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 *

191 related articles for article (PubMed ID: 6543897)

  • 1. Unclassified familial myopathy resembling Steinert disease, without myotonia.
    Telerman-Toppet N; Khoubesserian P; Bacq M; Durdu J; Lambelin D; Lousberg G; Coërs C
    Muscle Nerve; 1984; 7(6):439-41. PubMed ID: 6543897
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The clinical and myopathological features of oculopharyngodistal myopathy in a Chinese family.
    Lu H; Luan X; Yuan Y; Dong M; Sun W; Yan C
    Neuropathology; 2008 Dec; 28(6):599-603. PubMed ID: 18503509
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial myopathy associated with tubular aggregates--report of two siblings].
    Ikeuchi T; Anezaki T; Ishiguro H; Tanaka M; Tanaka K; Tsuji S
    Rinsho Shinkeigaku; 1995 Sep; 35(9):1016-20. PubMed ID: 8565338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial form of centronuclear myopathy in the adult].
    Pépin B; Mikol J; Goldstein B; Haguenau M; Godlewski S
    Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Myotonic dystrophy-like disease in a dog.
    Simpson ST; Braund KG
    J Am Vet Med Assoc; 1985 Mar; 186(5):495-8. PubMed ID: 3972711
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship.
    Horowitz SH; Schmalbruch H
    Muscle Nerve; 1994 Feb; 17(2):151-60. PubMed ID: 8114783
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial myalgic myopathy.
    Roy EP; Riggs JE; Crosby TW; Gutmann L; Schochet SS
    W V Med J; 1988 Oct; 84(10):456-9. PubMed ID: 3188494
    [No Abstract]   [Full Text] [Related]  

  • 8. Malignant hyperpyrexia myopathy.
    Harriman DG; Sumner DW; Ellis FR
    Q J Med; 1973 Oct; 42(168):639-64. PubMed ID: 4802524
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hreditary myopathies].
    Kuhn E
    Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097
    [No Abstract]   [Full Text] [Related]  

  • 10. [A case of myotonic dystrophy showing proximal dominant muscle involvement but not myotonia].
    Mihori A; Miyauchi H; Kaneda K; Nakayama M; Ono S; Shimizu N
    Rinsho Shinkeigaku; 1999 Apr; 39(4):461-4. PubMed ID: 10391974
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
    Rosing HS; Hopkins LC; Wallace DC; Epstein CM; Weidenheim K
    Ann Neurol; 1985 Mar; 17(3):228-37. PubMed ID: 3922281
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myotubular myopathy associated with cataract and electrical myotonia.
    Hawkes CH; Absolon MJ
    J Neurol Neurosurg Psychiatry; 1975 Aug; 38(8):761-4. PubMed ID: 1185197
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
    Le Ber I; Martinez M; Campion D; Laquerrière A; Bétard C; Bassez G; Girard C; Saugier-Veber P; Raux G; Sergeant N; Magnier P; Maisonobe T; Eymard B; Duyckaerts C; Delacourte A; Frebourg T; Hannequin D
    Brain; 2004 Sep; 127(Pt 9):1979-92. PubMed ID: 15215218
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial myopathy with exclusively cardiac clinical expression].
    Morand P; Bienvenu P; Daumas PL; Kieffer A; Muh JP; Raynaud R
    Arch Mal Coeur Vaiss; 1977 Oct; 70(10):1097-103. PubMed ID: 413519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sarcoid myopathy presenting with diaphragm weakness.
    Dewberry RG; Schneider BF; Cale WF; Phillips LH
    Muscle Nerve; 1993 Aug; 16(8):832-5. PubMed ID: 8332135
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cardiac pathology in chronic myopathy, with particular reference to dystrophia myotonica.
    Franks AJ
    J Pathol; 1978 Aug; 125(4):213-7. PubMed ID: 722403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene.
    Bergman JE; Veenstra-Knol HE; van Essen AJ; van Ravenswaaij CM; den Dunnen WF; van den Wijngaard A; van Tintelen JP
    Eur J Med Genet; 2007; 50(5):355-66. PubMed ID: 17720647
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Proximal myotonial myopathy (PROMM): clinical and histology study].
    Bassez G; Attarian S; Laforêt P; Azulay JP; Rouche A; Ferrer X; Urtizberea JA; Pellissier JF; Duboc D; Fardeau M; Pouget J; Eymard B
    Rev Neurol (Paris); 2001 Feb; 157(2):209-18. PubMed ID: 11283467
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical analysis of familial forms of myasthenia].
    Strokov IA; Verbitskiĭ AM; Kvirkveliia NB; Gekht BM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):321-6. PubMed ID: 3705835
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.