221 related articles for article (PubMed ID: 10399862)
1. Myotonic dystrophy and proximal myotonic myophathy.
Ricker K
J Neurol; 1999 May; 246(5):334-8. PubMed ID: 10399862
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. The myotonic dystrophies.
Thornton C
Semin Neurol; 1999; 19(1):25-33. PubMed ID: 10711986
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. 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]
7. 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]
8. Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMM.
Sun C; Henriksen OA; Tranebjaerg L
Clin Genet; 1999 Dec; 56(6):457-61. PubMed ID: 10665666
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
Bachinski LL; Udd B; Meola G; Sansone V; Bassez G; Eymard B; Thornton CA; Moxley RT; Harper PS; Rogers MT; Jurkat-Rott K; Lehmann-Horn F; Wieser T; Gamez J; Navarro C; Bottani A; Kohler A; Shriver MD; Sallinen R; Wessman M; Zhang S; Wright FA; Krahe R
Am J Hum Genet; 2003 Oct; 73(4):835-48. PubMed ID: 12970845
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?
Abbruzzese C; Krahe R; Liguori M; Tessarolo D; Siciliano MJ; Ashizawa T; Giacanelli M
J Neurol; 1996 Oct; 243(10):715-21. PubMed ID: 8923304
[TBL] [Abstract][Full Text] [Related]
14. Proximal myotonic myopathy. Analysis of 3 Swedish cases.
Schuitevoerder K; Ansved T; Solders G; Borg K
Acta Neurol Scand; 1997 Oct; 96(4):266-70. PubMed ID: 9325482
[TBL] [Abstract][Full Text] [Related]
15. A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature.
Meola G; Sansone V
Ital J Neurol Sci; 1996 Oct; 17(5):347-53. PubMed ID: 8933228
[TBL] [Abstract][Full Text] [Related]
16. Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.
Schneider C; Ziegler A; Ricker K; Grimm T; Kress W; Reimers CD; Meinck H; Reiners K; Toyka KV
Neurology; 2000 Aug; 55(3):383-8. PubMed ID: 10932272
[TBL] [Abstract][Full Text] [Related]
17. [DNA diagnosis in myotonic dystrophy].
Tachi N
Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
