E-LIB Suche - Ergebnisse für: Smets, Tine

1

Segmental testicular infarction: a case report:

Smets, Tine ; Reichman, Gina ; Michielsen, Dirk P. J.
Journal of Medical Case Reports. 11 (2017) 1 - p. , 2017

2

Pediatric Otoplasty: An Evaluation of the Surgical Techniqu..:

Tine Smets ; Frans Gordts ; Ina Foulon
http://www.b-ent.be/en/pediatric-otoplasty-an-evaluation-of-the-surgical-technique-results-patient-satisfaction-and-influence-of-a-medical-fee-131120. , 2023

Link: https://doi.org/10.5152/..

3

Segmental testicular infarction: a case report:

Tine Smets ; Gina Reichman ; Dirk P. J. Michielsen
http://link.springer.com/article/10.1186/s13256-017-1308-1. , 2017

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

4

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

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

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

5

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/..

6

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/..

7

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/..

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

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/..

10

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/..

11

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/..

12

KCNQ2 encephalopathy: Emerging phenotype of a neonatal epil..:

Weckhuysen, Sarah ; Mandelstam, Simone ; Suls, Arvid...
Annals of Neurology. 71 (2012) 1 - p. 15-25 , 2012

Link: https://doi.org/10.1002/..

13

TheSCN1Avariant database: a novel research and diagnostic t..:

Claes, Lieve RF ; Deprez, Liesbet ; Suls, Arvid...
Human Mutation. 30 (2009) 10 - p. E904-E920 , 2009

Link: https://doi.org/10.1002/..

14

REEP1 mutation spectrum and genotype/phenotype correlation ..:

Beetz, Christian ; Schüle, Rebecca ; Deconinck, Tine...
Brain. 131 (2008) 4 - p. 1078-1086 , 2008

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

15

Synthesis and Anti-Angiogenic Activity of 6-(1,2,4-Thiadiaz..:

Bongartz, Jean-Pierre ; Stokbroekx, Raymond ; Van der Aa, Marcel...
Bioorganic & Medicinal Chemistry Letters. 12 (2002) 4 - p. 589-591 , 2002

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