Cohn RD - Search Results

1

Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.

Franz WM, Müller M, Müller OJ, Herrmann R, Rothmann T, Cremer M, Cohn RD, Voit T, Katus HA. Franz WM, et al. Among authors: cohn rd. Lancet. 2000 May 20;355(9217):1781-5. doi: 10.1016/S0140-6736(00)02266-2. Lancet. 2000. PMID: 10832829

2

Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle.

Cohn RD, Mayer U, Saher G, Herrmann R, van der Flier A, Sonnenberg A, Sorokin L, Voit T. Cohn RD, et al. J Neurol Sci. 1999 Mar 1;163(2):140-52. doi: 10.1016/s0022-510x(99)00012-x. J Neurol Sci. 1999. PMID: 10371075

3

Changes of laminin beta 2 chain expression in congenital muscular dystrophy.

Cohn RD, Herrmann R, Wewer UM, Voit T. Cohn RD, et al. Neuromuscul Disord. 1997 Sep;7(6-7):373-8. doi: 10.1016/s0960-8966(97)00072-2. Neuromuscul Disord. 1997. PMID: 9327401

4

Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases.

Cohn RD, Herrmann R, Sorokin L, Wewer UM, Voit T. Cohn RD, et al. Neurology. 1998 Jul;51(1):94-100. doi: 10.1212/wnl.51.1.94. Neurology. 1998. PMID: 9674785

5

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation.

Voit T, Cohn RD, Sperner J, Leube B, Sorokin L, Toda T, Herrmann R. Voit T, et al. Among authors: cohn rd. Neuromuscul Disord. 1999 Mar;9(2):95-101. doi: 10.1016/s0960-8966(98)00091-1. Neuromuscul Disord. 1999. PMID: 10220864

6

Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus.

Voit T, Kutz P, Leube B, Neuen-Jacob E, Schröder JM, Cavallotti D, Vaccario ML, Schaper J, Broich P, Cohn R, Baethmann M, Göhlich-Ratmann G, Scoppetta C, Herrmann R. Voit T, et al. Neuromuscul Disord. 2001 Jan;11(1):11-9. doi: 10.1016/s0960-8966(00)00158-9. Neuromuscul Disord. 2001. PMID: 11166161

7

Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.

Cohn RD, Gillessen-Kaesbach G, Dobyns WB, Kahn T, Lenard HG, Voit T. Cohn RD, et al. Am J Med Genet. 1996 May 3;63(1):314-7. doi: 10.1002/(SICI)1096-8628(19960503)63:1<314::AID-AJMG52>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723127

8

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.

Coral-Vazquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, Davisson RL, Straub V, Barresi R, Bansal D, Hrstka RF, Williamson R, Campbell KP. Coral-Vazquez R, et al. Among authors: cohn rd. Cell. 1999 Aug 20;98(4):465-74. doi: 10.1016/s0092-8674(00)81975-3. Cell. 1999. PMID: 10481911 Free article.

9

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.

Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Durbeej M, et al. Among authors: cohn rd. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176 Free article.

10

Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.

Cohn RD, Durbeej M, Moore SA, Coral-Vazquez R, Prouty S, Campbell KP. Cohn RD, et al. J Clin Invest. 2001 Jan;107(2):R1-7. doi: 10.1172/JCI11642. J Clin Invest. 2001. PMID: 11160141 Free PMC article.

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