|
π
|
KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
23 auth.
S. Weckhuysen,
S. Mandelstam,
A. Suls,
D. Audenaert,
T. Deconinck,
L. Claes,
L. Deprez,
K. Smets,
D. Hristova,
I. Yordanova,
...
A. Jordanova,
B. Ceulemans,
A. Jansen,
D. Hasaerts,
F. Roelens,
L. Lagae,
S. Yendle,
Thorsten Stanley,
S. Heron,
J. Mulley,
S. Berkovic,
I. Scheffer,
P. de Jonghe
|
8 |
2012 |
8
π
|
|
π
|
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
27 auth.
A. Suls,
Peter Dedeken,
K. Goffin,
H. Van Esch,
P. Dupont,
D. Cassiman,
J. Kempfle,
Thomas V. Wuttke,
Y. Weber,
H. Lerche,
Z. Afawi,
W. Vandenberghe,
A. Korczyn,
S. Berkovic,
D. Ekstein,
...
S. Kivity,
P. Ryvlin,
L. Claes,
L. Deprez,
S. Maljevic,
Alberto Vargas,
T. Van Dyck,
D. Goossens,
J. Del-Favero,
K. Van Laere,
P. de Jonghe,
W. van Paesschen
|
8 |
2008 |
8
π
|
|
π
|
Earlyβonset absence epilepsy caused by mutations in the glucose transporter GLUT1
15 auth.
A. Suls,
S. Mullen,
Y. Weber,
K. Verhaert,
B. Ceulemans,
R. Guerrini,
Thomas V. Wuttke,
Alberto Salvo-Vargas,
L. Deprez,
L. Claes,
...
A. Jordanova,
S. Berkovic,
H. Lerche,
P. de Jonghe,
I. Scheffer
|
8 |
2009 |
8
π
|
|
π
|
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
16 auth.
Y. Liao,
L. Deprez,
S. Maljevic,
J. Pitsch,
L. Claes,
D. Hristova,
A. Jordanova,
S. AlaβMello,
A. Bellan-Koch,
Dragica Blazevic,
...
S. Schubert,
E. Thomas,
S. Petrou,
A. Becker,
P. de Jonghe,
H. Lerche
|
7 |
2010 |
7
π
|
|
π¦
|
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations
17 auth.
L. Deprez,
S. Weckhuysen,
Philip Holmgren,
A. Suls,
T. Dyck,
D. Goossens,
J. Del-Favero,
Anna C. Jansen,
K. Verhaert,
L. Lagae,
...
A. Jordanova,
R. Coster,
S. Yendle,
S. Berkovic,
I. Scheffer,
B. Ceulemans,
P. Jonghe
|
7 |
2010 |
7
π¦
|
|
π
|
A novel GABRG2 mutation associated with febrile seizures
11 auth.
D. Audenaert,
E. Schwartz,
K. Claeys,
L. Claes,
L. Deprez,
A. Suls,
...
T. Dyck,
L. Lagae,
C. Broeckhoven,
R. L. MacDonald,
P. Jonghe
|
7 |
2006 |
7
π
|
|
π
|
Microdeletions involving the SCN1A gene may be common in SCN1Aβmutationβnegative SMEI patients
20 auth.
A. Suls,
K. Claeys,
D. Goossens,
Boris Harding,
R. Luijk,
Stefaan Scheers,
L. Deprez,
D. Audenaert,
T. Dyck,
S. Beeckmans,
...
Iris Smouts,
B. Ceulemans,
L. Lagae,
G. Buyse,
N. BariΕ‘iΔ,
J. Misson,
J. Wauters,
J. Del-Favero,
P. de Jonghe,
L. Claes
|
6 |
2006 |
6
π
|
|
π
|
The SCN1A variant database: a novel research and diagnostic tool
9 auth.
L. Claes,
L. Deprez,
A. Suls,
J. Baets,
K. Smets,
T. Van Dyck,
...
T. Deconinck,
A. Jordanova,
P. de Jonghe
|
6 |
2009 |
6
π
|
|
π¦
|
Epilepsy as part of the phenotype associated with ATP1A2 mutations
12 auth.
L. Deprez,
S. Weckhuysen,
K. Peeters,
T. Deconinck,
K. Claeys,
L. Claes,
...
A. Suls,
T. Van Dyck,
A. Palmini,
G. Matthijs,
W. van Paesschen,
P. de Jonghe
|
6 |
2008 |
6
π¦
|
|
π¦
|
Genetics of epilepsy syndromes starting in the first year of life
L. Deprez,
A. Jansen,
P. de Jonghe
|
6 |
2009 |
6
π¦
|
