Výsledky vyhledávání - Danielle M. Andrade
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Microinjection of GABAergic agents into the anterior nucleus of the thalamus modulates pilocarpine-induced seizures and status epilepticus Autor Simone Bittencourt, Francisco Paulino Dubiela, Claudio M. Queiroz, Luciene Covolan, Danielle M. Andrade, Andrés M. Lozano, Luiz E. Mello, Clement Hamani
Vydáno 2010Artigo -
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Neurocognitive and Seizure Outcomes of Selective Amygdalohippocampectomy versus Anterior Temporal Lobectomy for Mesial Temporal Lobe Epilepsy Autor Alireza Mansouri, Aria Fallah, Mary Pat McAndrews, Mélanie Cohn, Diana Mayor, Danielle M. Andrade, Peter L. Carlen, J. Martin del Campo, Peter Tai, Richard Wennberg, Taufik A. Valiante
Vydáno 2014Artigo -
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Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature Autor Chelsea Lowther, Gregory Costain, Dimitri J. Stavropoulos, Rebecca Melvin, Candice K. Silversides, Danielle M. Andrade, Joyce So, Hanna Faghfoury, Anath C. Lionel, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett
Vydáno 2014Revisão -
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Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome Autor Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J. Gazzellone, Nancy J. Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W.C. Chow, Danielle M. Andrade, Brendan J. Frey, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett
Vydáno 2015Artigo -
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Global characterization of copy number variants in epilepsy patients from whole genome sequencing Autor Jean Monlong, Simon Girard, Caroline Meloche, Maxime Cadieux‐Dion, Danielle M. Andrade, Ron G. Lafrenière, Micheline Gravel, Dan Spiegelman, Alexandre Dionne‐Laporte, Cyrus Boelman, Fadi F. Hamdan, Jacques L. Michaud, Guy A. Rouleau, Berge A. Minassian, Guillaume Bourque, Patrick Cossette
Vydáno 2018Artigo -
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How can transition to adult care be best orchestrated for adolescents with epilepsy? Autor Peter Camfield, Danielle M. Andrade, Carole S. Camfield, Jaime Carrizosa, Richard Appleton, Michel Baulac, Lawrence W. Brown, Eleonor Ben Menachem, J. Helen Cross, Isabelle Desguerre, Christina Grant, Hassan Hosny, Laura Jurasek, Marco Mula, Margarete Pfäfflin, Sylvain Rheims, Howard Ring, Renée A. Shellhaas, Kollencheri Puthenveettil Vinayan, Elaine Wirrell, Rima Nabbout
Vydáno 2019Revisão -
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Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability Autor Rosalind Law, Tracy Dixon‐Salazar, Julie Jerber, Na Cai, Ansar Ahmed Abbasi, Maha S. Zaki, Kirti Mittal, Stacey Gabriel, Muhammad Rafiq, Valeed Khan, Maria Nguyen, Ghazanfar Ali, Brett Copeland, Eric Scott, Nasim Vasli, Anna Mikhailov, Muhammad Nasim Khan, Danielle M. Andrade, Muhammad Ayaz, Muhammad Ansar, Muhammad Ayub, John B. Vincent, Joseph G. Gleeson
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Medicine
Epilepsy
Biology
Psychiatry
Genetics
Gene
Internal medicine
Neuroscience
Psychology
Disease
Phenotype
Pediatrics
Genome
Copy-number variation
Bioinformatics
Mutation
Pathology
Computational biology
Deletion syndrome
Dravet syndrome
Environmental health
Exome sequencing
Health care
Intellectual disability
Law
Political science
Population
Computer science
Coronavirus disease 2019 (COVID-19)
DiGeorge syndrome