Результати пошуку - Srour, Myriam
- Показ 1 - 20 результатів із 36
- На наступну сторінку
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Psychopharmacology of Tic Disorders за авторством Srour, Myriam, Lespérance, Paul, Richer, Francois, Chouinard, Sylvain
Опубліковано 2008Текст -
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Hemiconvulsion‐Hemiplegia‐Epilepsy in a girl with cobalamin C deficiency за авторством Myers, Kenneth A., Dudley, Roy WR., Srour, Myriam
Опубліковано 2018Текст -
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Teaching NeuroImages: CLOVES Syndrome за авторством Collins, Meagan, Krochmalnek, Eric, Alsubhi, Sarah, Srour, Myriam
Опубліковано 2021Текст -
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Acute Hemorrhagic Encephalitis Responding to Combined Decompressive Craniectomy, Intravenous Immunoglobulin, and Corticosteroid Therapies: Association with Novel RANBP2 Variant за авторством Alawadhi, Abdulla, Saint-Martin, Christine, Bhanji, Farhan, Srour, Myriam, Atkinson, Jeffrey, Sébire, Guillaume
Опубліковано 2018Текст -
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Antenatal corticosteroid administration and early school age child development: A regression discontinuity study in British Columbia, Canada за авторством Hutcheon, Jennifer A., Harper, Sam, Liauw, Jessica, Skoll, M. Amanda, Srour, Myriam, Strumpf, Erin C.
Опубліковано 2020Текст -
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Homozygous deletion of Tenascin-R in a patient with intellectual disability за авторством Dufresne, David, Hamdan, Fadi F, Rosenfeld, Jill A, Torchia, Beth, Rosenblatt, Bernard, Michaud, Jacques L, Srour, Myriam
Опубліковано 2012Текст -
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A Novel De Novo Variant in DYNC1H1 Causes Spinal Muscular Atrophy Lower Extremity Predominant in Identical Twins: A Case Report за авторством Derksen, Alexa, Mirchi, Amytice, Tran, Luan T., Cao-Lei, Lei, Oskoui, Maryam, Srour, Myriam, Poulin, Chantal, Bernard, Geneviève
Опубліковано 2021Текст -
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Antenatal corticosteroid administration and attention-deficit/hyperactivity disorder in childhood: a regression discontinuity study за авторством Hutcheon, Jennifer A., Strumpf, Erin C., Liauw, Jessica, Skoll, M. Amanda, Socha, Peter, Srour, Myriam, Ting, Joseph Y., Harper, Sam
Опубліковано 2022Текст -
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SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay за авторством D’Amours, Guylaine, Langlois, Mathieu, Mathonnet, Géraldine, Fetni, Raouf, Nizard, Sonia, Srour, Myriam, Tihy, Frédérique, S Phillips, Michael, L Michaud, Jacques, Lemyre, Emmanuelle
Опубліковано 2014Текст -
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Congenital Mirror Movements in a New Italian Family за авторством Fasano, Alfonso, Bologna, Matteo, Iezzi, Ennio, Pavone, Luigi, Srour, Myriam, Di Biasio, Francesca, Grillea, Giovanni, Rouleau, Guy A., Levert, Annie, Sebastiano, Fabio, Colonnese, Claudio, Berardelli, Alfredo
Опубліковано 2014Текст -
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Status Epilepticus Manifested as Continuous Epileptic Spasms за авторством Liao, Jianxiang, Huang, Tieshuan, Srour, Myriam, Xiao, Yuhan, Chen, Yan, Lin, Sufang, Chen, Li, Hu, Yan, Men, Lina, Wen, Jialun, Li, Bing, Wen, Feiqiu, Xiong, Lan
Опубліковано 2020Текст -
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Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and Epilepsy за авторством Srour, Myriam, Shimokawa, Noriaki, Hamdan, Fadi F., Nassif, Christina, Poulin, Chantal, Al Gazali, Lihadh, Rosenfeld, Jill A., Koibuchi, Noriyuki, Rouleau, Guy A., Al Shamsi, Aisha, Michaud, Jacques L.
Опубліковано 2017Текст -
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Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia за авторством Srour, Myriam, Chitayat, David, Caron, Véronique, Chassaing, Nicolas, Bitoun, Pierre, Patry, Lysanne, Cordier, Marie-Pierre, Capo-Chichi, José-Mario, Francannet, Christine, Calvas, Patrick, Ragge, Nicola, Dobrzeniecka, Sylvia, Hamdan, Fadi F., Rouleau, Guy A., Tremblay, André, Michaud, Jacques L.
Опубліковано 2013Текст -
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Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia за авторством Srour, Myriam, Chitayat, David, Caron, Véronique, Chassaing, Nicolas, Bitoun, Pierre, Patry, Lysanne, Cordier, Marie-Pierre, Capo-Chichi, José-Mario, Francannet, Christine, Calvas, Patrick, Ragge, Nicola, Dobrzeniecka, Sylvia, Hamdan, Fadi F., Rouleau, Guy A., Tremblay, André, Michaud, Jacques L.
Опубліковано 2013Текст -
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De Novo Mutations in Moderate or Severe Intellectual Disability за авторством Hamdan, Fadi F., Srour, Myriam, Capo-Chichi, Jose-Mario, Daoud, Hussein, Nassif, Christina, Patry, Lysanne, Massicotte, Christine, Ambalavanan, Amirthagowri, Spiegelman, Dan, Diallo, Ousmane, Henrion, Edouard, Dionne-Laporte, Alexandre, Fougerat, Anne, Pshezhetsky, Alexey V., Venkateswaran, Sunita, Rouleau, Guy A., Michaud, Jacques L.
Опубліковано 2014Текст -
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Mesocorticolimbic Connectivity and Volumetric Alterations in DCC Mutation Carriers за авторством Vosberg, Daniel E., Zhang, Yu, Menegaux, Aurore, Chalupa, Amanda, Manitt, Colleen, Zehntner, Simone, Eng, Conrad, DeDuck, Kristina, Allard, Dominique, Durand, France, Dagher, Alain, Benkelfat, Chawki, Srour, Myriam, Joober, Ridha, Lepore, Franco, Rouleau, Guy, Théoret, Hugo, Bedell, Barry J., Flores, Cecilia, Leyton, Marco
Опубліковано 2018Текст -
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Age-related injury responses of human oligodendrocytes to metabolic insults: link to BCL-2 and autophagy pathways за авторством Fernandes, Milton Guilherme Forestieri, Luo, Julia Xiao Xuan, Cui, Qiao-Ling, Perlman, Kelly, Pernin, Florian, Yaqubi, Moein, Hall, Jeffery A., Dudley, Roy, Srour, Myriam, Couturier, Charles P., Petrecca, Kevin, Larochelle, Catherine, Healy, Luke M., Stratton, Jo Anne, Kennedy, Timothy E., Antel, Jack P.
Опубліковано 2021Текст -
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Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic за авторством Amir Yazdani, Pouneh, St-Jean, Marie-Lou, Matovic, Sara, Spahr, Aaron, Tran, Luan T., Boucher, Renée-Myriam, Poulin, Chantal, Osterman, Bradley, Srour, Myriam, Rosenblatt, Bernard, Chenier, Sébastien, Soucy, Jean-Francois, Laberge, Anne-Marie, Braverman, Nancy, D’Agostino, Maria Daniela, Nguyen, Cam-Tu Emilie, Morsa, Maxime, Bernard, Geneviève
Опубліковано 2022Текст