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 *

113 related articles for article (PubMed ID: 7249470)

  • 41. [Dystroglycan linkage and muscular dystrophy].
    Shimizu T
    Rinsho Shinkeigaku; 2002 Nov; 42(11):1091-4. PubMed ID: 12784674
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Causes of death in Fukuyama congenital muscular dystrophy].
    Ishihara T; Yoshitake S; Aoyagi T; Nonaka I; Sugita H
    Rinsho Shinkeigaku; 1984 Oct; 24(10):968-74. PubMed ID: 6518697
    [No Abstract]   [Full Text] [Related]  

  • 43. [Updates in muscular dystrophies].
    Erazo-Torricelli R
    Rev Neurol; 2004 Nov 1-15; 39(9):860-71. PubMed ID: 15543503
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Becker muscular dystrophy: clinical analysis, genetic and pathologic correlations].
    Colomer J
    Rev Neurol; 1995; 23 Suppl 3():S408-9. PubMed ID: 7497323
    [No Abstract]   [Full Text] [Related]  

  • 45. EMG and nerve conduction studies in children with congenital muscular dystrophy.
    Quijano-Roy S; Renault F; Romero N; Guicheney P; Fardeau M; Estournet B
    Muscle Nerve; 2004 Feb; 29(2):292-9. PubMed ID: 14755496
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Quantitative electromyography. Its application to progressive muscular dystrophy.
    Hirose K; Uono M; Sobue I
    Electromyogr Clin Neurophysiol; 1974; 14(4):355-63. PubMed ID: 4452339
    [No Abstract]   [Full Text] [Related]  

  • 47. [Masticatory performance in patients with progressive muscular dystrophy (author's transl)].
    Hamada T; Imada K; Kobayashi M; Yamada S
    Hiroshima Daigaku Shigaku Zasshi; 1976; 8(1):61-4. PubMed ID: 1069806
    [No Abstract]   [Full Text] [Related]  

  • 48. Is the central nervous system ever involved in muscular dystrophy?
    Sen S; Chakravarty A
    J Assoc Physicians India; 1976 Aug; 24(8):477-81. PubMed ID: 1025129
    [No Abstract]   [Full Text] [Related]  

  • 49. [Intelligence scale and the electroencephalogram in progressive muscular dystrophy].
    Tomonaga M; Muro T; Kito S
    Iryo; 1967 Jul; 21(7):800-6. PubMed ID: 5582475
    [No Abstract]   [Full Text] [Related]  

  • 50. [General anesthesia for progressive muscular dystrophy patients (author's transl)].
    Koshiyama K; Kuwahara O; Tanaka H; Nakashima A
    Masui; 1979 Apr; 28(4):415-20. PubMed ID: 439384
    [No Abstract]   [Full Text] [Related]  

  • 51. Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis.
    Kondo E; Saito K; Toda T; Osawa M; Yamamoto T; Kobayashi M; Fukuyama Y
    Am J Med Genet; 1996 Dec; 66(2):169-74. PubMed ID: 8958324
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prenatal diagnosis of Fukuyama congenital muscular dystrophy.
    Saito K
    Prenat Diagn; 2006 May; 26(5):415-7. PubMed ID: 16570239
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.
    Yoshioka M; Higuchi Y; Fujii T; Aiba H; Toda T
    Brain Dev; 2008 Jan; 30(1):59-67. PubMed ID: 17597323
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Other non-Fukuyama congenital muscular dystrophy].
    Hayashi YK
    Ryoikibetsu Shokogun Shirizu; 2001; (35):111-3. PubMed ID: 11555884
    [No Abstract]   [Full Text] [Related]  

  • 55. Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.
    Okada M; Kawahara G; Noguchi S; Sugie K; Murayama K; Nonaka I; Hayashi YK; Nishino I
    Neurology; 2007 Sep; 69(10):1035-42. PubMed ID: 17785673
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries.
    Kirschner J; Bönnemann CG
    Arch Neurol; 2004 Feb; 61(2):189-99. PubMed ID: 14967765
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [The place of electromyography in the diagnosis of myopathy in children].
    Raimbault J; Renault F; Laget P
    Ann Pediatr (Paris); 1977; 24(6-7):451-8. PubMed ID: 16211924
    [No Abstract]   [Full Text] [Related]  

  • 58. [Heterogeneity of muscular dystrophy].
    Zellweger H; Pavone L; Ionasescu V; Conway T
    Minerva Med; 1972 Feb; 63(11):649-65. PubMed ID: 4551970
    [No Abstract]   [Full Text] [Related]  

  • 59. [The life spans, cause of death and pathological findings of Fukuyama type congenital muscular dystrophy--analysis of 24 autopsy cases].
    Mukoyama M; Hizawa K; Kagawa N; Takahashi K
    Rinsho Shinkeigaku; 1993 Nov; 33(11):1154-6. PubMed ID: 8124873
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Evoked electromyographical studies on the neuromuscular junction in progressive muscular dystrophy.
    Shibata N
    Sapporo Igaku Zasshi; 1968; 33(4):281-95. PubMed ID: 5750821
    [No Abstract]   [Full Text] [Related]  

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