Grimm T - Search Results

1

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. Schneider C, et al. Among authors: grimm t. Neuromuscul Disord. 2001 Jul;11(5):485-8. doi: 10.1016/s0960-8966(00)00218-2. Neuromuscul Disord. 2001. PMID: 11404122

2

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. Kress W, et al. Among authors: grimm t. Neuromuscul Disord. 2000 Oct;10(7):478-80. doi: 10.1016/s0960-8966(00)00129-2. Neuromuscul Disord. 2000. PMID: 10996776

3

Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM).

Schneider C, Grimm T, Kress W, Sommer C, Müller CR. Schneider C, et al. Among authors: grimm t. Neuromuscul Disord. 2000 Oct;10(7):481-3. doi: 10.1016/s0960-8966(00)00115-2. Neuromuscul Disord. 2000. PMID: 10996777

4

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: grimm t. Neurology. 2000 Aug 8;55(3):383-8. doi: 10.1212/wnl.55.3.383. Neurology. 2000. PMID: 10932272

5

Linkage of proximal myotonic myopathy to chromosome 3q.

Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR. Ricker K, et al. Among authors: grimm t. Neurology. 1999 Jan 1;52(1):170-1. doi: 10.1212/wnl.52.1.170. Neurology. 1999. PMID: 9921867

6

Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.

Grimm T, Kress W, Meng G, Müller CR. Grimm T, et al. Acta Myol. 2012 Dec;31(3):179-83. Acta Myol. 2012. PMID: 23620649 Free PMC article.

7

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec I, Kress W, Meng G, Müller B, Müller CR, Grimm T. Stec I, et al. Among authors: grimm t. J Med Genet. 1995 Dec;32(12):930-3. doi: 10.1136/jmg.32.12.930. J Med Genet. 1995. PMID: 8825917 Free PMC article.

8

Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19.

Kausch K, Lehmann-Horn F, Janka M, Wieringa B, Grimm T, Müller CR. Kausch K, et al. Among authors: grimm t. Genomics. 1991 Jul;10(3):765-9. doi: 10.1016/0888-7543(91)90461-m. Genomics. 1991. PMID: 1889818

9

Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy.

Grimm T, Müller B, Müller CR, Janka M. Grimm T, et al. J Med Genet. 1990 Nov;27(11):683-7. doi: 10.1136/jmg.27.11.683. J Med Genet. 1990. PMID: 2277383 Free PMC article.

10

Parental source effect on inherited mutations in the dystrophin gene of mice and humans.

Kress W, Grimm T, Müller CR, Keller H, Bittner R. Kress W, et al. Among authors: grimm t. Acta Genet Med Gemellol (Roma). 1996;45(1-2):251-3. doi: 10.1017/s0001566000001409. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872041 No abstract available.

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