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Showing 1–3 of 3 results
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Research |
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
- Kevin P Kenna
- , Perry T C van Doormaal
- , Annelot M Dekker
- , Nicola Ticozzi
- , Brendan J Kenna
- , Frank P Diekstra
- , Wouter van Rheenen
- , Kristel R van Eijk
- , Ashley R Jones
- , Pamela Keagle
- , Aleksey Shatunov
- , William Sproviero
- , Bradley N Smith
- , Michael A van Es
- , Simon D Topp
- , Aoife Kenna
- , Jack W Miller
- , Claudia Fallini
- , Cinzia Tiloca
- , Russell L McLaughlin
- , Caroline Vance
- , Claire Troakes
- , Claudia Colombrita
- , Gabriele Mora
- , Andrea Calvo
- , Federico Verde
- , Safa Al-Sarraj
- , Andrew King
- , Daniela Calini
- , Jacqueline de Belleroche
- , Frank Baas
- , Anneke J van der Kooi
- , Marianne de Visser
- , Anneloor L M A ten Asbroek
- , Peter C Sapp
- , Diane McKenna-Yasek
- , Meraida Polak
- , Seneshaw Asress
- , José Luis Muñoz-Blanco
- , Tim M Strom
- , Thomas Meitinger
- , Karen E Morrison
- , Sandra D'Alfonso
- , Letizia Mazzini
- , Giacomo P Comi
- , Roberto Del Bo
- , Mauro Ceroni
- , Stella Gagliardi
- , Giorgia Querin
- , Cinzia Bertolin
- , Viviana Pensato
- , Barbara Castellotti
- , Stefania Corti
- , Cristina Cereda
- , Lucia Corrado
- , Gianni Sorarù
- , Giuseppe Lauria
- , Kelly L Williams
- , P Nigel Leigh
- , Garth A Nicholson
- , Ian P Blair
- , Claire S Leblond
- , Patrick A Dion
- , Guy A Rouleau
- , Hardev Pall
- , Pamela J Shaw
- , Martin R Turner
- , Kevin Talbot
- , Franco Taroni
- , Kevin B Boylan
- , Marka Van Blitterswijk
- , Rosa Rademakers
- , Jesús Esteban-Pérez
- , Alberto García-Redondo
- , Phillip Van Damme
- , Wim Robberecht
- , Adriano Chio
- , Cinzia Gellera
- , Carsten Drepper
- , Michael Sendtner
- , Antonia Ratti
- , Jonathan D Glass
- , Jesús S Mora
- , Nazli A Basak
- , Orla Hardiman
- , Albert C Ludolph
- , Peter M Andersen
- , Jochen H Weishaupt
- , Robert H Brown Jr
- , Ammar Al-Chalabi
- , Vincenzo Silani
- , Christopher E Shaw
- , Leonard H van den Berg
- , Jan H Veldink
- & John E Landers
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Research |
The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
- Bradley N Smith
- , Stephen Newhouse
- , Aleksey Shatunov
- , Caroline Vance
- , Simon Topp
- , Lauren Johnson
- , Jack Miller
- , Younbok Lee
- , Claire Troakes
- , Kirsten M Scott
- , Ashley Jones
- , Ian Gray
- , Jamie Wright
- , Tibor Hortobágyi
- , Safa Al-Sarraj
- , Boris Rogelj
- , John Powell
- , Michelle Lupton
- , Simon Lovestone
- , Peter C Sapp
- , Markus Weber
- , Peter J Nestor
- , Helenius J Schelhaas
- , Anneloor ALM ten Asbroek
- , Vincenzo Silani
- , Cinzia Gellera
- , Franco Taroni
- , Nicola Ticozzi
- , Leonard Van den Berg
- , Jan Veldink
- , Phillip Van Damme
- , Wim Robberecht
- , Pamela J Shaw
- , Janine Kirby
- , Hardev Pall
- , Karen E Morrison
- , Alex Morris
- , Jacqueline de Belleroche
- , J M B Vianney de Jong
- , Frank Baas
- , Peter M Andersen
- , John Landers
- , Robert H Brown Jr
- , Michael E Weale
- , Ammar Al-Chalabi
- & Christopher E Shaw
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Research |
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
- Chi-Hong Wu
- , Claudia Fallini
- , Nicola Ticozzi
- , Pamela J. Keagle
- , Peter C. Sapp
- , Katarzyna Piotrowska
- , Patrick Lowe
- , Max Koppers
- , Diane McKenna-Yasek
- , Desiree M. Baron
- , Jason E. Kost
- , Paloma Gonzalez-Perez
- , Andrew D. Fox
- , Jenni Adams
- , Franco Taroni
- , Cinzia Tiloca
- , Ashley Lyn Leclerc
- , Shawn C. Chafe
- , Dev Mangroo
- , Melissa J. Moore
- , Jill A. Zitzewitz
- , Zuo-Shang Xu
- , Leonard H. van den Berg
- , Jonathan D. Glass
- , Gabriele Siciliano
- , Elizabeth T. Cirulli
- , David B. Goldstein
- , Francois Salachas
- , Vincent Meininger
- , Wilfried Rossoll
- , Antonia Ratti
- , Cinzia Gellera
- , Daryl A. Bosco
- , Gary J. Bassell
- , Vincenzo Silani
- , Vivian E. Drory
- , Robert H. Brown Jr
- & John E. Landers
