Jocelyn LAPORTE

Publications

• 2017

  • 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

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • Antisense oligonucleotide-mediated Dnm2 knockdown prevents and reverts myotubular myopathy in mice

    • Hichem Tasfaout
    • Suzie Buono
    • Shuling Guo
    • Christine Kretz
    • Nadia Messaddeq
    • Sheri Booten
    • Sarah Greenlee
    • Brett Monia
    • Belinda Cowling
    • Jocelyn Laporte

    Nature Communications ; Volume: 8 ; Page: 15661

    HAL DOI

  • ORAI1 mutations with distinct channel gating defects in tubular aggregate myopathy

    • Johann Bohm
    • Monica Bulla
    • Jill Urquhart
    • Edoardo Malfatti
    • Simon Williams
    • James O'Sullivan
    • Anastazja Szlauer
    • Catherine Koch
    • Giovanni Baranello
    • Martin Mora
    • Michela Ripolone
    • Raffaella Violano
    • Maurizio Moggio
    • Helen Kingston
    • Timothy Dawson
    • Christian Degoede
    • John Nixon
    • Anne Boland
    • Jean-François Deleuze
    • Norma Romero
    • ...

    Human Mutation ; Volume: 38 ; Page: 426-438

    HAL DOI

  • 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

    HAL DOI

  • CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy

    • Johann Bohm
    • Xavière Lornage
    • Frédéric Chevessier
    • Catherine Birck
    • Simona Zanotti
    • Paola Cudia
    • Monica Bulla
    • Florence Granger
    • Mai Thao Bui
    • Maxime Sartori
    • Christiane Schneider-Gold
    • Edoardo Malfatti
    • Norma Romero
    • Marina Mora
    • Jocelyn Laporte

    Acta Neuropathologica ; Volume: 135 ; Page: 149-151

    HAL DOI

  • Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems

    • Gemma Walmsley
    • Stéphane Blot
    • Kerrie Venner
    • Caroline Sewry
    • Jocelyn Laporte
    • Jordan Blondelle
    • Inès Barthélémy
    • Marie Maurer
    • Nicolas Blanchard-Gutton
    • Fanny Pilot-Storck
    • Laurent L. Tiret
    • Richard Piercy

    American Journal of Pathology ; Volume: 187 ; Page: 441-456

    HAL DOI

• 2016

  • Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion

    • Nasim Vasli
    • Elizabeth Harris
    • Jason Karamchandani
    • Eric Bareke
    • Jacek Majewski
    • Norma B. Romero
    • Tanya Stojkovic
    • Rita Barresi
    • Hichem Tasfaout
    • Richard Charlton
    • Edoardo Malfatti
    • Johann Böhm
    • Chiara Marini-Bettolo
    • Karine Choquet
    • Marie-Josée Dicaire
    • Yi-Hong Shao
    • Ana Topf
    • Erin O’ferrall
    • Bruno Eymard
    • Volker Straub
    • ...

    Brain - A Journal of Neurology ; Volume: 140 ; Page: 37-48

    HAL DOI