Reiners K - Search Results

1

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. Ricker K, et al. Among authors: reiners k. Arch Neurol. 1995 Jan;52(1):25-31. doi: 10.1001/archneur.1995.00540250029009. Arch Neurol. 1995. PMID: 7826272

2

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. Schneider C, et al. Among authors: reiners k. Neurology. 2000 Aug 8;55(3):383-8. doi: 10.1212/wnl.55.3.383. Neurology. 2000. PMID: 10932272

3

[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. Schneider C, et al. Among authors: reiners k. Nervenarzt. 2001 Aug;72(8):618-24. doi: 10.1007/s001150170061. Nervenarzt. 2001. PMID: 11519202 Review. German.

4

Assessment of cardiovascular autonomic function in myotonic dystrophy type 2 (DM2/PROMM).

Flachenecker P, Schneider C, Cursiefen S, Ricker K, Toyka KV, Reiners K. Flachenecker P, et al. Among authors: reiners k. Neuromuscul Disord. 2003 May;13(4):289-93. doi: 10.1016/s0960-8966(02)00277-8. Neuromuscul Disord. 2003. PMID: 12868497

5

Musculoskeletal pain in patients with myotonic dystrophy type 2.

George A, Schneider-Gold C, Zier S, Reiners K, Sommer C. George A, et al. Among authors: reiners k. Arch Neurol. 2004 Dec;61(12):1938-42. doi: 10.1001/archneur.61.12.1938. Arch Neurol. 2004. PMID: 15596616

6

Mycophenolate mofetil in the therapy of severe myasthenia gravis.

Schneider C, Gold R, Reiners K, Toyka KV. Schneider C, et al. Among authors: reiners k. Eur Neurol. 2001;46(2):79-82. doi: 10.1159/000050768. Eur Neurol. 2001. PMID: 11528156

7

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. Schneider-Gold C, et al. Among authors: reiners k. Neurology. 2003 Feb 11;60(3):500-2. doi: 10.1212/01.wnl.0000044405.29988.e1. Neurology. 2003. PMID: 12578937 Clinical Trial.

8

LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments.

Reilich P, Petersen JA, Vielhaber S, Mawrin C, Schneider-Gold C, Sommer C, Reiners K, Deschauer M, Pongratz D, Lochmüller H, Walter MC. Reilich P, et al. Among authors: reiners k. Acta Myol. 2006 Oct;25(2):73-6. Acta Myol. 2006. PMID: 18593008

9

Involvement of the visual pathway in hereditary neuropathy with liability to pressure palsies.

Schneider C, Reiners K, Friedl W, Ebner R, Toyka KV. Schneider C, et al. Among authors: reiners k. J Neurol. 2000 Mar;247(3):222-3. doi: 10.1007/s004150050569. J Neurol. 2000. PMID: 10787121 No abstract available.

10

Camptocormia in Parkinson's disease mimicked by focal myositis of the paraspinal muscles.

Wunderlich S, Csoti I, Reiners K, Günthner-Lengsfeld T, Schneider C, Becker G, Naumann M. Wunderlich S, et al. Among authors: reiners k. Mov Disord. 2002 May;17(3):598-600. doi: 10.1002/mds.10110. Mov Disord. 2002. PMID: 12112214

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