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 *

163 related articles for article (PubMed ID: 24710723)

  • 1. Laing early-onset distal myopathy in a Belgian family.
    Van den Bergh PY; Martin JJ; Lecouvet F; Udd B; Schmedding E
    Acta Neurol Belg; 2014 Dec; 114(4):253-6. PubMed ID: 24710723
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient.
    Dubourg O; Maisonobe T; Behin A; Suominen T; Raheem O; Penttilä S; Parton M; Eymard B; Dahl A; Udd B
    J Neurol; 2011 Jun; 258(6):1157-63. PubMed ID: 21279644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New phenotype and pathology features in MYH7-related distal myopathy.
    Tasca G; Ricci E; Penttilä S; Monforte M; Giglio V; Ottaviani P; Camastra G; Silvestri G; Udd B
    Neuromuscul Disord; 2012 Jul; 22(7):640-7. PubMed ID: 22521714
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathy.
    Muelas N; Hackman P; Luque H; Garcés-Sánchez M; Azorín I; Suominen T; Sevilla T; Mayordomo F; Gómez L; Martí P; María Millán J; Udd B; Vílchez JJ
    Neurology; 2010 Aug; 75(8):732-41. PubMed ID: 20733148
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family.
    Lefter S; Hardiman O; McLaughlin RL; Murphy SM; Farrell M; Ryan AM
    Neuromuscul Disord; 2015 Feb; 25(2):155-60. PubMed ID: 25447691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathy.
    Komlósi K; Hadzsiev K; Garbes L; Martínez Carrera LA; Pál E; Sigurðsson JH; Magnusson O; Melegh B; Wirth B
    Neuromuscul Disord; 2014 Feb; 24(2):156-61. PubMed ID: 24300783
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement.
    Park JM; Kim YJ; Yoo JH; Hong YB; Park JH; Koo H; Chung KW; Choi BO
    Neuromuscul Disord; 2013 Jul; 23(7):580-6. PubMed ID: 23707328
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
    Overeem S; Schelhaas HJ; Blijham PJ; Grootscholten MI; ter Laak HJ; Timmermans J; van den Wijngaard A; Zwarts MJ
    Neuromuscul Disord; 2007 Jun; 17(6):490-3. PubMed ID: 17383184
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy.
    Lamont PJ; Udd B; Mastaglia FL; de Visser M; Hedera P; Voit T; Bridges LR; Fabian V; Rozemuller A; Laing NG
    J Neurol Neurosurg Psychiatry; 2006 Feb; 77(2):208-15. PubMed ID: 16103042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture.
    Feinstein-Linial M; Buvoli M; Buvoli A; Sadeh M; Dabby R; Straussberg R; Shelef I; Dayan D; Leinwand LA; Birk OS
    BMC Med Genet; 2016 Aug; 17(1):57. PubMed ID: 27519903
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Laing distal myopathy with a novel mutation in exon 34 of the MYH7 gene.
    Ferbert A; Zibat A; Rautenstrauß B; Kress W; Hügens-Penzel M; Weis J; Shah Y; Roth C
    Neuromuscul Disord; 2016 Sep; 26(9):598-603. PubMed ID: 27469267
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distal myopathy with coexisting heterozygous TIA1 and MYH7 Variants.
    Brand P; Dyck PJ; Liu J; Berini S; Selcen D; Milone M
    Neuromuscul Disord; 2016 Aug; 26(8):511-5. PubMed ID: 27282841
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A case of Japanese Laing type distal myopathy with a mutation in MYH7 gene].
    Hara K; Miyata H; Nishino I
    Rinsho Shinkeigaku; 2019 Dec; 59(12):823-828. PubMed ID: 31761835
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two families with MYH7 distal myopathy associated with cardiomyopathy and core formations.
    Naddaf E; Waclawik AJ
    J Clin Neuromuscul Dis; 2015 Mar; 16(3):164-9. PubMed ID: 25695922
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations.
    Yu M; Zhu Y; Lu Y; Lv H; Zhang W; Yuan Y; Wang Z
    Orphanet J Rare Dis; 2020 Dec; 15(1):344. PubMed ID: 33298082
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
    Bánfai Z; Hadzsiev K; Pál E; Komlósi K; Melegh M; Balikó L; Melegh B
    BMC Med Genet; 2017 Sep; 18(1):105. PubMed ID: 28927399
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
    Meredith C; Herrmann R; Parry C; Liyanage K; Dye DE; Durling HJ; Duff RM; Beckman K; de Visser M; van der Graaff MM; Hedera P; Fink JK; Petty EM; Lamont P; Fabian V; Bridges L; Voit T; Mastaglia FL; Laing NG
    Am J Hum Genet; 2004 Oct; 75(4):703-8. PubMed ID: 15322983
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.
    Homayoun H; Khavandgar S; Hoover JM; Mohsen AW; Vockley J; Lacomis D; Clemens PR
    Neuromuscul Disord; 2011 Mar; 21(3):219-22. PubMed ID: 21211974
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.
    Lamont PJ; Wallefeld W; Hilton-Jones D; Udd B; Argov Z; Barboi AC; Bonneman C; Boycott KM; Bushby K; Connolly AM; Davies N; Beggs AH; Cox GF; Dastgir J; DeChene ET; Gooding R; Jungbluth H; Muelas N; Palmio J; Penttilä S; Schmedding E; Suominen T; Straub V; Staples C; Van den Bergh PY; Vilchez JJ; Wagner KR; Wheeler PG; Wraige E; Laing NG
    Hum Mutat; 2014 Jul; 35(7):868-79. PubMed ID: 24664454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain.
    Carbonell-Corvillo P; Tristán-Clavijo E; Cabrera-Serrano M; Servián-Morilla E; García-Martín G; Villarreal-Pérez L; Rivas-Infante E; Area-Gómez E; Chamorro-Muñoz MI; Gil-Gálvez A; Miranda-Vizuete A; Martinez-Mir A; Laing N; Paradas C
    Neuromuscul Disord; 2018 Oct; 28(10):828-836. PubMed ID: 30166250
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.