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 *

114 related articles for article (PubMed ID: 36381256)

  • 1. Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia.
    Lace B; Micule I; Kenina V; Setlere S; Strautmanis J; Kazaine I; Taurina G; Murmane D; Grinfelde I; Kornejeva L; Krumina Z; Sterna O; Radovica-Spalvina I; Vasiljeva I; Gailite L; Stavusis J; Livcane D; Kidere D; Malniece I; Inashkina I
    Neurol Genet; 2022 Jun; 8(3):e685. PubMed ID: 36381256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.
    Inashkina I; Jankevics E; Stavusis J; Vasiljeva I; Viksne K; Micule I; Strautmanis J; Naudina MS; Cimbalistiene L; Kucinskas V; Krumina A; Utkus A; Burnyte B; Matuleviciene A; Lace B
    BMC Musculoskelet Disord; 2016 May; 17():200. PubMed ID: 27142102
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
    Megarbane A; Bizzari S; Deepthi A; Sabbagh S; Mansour H; Chouery E; Hmaimess G; Jabbour R; Mehawej C; Alame S; Hani A; Hasbini D; Ghanem I; Koussa S; Al-Ali MT; Obeid M; Talea DB; Lefranc G; Lévy N; Leturcq F; El Hayek S; Delague V; Urtizberea JA
    J Neuromuscul Dis; 2022; 9(1):193-210. PubMed ID: 34602496
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The prevalence of hereditary neuromuscular disorders in Northern Norway.
    Müller KI; Ghelue MV; Lund I; Jonsrud C; Arntzen KA
    Brain Behav; 2021 Jan; 11(1):e01948. PubMed ID: 33185984
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Epidemiology of Neuromuscular Disorders: A Comprehensive Overview of the Literature.
    Deenen JC; Horlings CG; Verschuuren JJ; Verbeek AL; van Engelen BG
    J Neuromuscul Dis; 2015; 2(1):73-85. PubMed ID: 28198707
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population.
    Norwood FL; Harling C; Chinnery PF; Eagle M; Bushby K; Straub V
    Brain; 2009 Nov; 132(Pt 11):3175-86. PubMed ID: 19767415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation.
    Pantoja-Melendez CA; Miranda-Duarte A; Roque-Ramirez B; Zenteno JC
    PLoS One; 2017; 12(1):e0170280. PubMed ID: 28103310
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Respiratory muscle training in children and adults with neuromuscular disease.
    Silva IS; Pedrosa R; Azevedo IG; Forbes AM; Fregonezi GA; Dourado Junior ME; Lima SR; Ferreira GM
    Cochrane Database Syst Rev; 2019 Sep; 9(9):CD011711. PubMed ID: 31487757
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The SMN1 common variant c.22 dupA in Chinese patients causes spinal muscular atrophy by nonsense-mediated mRNA decay in humans.
    Bai J; Qu Y; Cao Y; Yang L; Ge L; Jin Y; Wang H; Song F
    Gene; 2018 Feb; 644():49-55. PubMed ID: 29080838
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Advances in imaging of brain abnormalities in neuromuscular disease.
    Angelini C; Pinzan E
    Ther Adv Neurol Disord; 2019; 12():1756286419845567. PubMed ID: 31105770
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 Individuals.
    Bowen BM; Truty R; Aradhya S; Bristow SL; Johnson BA; Morales A; Tan CA; Westbrook MJ; Winder TL; Chavez JC
    Front Neurol; 2021; 12():663911. PubMed ID: 34025568
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy.
    Liang WC; Jong YJ; Wang CH; Wang CH; Tian X; Chen WZ; Kan TM; Minami N; Nishino I; Wong LC
    Orphanet J Rare Dis; 2020 Jun; 15(1):160. PubMed ID: 32576226
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exercise biology of neuromuscular disorders.
    Ng SY; Manta A; Ljubicic V
    Appl Physiol Nutr Metab; 2018 Nov; 43(11):1194-1206. PubMed ID: 29944848
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Population frequencies of inherited neuromuscular diseases--a world survey.
    Emery AE
    Neuromuscul Disord; 1991; 1(1):19-29. PubMed ID: 1822774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic.
    Stehlíková K; Skálová D; Zídková J; Haberlová J; Voháňka S; Mazanec R; Mrázová L; Vondráček P; Ošlejšková H; Zámečník J; Honzík T; Zeman J; Magner M; Šišková D; Langová M; Gregor V; Godava M; Smolka V; Fajkusová L
    Clin Genet; 2017 Mar; 91(3):463-469. PubMed ID: 27447704
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A hospital based epidemiological study of genetically determined muscle disease in south western Norway.
    Husebye SA; Rebne CB; Stokland AE; Sanaker PS; Bindoff LA
    Neuromuscul Disord; 2020 Mar; 30(3):181-185. PubMed ID: 32146000
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of muscular dystrophies: our experience in Mexico.
    Escobar-Cedillo RE; López-Hernández L; Miranda-Duarte A; Curiel-Leal MD; Suarez-Ocón A; Sánchez-Chapul L; Berenice Luna-Angulo A; Ávila-Ramírez G; López-Hernández JA; Gómez-Díaz B
    Folia Neuropathol; 2021; 59(3):276-283. PubMed ID: 34628793
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction
    Alcántara-Ortigoza MA; Reyna-Fabián ME; González-Del Angel A; Estandia-Ortega B; Bermúdez-López C; Cruz-Miranda GM; Ruíz-García M
    Genes (Basel); 2019 Oct; 10(11):. PubMed ID: 31671740
    [TBL] [Abstract][Full Text] [Related]  

  • 19. What we do not know about pregnancy in hereditary neuromuscular disorders.
    Argov Z; de Visser M
    Neuromuscul Disord; 2009 Oct; 19(10):675-9. PubMed ID: 19692244
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A review of the genetic spectrum of hereditary spastic paraplegias, inherited neuropathies and spinal muscular atrophies in Africans.
    Mahungu AC; Monnakgotla N; Nel M; Heckmann JM
    Orphanet J Rare Dis; 2022 Mar; 17(1):133. PubMed ID: 35331287
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.