U. Walther-Louvier
发表
F. Rivier,
F. Chapon,
C. Richelme,
2019,
Orphanet Journal of Rare Diseases.
S. Lehmann,
M. Koenig,
F. Rivier,
2020,
Neuromuscular Disorders.
V. Fraix,
L. Kremer,
M. Koenig,
2021,
Genetics in Medicine.
F. Rivier,
P. Cintas,
C. Cancés,
2021,
Neuropediatrics.
M. Koenig,
F. Rivier,
E. Malfatti,
2021,
Genes.
F. Rivier,
C. Richelme,
G. Bassez,
2019,
Neurology.
C. Richelme,
P. Sabouraud,
S. Quijano-roy,
2020,
Orphanet Journal of Rare Diseases.
S. Quijano-roy,
C. Barnérias,
I. Desguerre,
2022,
Neurology.
F. Rivier,
M. Cossée,
J. Rendu,
2021,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
R. Porcher,
D. Annane,
P. Ravaud,
2021,
European heart journal.
F. Rivier,
E. Uro-Coste,
C. Espil,
2016,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
N. Lévy,
P. Latour,
T. Stojkovic,
2022,
Clinical genetics.
R. Porcher,
É. Marijon,
A. Lazarus,
2019,
Circulation.
M. Koenig,
F. Rivier,
M. Cossée,
2018,
The Journal of molecular diagnostics : JMD.
Y. Péréon,
P. Cintas,
C. Barnérias,
2023,
Neuromuscular Disorders.
F. Rivier,
U. Walther-Louvier,
É. Baudou,
2018,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
G. Rondouin,
F. Rivier,
B. Echenne,
2014,
Multiple sclerosis.
F. Rivier,
J. Lefranc,
G. Touati,
2023,
European journal of neurology.