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 *

98 related articles for article (PubMed ID: 2294956)

  • 41. [Congenital desproportion of various types of muscle fiber, with relative small size of type I fibers. Morphological documents on muscle biopsies in 3 members of the same family].
    Fardeau M; Harpey JP; Caille B
    Rev Neurol (Paris); 1975 Nov; 131(11):745-66. PubMed ID: 130671
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook.
    Cavanagh NP; Lake BD; McMeniman P
    Arch Dis Child; 1979 Oct; 54(10):735-43. PubMed ID: 507896
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Congenital fiber type disproportion: severe form with marked improvement.
    Tsuji M; Higuchi Y; Shiraishi K; Mitsuyoshi I; Hattori H
    Pediatr Neurol; 1999 Sep; 21(3):658-60. PubMed ID: 10513694
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Congenital disproportion of fiber types. Study of a family].
    Gobernado JM; Riva C; Zaragoza E; Gimeno A; Anaya A
    Arch Neurobiol (Madr); 1980; 43(3):147-64. PubMed ID: 7458538
    [No Abstract]   [Full Text] [Related]  

  • 45. [Congenital myopathy without specific muscle pathologic features. Case report].
    Yuza F; Tatsuno M; Okuyama K; Nonaka I
    No To Hattatsu; 1986 Jan; 18(1):70-2. PubMed ID: 3718775
    [No Abstract]   [Full Text] [Related]  

  • 46. Congenital blepharophimosis, joint contractures, and muscular hypotonia.
    Fitch N; Karpati G; Pinsky L
    Neurology; 1971 Dec; 21(12):1214-20. PubMed ID: 5167313
    [No Abstract]   [Full Text] [Related]  

  • 47. Mitochondria-lipid-glycogen (MLG) disease of muscle: a morphologically regressive congenital myopathy.
    Jerusalem F; Angelini C; Engel AG; Groover RV
    Trans Am Neurol Assoc; 1973; 98():89-93. PubMed ID: 4784980
    [No Abstract]   [Full Text] [Related]  

  • 48. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].
    Yamamoto T; Kitada T; Hirasawa E; Mori H; Mizuno Y
    No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model.
    Engel WK; Gold GN; Karpati G
    Arch Neurol; 1968 Apr; 18(4):435-44. PubMed ID: 4230186
    [No Abstract]   [Full Text] [Related]  

  • 50. [Centronuclear (myotubular) myopathy: a case report].
    Reed UC; Tsanaclis AM; Ferreira LM; Carvalho MS; Diament A; Levy JA
    Rev Hosp Clin Fac Med Sao Paulo; 1992; 47(5):237-9. PubMed ID: 1340609
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
    Floriach-Robert M; Cabello A; Simón De Las Heras R; Mateos Beato F
    Neurologia; 2001; 16(6):245-53. PubMed ID: 11423041
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria (author's transl)].
    Okamura K; Nagae K; Omae T; Mita T
    Rinsho Shinkeigaku; 1975 Apr; 15(4):177-83. PubMed ID: 1170056
    [No Abstract]   [Full Text] [Related]  

  • 53. Congenital hypotonia revisited.
    Brooke MH; Carroll JE; Ringel SP
    Muscle Nerve; 1979; 2(2):84-100. PubMed ID: 397413
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Minimal change myopathy: report of a case.
    Tzeng CY; Jong YJ; Chiang CH; Chaou WT
    J Formos Med Assoc; 1990 Dec; 89(12):1099-102. PubMed ID: 1982682
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [A case of nemaline myopathy studied over a period of nine years (author's transl)].
    Pou-Serradell A; Navarro C
    Rev Neurol (Paris); 1978 Apr; 134(4):295-302. PubMed ID: 725401
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Congenital myopathies].
    Vallat JM; Vital C; Le Blanc M
    Bord Med; 1972 Nov; 5(18):2439-51. PubMed ID: 4661890
    [No Abstract]   [Full Text] [Related]  

  • 57. Congenital myopathy with uniform type 1 fiber predominance and type 2 fiber hypoplasia: report of one case.
    Huang ML; Tsai CH; Lee CC
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(1):62-4. PubMed ID: 9553297
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Congenital fiber type disproportion. Report of an atypical case and review of the literature].
    Cañete Estrada R; Peña Amaro J; García Hortelano MT; Sánchez Polaina R; Burón Romero A; Romanos Lezcano A
    An Esp Pediatr; 1991 Oct; 35(4):265-7. PubMed ID: 1763856
    [No Abstract]   [Full Text] [Related]  

  • 59. Central core disease--a case report.
    Myong NH; Suh YL; Chi JG; Hwang YS
    J Korean Med Sci; 1993 Jun; 8(3):235-40. PubMed ID: 8240757
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Multicore disease. Report of a case with lack of fibre type differentiation.
    Taratuto AL; Sfaello ZM; Rezzonico C; Morales RC
    Neuropadiatrie; 1978 Aug; 9(3):285-97. PubMed ID: 213746
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.