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 *

146 related articles for article (PubMed ID: 8741360)

  • 21. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
    Schmitt HP; Krause KH
    Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
    van Overveld PG; Enthoven L; Ricci E; Rossi M; Felicetti L; Jeanpierre M; Winokur ST; Frants RR; Padberg GW; van der Maarel SM
    Ann Neurol; 2005 Oct; 58(4):569-76. PubMed ID: 16178028
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Beevor's sign and facioscapulohumeral dystrophy.
    Awerbuch GI; Nigro MA; Wishnow R
    Arch Neurol; 1990 Nov; 47(11):1208-9. PubMed ID: 2146943
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Permanent muscle weakness in McArdle disease.
    Nadaj-Pakleza AA; Vincitorio CM; Laforêt P; Eymard B; Dion E; Teijeira S; Vietez I; Jeanpierre M; Navarro C; Stojkovic T
    Muscle Nerve; 2009 Sep; 40(3):350-7. PubMed ID: 19670320
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies.
    Morosetti R; Mirabella M; Gliubizzi C; Broccolini A; Sancricca C; Pescatori M; Gidaro T; Tasca G; Frusciante R; Tonali PA; Cossu G; Ricci E
    Stem Cells; 2007 Dec; 25(12):3173-82. PubMed ID: 17761758
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Differential diagnosis of scapuloperoneal syndrome.
    Milanov I; Ishpekova B
    Electromyogr Clin Neurophysiol; 1997 Mar; 37(2):73-8. PubMed ID: 9098670
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Diagnosing and managing muscular dystrophy.
    Orrell RW
    Practitioner; 2012 Sep; 256(1754):21-4, 2-3. PubMed ID: 23252132
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The study of deafness in patients with facioscapulohumeral dystrophy].
    Sánchez-Alcón MD; Pérez Garrigues H; Vílchez J; Casanova B; Morera C
    Acta Otorrinolaringol Esp; 1994; 45(2):79-82. PubMed ID: 8086213
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Gene hunting of facioscapulohumeral muscular dystrophy].
    Song MD; Arahata K
    No To Shinkei; 1996 Apr; 48(4):307-13. PubMed ID: 8679326
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. [A clinical trial of creatine monohydrate in muscular dystrophy patients].
    Matsumura T; Yokoe M; Nakamori M; Hattori N; Saito T; Nozaki S; Fujimura H; Shinno S
    Rinsho Shinkeigaku; 2004 Oct; 44(10):661-6. PubMed ID: 15568480
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. 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]  

  • 34. Prosthetic treatment of a patient with facioscapulohumeral muscular dystrophy: a clinical report.
    Güler AU; Ceylan G; Ozkoç O; Aydiin M; Cengiz N
    J Prosthet Dent; 2003 Oct; 90(4):321-4. PubMed ID: 14564285
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Acupuncture Improves the Facial Muscular Function in a Case of Facioscapulohumeral Muscular Dystrophy.
    Liu Y; Xiao F; Liang X
    J Acupunct Meridian Stud; 2019 Apr; 12(2):73-76. PubMed ID: 30508665
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Epidemiology and clinical polymorphism of the humero-scapulo-facial form of progressive muscular dystrophy].
    Sattarova SK; Guliaeva AE; Khannanova FK
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):23-7. PubMed ID: 2163162
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
    Butz M; Koch MC; Müller-Felber W; Lemmers RJ; van der Maarel SM; Schreiber H
    J Neurol; 2003 Aug; 250(8):932-7. PubMed ID: 12928911
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Facioscapulohumeral muscular dystrophy with congenital absence of sternocleidomastoid muscles.
    Penchaszadeh V
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):116-7. PubMed ID: 5173120
    [No Abstract]   [Full Text] [Related]  

  • 40. [Association of dystrophinopathy with facial-scapular-humeral dystrophy in the same family].
    Serrano PJ; García Pérez A; Vilches RM; Mínguez A; Hernández Ramos FJ
    Rev Neurol; 1995; 23(120):301-3. PubMed ID: 7497180
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.