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 *

42 related articles for article (PubMed ID: 7210305)

  • 1. [Genetic study of myopathies in Tunisia].
    Hamida MB; Marakchi D
    Union Med Can; 1980 Nov; 109(11):1609-28. PubMed ID: 7210305
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. [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]  

  • 4. [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]  

  • 5. Genetic-epidemiological studies of muscular dystrophy on a sample of population in Romania. I. Incidence of disease, genetic transmission, sporadic factor, sex involvement, gene manifestations in heterozygotes, onset in muscular distrophy.
    Badiu G
    Rev Roum Neurol; 1973; 10(6):519-30. PubMed ID: 4771090
    [No 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. [Protopathic myopathies. Progressive muscular dystrophy].
    Enrique Azurduy N; Solis Padilla A
    Neurocirugia; 1969; 27(1):49-55. PubMed ID: 5385658
    [No Abstract]   [Full Text] [Related]  

  • 8. The limb-girdle muscular dystrophies.
    Bushby K
    Eur J Paediatr Neurol; 2001; 5(5):213-4. PubMed ID: 11585112
    [No Abstract]   [Full Text] [Related]  

  • 9. [Renewed interest in muscular dystrophy].
    Eymard B
    Rev Prat; 2001 Feb; 51(3):262-9. PubMed ID: 11265422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
    Fardeau M; Matsumura K; Tomé FM; Collin H; Leturcq F; Kaplan JC; Campbell KP
    C R Acad Sci III; 1993 Aug; 316(8):799-804. PubMed ID: 8044705
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Autosomal recessive limb-girdle muscular dystrophy probably linked to chromosome 15].
    Noguera Moya A; Lorenzo Sanz G; García Villanueva M; Benítez J; Aparicio Méix JM
    An Esp Pediatr; 1996 Mar; 44(3):267-9. PubMed ID: 8830604
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetics of childhood spinal muscular atrophy.
    Winsor EJ; Murphy EG; Thompson MW; Reed TE
    J Med Genet; 1971 Jun; 8(2):143-8. PubMed ID: 5096536
    [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. The limb-girdle muscular dystrophies: diagnostic guidelines.
    Bushby KM
    Eur J Paediatr Neurol; 1999; 3(2):53-8. PubMed ID: 10700539
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Duchenne muscular dystrophy: clinico-pathologic study of 10 families from South Tunisia].
    Mhiri C; Triki C; Fakhfakh F; Chouayakh F; Fki I; Jlidi R; Ayadi H; Zouari N
    Tunis Med; 1996 Feb; 74(2):85-92. PubMed ID: 9507303
    [No Abstract]   [Full Text] [Related]  

  • 16. Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
    Illarioshkin SN; Ivanova-Smolenskaya IA; Tanaka H; Poleshchuk VV; Markova ED; Tsuji S
    Genomics; 1997 Jun; 42(2):345-8. PubMed ID: 9192858
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13].
    Illarioshkin SN; Ivanova-Smolenskaia IA; Dimborskaia SA; Poleshchuk VV; Markova ED; Slominskiĭ PA; Bulaeva KB; Tsudzi Sh
    Genetika; 1997 Nov; 33(11):1551-8. PubMed ID: 9480219
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inherited myopathies and muscular dystrophies.
    Cardamone M; Darras BT; Ryan MM
    Semin Neurol; 2008 Apr; 28(2):250-9. PubMed ID: 18351526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A geno-geographic study of myopathy patients in various areas of the Kalinin region].
    Artemchuk NL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(6):807-10. PubMed ID: 4243650
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic studies and molecular structures: the dystrophin associated complex.
    Beckmann JS
    Hum Mol Genet; 1996 Jul; 5(7):865-7. PubMed ID: 8817320
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.