Bilaketaren emaitzak - Matthew Zemel
- Erakusten 1 - 4 emaitzak -- 4
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1
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy nork Borislav Dejanovic, Tania Djémié, Nora Grünewald, Arvid Suls, Vanessa Kress, Florian Hetsch, Dana Craiu, Matthew Zemel, Padhraig Gormley, Dennis Lal, Candace T. Myers, Heather C. Mefford, Aarno Palotie, Ingo Helbig, Jochen C. Meier, Peter De Jonghe, Sarah Weckhuysen, Günter Schwarz
Argitaratua 2015Artigo -
2
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene <i><scp>WDR</scp>45</i> nork Gemma L. Carvill, Aijie Liu, Simone Mandelstam, Amy L. Schneider, Amy Lacroix, Matthew Zemel, Jacinta M. McMahon, Luis Bello‐Espinosa, Mark T. Mackay, Geoff Wallace, Michaela Waak, Jing Zhang, Cheng Yang, Stephen Malone, Yuehua Zhang, Heather C. Mefford, Ingrid E. Scheffer
Argitaratua 2017Artigo -
3
Epileptic spasms are a feature of <i>DEPDC5</i> mTORopathy nork Gemma L. Carvill, Douglas E. Crompton, Brigid M. Regan, Jacinta M. McMahon, Julia Saykally, Matthew Zemel, Amy L. Schneider, Leanne M. Dibbens, Katherine B. Howell, Simone Mandelstam, Richard J. Leventer, A. Simon Harvey, Saul A. Mullen, Samuel F. Berkovic, Joseph Sullivan, Ingrid E. Scheffer, Heather C. Mefford
Argitaratua 2015Artigo -
4
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures nork Gemma L. Carvill, Jacinta M. McMahon, Amy L. Schneider, Matthew Zemel, Candace T. Myers, Julia Saykally, John Nguyen, Angela Robbiano, Federico Zara, Nicola Specchio, Oriano Mecarelli, Robert L. Smith, Richard J. Leventer, Rikke S. Møller, Marina Nikanorova, Petia Dimova, Albena Jordanova, Steven Petrou, Ingo Helbig, Pasquale Striano, Sarah Weckhuysen, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford
Argitaratua 2015Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Medicine
Biology
Epilepsy
Gene
Genetics
Disease
Internal medicine
Pathology
Pediatrics
Phenotype
Psychiatry
Age of onset
Cohort
Computer science
Cortical dysplasia
Dysplasia
Dystonia
Encephalopathy
GABA transporter
Global developmental delay
Library science
Missense mutation
Myoclonic epilepsy
Neurodegeneration
Neurogenetics
Neuroscience
Pediatric Neurology
Transporter
West Syndrome