G. Rudolf
发表
Edouard Hirsch,
Dalila Pinto,
D. Pinto,
2005,
Human molecular genetics.
G. Rudolf,
M. Valenti,
J. Motte,
2004
.
P. Genton,
Ying-Hui Fu,
A. Hunter,
2012,
Neurology.
W. Chung,
N. Drouot,
C. Blauwendraat,
2020,
Annals of neurology.
M. Koenig,
S. Kremer,
I. Namer,
2017,
Journal of Neurology.
M. Sitbon,
D. Campion,
D. Hannequin,
2016,
Journal of Neurology.
A. Ioannides,
P. Striano,
Katsuhiro Kobayashi,
2016,
Epileptic disorders : international epilepsy journal with videotape.
N. Drouot,
P. Burbaud,
L. Cif,
2020,
Parkinsonism & related disorders.
A. Pagnamenta,
N. Drouot,
I. Sumara,
2016,
Nature Genetics.
L. Kappos,
T. Derfuss,
R. Lindberg,
2015,
Journal of Neuroinflammation.
P Kahane,
P. Kahane,
C. Marescaux,
2000,
Brain : a journal of neurology.
P. Kind,
J. Hentschel,
D. Mitter,
2018,
Brain : a journal of neurology.
Enrico Amico,
Philippe Allain,
Mark Mühlau,
2017,
The Lancet. Neurology.
B. Lhermitte,
A. Echaniz-Laguna,
C. Marelli,
2021,
Journal of Neurology.
S. Froelich,
A. Arzimanoglou,
E. Hirsch,
2006,
Epileptic disorders : international epilepsy journal with videotape.
I. Namer,
M. Anheim,
G. Rudolf,
2014,
Journal of Neurology.
Conditional switching of KIF2A mutation provides new insights into cortical malformations pathogeny.
N. Drouot,
H. Meziane,
B. Yalcin,
2020,
Human molecular genetics.
Thomas Bourgeron,
Christopher Schröder,
Bernhard Horsthemke,
2019,
Nature Communications.
F. Blanc,
G. Rudolf,
J. de Seze,
2013,
Clinical & developmental immunology.
G. Carvill,
I. Scheffer,
H. Mefford,
2016,
European Journal of Human Genetics.
A. Echaniz-Laguna,
C. Andres,
P. Corcia,
2015,
PloS one.
A. Echaniz-Laguna,
G. Bierry,
G. Rudolf,
2016,
Journal of neuromuscular diseases.
R. Miles,
M. Baulac,
C. Marescaux,
2013,
Nature Genetics.
A. Biraben,
F. Bartolomei,
P. Striano,
2018,
Genetics in Medicine.
Anne de Saint Martin,
N. Burnashev,
T. Tsintsadze,
2013,
Nature Genetics.
E. Hirsch,
G. Rudolf,
C. Seegmuller,
2014,
Epilepsia.
J. Chelly,
M. Anheim,
G. Rudolf,
2017,
Parkinsonism & related disorders.
Marie-Noëlle Metz-Lutz,
Edouard Hirsch,
Sandrine Pereira,
2006,
Human molecular genetics.
S. Antonarakis,
P. Ryvlin,
A. Crespel,
2015,
Human molecular genetics.
Krista,
Malika,
S. Antonarakis,
2015
.
P. Kuhn,
T. Frebourg,
G. Rudolf,
2009,
The New England journal of medicine.
E. Hirsch,
G. Rudolf,
M. Valenti,
2006,
Epilepsia.
F. Blanc,
F. Lolli,
A. Papini,
2013,
Journal of peptide science : an official publication of the European Peptide Society.
M. Amador,
G. Stevanin,
J. Antoine,
2019,
Neurology: Genetics.
P. Cabre,
G. Rudolf,
S. Allouche,
2014,
Multiple sclerosis and related disorders.
N. Drouot,
M. Baulac,
M. Habert,
2020,
Movement disorders : official journal of the Movement Disorder Society.
Meghan C Towne,
Sharyn A. Lincoln,
Stephan J Sanders,
2017,
American journal of human genetics.
L. Kappos,
T. Derfuss,
R. Lindberg,
2015,
Journal of Neuroinflammation.
Adrian Danek,
Nicholas W. Wood,
Andrea H. Németh,
2001,
Nature Genetics.
R. Møller,
H. Hjalgrim,
E. Hirsch,
2019,
Epileptic disorders : international epilepsy journal with videotape.
M. Loriot,
R. Favre,
G. Rudolf,
2003,
Clinical genetics.
J. Jankovic,
A. Bowcock,
K. Bhatia,
2012,
Cell reports.
N. Drouot,
M. Vidailhet,
L. Cif,
2022,
Movement disorders : official journal of the Movement Disorder Society.
I. Scheffer,
C. Elger,
S. Lorenz,
2006,
Epilepsia.
D. Gauguier,
C. Marescaux,
M. Lathrop,
2004,
Epilepsia.
V. Biancalana,
O. Caron,
G. Rudolf,
2008,
European journal of medical genetics.
P. Ryvlin,
L. Maillard,
P. Genton,
2010,
Epilepsia.
Y. Ben-Ari,
N. Burnashev,
A. Represa,
2013,
Brain : a journal of neurology.
P. Ryvlin,
A. Arzimanoglou,
E. Hirsch,
2014,
Epilepsia.
Edouard Hirsch,
Simon E Fisher,
S. Fisher,
2010,
Human molecular genetics.
E. Hirsch,
G. Rudolf,
M. Valenti,
2009,
Epilepsia.
Edouard Hirsch,
Damien Sanlaville,
Alexis Arzimanoglou,
2012,
Epilepsia.
G. Lathrop,
P. Dessen,
V. Lazar,
2010,
PloS one.
M Farrall,
A Danek,
A. Monaco,
1997,
American journal of human genetics.
N. Drouot,
M. Koenig,
J. Mandel,
2018,
JAMA neurology.
Tommaso Pippucci,
Josemir W. Sander,
Edouard Hirsch,
2019,
Nature Communications.
P. Vermersch,
I. Fajardy,
S. Vukusic,
2009,
Multiple sclerosis.
R. Abou Jamra,
M. V. van Slegtenhorst,
C. Goizet,
2020,
Molecular genetics & genomic medicine.
D. Pinto,
I. Scheffer,
P. Striano,
2010,
Epilepsy Research.
Lynch,
J. Jankovic,
A. Bowcock,
2012
.
C. Marescaux,
M. Metz-Lutz,
E. Hirsch,
2001,
Neurology.
A. Boland,
P. Nitschké,
J. Deleuze,
2020,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
K. Strauch,
S. Lorenz,
U. Stephani,
2005,
Annals of neurology.
N. Drouot,
Y. Hérault,
B. Yalcin,
2019,
Nature Communications.
N. Drouot,
L. Minotti,
P. Kahane,
2020,
European Journal of Human Genetics.
I. Scheffer,
J. Gécz,
P. Striano,
2016,
Human Genetics.
F. Durif,
D. Campion,
D. Hannequin,
2014,
neurogenetics.
M. Koenig,
W. Meissner,
A. Eusebio,
2016,
Movement disorders : official journal of the Movement Disorder Society.
P. Paquier,
P. van Bogaert,
G. Rudolf,
2017,
Epileptic disorders : international epilepsy journal with videotape.
I. Namer,
F. Moussallieh,
K. Elbayed,
2014,
Multiple sclerosis.
Anne de Saint Martin,
P. Maquet,
C. Marescaux,
2006,
Epilepsy Research.
I. Scheffer,
J. Gécz,
P. Striano,
2016,
Human Genetics.
M. Schaeffer,
J. Chelly,
M. Anheim,
2016,
BMC Neurology.
J. Serratosa,
C. Tassinari,
G. Rubboli,
2020,
Clinical Neurophysiology.
N. Drouot,
J. Chelly,
A. Piton,
2022,
Movement disorders : official journal of the Movement Disorder Society.
W. Chung,
N. Drouot,
C. Blauwendraat,
2020,
Annals of neurology.
N. Drouot,
Y. Hérault,
B. Yalcin,
2019,
Nature Communications.
Anne de Saint Martin,
A. Biraben,
F. Bartolomei,
2018,
Genetics in Medicine.
C. Marescaux,
L. Vercueil,
B. Goichot,
2010,
Clinical genetics.
P. Genton,
Ying-Hui Fu,
A. Hunter,
2012,
Neurology.
P. Ryvlin,
L. Maillard,
P. Genton,
2010,
Epilepsia.
E. Hirsch,
G. Rudolf,
M. Valenti,
2009,
Epilepsia.
A. Papini,
P. Rovero,
G. Rudolf,
2012
.