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Multiexon deletions account for 15% of congenital myasthenic...
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Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing Karen Gaudon,1 Isabelle Pe´nisson-Besnier,2 ...
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Researchgate: Karen Gaudon
Paris, France
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authors:"Karen Gaudon" - Search | Paperity
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CiteSeerX — MUSK, a new target for mutations causing congenital...
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BibTeX @ARTICLE{Faraut04musk,a, author = {Brice Faraut and Aymeric Ravel-chapuis and Pascale Richard and Karen Gaudon and Ra Prioleau and Ruth Herbst and Evelyne ...
MUSK, a new target for mutations causing congenital myasthenic...
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congenital myasthenic syndrome. Fre. ´. de. ´. ric Chevessier. 1. , Brice Faraut. 1. , Aymeric Ravel-Chapuis. 2. , Pascale Richard. 1,3. ,. Karen Gaudon. 1,3. , Ste.
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Karen Gaudon's Research | CureHunter
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Karen Gaudon Selected Research. Karen Gaudon Research Topics. Disease. 5, Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital)
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Identification of an agrin mutation that causes congenital myasthenia...
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Identification of an agrin mutation that causes congenital myasthenia and affects synapse function C Huzé, S Bauché, P Richard, F Chevessier, E Goillot,
Evolutionary Psychology News - Yahoo Groups
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... Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, ...
Gaudon - Names Encyclopedia
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Karen Gaudon (1) Marion Gaudon (1) Yvette Gaudon (1) Solenn Gaudon (1) Yves Gaudon (1) Johan Gaudon (1) Laurence Gaudon (1) Gilbert Gaudon (1) Germaine Gaudon (1)
A synonymous CHRNE mutation responsible for an aberrant splicing...
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Karen Gaudon. Inserm, U582, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière and Université Pierre et Marie Curie Paris 6, Paris, ...
PLOS ONE: A Mutation Causes MuSK Reduced Sensitivity to Agrin and...
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Affiliation: Medical University of Vienna, Center for Brain Research, Vienna, Austria. X. Karen Gaudon,. Affiliation: APHP, UF Cardiogénétique ...
Identification of an agrin mutation that causes congenital myasthenia...
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We report the case of a congenital myasthenic syndrome due to a mutation in AGRN, the gene encoding agrin, an extracellular matrix molecule released by the...
A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital...
hal.sorbonne-universite.fr
Asma Ben Ammar 1, 2 Payam Soltanzadeh 1 Stéphanie Bauché 1 Pascale Richard 3 Evelyne Goillot 4 Ruth Herbst 5Karen Gaudon
Biologie Aujourd'hui
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Biologie Aujourd'hui, anciennement Journal de la Société de Biologie, Organe officiel de la Société de Biologie
Altmetric – A Mutation Causes MuSK Reduced Sensitivity to Agrin and...
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by Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Hu Jan
Pascale.Richard - Publications List
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Pascale Richard, Karen Gaudon, Emmanuel Fournier, Christopher Jackson, Stéphanie Bauch é,
sommaire 199_1
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Frédéric Chevessier 1, Brice Faraut 1, Aymeric Ravel-Chapuis 2, Pascale Richard 1,3, Karen Gaudon 1,3, Stéphanie Bauché 1, Cassandra Prioleau 1
Session Simultanée èmes Assises de Génétique Humaine et -...
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Session Simultanée èmes Assises de Génétique Humaine et
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{php:anteprima(a:3:{i:0;s:446:"Caroline Huze´,1 Stephanie Bauche´,2,3,4 Pascale Richard,5 Frederic Chevessier,2,6 Evelyne Goillot,1 Karen Gaudon,5 Asma ...
مقاله جهش در مشک باعث سندرم میاستنیک مادرزادی - سایپرز، باش
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مقاله , در Journal of Physiology-Paris () توسط Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, Pascale Richard, Karen Gaudon, Stéphanie Bauché, ...
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