BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 29735511)

  • 21. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.
    Nguyen K; Bassez G; Krahn M; Bernard R; Laforêt P; Labelle V; Urtizberea JA; Figarella-Branger D; Romero N; Attarian S; Leturcq F; Pouget J; Lévy N; Eymard B
    Arch Neurol; 2007 Aug; 64(8):1176-82. PubMed ID: 17698709
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Axial muscle involvement in patients with limb girdle muscular dystrophy type R9.
    Revsbech KL; Rudolf K; Sheikh AM; Khawajazada T; de Stricker Borch J; Dahlqvist JR; Løkken N; Witting N; Vissing J
    Muscle Nerve; 2022 Apr; 65(4):405-414. PubMed ID: 35020210
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Muscle MRI patterns for limb girdle muscle dystrophies: systematic review.
    Alawneh I; Stosic A; Gonorazky H
    J Neurol; 2023 Aug; 270(8):3946-3957. PubMed ID: 37129643
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Muscle MRI findings in limb girdle muscular dystrophy type 2L.
    Sarkozy A; Deschauer M; Carlier RY; Schrank B; Seeger J; Walter MC; Schoser B; Reilich P; Leturq F; Radunovic A; Behin A; Laforet P; Eymard B; Schreiber H; Hicks D; Vaidya SS; Gläser D; Carlier PG; Bushby K; Lochmüller H; Straub V
    Neuromuscul Disord; 2012 Oct; 22 Suppl 2():S122-9. PubMed ID: 22980763
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical Muscle Testing Compared with Whole-Body Magnetic Resonance Imaging in Facio-scapulo-humeral Muscular Dystrophy.
    Regula JU; Jestaedt L; Jende F; Bartsch A; Meinck HM; Weber MA
    Clin Neuroradiol; 2016 Dec; 26(4):445-455. PubMed ID: 25860436
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adding quantitative muscle MRI to the FSHD clinical trial toolbox.
    Mul K; Vincenten SCC; Voermans NC; Lemmers RJLF; van der Vliet PJ; van der Maarel SM; Padberg GW; Horlings CGC; van Engelen BGM
    Neurology; 2017 Nov; 89(20):2057-2065. PubMed ID: 29030457
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characteristic Posterior-dominant Lower Limb Muscle Involvement in Limb-girdle Muscular Dystrophy due to a DNAJB6 Phe93Leu Mutation.
    Kojima Y; Noto YI; Takewaki D; Tokuda N; Shiga K; Hamano A; Mizuta I; Muranishi M; Kasai T; Nakagawa M; Mizuno T
    Intern Med; 2017 Sep; 56(17):2347-2351. PubMed ID: 28794355
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Dysferlinopathy Promotes an Intramuscle Expansion of Macrophages with a Cyto-Destructive Phenotype.
    Baek JH; Many GM; Evesson FJ; Kelley VR
    Am J Pathol; 2017 Jun; 187(6):1245-1257. PubMed ID: 28412297
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies.
    Ten Dam L; van der Kooi AJ; Rövekamp F; Linssen WH; de Visser M
    Neuromuscul Disord; 2014 Dec; 24(12):1097-102. PubMed ID: 25176504
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies.
    Peric S; Maksimovic R; Banko B; Durdic M; Bjelica B; Bozovic I; Balcik Y; Pesovic J; Savic-Pavicevic D; Rakocevic-Stojanovic V
    J Neurol; 2017 Sep; 264(9):1899-1908. PubMed ID: 28756605
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Limb-girdle muscular dystrophy type 2B: An unusual cause of proximal muscular weakness in Saudi Arabia.
    Algahtani H; Shirah B; Alassiri AH; Habib BA; Almuhanna R; Ahamed MF
    J Back Musculoskelet Rehabil; 2018; 31(5):999-1004. PubMed ID: 29966189
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal study.
    Willis TA; Hollingsworth KG; Coombs A; Sveen ML; Andersen S; Stojkovic T; Eagle M; Mayhew A; de Sousa PL; Dewar L; Morrow JM; Sinclair CD; Thornton JS; Bushby K; Lochmüller H; Hanna MG; Hogrel JY; Carlier PG; Vissing J; Straub V
    PLoS One; 2013; 8(8):e70993. PubMed ID: 23967145
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Three novel recessive DYSF mutations identified in three patients with muscular dystrophy, limb-girdle, type 2B.
    Okubo M; Iida A; Hayashi S; Mori-Yoshimura M; Oya Y; Watanabe A; Arahata H; El Sherif R; Noguchi S; Nishino I
    J Neurol Sci; 2018 Dec; 395():169-171. PubMed ID: 30366248
    [No Abstract]   [Full Text] [Related]  

  • 34. 'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1D.
    Sandell SM; Mahjneh I; Palmio J; Tasca G; Ricci E; Udd BA
    Eur J Neurol; 2013 Dec; 20(12):1553-9. PubMed ID: 23865856
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy.
    Moore U; Fernández-Simón E; Schiava M; Cox D; Gordish-Dressman H; James MK; Mayhew A; Wilson I; Guglieri M; Rufibach L; Blamire A; Carlier PG; Mori-Yoshimura M; Day JW; Jones KJ; Bharucha-Goebel DX; Salort-Campana E; Pestronk A; Walter MC; Paradas C; Stojkovic T; Bravver E; Pegoraro E; Mendell JR; Bushby K; Diaz-Manera J; Straub V;
    Neuromuscul Disord; 2023 Feb; 33(2):199-207. PubMed ID: 36689846
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Leg Muscle Involvement in Facioscapulohumeral Muscular Dystrophy: Comparison between Facioscapulohumeral Muscular Dystrophy Types 1 and 2.
    Mair D; Huegens-Penzel M; Kress W; Roth C; Ferbert A
    Eur Neurol; 2017; 77(1-2):32-39. PubMed ID: 27855411
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis.
    Domínguez-González C; Fernández-Torrón R; Moore U; de Fuenmayor-Fernández de la Hoz CP; Vélez-Gómez B; Cabezas JA; Alonso-Pérez J; González-Mera L; Olivé M; García-García J; Moris G; León Hernández JC; Muelas N; Servian-Morilla E; Martin MA; Díaz-Manera J; Paradas C
    J Neurol; 2022 Jul; 269(7):3550-3562. PubMed ID: 35286480
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical and magnetic resonance imaging features of 'diamond on quadriceps' sign in dysferlinopathy.
    Pradhan S
    Neurol India; 2009; 57(2):172-5. PubMed ID: 19439848
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dysferlinopathy in Iran: Clinical and genetic report.
    Fatehi F; Nafissi S; Urtizberea JA; Blanck-Labelle V; Lévy N; Krahn M; Dbouk MB; Attarian S
    J Neurol Sci; 2015 Dec; 359(1-2):256-9. PubMed ID: 26671124
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern.
    Polavarapu K; Manjunath M; Preethish-Kumar V; Sekar D; Vengalil S; Thomas P; Sathyaprabha TN; Bharath RD; Nalini A
    Neuromuscul Disord; 2016 Nov; 26(11):768-774. PubMed ID: 27666775
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.