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 *

141 related articles for article (PubMed ID: 7400780)

  • 1. [Duchenne muscular dystrophy in Tunesia: 31 cases in 13 families with autosomal recessive inheritance].
    Ben Hamida M; Marrakchi D
    J Genet Hum; 1980 Mar; 28(1):1-9. PubMed ID: 7400780
    [No Abstract]   [Full Text] [Related]  

  • 2. Girls with muscular dystrophy.
    Reddy BK; Kumari CK; Reddy MV; Reddi OS
    Acta Anthropogenet; 1984; 8(3-4):209-16. PubMed ID: 6545753
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
    Ben Othmane K; Ben Hamida M; Pericak-Vance MA; Ben Hamida C; Blel S; Carter SC; Bowcock AM; Petruhkin K; Gilliam TC; Roses AD
    Nat Genet; 1992 Dec; 2(4):315-7. PubMed ID: 1303286
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance.
    Zatz M; Passos-Bueno MR; Rapaport D
    Am J Med Genet; 1989 Mar; 32(3):407-10. PubMed ID: 2658592
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M; Attia N; Chabouni H; Fardeau M
    Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
    Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia.
    Ben Hamida M; Fardeau M; Attia N
    Muscle Nerve; 1983 Sep; 6(7):469-80. PubMed ID: 6633560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.
    Kawai H; Akaike M; Endo T; Adachi K; Inui T; Mitsui T; Kashiwagi S; Fujiwara T; Okuno S; Shin S
    J Clin Invest; 1995 Sep; 96(3):1202-7. PubMed ID: 7657792
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance.
    Niemi KM; Sommer H; Kero M; Kanerva L; Haltia M
    Arch Dermatol; 1988 Apr; 124(4):551-4. PubMed ID: 3355199
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Problems associated with female conductors of hereditary X-chromosomal recessive muscular dystrophy (Duchenne type)].
    Gundlach HJ; Pelz L; Ernst K
    Psychiatr Neurol Med Psychol (Leipz); 1974 Nov; 26(11):693-8. PubMed ID: 4449906
    [No Abstract]   [Full Text] [Related]  

  • 11. [Autosomal recessive distal muscular dystrophy--a new type of distal muscular dystrophy observed characteristically in Japan].
    Miyoshi K; Iwasa M; Kawai H; Sasaki N; Kusaka K; Yagita M; Hiasa M; Tada Y
    Nihon Rinsho; 1977 Nov; 35(11):3922-8. PubMed ID: 599673
    [No Abstract]   [Full Text] [Related]  

  • 12. Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate.
    Bader PI; Bender CJ; Creason MT; Conn PS; Townsend DW
    Am J Med Genet; 1982 Jul; 12(3):255-69. PubMed ID: 7114089
    [No Abstract]   [Full Text] [Related]  

  • 13. Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.
    Louhichi N; Richard P; Triki CH; Meziou M; Ayadi H; Guicheney P; Fakhfakh F
    Arch Inst Pasteur Tunis; 2006; 83(1-4):19-23. PubMed ID: 19388593
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duchenne-like muscular dystrophy in the Arabs.
    Zatz M; Passos-Bueno MR; Rapaport D
    Am J Med Genet; 1990 Oct; 37(2):289-90. PubMed ID: 2248301
    [No Abstract]   [Full Text] [Related]  

  • 15. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy].
    Endo T; Akaike M; Kawai H; Matsumura K; Saito S
    Rinsho Shinkeigaku; 1996 Mar; 36(3):415-22. PubMed ID: 8741343
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Severe autosomal recessive myopathies in children in Tunisia].
    Ben Hamida M
    Bull Acad Natl Med; 1984; 168(7-8):937-40. PubMed ID: 6398752
    [No Abstract]   [Full Text] [Related]  

  • 17. Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.
    el Kerch F; Sefiani A; Azibi K; Boutaleb N; Yahyaoui M; Bentahila A; Vinet MC; Leturcq F; Bachner L; Beckmann J
    J Med Genet; 1994 Apr; 31(4):342-3. PubMed ID: 8071965
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A; Yoshida K; Ikeda S
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases].
    García-García D; Teijeira-Bautista S; Fernández-Rodríguez JM; Flores-Calvete J; Sánchez-Espíldora P; Fernández-Couto D; Cimas-Hernando I; Teijeiro-Ferreira A; Fernández-Hojas R; Brasa-Fernández Fierros J; Martínez de Alegría A; Escribano-Arias JL; Núñez-Delgado M; Navarro-Fernández Balbuena C
    Rev Neurol; 1998 Jun; 26(154):905-11. PubMed ID: 9658457
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Progressive muscular dystrophy: 2 adult cases.
    Belcher DW
    Ethiop Med J; 1970 Jul; 8(3):141-6. PubMed ID: 5520295
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.