E-LIB Suche - Ergebnisse für: Smets, Katrien

1

FAHN/SPG35: a narrow phenotypic spectrum across disease cla..:

Rattay, Tim W ; Lindig, Tobias ; Baets, Jonathan...
Brain. 142 (2019) 6 - p. 1561-1572 , 2019

2

Eccrine porocarcinoma of the scalp: diagnosis and importanc..:

De Fré, Maxime ; Smets, Katrien ; Ulicki, Michal...
European Journal of Plastic Surgery. 42 (2019) 6 - p. 623-627 , 2019

Link: https://doi.org/10.1007/..

3

Occupational airborne allergic contact dermatitis caused by..:

Aerts, Olivier ; Mangodt, Evelyne ; Smets, Katrien...
Contact Dermatitis. 80 (2018) 1 - p. 71-73 , 2018

Link: https://doi.org/10.1111/..

4

STUB1/CHIP mutations cause Gordon Holmes syndrome as part o..:

Hayer, Stefanie Nicole ; Deconinck, Tine ; Bender, Benjamin...
Orphanet Journal of Rare Diseases. 12 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

5

Hereditary spastic paraplegia type 5: natural history, biom..:

Schöls, Ludger ; Rattay, Tim W ; Martus, Peter...
Brain. 140 (2017) 12 - p. 3112-3127 , 2017

Link: https://doi.org/10.1093/..

6

Investigating the role of ALS genes CHCHD10 and TUBA4A in B..:

Perrone, Federica ; Nguyen, Hung Phuoc ; Van Mossevelde, Sara...
Neurobiology of Aging. 51 (2017) - p. 177.e9-177.e16 , 2017

Link: https://doi.org/10.1016/..

7

SYNE1 ataxia is a common recessive ataxia with major non-ce..:

Synofzik, Matthis ; Smets, Katrien ; Mallaret, Martial...
Brain. 139 (2016) 5 - p. 1378-1393 , 2016

Link: https://doi.org/10.1093/..

8

Motor neuron degeneration in spastic paraplegia 11 mimics a..:

Denora, Paola S. ; Smets, Katrien ; Zolfanelli, Federica...
Brain. , 2016

Link: https://doi.org/10.1093/..

9

Automated non-EEG based seizure detection: Do users have a ..:

Van de Vel, Anouk ; Smets, Katrien ; Wouters, Kristien.
Epilepsy & Behavior. 62 (2016) - p. 121-128 , 2016

Link: https://doi.org/10.1016/..

10

The spectrum of epilepsy caused by POLG mutations:

Janssen, Wouter ; Quaegebeur, Annelies ; Van Goethem, Gert...
Acta Neurologica Belgica. 116 (2015) 1 - p. 17-25 , 2015

Link: https://doi.org/10.1007/..

11

First de novo KCND3 mutation causes severe Kv4.3 channel dy..:

Smets, Katrien ; Duarri, Anna ; Deconinck, Tine...
BMC Medical Genetics. 16 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

12

Loss ofTBK1is a frequent cause of frontotemporal dementia i..:

Gijselinck, Ilse ; Van Mossevelde, Sara ; van der Zee, Julie...
Neurology. 85 (2015) 24 - p. 2116-2125 , 2015

Link: https://doi.org/10.1212/..

13

Rare mutations in SQSTM1 modify susceptibility to frontotem..:

van der Zee, Julie ; Van Langenhove, Tim ; Kovacs, Gabor G....
Acta Neuropathologica. 128 (2014) 3 - p. 397-410 , 2014

Link: https://doi.org/10.1007/..

14

Partial deletion ofAFG3L2causing spinocerebellar ataxia typ..:

Smets, Katrien ; Deconinck, Tine ; Baets, Jonathan...
Neurology. 82 (2014) 23 - p. 2092-2100 , 2014

Link: https://doi.org/10.1212/..

15

First line management of prolonged convulsive seizures in c..:

De Waele, Liesbeth ; Boon, Paul ; Ceulemans, Berten...
Acta Neurologica Belgica. 113 (2013) 4 - p. 375-380 , 2013

Link: https://doi.org/10.1007/..