Genetic Mechanisms Behind Severe Psychotic Reactions to Levetiracetam

por Andrade, Danielle M.
Publicado 2022

Somatic Variants and Surgical Epilepsies: Search and You Will Find

por Andrade, Danielle M.
Publicado 2023

Is There a Continuum Between Acute Symptomatic Seizures Secondary to Autoimmune Encephalitis and Autoimmune-Associated Epilepsy?

por Andrade, Danielle M.
Publicado 2023

Time Is Brain: The Importance of an Accurate SCN1A Prediction Score in the Era of Precision Medicine

por Andrade, Danielle M.
Publicado 2022

Myopathic dysphagia caused by thyrotoxicosis: a case report and review of the literature

por Alwithenani, Raad, Andrade, Danielle M, Zhang, Lingxin, Gomez-Hernandez, Karen E
Publicado 2022

Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation

por Nascimento, Fábio A., Borlot, Felippe, Cossette, Patrick, Minassian, Berge A., Andrade, Danielle M.
Publicado 2015

Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults

por Tabarestani, Sepideh, Varriano, Brenda, Rawal, Sapna, France Morel, Chantal, Carmela Tartaglia, Maria, Andrade, Danielle M.
Publicado 2020

Imaging in medically refractory epilepsy at 3 Tesla: a 13-year tertiary adult epilepsy center experience

por Hainc, Nicolin, McAndrews, Mary Pat, Valiante, Taufik, Andrade, Danielle M., Wennberg, Richard, Krings, Timo
Publicado 2022

GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis

por Day, Gregory S., Prüss, Harald, Benseler, Susanne M., Paton, Tara A., Paterson, Andrew D., Andrade, Danielle M.
Publicado 2015

Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome

por Selvarajah, Arunan, Gorodetsky, Carolina, Marques, Paula, Zulfiqar Ali, Quratulain, Berg, Anne T., Fasano, Alfonso, Andrade, Danielle M.
Publicado 2022

Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration

por Rezazadeh, Arezoo, Bercovici, Eduard, Kiehl, Tim‐Rasmus, Chow, Eva W., Krings, Timo, Bassett, Anne S., Andrade, Danielle M.
Publicado 2018

Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with...

por Thompson, Miles D., Li, Xueying, Spencer-Manzon, Michele, Andrade, Danielle M., Murakami, Yoshiko, Kinoshita, Taroh, Carpenter, Thomas O.
Publicado 2023

Progressive myoclonus epilepsy associated with SACS gene mutations

por Nascimento, Fábio A., Canafoglia, Laura, Aljaafari, Danah, Muona, Mikko, Lehesjoki, Anna-Elina, Berkovic, Samuel F., Franceschetti, Silvana, Andrade, Danielle M.
Publicado 2016

Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome

por Cheung, Evelyn Ning Man, George, Susan R, Costain, Gary A, Andrade, Danielle M, Chow, Eva W C, Silversides, Candice K, Bassett, Anne S
Publicado 2014

Adult Phenotype of SYNGAP1-DEE

por Rong, Marlene, Benke, Tim, Zulfiqar Ali, Quratulain, Aledo-Serrano, Ángel, Bayat, Allan, Rossi, Alessandra, Devinsky, Orrin, Qaiser, Farah, Ali, Anum S., Fasano, Alfonso, Bassett, Anne S., Andrade, Danielle M.
Publicado 2023

Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control study

por Rafiee, Marjan, Patel, Kramay, Groppe, David M., Andrade, Danielle M., Bercovici, Eduard, Bui, Esther, Carlen, Peter L., Reid, Aylin, Tai, Peter, Weaver, Donald, Wennberg, Richard, Valiante, Taufik A.
Publicado 2020

COVID‐19 vaccine in patients with Dravet syndrome: Observations and real‐world experiences

por Hood, Veronica, Berg, Anne T., Knupp, Kelly G., Koh, Sookyong, Laux, Linda, Meskis, Mary Anne, Zulfiqar‐Ali, Quratulain, Perry, M. Scott, Scheffer, Ingrid E., Sullivan, Joseph, Wirrell, Elaine, Andrade, Danielle M.
Publicado 2022

Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome

por Qaiser, Farah, Sadoway, Tara, Yin, Yue, Zulfiqar Ali, Quratulain, Nguyen, Charlotte M, Shum, Natalie, Backstrom, Ian, Marques, Paula T, Tabarestani, Sepideh, Munhoz, Renato P, Krings, Timo, Pearson, Christopher E, Yuen, Ryan K C, Andrade, Danielle M
Publicado 2021

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

por Merico, Daniele, Zarrei, Mehdi, Costain, Gregory, Ogura, Lucas, Alipanahi, Babak, Gazzellone, Matthew J., Butcher, Nancy J., Thiruvahindrapuram, Bhooma, Nalpathamkalam, Thomas, Chow, Eva W. C., Andrade, Danielle M., Frey, Brendan J., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Publicado 2015

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

por Monlong, Jean, Girard, Simon L., Meloche, Caroline, Cadieux-Dion, Maxime, Andrade, Danielle M., Lafreniere, Ron G., Gravel, Micheline, Spiegelman, Dan, Dionne-Laporte, Alexandre, Boelman, Cyrus, Hamdan, Fadi F., Michaud, Jacques L., Rouleau, Guy, Minassian, Berge A., Bourque, Guillaume, Cossette, Patrick
Publicado 2018