BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 11985390)

  • 21. Distribution of extremity muscle weakness in myasthenia gravis: sparing of tibialis anterior muscle.
    Oztürk A; Deymeer F; Serdaroğlu P; Parman Y; Ozdemir C
    Acta Myol; 2003 Sep; 22(2):58-60. PubMed ID: 14959565
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Facioscapulohumeral muscular dystrophy: Report of seven patients].
    Cea G; Jiménez D
    Rev Med Chil; 2015 Mar; 143(3):304-9. PubMed ID: 26005816
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Selective Triceps Muscle Weakness in Myasthenia Gravis is Under-Recognized.
    Domingo CA; Landau ME; Campbell WW
    J Clin Neuromuscul Dis; 2016 Dec; 18(2):103-104. PubMed ID: 27861226
    [No Abstract]   [Full Text] [Related]  

  • 24. Isolated bilateral triceps muscle weakness as a presenting complaint in myasthenia gravis: A review.
    Thilak MR; Prabhu AN; Rao K SS; Vasantbhai MJ
    Neurol India; 2019; 67(2):566-568. PubMed ID: 31085879
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years.
    Ramos VF; Thaisetthawatkul P
    Age Ageing; 2012 Mar; 41(2):273-4. PubMed ID: 21795275
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Distal myasthenia gravis.
    Renard D; Castelnovo G; Labauge P
    Acta Neurol Belg; 2008 Sep; 108(3):107-8. PubMed ID: 19115675
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy.
    Korngut L; Siu VM; Venance SL; Levin S; Ray P; Lemmers RJ; Keith J; Campbell C
    Neuromuscul Disord; 2008 Jul; 18(7):579-82. PubMed ID: 18586493
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Facioscapulohumeral muscular dystrophy].
    Nakagawa M; Higuchi I
    Ryoikibetsu Shokogun Shirizu; 2001; (35):39-45. PubMed ID: 11555966
    [No Abstract]   [Full Text] [Related]  

  • 32. Facioscapulohumeral dystrophy.
    Kissel JT
    Semin Neurol; 1999; 19(1):35-43. PubMed ID: 10711987
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Focal and other unusual presentations of facioscapulohumeral muscular dystrophy.
    Hassan A; Jones LK; Milone M; Kumar N
    Muscle Nerve; 2012 Sep; 46(3):421-5. PubMed ID: 22907234
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy.
    Sheth VS; Shapiro MJ
    Arch Ophthalmol; 2008 May; 126(5):745-6; author reply 746. PubMed ID: 18474804
    [No Abstract]   [Full Text] [Related]  

  • 36. Respiratory pattern in a FSHD pediatric population.
    Trucco F; Pedemonte M; Fiorillo C; Tacchetti P; Brisca G; Bruno C; Minetti C
    Respir Med; 2016 Oct; 119():78-80. PubMed ID: 27692152
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Unique Case of Type-1 Facioscapulohumeral Muscular Dystrophy and Sarcomeric Hypertrophic Cardiomyopathy.
    Lima da Silva G; Guimarães T; Pinto FJ; Brito D
    Rev Esp Cardiol (Engl Ed); 2018 Sep; 71(9):765-766. PubMed ID: 28697927
    [No Abstract]   [Full Text] [Related]  

  • 38. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child.
    Shields CL; Zahler J; Falk N; Furuta M; Eagle RC; Espinosa LE; Fischer PR; Shields JA
    Arch Ophthalmol; 2007 Jun; 125(6):840-2. PubMed ID: 17563001
    [No Abstract]   [Full Text] [Related]  

  • 39. Patient page. Exercise is safe and beneficial for people with facioscapulohumeral muscular dystrophy.
    Brey RL
    Neurology; 2005 Mar; 64(6):E22. PubMed ID: 15781802
    [No Abstract]   [Full Text] [Related]  

  • 40. Diagnostic challenges in facioscapulohumeral muscular dystrophy.
    Sacconi S; Salviati L; Bourget I; Figarella D; Péréon Y; Lemmers R; van der Maarel S; Desnuelle C
    Neurology; 2006 Oct; 67(8):1464-6. PubMed ID: 17060574
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.