BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 19049553)

  • 21. A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment.
    Dorobek M; Kabzińska D
    Eur J Paediatr Neurol; 2004; 8(6):313-6. PubMed ID: 15542386
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Facioscapulohumeral muscular dystrophy with EcoRI/BlnI fragment size of more than 32 kb.
    Vielhaber S; Jakubiczka S; Schröder JM; Sailer M; Feistner H; Heinze HJ; Wieacker P; Bettecken T
    Muscle Nerve; 2002 Apr; 25(4):540-8. PubMed ID: 11932972
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
    Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
    J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Genetic investigations in facioscapulohumeral muscular dystrophy: a preliminary report].
    Dorobek M; Kabzińska D; Ryniewicz B; Fidziańska-Dolot A; Hausmanowa-Petrusewicz I
    Neurol Neurochir Pol; 2004; 38(2):83-8. PubMed ID: 15307599
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe phenotype in infantile facioscapulohumeral muscular dystrophy.
    Klinge L; Eagle M; Haggerty ID; Roberts CE; Straub V; Bushby KM
    Neuromuscul Disord; 2006 Oct; 16(9-10):553-8. PubMed ID: 16934468
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.
    Goto K; Nishino I; Hayashi YK
    Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD).
    Wood-Allum C; Brennan P; Hewitt M; Lowe J; Tyfield L; Wills A
    Neuropathol Appl Neurobiol; 2004 Apr; 30(2):188-91. PubMed ID: 15043716
    [No Abstract]   [Full Text] [Related]  

  • 28. Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy.
    Vitelli F; Villanova M; Malandrini A; Bruttini M; Piccini M; Merlini L; Guazzi G; Renieri A
    Muscle Nerve; 1999 Oct; 22(10):1437-41. PubMed ID: 10487912
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophy.
    Lutz KL; Holte L; Kliethermes SA; Stephan C; Mathews KD
    Neurology; 2013 Oct; 81(16):1374-7. PubMed ID: 24042093
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Facioscapulohumeral muscular dystrophy.
    Tawil R
    Curr Neurol Neurosci Rep; 2004 Jan; 4(1):51-4. PubMed ID: 14683629
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Isolated facial diplegia and very late-onset myopathy in two siblings: atypical presentations of facioscapulohumeral dystrophy.
    Figueroa JJ; Chapin JE
    J Neurol; 2010 Mar; 257(3):444-6. PubMed ID: 19826857
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy.
    Reilich P; Schramm N; Schoser B; Schneiderat P; Strigl-Pill N; Müller-Höcker J; Kress W; Ferbert A; Rudnik-Schöneborn S; Noth J; Lochmüller H; Weis J; Walter MC
    J Neurol; 2010 Jul; 257(7):1108-18. PubMed ID: 20146070
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophy.
    Dmitriev P; Lipinski M; Vassetzky YS
    Neuromuscul Disord; 2009 Jan; 19(1):17-20. PubMed ID: 18974002
    [TBL] [Abstract][Full Text] [Related]  

  • 34. FSHD-like patients without 4q35 deletion.
    Yamanaka G; Goto K; Ishihara T; Oya Y; Miyajima T; Hoshika A; Nishino I; Hayashi YK
    J Neurol Sci; 2004 Apr; 219(1-2):89-93. PubMed ID: 15050443
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Facio-scapula-humeral muscular dystrophy: clinical picture and molecular genetics].
    Dorobek M
    Neurol Neurochir Pol; 2003; 37(1):151-9. PubMed ID: 12910837
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tongue atrophy in facioscapulohumeral muscular dystrophy.
    Yamanaka G; Goto K; Matsumura T; Funakoshi M; Komori T; Hayashi YK; Arahata K
    Neurology; 2001 Aug; 57(4):733-5. PubMed ID: 11524495
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy.
    Pastorello E; Cao M; Trevisan CP
    Clin Neurol Neurosurg; 2012 Apr; 114(3):230-4. PubMed ID: 22079131
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Compound heterozygosity in a South African patient with facioscapulohumeral muscular dystrophy.
    Olckers A; van der Merwe A; Wayne Towers G; Retief CF; Honey E; Schutte CM
    Neuromuscul Disord; 2012 Aug; 22(8):728-34. PubMed ID: 22652079
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion.
    Felice KJ; Moore SA
    Muscle Nerve; 2001 Mar; 24(3):352-6. PubMed ID: 11353419
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Facioscapulohumeral muscular dystrophy.
    Tawil R; Van Der Maarel SM
    Muscle Nerve; 2006 Jul; 34(1):1-15. PubMed ID: 16508966
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.