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 *

58 related articles for article (PubMed ID: 5360953)

  • 21. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance].
    Grinio LP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1621-4. PubMed ID: 7324662
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Localized continuous muscular activity secondary to radioculopathy S1 with shin hypertrophy and focal myositis].
    Pérez Errazquin F; Quesada J; Chinchón I; Segura D; Bautista J
    Neurologia; 1999 Apr; 14(4):193-5. PubMed ID: 10363496
    [No Abstract]   [Full Text] [Related]  

  • 23. [Clinical study of one family of central core disease (author's transl)].
    Fukunaga H; Kitano H; Tokunaga H; Okatsu Y; Igata A
    Rinsho Shinkeigaku; 1980 Apr; 20(4):248-54. PubMed ID: 7408328
    [No Abstract]   [Full Text] [Related]  

  • 24. [Glycogenosis type III with peripheral nerve disorder and muscular hypertrophy in an adult].
    Hokezu Y; Nagamatsu K; Nakagawa M; Osame M; Ohnishi A
    Rinsho Shinkeigaku; 1983 Jun; 23(6):473-9. PubMed ID: 6317246
    [No Abstract]   [Full Text] [Related]  

  • 25. [Karyologic studies in muscle diseases].
    Badurska B; Prot J
    Pol Tyg Lek; 1969 Mar; 24(13):476-8. PubMed ID: 5790554
    [No Abstract]   [Full Text] [Related]  

  • 26. [Gene errors in muscular diseases].
    Somer H; Auranen M
    Duodecim; 1997; 113(18):1795-802. PubMed ID: 10892072
    [No Abstract]   [Full Text] [Related]  

  • 27. [Congenital ophthalmomyopathy].
    Frazzetto F; Streiff EB; Forssmann WG
    Ann Ocul (Paris); 1969 Dec; 202(12):1217-53. PubMed ID: 5404748
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. [Progressive chronic ophthalmoplegia. (Clinical, biochemical, histological and electromyographic findings in a family with primary ocular myopathy)].
    Bernardi G; Bonanni R; Vasconetto C
    Atti Accad Fisiocrit Siena Med Fis; 1968; 17(2):1093-105. PubMed ID: 5760318
    [No Abstract]   [Full Text] [Related]  

  • 30. Muscle hypertrophy secondary to the tethered cord syndrome.
    Bertorini T; Woodhouse C; Horner L
    Muscle Nerve; 1994 Mar; 17(3):331-5. PubMed ID: 8107711
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Consequences of mutations within the C terminus of the FHL1 gene.
    Schoser B; Goebel HH; Janisch I; Quasthoff S; Rother J; Bergmann M; Müller-Felber W; Windpassinger C
    Neurology; 2009 Aug; 73(7):543-51. PubMed ID: 19687455
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Changes in the activity of blood serum enzymes in relatives of children with myopathy].
    Grinio LP
    Vopr Med Khim; 1966; 12(6):600-3. PubMed ID: 6000902
    [No Abstract]   [Full Text] [Related]  

  • 33. [Hypertrophia musculorum vera].
    Cosi V; Tonali P
    Riv Neurobiol; 1965; 11(4):791-812. PubMed ID: 5888029
    [No Abstract]   [Full Text] [Related]  

  • 34. Molecular, cellular and physiological investigation of myostatin propeptide-mediated muscle growth in adult mice.
    Matsakas A; Foster K; Otto A; Macharia R; Elashry MI; Feist S; Graham I; Foster H; Yaworsky P; Walsh F; Dickson G; Patel K
    Neuromuscul Disord; 2009 Jul; 19(7):489-99. PubMed ID: 19541486
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)].
    Fujimori N; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1980 Jun; 20(6):423-9. PubMed ID: 7408341
    [No Abstract]   [Full Text] [Related]  

  • 36. [A case of myotubular myopathy with autosomal dominant inheritance (author's transl)].
    Wakabayashi Y; Arimura Y; Sawaguchi Y; Koike H; Yoshino Y
    No To Shinkei; 1980 Jul; 32(7):715-22. PubMed ID: 7407023
    [No Abstract]   [Full Text] [Related]  

  • 37. A novel missense mutation in the caveolin-3 gene in rippling muscle disease.
    Lorenzoni PJ; Scola RH; Vieira N; Vainzof M; Carsten AL; Werneck LC
    Muscle Nerve; 2007 Aug; 36(2):258-60. PubMed ID: 17405141
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rippling muscle disease.
    Roberts HL; Day B; Lo H; McLean C; North K
    J Clin Neurosci; 2006 Jun; 13(5):576-8. PubMed ID: 16723230
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Non-muscular aspects of muscular disorders in children.
    Spiro AJ
    Pediatr Ann; 1984 Feb; 13(2):117-8, 120, 122. PubMed ID: 6200822
    [No Abstract]   [Full Text] [Related]  

  • 40. Hereditary myopathies.
    Emery AE
    Clin Orthop Relat Res; 1964; 33():164-73. PubMed ID: 5889019
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.