L. De Waele
发表
L. Lagae,
D. Mekahli,
L. de Waele,
2015,
Pediatric Nephrology.
L. Servais,
L. de Waele,
Theodora Markati,
2021,
Frontiers in Pharmacology.
L. Servais,
J. Hogrel,
P. Carlier,
2020,
Annals of clinical and translational neurology.
L. Servais,
J. Hogrel,
P. Carlier,
2018,
PloS one.
L. Lagae,
A. Vanderver,
K. Devriendt,
2015,
American journal of medical genetics. Part A.
Martin A. M. Reijns,
Y. Crow,
H. Van Esch,
2020,
Nature Genetics.
E. Mercuri,
L. Servais,
C. Straathof,
2019,
Neuromuscular Disorders.
A. Byars,
S. Gardner-Lubbe,
R. Waltereit,
2022,
Frontiers in Psychiatry.
M. Jaatun,
K. Katanyuwong,
E. Pataraia,
2018,
Orphanet Journal of Rare Diseases.
L. Lagae,
A. Vanderver,
J. Tolmie,
2014,
Nature Genetics.
Susan M. Schlenner,
M. R. Baker,
A. Liston,
2022,
Cellular & Molecular Immunology.
G. Comi,
E. Zanoteli,
N. Goemans,
2022,
Orphanet Journal of Rare Diseases.
H. Feys,
K. Klingels,
N. Goemans,
2019,
Neuromuscular Disorders.
A. Uyttebroeck,
C. Sleurs,
L. de Waele,
2021,
The Cerebellum.
A. Uyttebroeck,
C. Sleurs,
L. de Waele,
2021,
The Cerebellum.
M. Jaatun,
K. Katanyuwong,
P. Kwan,
2018,
Epilepsia open.
K. Desloovere,
C. Verfaillie,
K. Sipido,
2021,
bioRxiv.
T. de Ravel,
A. Corveleyn,
L. de Catte,
2017,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
P. van Damme,
C. Verfaillie,
H. V. van Duyvenvoorde,
2019,
Translational Psychiatry.
C. Verfaillie,
K. Sipido,
M. Sampaolesi,
2017,
Stem cells international.
E. Mazzone,
L. Servais,
O. Boespflug-Tanguy,
2022,
European journal of neurology.
D. Abramowicz,
P. Van Gaal,
L. de Waele,
2018,
Acta clinica Belgica.
B. Bammens,
D. Mekahli,
P. Janssens,
2018,
Pediatric Nephrology.
J. Wilson,
Lieven Thorrez,
T. VandenDriessche,
2006,
Journal of thrombosis and haemostasis : JTH.
C. von Kalle,
A. Annoni,
L. Naldini,
2011,
Hepatology.
M. R. Baker,
A. Liston,
I. Serysheva,
2021,
medRxiv.
M. Sampaolesi,
R. Gijsbers,
R. Derua,
2022,
Frontiers in Immunology.
C. Verfaillie,
C. Deroose,
O. Gheysens,
2016,
Stem cells international.
A. Byars,
M. Sahin,
S. Gardner-Lubbe,
2022,
Journal of neurodevelopmental disorders.
M. Sahin,
S. Gardner-Lubbe,
P. D. de Vries,
2021,
Orphanet Journal of Rare Diseases.
G. Molenberghs,
K. Desloovere,
A. Van Campenhout,
2022,
Frontiers in Human Neuroscience.
L. Thomas,
M. Nellist,
J. Sampson,
2023,
Human Mutation.
H. Firth,
P. Striano,
M. Haeusler,
2021,
medRxiv.
K. Devriendt,
L. de Waele,
M. Holvoet,
2021,
Clinical dysmorphology.
D. Mekahli,
E. Levtchenko,
S. De Rechter,
2015,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
K. Jansen,
A. Corveleyn,
I. Meyts,
2022,
Neurology.
K. Bushby,
F. Muntoni,
A. Schapira,
2013,
Human mutation.
L. Lagae,
A. Vanderver,
R. Schiffmann,
2016,
Nature Genetics.
L. Lagae,
B. Dan,
P. Boon,
2013,
Acta Neurologica Belgica.
M. Jaatun,
K. Katanyuwong,
E. Pataraia,
2021,
Orphanet Journal of Rare Diseases.
A. Byars,
S. Gardner-Lubbe,
R. Waltereit,
2023,
Journal of Neurodevelopmental Disorders.
A. Byars,
S. Gardner-Lubbe,
R. Waltereit,
2023,
Pediatric neurology.
N. Goemans,
K. Luyckx,
J. Lemiere,
2022,
Clinical child psychology and psychiatry.
S. Mehta,
Y. Crow,
D. Clifford,
2020,
American journal of medical genetics. Part A.
N. Absalom,
R. Møller,
K. Jansen,
2020,
Brain communications.
O. Witt,
S. Jóźwiak,
J. Pedespan,
2016,
BMC Neurology.
K. Desloovere,
A. Van Campenhout,
N. Goemans,
2022,
Frontiers in Physiology.
N. Goemans,
J. Hendriksen,
R. Vermeulen,
2023,
Neuromuscular Disorders.
N. Doorenweerd,
S. Geuens,
L. De Waele,
2024,
Journal of neuromuscular diseases.
B. Ceulemans,
N. Deconinck,
L. de Waele,
2017,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.