Literature DB >> 12398845

98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The Netherlands.

F Muntoni1, E Bertini, C Bönnemann, M Brockington, S Brown, K Bushby, M Fiszman, C Körner, E Mercuri, L Merlini, J Hewitt, S Quijano-Roy, N Romero, S Squarzoni, C A Sewry, V Straub, H Topaloglu, G Haliloglu, T Voit, U Wewer, P Guicheney.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12398845     DOI: 10.1016/s0960-8966(02)00068-8

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


× No keyword cloud information.
  6 in total

Review 1.  The congenital muscular dystrophies: recent advances and molecular insights.

Authors:  Jerry R Mendell; Daniel R Boué; Paul T Martin
Journal:  Pediatr Dev Pathol       Date:  2006 Nov-Dec

2.  Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A.

Authors:  Ajay Kumar; Jenny Yamauchi; Tanya Girgenrath; Mahasweta Girgenrath
Journal:  Hum Mol Genet       Date:  2011-03-26       Impact factor: 6.150

Review 3.  Collagen VI related muscle disorders.

Authors:  A K Lampe; K M D Bushby
Journal:  J Med Genet       Date:  2005-09       Impact factor: 6.318

4.  Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI.

Authors:  Claudia C Leite; Leandro T Lucato; Maria G M Martin; Lucio G Ferreira; Maria B D Resende; Mary S Carvalho; Suely K N Marie; J Randy Jinkins; Umbertina C Reed
Journal:  Pediatr Radiol       Date:  2005-03-05

5.  New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.

Authors:  Te-Cheng Pan; Rui-Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bönnemann; Mon-Li Chu
Journal:  Am J Hum Genet       Date:  2003-07-01       Impact factor: 11.025

6.  Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy.

Authors:  Yan-Zhi Zhang; Dan-Hua Zhao; Hai-Po Yang; Ai-Jie Liu; Xing-Zhi Chang; Dao-Jun Hong; Carsten Bonnemann; Yun Yuan; Xi-Ru Wu; Hui Xiong
Journal:  World J Pediatr       Date:  2014-05-07       Impact factor: 2.764

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.