclusions.
    Sharma MC; Schultze C; von Moers A; Stoltenburg-Didinger G; Shin YS; Podskarbi T; Isenhardt K; Tews DS; Goebel HH
    Acta Neuropathol; 2005 Aug; 110(2):151-7. PubMed ID: 15986226
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparison of histopathologic criteria and skeletal muscle fixation techniques for the diagnosis of polysaccharide storage myopathy in horses.
    Firshman AM; Valberg SJ; Bender JB; Annandale EJ; Hayden DW
    Vet Pathol; 2006 May; 43(3):257-69. PubMed ID: 16672572
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.