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 *

232 related articles for article (PubMed ID: 580714)

  • 41. Quantitative histopathology in congenital myopathies.
    Micaglio G; Ceccato MB; Trevisan C; Angelini C
    Riv Neurol; 1987; 57(4):261-8. PubMed ID: 3317765
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [A case of myopathy with ulcerative colitis].
    Hasegawa H; Hasegawa K; Saito T; Kowa H; Nonaka I
    Rinsho Shinkeigaku; 1990 Feb; 30(2):184-8. PubMed ID: 2350931
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [An unusual myopathy: the so-called congenital fiber-type disproportion].
    Lössner J; Ziegan J; Oertel G
    Z Gesamte Inn Med; 1979 Nov; 34(22):685-7. PubMed ID: 549303
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Nemaline myopathy (congenital rod disease) - clinical picture, histology, and histochemistry].
    Voncina D; Tivadar I; Dekleva A
    Neurologija; 1978; 26(1-4):169-74. PubMed ID: 754016
    [No Abstract]   [Full Text] [Related]  

  • 45. Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.
    Kley RA; Hellenbroich Y; van der Ven PF; Fürst DO; Huebner A; Bruchertseifer V; Peters SA; Heyer CM; Kirschner J; Schröder R; Fischer D; Müller K; Tolksdorf K; Eger K; Germing A; Brodherr T; Reum C; Walter MC; Lochmüller H; Ketelsen UP; Vorgerd M
    Brain; 2007 Dec; 130(Pt 12):3250-64. PubMed ID: 18055494
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line.
    Pellegrini G; Barbieri S; Moggio M; Cheldi A; Scarlato G; Minetti C
    Neuropediatrics; 1985 Aug; 16(3):162-6. PubMed ID: 4047349
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Clinical and pathological studies on two patients with adult-onset nemaline myopathy].
    Maruyama T; Hanyu N; Maruyama K; Takeda S; Yanagisawa N; Nonaka I
    Rinsho Shinkeigaku; 1990 Jul; 30(7):738-44. PubMed ID: 2173650
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Fiber type disproportion in nemaline myopathy.
    Huang CC; Lee CC; Chen SS
    Zhonghua Yi Xue Za Zhi (Taipei); 1989 Apr; 43(4):229-32. PubMed ID: 2804774
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Congenital myopathies.
    Romero NB; Clarke NF
    Handb Clin Neurol; 2013; 113():1321-36. PubMed ID: 23622357
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.
    Biral D; Damiani E; Scarpini E; Bet L; Bresolin N; Moggio M; Pellegrini G; Barbieri S; Scarlato G
    Neurology; 1987 Oct; 37(10):1658-62. PubMed ID: 3309721
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Early infant death in nemaline (rod) myopathy.
    Eeg-Olofsson O; Henriksson KG; Thornell LE; Wesström G
    Brain Dev; 1983; 5(1):53-7. PubMed ID: 6846734
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Immunofluorescence microscopy of a myopathy. alpha-Actinin is a major constituent of nemaline rods.
    Jockusch BM; Veldman H; Griffiths GW; van Oost BA; Jennekens FG
    Exp Cell Res; 1980 Jun; 127(2):409-20. PubMed ID: 6991264
    [No Abstract]   [Full Text] [Related]  

  • 53. [Two adult cases of nemaline myopathy presenting different clinical symptoms and CT findings].
    Tajima Y; Yoshida A; Ura S
    No To Shinkei; 2001 Jul; 53(7):653-8. PubMed ID: 11517491
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities.
    Fukunaga H; Osame M; Igata A
    J Neurol Sci; 1980 May; 46(2):169-77. PubMed ID: 6247453
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.
    Berger J; Tarakci H; Berger S; Li M; Hall TE; Arner A; Currie PD
    Dis Model Mech; 2014 Dec; 7(12):1407-15. PubMed ID: 25288681
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Nemaline myopathy. The origin of nemaline structures.
    Gonatas NK; Shy GM; Godfrey EH
    N Engl J Med; 1966 Mar; 274(10):535-9. PubMed ID: 5908457
    [No Abstract]   [Full Text] [Related]  

  • 57. Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathies.
    Coërs C; Telerman-Toppet N; Gérard JM; Szliwowski H; Bethlem J; van Wijngaarden GK
    Neurology; 1976 Nov; 26(11):1046-53. PubMed ID: 988511
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotype.
    Madigan NN; Polzin MJ; Cui G; Liewluck T; Alsharabati MH; Klein CJ; Windebank AJ; Mer G; Milone M
    Acta Neuropathol Commun; 2021 Apr; 9(1):79. PubMed ID: 33926564
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Progression in nemaline myopathy.
    Nonaka I; Ishiura S; Arahata K; Ishibashi-Ueda H; Maruyama T; Ii K
    Acta Neuropathol; 1989; 78(5):484-91. PubMed ID: 2683560
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Unusual course of nemaline myopathy.
    Hausmanowa-Petrusewicz I; Fidziańska A; Badurska B
    Neuromuscul Disord; 1992; 2(5-6):413-8. PubMed ID: 1300189
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.