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 *

119 related articles for article (PubMed ID: 3144876)

  • 61. [Distal and congenital myopathy with hypertrophy of the calves. Presence of mitochondrial anomalies].
    Lapresle J; Fardeau M; Godet-Guillain J
    J Neurol Sci; 1972 Sep; 17(1):87-102. PubMed ID: 4342520
    [No Abstract]   [Full Text] [Related]  

  • 62. Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature.
    Schochet SS; Zellweger H; Ionasescu V; McCormick WF
    J Neurol Sci; 1972 Jun; 16(2):215-28. PubMed ID: 5037445
    [No Abstract]   [Full Text] [Related]  

  • 63. Pleocore disease. Multi-minicore disease and focal loss of cross striations.
    Martin JJ; Bruyland M; Busch HF; Farriaux JP; Krivosic I; Ceuterick C
    Acta Neuropathol; 1986; 72(2):142-9. PubMed ID: 3825514
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Histochemistry and electron microscopy of muscle fibres in a case of congenital paramyotonia.
    Schiffer D; Giordana MT; Monga G; Mollo F
    J Neurol; 1976 Jan; 211(2):125-33. PubMed ID: 55468
    [TBL] [Abstract][Full Text] [Related]  

  • 65. 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]  

  • 66. 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]  

  • 67. Electrophysiological signs of myopathy as related with muscle biopsy.
    Buchthal F
    Acta Neurol (Napoli); 1977; 32(1):1-29. PubMed ID: 855688
    [No Abstract]   [Full Text] [Related]  

  • 68. Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosis.
    Ricoy JR; Cabello A
    J Neurol Neurosurg Psychiatry; 1985 Feb; 48(2):167-71. PubMed ID: 3981176
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy).
    Ohtaki E; Yamaguchi Y; Yamashita Y; Matsuishi T; Terasawa K; Katafuchi Y; Nonaka I
    Brain Dev; 1990; 12(4):427-30. PubMed ID: 2240464
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Pathology of congenital nemaline myopathy. A follow-up study.
    Wallgren-Pettersson C; Rapola J; Donner M
    J Neurol Sci; 1988 Feb; 83(2-3):243-57. PubMed ID: 3356991
    [TBL] [Abstract][Full Text] [Related]  

  • 71. [4 cases of congenital disproportion of histochemical types of muscle fibers].
    Bramini M; Carboni P; Giacanelli M; D'Amico A
    Riv Neurobiol; 1981; 27(34):771-5. PubMed ID: 7052689
    [No Abstract]   [Full Text] [Related]  

  • 72. Infantile centronuclear myopathy. Evidence suggesting incomplete innervation.
    Elder GB; Dean D; McComas AJ; Paes B; DeSa D
    J Neurol Sci; 1983 Jul; 60(1):79-88. PubMed ID: 6875615
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type.
    Gibbels E; Kellermann K; Schädlich HJ; Adams R; Haupt WF
    Acta Neuropathol; 1992; 83(4):371-8. PubMed ID: 1575014
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Congenital Lambert-Eaton myasthenic syndrome.
    Bady B; Chauplannaz G; Carrier H
    J Neurol Neurosurg Psychiatry; 1987 Apr; 50(4):476-8. PubMed ID: 3035103
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement.
    Lamminen AE
    Br J Radiol; 1990 Dec; 63(756):946-50. PubMed ID: 2268764
    [TBL] [Abstract][Full Text] [Related]  

  • 76. ["Central core" myopathy: report of a case].
    Werneck LC; Silvado CE
    Arq Neuropsiquiatr; 1981 Jun; 39(2):230-6. PubMed ID: 7283803
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [Study of a new observation of "nemaline myopathy". II. Ultrastructural findings].
    Fardeau M
    Acta Neuropathol; 1969; 13(3):250-66. PubMed ID: 4185117
    [No Abstract]   [Full Text] [Related]  

  • 78. Nemaline myopathy: comparative muscle histochemistry in the severe neonatal, moderate congenital, and adult-onset forms.
    Shimomura C; Nonaka I
    Pediatr Neurol; 1989; 5(1):25-31. PubMed ID: 2712935
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Pathology of the muscular dystrophies and the congenital nonprogressive myopathies.
    Armbrustmacher VW
    Pathol Annu; 1980; 15(Pt 1):301-33. PubMed ID: 7443308
    [No Abstract]   [Full Text] [Related]  

  • 80. [Centronuclear myopathy. Apropos of a new case].
    Dubois B; Martin JJ; Develter S; Guérin M; Loeuille GA; Debeugny P; Farriaux JP
    Sem Hop; 1983 Feb; 59(8):561-5. PubMed ID: 6302904
    [TBL] [Abstract][Full Text] [Related]  

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