Arama Sonuçları - Mathieu Milh
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- Sonraki Sayfaya Git
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Early patterns of activity in the developing cortex: Focus on the sensorimotor system Yazar: Roustem Khazipov, Mathieu Milh
Baskı/Yayın Bilgisi 2017Revisão -
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Rapid Cortical Oscillations and Early Motor Activity in Premature Human Neonate Yazar: Mathieu Milh, Anna Kaminśka, Catherine Huon, Alexandre Lapillonne, Yehezkel Ben‐Ari, Roustem Khazipov
Baskı/Yayın Bilgisi 2006Artigo -
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Altering cannabinoid signaling during development disrupts neuronal activity Yazar: Christophe Bernard, Mathieu Milh, Yury M. Morozov, Yehezkel Ben‐Ari, Tamás F. Freund, H. Gozlan
Baskı/Yayın Bilgisi 2005Artigo -
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Ongoing Epileptiform Activity in the Post-Ischemic Hippocampus Is Associated with a Permanent Shift of the Excitatory–Inhibitory Synaptic Balance in CA3 Pyramidal Neurons Yazar: Jérôme Epsztein, Mathieu Milh, Rachid Id Bihi, Isabel Jorquera, Yehezkel Ben‐Ari, Alfonso Represa, Valérie Crépel
Baskı/Yayın Bilgisi 2006Artigo -
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A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression‐burst enhances Kv7/M channel activity Yazar: Jérôme Devaux, Affef Abidi, Agathe Roubertie, Florence Molinari, Hélène Becq, Caroline Lacoste, Laurent Villard, Mathieu Milh, Laurent Aniksztejn
Baskı/Yayın Bilgisi 2016Artigo -
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Open‐label study to investigate the safety and efficacy of adjunctive perampanel in pediatric patients (4 to <12 years) with inadequately controlled focal seizures or generalize... Yazar: András Fogarasi, Robert Flamini, Mathieu Milh, Steven Phillips, Shinsaku Yoshitomi, Anna Patten, Takao Takase, Antonio Laurenza, Leock Y. Ngo
Baskı/Yayın Bilgisi 2020Artigo -
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A Conserved Switch in Sensory Processing Prepares Developing Neocortex for Vision Yazar: Matthew T. Colonnese, Anna Kaminśka, Marat Minlebaev, Mathieu Milh, Bernard Bloem, Sandra Lescure, G Moriette, Catherine Chiron, Yehezkel Ben‐Ari, Roustem Khazipov
Baskı/Yayın Bilgisi 2010Artigo -
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Auditory Stimuli Mimicking Ambient Sounds Drive Temporal “Delta-Brushes” in Premature Infants Yazar: Mathilde Chipaux, Matthew T. Colonnese, Audrey Mauguen, Laure Fellous, Mostafa Mokhtari, Oscar Lezcano, Mathieu Milh, Olivier Dulac, Catherine Chiron, Roustem Khazipov, Anna Kaminśka
Baskı/Yayın Bilgisi 2013Artigo -
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Novel Compound Heterozygous Mutations in<i>TBC</i><i>1</i><i>D</i><i>24</i>Cause Familial Malignant Migrating Partial Seizures of Infancy Yazar: Mathieu Milh, Antonio Falace, Nathalie Villeneuve, Nicola Vanni, Pierre Cacciagli, Stefania Assereto, Rima Nabbout, Fabio Benfenati, Federico Zara, B. Chabrol, Laurent Villard, Anna Fassio
Baskı/Yayın Bilgisi 2013Artigo -
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Recurrent mutations in the <i>CDKL5</i> gene: Genotype–phenotype relationships Yazar: Nadia Bahi‐Buisson, Nathalie Villeneuve, Emilie Caietta, Aurélia Jacquette, Hélène Maurey, Gert Matthijs, Hilde Van Esch, Andrée Delahaye‐Duriez, Anne Moncla, Mathieu Milh, Flore Zufferey, Bertrand Diebold, Thierry Bienvenu
Baskı/Yayın Bilgisi 2012Artigo -
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Variable clinical expression in patients with mosaicism for <i>KCNQ2</i> mutations Yazar: Mathieu Milh, Caroline Lacoste, Pierre Cacciagli, Affef Abidi, Julie Sutera-Sardo, Ilias Tzelepis, Estelle Colin, Catherine Badens, Alexandra Afenjar, Anne Dieux Coeslier, Thomas Dailland, Gaëtan Lesca, Nicole Philip, Laurent Villard
Baskı/Yayın Bilgisi 2015Artigo -
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Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations Yazar: Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane, Anna Kaminśka, Cécile Laroche, Marie Anne Barthez, Cyril Gitiaux, Céline Bartoli, Ana Borges-Correia, Pierre Cacciagli, Cécile Mignon‐Ravix, Hélène Cuberos, B. Chabrol, Laurent Villard
Baskı/Yayın Bilgisi 2011Artigo -
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Interictal stereotactic-EEG functional connectivity in refractory focal epilepsies Yazar: Stanislas Lagarde, Nicolas Roehri, Isabelle Lambert, Agnès Trebuchon, Aileen McGonigal, Romain Carron, Didier Scavarda, Mathieu Milh, Francesca Pizzo, Bruno Colombet, Bernard Giusiano, Samuel Médina Villalon, Maxime Guye, Christian Bénar, Fabrice Bartoloméi
Baskı/Yayın Bilgisi 2018Artigo -
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Stereoelectroencephalographic exploration and surgical outcome in Lennox–Gastaut syndrome Yazar: Soomi Cho, Julia Makhalova, Samuel Medina Villalon, Nathalie Villeneuve, Agnès Trébuchon, Manel Krouma, Didier Scavarda, Anne Lépine, Mathieu Milh, Romain Carron, Francesca Bonini, Géraldine Daquin, Sandrine Aubert, Stanislas Lagarde, Francesca Pizzo, Fabrice Bartoloméi
Baskı/Yayın Bilgisi 2025Artigo -
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Key clinical features to identify girls with CDKL5 mutations Yazar: Nadia Bahi‐Buisson, Juliette Nectoux, Haydeé Rosas‐Vargas, Mathieu Milh, Nathalie Boddaert, Benoı̂t Girard, Claude Cancès, Dorothée Ville, Alexandra Afenjar, Marlène Rio, Delphine Héron, Marie Ange N'Guyen Morel, Alexis Arzimanoglou, Christophe Philippe, Philippe Jonveaux, Jamel Chelly, Thierry Bienvenu
Baskı/Yayın Bilgisi 2008Artigo -
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Amitriptyline use in individuals with <i>KCNQ2/3</i> gain‐of‐function variants: A retrospective cohort study Yazar: Matthias De Wachter, Charissa Millevert, Joost Nicolai, Elisabeth A. Cats, Gerhard Kluger, Mathieu Milh, Robin Cloarec, Steffen Syrbe, Katrijn Arts, Katrien Jansen, Magdalena Krygier, Robert Śmigiel, Stéphane Auvin, Kern Olofson, Cathrine E. Gjerulfsen, Berten Ceulemans, Rikke S. Møller, Allan Bayat, Sarah Weckhuysen
Baskı/Yayın Bilgisi 2025Artigo -
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Depolarizing Actions of GABA in Immature Neurons Depend Neither on Ketone Bodies Nor on Pyruvate Yazar: Roman Tyzio, Camille Allène, Romain Nardou, Michel A. Picardo, Sumii Yamamoto, Sudhir Sivakumaran, Maddalena D. Caiati, Sylvain Rheims, Marat Minlebaev, Mathieu Milh, Pascal Ferré, Roustem Khazipov, Jean‐Louis Romette, Jean Lorquin, Rosa Cossart, Ilgam Khalilov, Astrid Nehlig, Enrico Cherubini, Yehezkel Ben‐Ari
Baskı/Yayın Bilgisi 2011Artigo
Arama Araçları:
İlgili Konular
Medicine
Biology
Neuroscience
Epilepsy
Genetics
Gene
Internal medicine
Pediatrics
Phenotype
Mutation
Psychiatry
Psychology
Electroencephalography
Encephalopathy
Ictal
Pathology
Receptor
Bioinformatics
Etiology
Intellectual disability
Microcephaly
Sensory system
Abnormality
Anesthesia
Biochemistry
Chemistry
Cohort
Corpus callosum
Endocrinology
Exome sequencing