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Items: 1 to 20 of 167

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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 3rd.

Arch Neurol. 1995 Jan;52(1):25-31.

PMID:
7826272
5.

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 3rd.

Neurology. 1994 Aug;44(8):1448-52.

PMID:
8058147
6.

[Proximal myotonic myopathy (PROMM). Clinical variability within a family].

Eger K, Schulte-Mattler WJ, Zierz S.

Nervenarzt. 1997 Oct;68(10):839-44. German.

PMID:
9441258
7.

Myotonic dystrophy and proximal myotonic myophathy.

Ricker K.

J Neurol. 1999 May;246(5):334-8. Review.

PMID:
10399862
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.

PMID:
10665666
9.

[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. French.

PMID:
11283467
10.

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.

PMID:
9829272
11.

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

Seznec H, Agbulut O, Sergeant N, Savouret C, Ghestem A, Tabti N, Willer JC, Ourth L, Duros C, Brisson E, Fouquet C, Butler-Browne G, Delacourte A, Junien C, Gourdon G.

Hum Mol Genet. 2001 Nov 1;10(23):2717-26.

12.

The myotonic dystrophies.

Thornton C.

Semin Neurol. 1999;19(1):25-33. Review.

PMID:
10711986
13.

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.

PMID:
10063831
14.

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 8;55(3):383-8.

PMID:
10932272
15.

Proximal myotonic myopathy: clinical, electrophysiological and pathological findings in a family.

Kohler A, Burkhard P, Hefft S, Bottani A, Pizzolato GP, Magistris MR.

Eur Neurol. 2000;43(1):50-3.

PMID:
10601809
16.

The expanding clinical and genetic spectrum of the myotonic dystrophies.

Ricker K.

Acta Neurol Belg. 2000 Sep;100(3):151-5.

PMID:
11098287
17.

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.

PMID:
9325482
18.

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.

PMID:
9008490
19.

Proximal myotonic myopathy (PROMM) presenting as myotonia during pregnancy.

Newman B, Meola G, O'Donovan DG, Schapira AH, Kingston H.

Neuromuscul Disord. 1999 May;9(3):144-9.

PMID:
10382907
20.

A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.

Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D.

Brain. 2004 Sep;127(Pt 9):1979-92. Epub 2004 Jun 23.

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