BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 308614)

  • 81. Carrier detection in Duchenne muscular dystrophy.
    Bundey S; Edwards JH; Insley J
    Lancet; 1979 Apr; 1(8121):881. PubMed ID: 86132
    [No Abstract]   [Full Text] [Related]  

  • 82. Epidemiology of muscular dystrophies in the Mediterranean area.
    Topaloglu H
    Acta Myol; 2013 Dec; 32(3):138-41. PubMed ID: 24803840
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.
    Roberts RG
    Lancet; 1991 Feb; 337(8739):504. PubMed ID: 1704092
    [No Abstract]   [Full Text] [Related]  

  • 84. No sex difference in mutations rates of Duchenne muscular dystrophy.
    Yasuda N; Kondô K
    J Med Genet; 1980 Apr; 17(2):106-11. PubMed ID: 7381863
    [TBL] [Abstract][Full Text] [Related]  

  • 85. CT of primary muscle diseases.
    Jiddane M; Gastaut JL; Pellissier JF; Pouget J; Serratrice G; Salamon G
    AJNR Am J Neuroradiol; 1983; 4(3):773-6. PubMed ID: 6410854
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Duchenne muscular dystrophy. Frequency of sporadic cases.
    Danieli GA; Barbujani G
    Hum Genet; 1984; 67(3):252-6. PubMed ID: 6469240
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Unspecific reactions of HLA-B antisera on fibroblasts from patients and carriers of Duchenne muscular dystrophy.
    Aragon de Kirbach ED; Willers I; Singh S; Goedde H
    Clin Genet; 1986 May; 29(5):369-73. PubMed ID: 3461893
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Becker muscular dystrophy: carrier detection by real-time ultrasound.
    Spiegler AW; Schindler S; Herrmann FH
    J Neurol; 1985; 232(5):307-9. PubMed ID: 3903058
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Duchenne muscular dystrophy.
    Edwards JH
    J Med Genet; 1984 Feb; 21(1):77. PubMed ID: 6694196
    [No Abstract]   [Full Text] [Related]  

  • 90. [Myotonic muscular dystrophy: diagnostic and eugenic problems].
    Grassi E; Moretti G; Tagliavini J; Marbini A; Juvarra G; Govoni E; Bragaglia MM; Rossi GL; Parma M
    Acta Biomed Ateneo Parmense; 1981; 52(5):187-95. PubMed ID: 6460404
    [No Abstract]   [Full Text] [Related]  

  • 91. Mutations in Duchenne muscular dystrophy.
    Hachinski V
    Arch Neurol; 1988 Jan; 45(1):87. PubMed ID: 3337682
    [No Abstract]   [Full Text] [Related]  

  • 92. Results of manual resistance exercise on a manifesting carrier of Duchenne muscular dystrophy. A case report.
    Bohannon RW; Jones PL
    Phys Ther; 1986 Jun; 66(6):973-5. PubMed ID: 3714817
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Hyperresponsivness of patients with clinical and premyopathic myotonic dystrophy to human growth hormone.
    Heymsfield SB; Bethel RA; Rudman D
    J Clin Endocrinol Metab; 1977 Jul; 45(1):147-58. PubMed ID: 874060
    [No Abstract]   [Full Text] [Related]  

  • 94. [Pseudohypertrophic muscular dystrophy type Duchenne].
    Cudny D
    Czas Stomatol; 1974 Mar; 27(3):247-50. PubMed ID: 4522193
    [No Abstract]   [Full Text] [Related]  

  • 95. Muscular dystrophy in young girls.
    Br Med J; 1970 Jun; 2(5712):745-6. PubMed ID: 5428735
    [No Abstract]   [Full Text] [Related]  

  • 96. The Becker type X-linked muscular dystrophy.
    Br Med J; 1976 Dec; 2(6050):1465-6. PubMed ID: 1000256
    [No Abstract]   [Full Text] [Related]  

  • 97. Diagnostic criteria for Duchenne and Becker muscular dystrophy.
    Miller G
    Neuromuscul Disord; 1992; 2(3):225. PubMed ID: 1483049
    [No Abstract]   [Full Text] [Related]  

  • 98. Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.
    Falk CT; Gilchrist JM; Pericak-Vance MA; Speer MC
    Am J Hum Genet; 1998 Apr; 62(4):941-9. PubMed ID: 9529338
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Evaluation of immunoregulatory cells in Duchenne muscular dystrophy and spinal muscular atrophy among African and Indian patients.
    Kiepiela P; Dawood AA; Moosa A; Coovadia HM; Coward P
    J Neurol Sci; 1988 Apr; 84(2-3):247-55. PubMed ID: 3259978
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Ligand-induced patching and capping of surface immunoglobulins.
    Loor F
    Methods Enzymol; 1984; 108():371-85. PubMed ID: 6396485
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.