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 *

116 related articles for article (PubMed ID: 33685096)

  • 1. [Facioscapulohumeral muscular dystrophy].
    Pospisilova J; Bjørnarå B; Bjørnarå KA
    Tidsskr Nor Laegeforen; 2021 Mar; 141(4):. PubMed ID: 33685096
    [No Abstract]   [Full Text] [Related]  

  • 2. Case Studies on the Genetic and Clinical Diagnosis of Facioscapulohumeral Muscular Dystrophy.
    Hamel J; Tawil R
    Neurol Clin; 2020 Aug; 38(3):529-540. PubMed ID: 32703466
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Facioscapulohumeral muscular dystrophy.
    Padberg GW; van Engelen BG
    Curr Opin Neurol; 2009 Oct; 22(5):539-42. PubMed ID: 19724227
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Facioscapulohumeral muscular dystrophy.
    Fitzsimons RB
    Curr Opin Neurol; 1999 Oct; 12(5):501-11. PubMed ID: 10590886
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Diagnostic image (53). Facioscapulohumeral muscle dystrophy].
    de Visser M
    Ned Tijdschr Geneeskd; 2001 Sep; 145(35):1690. PubMed ID: 11561486
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype.
    Tonini MM; Pavanello RC; Gurgel-Giannetti J; Lemmers RJ; van der Maarel SM; Frants RR; Zatz M
    J Med Genet; 2004 Feb; 41(2):e17. PubMed ID: 14757867
    [No Abstract]   [Full Text] [Related]  

  • 9. Application of Optical Genome Mapping to the Genetic Diagnosis of Facioscapulohumeral Muscular Dystrophy 1.
    Lee ST
    Ann Lab Med; 2024 Sep; 44(5):383-384. PubMed ID: 38845487
    [No Abstract]   [Full Text] [Related]  

  • 10. [Facioscapulohumeral muscular dystrophy - twelve cases from two pedigrees].
    An R; Xu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):402-3. PubMed ID: 24928028
    [No Abstract]   [Full Text] [Related]  

  • 11. Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis.
    Lemmers RJL ; de Kievit P; van Geel M; van der Wielen MJ; Bakker E; Padberg GW; Frants RR; van der Maarel SM
    Ann Neurol; 2001 Dec; 50(6):816-9. PubMed ID: 11761483
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy.
    Zouvelou V; Manta P; Kalfakis N; Evdokimidis I; Vassilopoulos D
    J Clin Neurosci; 2009 Sep; 16(9):1218-9. PubMed ID: 19502063
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Finding the Determinants of Disease Severity in Facioscapulohumeral Muscular Dystrophy.
    Tawil R
    Neurology; 2023 Jul; 101(3):97-98. PubMed ID: 37277202
    [No Abstract]   [Full Text] [Related]  

  • 14. Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy.
    Kolski HK; Leonard NJ; Lemmers RJ; Bamforth JS
    Muscle Nerve; 2008 Apr; 37(4):526-9. PubMed ID: 18059038
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Facioscapulohumeral dystrophy.
    Pandya S; King WM; Tawil R
    Phys Ther; 2008 Jan; 88(1):105-13. PubMed ID: 17986494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ventilatory support in facioscapulohumeral muscular dystrophy.
    Carter GT; Bird TD
    Neurology; 2005 Jan; 64(2):401; author reply 401. PubMed ID: 15668464
    [No Abstract]   [Full Text] [Related]  

  • 18. Subclinical facioscapulohumeral muscular dystrophy masquerading as bilateral Coats disease in a woman.
    Vance SK; Wald KJ; Sherman J; Freund KB
    Arch Ophthalmol; 2011 Jun; 129(6):807-9. PubMed ID: 21670353
    [No Abstract]   [Full Text] [Related]  

  • 19. Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.
    Rudnik-Schöneborn S; Weis J; Kress W; Häusler M; Zerres K
    Neuromuscul Disord; 2008 Nov; 18(11):881-5. PubMed ID: 18684626
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.
    Kekou K; Fryssira H; Sophocleous C; Mavrou A; Manta P; Metaxotou C
    Mol Cell Probes; 2005 Dec; 19(6):422-4. PubMed ID: 16144755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.