BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 20146070)

  • 1. 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]  

  • 2. Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.
    Neudecker S; Krasnianski M; Bahn E; Zierz S
    Acta Neuropathol; 2004 Sep; 108(3):257-9. PubMed ID: 15221332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
    Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].
    Jordan B; Müller-Reible C; Zierz S
    Nervenarzt; 2011 Jun; 82(6):712-22. PubMed ID: 21567298
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR
    Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Facioscapulohumeral dystrophy presenting as infantile facial diplegia and late-onset limb-girdle myopathy in members of the same family.
    Felice KJ; Jones JM; Conway SR
    Muscle Nerve; 2005 Sep; 32(3):368-72. PubMed ID: 15880682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Muscle MRI findings in facioscapulohumeral muscular dystrophy.
    Gerevini S; Scarlato M; Maggi L; Cava M; Caliendo G; Pasanisi B; Falini A; Previtali SC; Morandi L
    Eur Radiol; 2016 Mar; 26(3):693-705. PubMed ID: 26115655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromes.
    Schreiber O; Schneiderat P; Kress W; Rautenstrauss B; Senderek J; Schoser B; Walter MC
    BMC Med Genet; 2013 Sep; 14():92. PubMed ID: 24041033
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: a case study.
    Tsuji M; Kinoshita M; Imai Y; Kawamoto M; Kohara N
    Neuromuscul Disord; 2009 Feb; 19(2):140-2. PubMed ID: 19147353
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].
    Krasnianski M; Neudecker S; Eger K; Schulte-Mattler W; Zierz S
    Nervenarzt; 2003 Feb; 74(2):151-8. PubMed ID: 12596016
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
    Trevisan CP; Pastorello E; Tomelleri G; Vercelli L; Bruno C; Scapolan S; Siciliano G; Comacchio F
    Eur J Neurol; 2008 Dec; 15(12):1353-8. PubMed ID: 19049553
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Facioscapulohumeral muscular dystrophy 1 patients participating in the UK FSHD registry can be subdivided into 4 patterns of self-reported symptoms.
    Banerji CRS; Cammish P; Evangelista T; Zammit PS; Straub V; Marini-Bettolo C
    Neuromuscul Disord; 2020 Apr; 30(4):315-328. PubMed ID: 32327287
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [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]  

  • 20. Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
    Krasnianski M; Eger K; Neudecker S; Jakubiczka S; Zierz S
    Arch Neurol; 2003 Oct; 60(10):1421-5. PubMed ID: 14568813
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.