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LinkedIn: Sarah Weckhuysen - Belgium | LinkedIn
View Sarah Weckhuysen's (Belgium) professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Sarah ...
LinkedIn: Sarah Weckhuysen | LinkedIn
View Sarah’s full profile Then intensified research activities on genetics of epilepsy, Neurogenetics Group, VIB Department of Molecular Genetics, University of Antwerp, Belgium. Worked one year as a researcher at the ICM institute in Paris, and as neurologist-epileptologist in ...
Interests
'Italië: de schaduwkant van een zonovergoten land' - BOEKVOORSTELLING
www.wherevent.com
boekvoorstelling van Italië door Ine Roox inleiding door Harold Polis uitgever bij De Bezige Bij gesprek met de auteur en...
Gene linked with early epilepsy discovered -- ScienceDaily
www.sciencedaily.com
Certain types of early-onset epilepsy are caused by previously unknown mutations of a potassium channel gene, KCNA2. The mutations disrupt the electrical...
Families Lead Quest for Precision Medicine to Treat Rare Genetic...
www.prlog.org
Families Lead Quest for Precision Medicine to Treat Rare Genetic Disorder. Denver CO – October 12, – Families from around the US and across the globe will...
KCNQ2 Cure Alliance Foundation Formed to Educate and Advance Research...
www.prweb.com
... factors in our efforts to improve treatments and outcomes for patients affected by KCNQ2 encephalopathy,” said Dr. Sarah Weckhuysen, MD, ...
Business Profiles
Researchgate: Sarah Weckhuysen
Paris, France
Employees
About Sarah Weckhuysen | Sarah Weckhuysen | University of Antwerp
www.uantwerpen.be
You are here: UAntwerp · Staff; Sarah Weckhuysen ... België ua.be. Copyright
Publications Sarah Weckhuysen | Sarah Weckhuysen | University of...
www.uantwerpen.be
Sarah Weckhuysen · Publications · Research · My website. You are here: UAntwerp · Staff · Sarah Weckhuysen; Publications ...
Education
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
kclpure.kcl.ac.uk
... Markus Schilhabel ; Johanna A Jähn ; Hiltrud Muhle ; Rainer Boor ; Wim Van Paesschen ; Roberto Caraballo ; Natalio Fejerman ; Sarah Weckhuysen ; Peter ...
The phenotypic spectrum of SCN8A encephalopathy - Research Portal,...
kclpure.kcl.ac.uk
... Specchio and Tania Djémié and Sarah Weckhuysen and Niels Tommerup and Monica Troncoso and Ledia Troncoso and Andrea Bevot and Markus Wolff and ...
Books & Literature
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic...
biblio.ugent.be
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, ...
Pellock's Pediatric Epilepsy: Diagnosis and Therapy - Google Books
books.google.si
Now in its fourth edition, Pellock’s Pediatric Epilepsy: Diagnosis and Therapy remains the gold standard for diagnosis, treatment, classification, and...
Related Documents
Dr. sarah weckhuysen kcnq2 Cure summit professional track - Lean mor…
www.slideshare.net
Dr. Sarah Weckhuysen speaking at Denver KCNQ2 Cure summit professionals track at Children's Hospital of Colorado. More information at www.kcnq2summit.org
GRIN2B mutations in west syndrome and intellectual disability with...
www.deepdyve.com
and Sarah Weckhuysen, MD. 2,3,4. Objective: To identify novel epilepsy genes using a panel approach and describe the functional consequences of. mutations.
Scientific Publications
Clinical profile of patients with ATP1A3 mutations in Alternating...
ojrd.biomedcentral.com
... Sanjay Sisodiya, Boukje de Vries, Christophe Goubau, Sarah Weckhuysen, David Kemlink, Ingrid Scheffer, Gaëtan Lesca, Muriel Rabilloud, ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
www.ikmb.uni-kiel.de
... Johanna A Jähn, Hiltrud Muhle, Rainer Boor, Wim Van Paesschen, Roberto Caraballo, Natalio Fejerman, Sarah Weckhuysen, Peter De Jonghe, Jan Larsen, ...
Publications
Clinical profile of patients with ATP1A3 mutations in Alternating...
link.springer.com
... Christophe Goubau (8); Sarah Weckhuysen (9); David Kemlink (10); Ingrid Scheffer (11) (12); Gaëtan Lesca (13) (14); Muriel Rabilloud (15) ...
Epilepsy: Old Syndromes, New Genes | SpringerLink
link.springer.com
Next-generation sequencing technologies have tremendously increased the speed of gene discovery in monogenic epilepsies, enabling us to identify a genetic...
Reports & Statements
Exome shock with acute in-house deficiency | Beyond the Ion Channel
euroepinomics.wordpress.com
Sleep disturbances, double vision, writer’s cramp. As some of you might recall, I was not fully conscious during our Young Investigator’s meeting two weeks...
Pushing the button for the next exome sequencing round | Beyond the...
euroepinomics.wordpress.com
Galvanize. Last week, the EuroEPINOMICS RES working groups made the final decisions for the selection of trios for exome sequencing at the Sanger Centre,...
Miscellaneous
Sarah Weckhuysen | Université Paris-Sorbonne (Paris IV) - Academia.edu
paris-sorbonne.academia.edu
Academia.edu is a place to share and follow research.
sarah weckhuysen | Flickr
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sarah weckhuysen hasn't made any photos public yet. About · Jobs · Blog · Mobile · Developers · Guidelines · Feedback · Report abuse · Help forum · English.
Sarah Weckhuysen | Bari International Conference
www.epostersonline.com
Bari International Conference. Main menu. Home · Posters by ID · Posters by Title · Authors · Affiliations · Sessions · Topics. Search form. Sarah Weckhuysen ...
Altmetric – Mutations in GRIN2A cause idiopathic focal epilepsy with...
www.altmetric.com
... Rainer Boor, Wim Van Paesschen, Roberto Caraballo, Natalio Fejerman, Sarah Weckhuysen, Peter De Jonghe, Jan Larsen, Rikke S Møller, Helle Hjalgrim, ...
De novo mutations in HCN1 cause early infantile epileptic...
moh-it.pure.elsevier.com
... Cornelia Vogt ; Nady El Hajj ; Eberhard Schneider ; Arvid Suls ; Sarah Weckhuysen ; Padhraig Gormley ; Anna Elina Lehesjoki ; Peter De Jonghe ; Ingo Helbig ...
De novo mutations in HCN1 cause early infantile epileptic...
portal.findresearcher.sdu.dk
... Vogt and {El Hajj}, Nady and Eberhard Schneider and Arvid Suls and Sarah Weckhuysen and Padhraig Gormley and Anna-Elina Lehesjoki and {De Jonghe}, ...
De novo mutations in synaptic transmission genes including DNM1 cause...
experts.umn.edu
... Pasquale Striano ; Arvid Suls ; Tiina Talvik ; Sarah Von Spiczak ; Yvonne Weber ; Sarah Weckhuysen ; Federico Zara ; Bassel Abou-Khalil ; Brian K. Alldredge ...
Mito DB
mitodb.com
Katia Hardies, Carolien G F de Kovel, Sarah Weckhuysen, Bob Asselbergh, Thomas Geuens, Tine Deconinck, Abdelkrim Azmi, Patrick May, Eva Brilstra, ...
Epilepsy: Old Syndromes, New Genes - ProQuest
www.proquest.com
Epilepsy: Old Syndromes, New Genes. Sarah Weckhuysen & Christian M. Korff. Published online: 17 April 2014# Springer Science+Business Media New York ...
Members
iahcrc.net
Peter De Jonghe, Sarah Weckhuysen ). University Hospitals Leuven, Leuven, Belgium (Node BE01) Child Neurology (Prof. Gunnar Buyse). IAHCRC-CZ-SLO ...
Mutations in STX1B, encoding a presynaptic protein, cause...
www.bionity.com
... Almuth Caliebe, Inga Nagel, Bernard Kohl, Angela Kecskés, Maxime Jacmin, Katia Hardies, Sarah Weckhuysen, Erik Riesch, Thomas Dorn, ...
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with...
read.qxmd.com
... Marina Nikanorova, Petia Dimova, Albena Jordanova, Steven Petrou, Ingo Helbig, Pasquale Striano, Sarah Weckhuysen, Samuel F Berkovic ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
researchportal.helsinki.fi
... Markus Schilhabel ; Johanna A. Jaehn ; Hiltrud Muhle ; Rainer Boor ; Wim Van Paesschen ; Roberto Caraballo ; Natalio Fejerman ; Sarah Weckhuysen ; Peter ...
Pellock’s Pediatric Epilepsy: Diagnosis and Therapy, Fourth Edition
www.demosmedical.com
Department of Experimental and Clinical Pharmacology. University of Minnesota, Twin Cities. Minneapolis, Minnesota. Sarah Weckhuysen, MD, PhD. Sorbonne ...
Recessive loss-of-function mutations in AP4S1 cause mild...
researchportal.helsinki.fi
... Arvid Suls ; Rudy Balling ; Sarah Weckhuysen ; Peter De Jonghe ; Jennifer Hirst ; EuroEPINOMICS RES Consortium ; Anna-Elina Lehesjoki.
Publications of the week: Epilepsiome update, NPRL3, CHD2, and EXT2 |...
epilepsygenetics.net
The KCNQ2 post earlier this week was written by the KCNQ2 Epilepsiome team consisting of Sarah Weckhuysen, Maurizio Taglialatela, ...
Recessive mutations in SLC13A5 result in a loss of citrate transport...
academic.oup.com
Epileptic encephalopathies are a clinically and aetiologically heterogeneous subgroup of epilepsy syndromes. Hardies et al. establish independent evidence that
Scientific Advisory Board - KCNQ2 Cure Alliance
www.kcnq2cure.org
KCNQ2 Cure's SAB consists of Orrin Devinsky, Ingrid Scheffer, Petere De Johghe, David Goldstein, Sarah Weckhuysen, Steve White, and Ed Cooper
Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects...
journals.plos.org
Sarah Weckhuysen,. Affiliations University of Antwerp, Antwerp, Belgium, Neurogenetics Group, Department of Molecular Genetics, VIB, ...
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