BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 8664567)

  • 1. Proximal myotonic myopathy: mini-review of a recently delineated clinical disorder.
    MOxley RT
    Neuromuscul Disord; 1996 Mar; 6(2):87-93. PubMed ID: 8664567
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy.
    Ricker K; Koch MC; Lehmann-Horn F; Pongratz D; Speich N; Reiners K; Schneider C; Moxley RT
    Arch Neurol; 1995 Jan; 52(1):25-31. PubMed ID: 7826272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carrell-Krusen Symposium Invited Lecture-1997. Myotonic disorders in childhood: diagnosis and treatment.
    Moxley RT
    J Child Neurol; 1997 Feb; 12(2):116-29. PubMed ID: 9075021
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The expanding clinical and genetic spectrum of the myotonic dystrophies.
    Ricker K
    Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?
    Udd B; Krahe R; Wallgren-Pettersson C; Falck B; Kalimo H
    Neuromuscul Disord; 1997 Jun; 7(4):217-28. PubMed ID: 9196902
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).
    Day JW; Roelofs R; Leroy B; Pech I; Benzow K; Ranum LP
    Neuromuscul Disord; 1999 Jan; 9(1):19-27. PubMed ID: 10063831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Myotonic dystrophy (DM/Curschmann-Steinert disease) and proximal myotonic myopathy (PROMM/Ricker syndrome). Myotonic muscle diseases with multisystemic manifestations].
    Schneider C; Reiners K; Toyka KV
    Nervenarzt; 2001 Aug; 72(8):618-24. PubMed ID: 11519202
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The myotonic dystrophies.
    Thornton C
    Semin Neurol; 1999; 19(1):25-33. PubMed ID: 10711986
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.
    Meola G; Sansone V; Radice S; Skradski S; Ptacek L
    Neuromuscul Disord; 1996 May; 6(3):143-50. PubMed ID: 8784800
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromes.
    Schneider C; Wessig C; Müller CR; Brechtelsbauer D; Grimm T
    Neuromuscul Disord; 2001 Jul; 11(5):485-8. PubMed ID: 11404122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts.
    Ricker K; Koch MC; Lehmann-Horn F; Pongratz D; Otto M; Heine R; Moxley RT
    Neurology; 1994 Aug; 44(8):1448-52. PubMed ID: 8058147
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myotonic syndromes.
    Mankodi A; Thornton CA
    Curr Opin Neurol; 2002 Oct; 15(5):545-52. PubMed ID: 12351998
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Myotonic dystrophies.
    Meola G
    Curr Opin Neurol; 2000 Oct; 13(5):519-25. PubMed ID: 11073357
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.
    Meola G; Cardani R
    Neurol Sci; 2017 Apr; 38(4):535-546. PubMed ID: 28078562
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myotonic dystrophy.
    Jozefowicz RF; Griggs RC
    Neurol Clin; 1988 Aug; 6(3):455-72. PubMed ID: 3065594
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Myotonic dystrophies type 1 and 2: anesthetic care.
    Veyckemans F; Scholtes JL
    Paediatr Anaesth; 2013 Sep; 23(9):794-803. PubMed ID: 23384336
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and genetic heterogeneity in myotonic dystrophies.
    Meola G
    Muscle Nerve; 2000 Dec; 23(12):1789-99. PubMed ID: 11102902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Proximal myotonic myopathy (PROMM). Clinical variability within a family].
    Eger K; Schulte-Mattler WJ; Zierz S
    Nervenarzt; 1997 Oct; 68(10):839-44. PubMed ID: 9441258
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Proximal myotonial myopathy (PROMM): clinical and histology study].
    Bassez G; Attarian S; Laforêt P; Azulay JP; Rouche A; Ferrer X; Urtizberea JA; Pellissier JF; Duboc D; Fardeau M; Pouget J; Eymard B
    Rev Neurol (Paris); 2001 Feb; 157(2):209-18. PubMed ID: 11283467
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
    Kress W; Mueller-Myhsok B; Ricker K; Schneider C; Koch MC; Toyka KV; Mueller CR; Grimm T
    Neuromuscul Disord; 2000 Oct; 10(7):478-80. PubMed ID: 10996776
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.