120 related articles for article (PubMed ID: 10714590)
21. 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]
22. Hypothyroidism unmasking proximal myotonic myopathy.
Sansone V; Griggs RC; Moxley RT
Neuromuscul Disord; 2000 Mar; 10(3):165-72. PubMed ID: 10734262
[TBL] [Abstract][Full Text] [Related]
23. Musculoskeletal pain in patients with myotonic dystrophy type 2.
George A; Schneider-Gold C; Zier S; Reiners K; Sommer C
Arch Neurol; 2004 Dec; 61(12):1938-42. PubMed ID: 15596616
[TBL] [Abstract][Full Text] [Related]
24. [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]
25. A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
Bönsch D; Scheer P; Neumann C; Lang-Roth R; Seifert E; Storch P; Weiller C; Lamprecht-Dinnesen A; Deufel T
Eur J Hum Genet; 2001 Mar; 9(3):165-70. PubMed ID: 11313754
[TBL] [Abstract][Full Text] [Related]
26. PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
Bönsch D; Neumann C; Lang-Roth R; Witte O; Lamprecht-Dinnesen A; Deufel T
Clin Genet; 2003 Jan; 63(1):73-5. PubMed ID: 12519376
[No Abstract] [Full Text] [Related]
27. Proximal myotonic myopathy: clinical, neuropathologic, and molecular genetic features.
Eisenschenk S; Triggs WJ; Pearl GS; Rojiani AM
Ann Clin Lab Sci; 2001 Apr; 31(2):140-6. PubMed ID: 11337902
[TBL] [Abstract][Full Text] [Related]
28. Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy.
Meola G; Sansone V; Perani D; Colleluori A; Cappa S; Cotelli M; Fazio F; Thornton CA; Moxley RT
Neurology; 1999 Sep; 53(5):1042-50. PubMed ID: 10496264
[TBL] [Abstract][Full Text] [Related]
29. Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2.
Jakubiczka S; Vielhaber S; Kress W; Küpferling P; Reuner U; Kunath B; Wieacker P
Neurogenetics; 2004 Feb; 5(1):55-9. PubMed ID: 14666402
[TBL] [Abstract][Full Text] [Related]
30. PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness.
Phillips MF; Rogers MT; Barnetson R; Braun C; Harley HG; Myring J; Stevens D; Wiles CM; Harper PS
Neuromuscul Disord; 1998 Oct; 8(7):439-46. PubMed ID: 9829272
[TBL] [Abstract][Full Text] [Related]
31. Proximal myotonic myopathy with MRI white matter abnormalities of the brain.
Hund E; Jansen O; Koch MC; Ricker K; Fogel W; Niedermaier N; Otto M; Kuhn E; Meinck HM
Neurology; 1997 Jan; 48(1):33-7. PubMed ID: 9008490
[TBL] [Abstract][Full Text] [Related]
32. Genetic mapping of a second myotonic dystrophy locus.
Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. A patient with proximal myotonic myopathy and parkinsonism.
Chu K; Cho JW; Song EC; Jeon BS
Can J Neurol Sci; 2002 May; 29(2):188-90. PubMed ID: 12035844
[TBL] [Abstract][Full Text] [Related]
35. The myotonic dystrophies.
Thornton C
Semin Neurol; 1999; 19(1):25-33. PubMed ID: 10711986
[TBL] [Abstract][Full Text] [Related]
36. Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study.
Kassubek J; Juengling FD; Hoffmann S; Rosenbohm A; Kurt A; Jurkat-Rott K; Steinbach P; Wolf M; Ludolph AC; Lehmann-Horn F; Lerche H; Weber YG
Neurosci Lett; 2003 Sep; 348(2):73-6. PubMed ID: 12902021
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. [Musculoskeletal pain as the most prominent feature in myotonic dystrophy type 2].
George A; Schneider-Gold C; Reiners K; Sommer C
Schmerz; 2006 Sep; 20(5):388, 390-4, 396-7. PubMed ID: 16758212
[TBL] [Abstract][Full Text] [Related]
39. Creatine monohydrate in DM2/PROMM: a double-blind placebo-controlled clinical study. Proximal myotonic myopathy.
Schneider-Gold C; Beck M; Wessig C; George A; Kele H; Reiners K; Toyka KV
Neurology; 2003 Feb; 60(3):500-2. PubMed ID: 12578937
[TBL] [Abstract][Full Text] [Related]
40. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.
Korneluk RG; MacKenzie AE; Nakamura Y; Dubé I; Jacob P; Hunter AG
Genomics; 1989 Oct; 5(3):596-604. PubMed ID: 2613241
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
