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 *

116 related articles for article (PubMed ID: 7077346)

  • 21. Mitochondrial myopathy.
    Mechler F; Fawcett PR; Mastaglia FL; Hudgson P
    J Neurol Sci; 1981 May; 50(2):191-200. PubMed ID: 7229664
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial myopathy associated with Marfanoid features and multicores.
    Joyce DA; Mastaglia FL; Ojeda VJ; Spagnolo DV
    Aust N Z J Med; 1984 Aug; 14(4):495-9. PubMed ID: 6596064
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
    Berciano J; Gallardo E; Domínguez-Perles R; Gallardo E; García A; García-Barredo R; Combarros O; Infante J; Illa I
    J Neurol Neurosurg Psychiatry; 2008 Feb; 79(2):205-8. PubMed ID: 17698502
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biochemical, histological and electron microscopical study of experimentally induced cortisone myopathy.
    Luca N; Hategan D; Anghelescu N; Alexianu M; Petrovici A
    Neurol Psychiatr (Bucur); 1977; 15(1):57-63. PubMed ID: 877496
    [No Abstract]   [Full Text] [Related]  

  • 25. [Central core disease. Two cases with histoenzymology, electron microscopy and review of the literature (author's transl)].
    Pages A; Pages M
    Ann Pathol; 1981; 1(1):38-47. PubMed ID: 7018506
    [TBL] [Abstract][Full Text] [Related]  

  • 26. On a dominantly inherited myopathy with tubular aggregates.
    Martin JJ; Ceuterick C; Van Goethem G
    Neuromuscul Disord; 1997 Dec; 7(8):512-20. PubMed ID: 9447609
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Multicore disease in twins.
    Heffner R; Cohen M; Duffner P; Daigler G
    J Neurol Neurosurg Psychiatry; 1976 Jun; 39(6):602-6. PubMed ID: 985853
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new type of distal myopathy in two brothers.
    Kuhn E; Schröder JM
    J Neurol; 1981; 226(3):181-5. PubMed ID: 6172565
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Observations on central core disease.
    Bethlem J; van Wijngaarden GK; Meijer AE; Fleury P
    J Neurol Sci; 1971 Nov; 14(3):293-9. PubMed ID: 5135336
    [No Abstract]   [Full Text] [Related]  

  • 31. Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres.
    Bethlem J; van Gool J; Hülsmann WC; Meijer AE
    Brain; 1966 Sep; 89(3):569-88. PubMed ID: 4224150
    [No Abstract]   [Full Text] [Related]  

  • 32. Nemaline (rod) myopathy: the need for histochemical evaluation of affected families.
    Bender AN; Willner JP
    Ann Neurol; 1978 Jul; 4(1):37-42. PubMed ID: 697323
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Multicore myopathy: not always a benign entity.
    Shuaib A; Martin JM; Mitchell LB; Brownell AK
    Can J Neurol Sci; 1988 Feb; 15(1):10-4. PubMed ID: 3345455
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Type distribution of muscle fibres and their ultrastructure related to intracellular elemental composition as revealed by energy dispersive X-ray microanalysis. A study of multicore myopathy.
    Edström L; Mair WG; Wroblewski R; Hovmöller M; Malm G
    J Neurol Sci; 1986 Nov; 76(1):31-48. PubMed ID: 3783187
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chronic lactic acidosis in association with myopathy.
    Terlow MJ; Lake BD; Lloyd JK
    Arch Dis Child; 1973 Jun; 48(6):489-92. PubMed ID: 4712783
    [No Abstract]   [Full Text] [Related]  

  • 36. Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study.
    Kamieniecka Z
    Acta Neurol Scand; 1977 Jan; 55(1):57-75. PubMed ID: 65099
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [A case of mitochondrial myopathy with nemaline rods accompanied by a partial deficiency of cytochrome c oxidase].
    Kitagawa Y; Ishihara T; Koga Y; Hanada T; Irimajiri S
    Rinsho Shinkeigaku; 1988 Apr; 28(4):388-95. PubMed ID: 2850881
    [No Abstract]   [Full Text] [Related]  

  • 38. Severe neonatal centronuclear myopathy with autosomal dominant inheritance.
    Torres CF; Griggs RC; Goetz JP
    Arch Neurol; 1985 Oct; 42(10):1011-4. PubMed ID: 2994607
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Bethlem myopathy: early-onset benign autosomal dominant myopathy with contractures. Description of two new families.
    Merlini L; Morandi L; Granata C; Ballestrazzi A
    Neuromuscul Disord; 1994; 4(5-6):503-11. PubMed ID: 7881296
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Nemaline myopathy: a report of two siblings as evidence of autosomal recessive inheritance of the infantile type.
    Cartwright JD; Castle DJ; Duffield MG; Reef I
    Postgrad Med J; 1990 Nov; 66(781):962-4. PubMed ID: 2267214
    [TBL] [Abstract][Full Text] [Related]  

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