Pathophysiology of neuromuscular diseases
Team Leader : Jocelyn LAPORTE
Department : Translational medecine and neurogenetics
Valérie BIANCALANA
Researcher
valerie.biancalana@igbmc.fr
Research team(s)
Research subgroup(s)
Publications
2018
Article in a journal
Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy
- Valérie Biancalana
- Norma Romero
- Inger Johanne Thuestad
- Jaakko Ignatius
- Janne Kataja
- Maria Gardberg
- Dephine Héron
- Edoardo Malfatti
- Anders Oldfors
- Jocelyn Laporte
Acta Neuropathologica Communications ; Volume: 6
Article in a journal
A Roma founder BIN1 mutation causes a novel phenotype of centronuclear myopathy with rigid spine
- Macarena Cabrera-Serrano
- Fabiola Mavillard
- Valerie Biancalana
- Eloy Rivas
- Bharti Morar
- Aurelio Hernandez-Lain
- Montse Olive
- Nuria Muelas
- Eduardo Khan
- Alejandra Carvajal
- Pablo Quiroga
- Jordi Diaz-Manera
- Mark Davis
- Rainiero Avila
- Cristina Dominguez
- Norma Romero
- Juan Vilchez
- David Comas
- Nigel Laing
- Jocelyn Laporte
- ...
Neurology ; Volume: 91 ; Page: 339-348
Article in a journal
An integrated modelling methodology for estimating the prevalence of centronuclear myopathy
- I Vandersmissen
- Valerie Biancalana
- L Servais
- J Dowling
- G Vander Stichele
- S van Rooijen
- L Thielemans
Neuromuscul Disord ; Volume: 28 ; Page: 766-777
2017
Article in a journal
Recessive myopalladin mutations cause congenital cap myopathy with unusual rods
- E. Malfatti
- X. Lornage
- C. Chéraud
- R. Schneider
- V. Biancalana
- J. Cuisset
- M. Garibaldi
- B. Eymard
- M. Fardeau
- A. Boland
- J. Deleuze
- J. Thompson
- J. Böhm
- N. Romero
- J. Laporte
Neuromuscular Disorders ; Volume: 27 ; Page: S185
Article in a journal
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy
- Vanessa Schartner
- Norma Romero
- Sandra Donkervoort
- Susan Treves
- Pinki Munot
- Tyler Pierson
- Ivana Dabaj
- Edoardo Malfatti
- Irina Zaharieva
- Francesco Zorzato
- Osario Abath Neto
- Guy Brochier
- Xavière Lornage
- Bruno Eymard
- Ana Taratuto
- Johann Böhm
- Hernan Gonorazky
- Leigh Ramos-Platt
- Lucy Feng
- Rahul Phadke
- ...
Acta Neuropathologica ; Volume: 133 ; Page: 517-533
Article in a journal
Dominant Centronuclear Myopathy with Early Childhood Onset due to a Novel Mutation in BIN1
- Carlyn Kouwenberg
- Johann Bohm
- Corrie Erasmus
- Irene van Balken
- Sandra Vos
- Benno Kusters
- Erik Kamsteeg
- Valerie Biancalana
- Catherine Koch
- Nicolas Dondaine
- Jocelyn Laporte
- Nicol Voermans
Journal of Neuromuscular Diseases ; Volume: 4 ; Page: 349-355
Article in a journal
HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy
- Yon Andoni Echaniz-Laguna
- Xavière Lornage
- Beatrice Lannes
- Raphael Schneider
- Guillaume Bierry
- Nicolas Dondaine
- Anne Boland
- J Deleuze
- Johann Bohm
- Julie D. Thompson
- Jocelyn Laporte
- Valerie Biancalana
Acta Neuropathologica ; Volume: 134 ; Page: 163-165
Article in a journal
Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation
- Osorio Abath Neto
- Carlos Heise
- Cristiane de Araújo Martins Moreno
- Eduardo de Paula Estephan
- Lilia Mesrob
- Doris Lechner
- Anne Boland
- Jean-François Deleuze
- Acary Souza Bulle Oliveira
- Umbertina Reed
- Valerie Biancalana
- Jocelyn Laporte
- Edmar Zanoteli
Canadian Journal of Neurological Sciences ; Volume: 44 ; Page: 125-127
Article in a journal
Recessive MYPN mutations cause cap myopathy with occasional nemaline rods
- Xavière Lornage
- Edoardo Malfatti
- Raphael Schneider
- Valerie Biancalana
- Jean Cuisset
- Matteo Garibaldi
- Bruno Eymard
- Michel Fardeau
- Anne Boland
- Jean Deleuze
- Julie D. Thompson
- Robert Carlier
- Johann Bohm
- Norma Romero
- Jocelyn Laporte
Ann Neurol ; Volume: 81 ; Page: 467-473
2016
Article in a journal
A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels
- O. Abath Neto
- M. R. Silva
- A. Martins Cde
- S. Oliveira Ade
- U. C. Reed
- Valérie Biancalana
- J. B. Pesquero
- Jocelyn Laporte
- E. Zanoteli
Pediatric neurology ; Volume: 58 ; Page: 107-12