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[BOOK] Fiber optic sensors: an introduction for engineers and scientists

E Udd… - 2011 - books.google.com
Copyright Ó 2011 by John Wiley & Sons, Inc. All rights reserved. Published by John Wiley &
Sons, Inc., Hoboken, New Jersey Published simultaneously in Canada No part of this publication
may be reproduced, stored in a retrieval system, or transmitted in any form or by any ...
Cited by 297 - Related articles - All 6 versions

Population frequency of myotonic dystrophy

[PDF] from cnrs.frB Udd, T Suominen, LL Bachinski, S Auvinen… - 2011 - peer.ccsd.cnrs.fr
... Biomedical Sciences, Houston, TX, USA 8. Bjarne Udd,1,4,10,11* 1Neuromuscular Research
Unit, University of Tampere, 33520 ... Bjarne Udd, MD, Ph.D., Tel: +358 9 19125075; Fax: +358
9 19125073; Email: bjarne.udd@netikka.fi peer-00618486, version 1 - 2 Sep 2011 ...

Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy.

…, JE Landers, RH Brown Jr, B Udd… - American journal of …, 2011 - ncbi.nlm.nih.gov
Linkage analysis of the dominant distal myopathy we previously identified in a large Australian
family demonstrated one significant linkage region located on chromosome 7 and encompassing
18.6 Mbp and 151 genes. The strongest candidate gene was FLNC because filamin C, ...

Normal muscle MRI does not preclude increased connective tissue in muscle of recessive myotonia congenita

…, T Suominen, S Penttilä, B Udd… - Acta Neurologica …, 2011 - Wiley Online Library
... How to Cite. Hilbert, P., Frank, S., Raheem, O., Suominen, T., Penttilä, S., Udd, B. and Fischer,
D. (2011), Normal muscle MRI does not preclude increased connective tissue in muscle of
recessive myotonia congenita. Acta Neurologica Scandinavica, 124: 146–147. ...
All 2 versions

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy

…, D Auboeuf, L Garcia, P Zimmermann, B Udd… - Nature Medicine, 2011 - nature.com
Myotonic dystrophy is the most common muscular dystrophy in adults and the first recognized
example of an RNA-mediated disease. Congenital myotonic dystrophy (CDM1) and myotonic
dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant ...
Cited by 3 - All 3 versions

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