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 *

88 related articles for article (PubMed ID: 9855539)

  • 1. The first European family with tibial muscular dystrophy outside the Finnish population.
    de Seze J; Udd B; Haravuori H; Sablonnière B; Maurage CA; Hurtevent JF; Boutry N; Stojkovic T; Schraen S; Petit H; Vermersch P
    Neurology; 1998 Dec; 51(6):1746-8. PubMed ID: 9855539
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Tibial muscular dystrophy. A rare form of distal myopathy].
    de Seze J; Udd B; Vermersch P
    Rev Neurol (Paris); 1999 Apr; 155(4):296-305. PubMed ID: 10367327
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assignment of the tibial muscular dystrophy locus to chromosome 2q31.
    Haravuori H; Mäkelä-Bengs P; Udd B; Partanen J; Pulkkinen L; Somer H; Peltonen L
    Am J Hum Genet; 1998 Mar; 62(3):620-6. PubMed ID: 9497249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31.
    Udd B; Haravuori H; Kalimo H; Partanen J; Pulkkinen L; Paetau A; Peltonen L; Somer H
    Neuromuscul Disord; 1998 Jun; 8(5):327-32. PubMed ID: 9673987
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tibial muscular dystrophy in a Belgian family.
    Van den Bergh PY; Bouquiaux O; Verellen C; Marchand S; Richard I; Hackman P; Udd B
    Ann Neurol; 2003 Aug; 54(2):248-51. PubMed ID: 12891679
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage analyses in tibial muscular dystrophy.
    Nokelainen P; Udd B; Somer H; Peltonen L
    Hum Hered; 1996; 46(2):98-107. PubMed ID: 8666419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.
    Illarioshkin SN; Ivanova-Smolenskaya IA; Tanaka H; Vereshchagin NV; Markova ED; Poleshchuk VV; Lozhnikova SM; Sukhorukov VS; Limborska SA; Slominsky PA; Bulayeva KB; Tsuji S
    Brain; 1996 Dec; 119 ( Pt 6)():1895-909. PubMed ID: 9009996
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.
    Haravuori H; Vihola A; Straub V; Auranen M; Richard I; Marchand S; Voit T; Labeit S; Somer H; Peltonen L; Beckmann JS; Udd B
    Neurology; 2001 Apr; 56(7):869-77. PubMed ID: 11294923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients.
    Udd B; Partanen J; Halonen P; Falck B; Hakamies L; Heikkilä H; Ingo S; Kalimo H; Kääriäinen H; Laulumaa V
    Arch Neurol; 1993 Jun; 50(6):604-8. PubMed ID: 8503797
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.
    Hackman P; Vihola A; Haravuori H; Marchand S; Sarparanta J; De Seze J; Labeit S; Witt C; Peltonen L; Richard I; Udd B
    Am J Hum Genet; 2002 Sep; 71(3):492-500. PubMed ID: 12145747
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early onset chromosome 14-linked distal myopathy (Laing).
    Mastaglia FL; Phillips BA; Cala LA; Meredith C; Egli S; Akkari PA; Laing NG
    Neuromuscul Disord; 2002 May; 12(4):350-7. PubMed ID: 12062252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A distinct phenotype of distal myopathy in a large Finnish family.
    Mahjneh I; Haravuori H; Paetau A; Anderson LV; Saarinen A; Udd B; Somer H
    Neurology; 2003 Jul; 61(1):87-92. PubMed ID: 12847162
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.
    Bejaoui K; Hirabayashi K; Hentati F; Haines JL; Ben Hamida C; Belal S; Miller RG; McKenna-Yasek D; Weissenbach J; Rowland LP
    Neurology; 1995 Apr; 45(4):768-72. PubMed ID: 7723968
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
    Weiler T; Greenberg CR; Nylen E; Halliday W; Morgan K; Eggertson D; Wrogemann K
    Am J Hum Genet; 1996 Oct; 59(4):872-8. PubMed ID: 8808603
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic heterogeneity in Miyoshi-type distal muscular dystrophy.
    Linssen WH; de Visser M; Notermans NC; Vreyling JP; Van Doorn PA; Wokke JH; Baas F; Bolhuis PA
    Neuromuscul Disord; 1998 Jun; 8(5):317-20. PubMed ID: 9673985
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
    Bashir R; Keers S; Strachan T; Passos-Bueno R; Zatz M; Weissenbach J; Le Paslier D; Meisler M; Bushby K
    Genomics; 1996 Apr; 33(1):46-52. PubMed ID: 8617508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy.
    Udd B; Rapola J; Nokelainen P; Arikawa E; Somer H
    J Neurol Sci; 1992 Dec; 113(2):214-21. PubMed ID: 1487757
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR; Moreira ES; Vainzof M; Chamberlain J; Marie SK; Pereira L; Akiyama J; Roberds SL; Campbell KP; Zatz M
    Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 5.