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换一批
作者：
Claire,Bar [1]
;
Delphine,Breuillard [1]
;
Mathieu,Kuchenbuch [1]
;
Mélanie,Jennesson [2]
;
Gwenaël,Le Guyader [3]
;
Hervé,Isnard [4]
;
Anne,Rolland [5]
;
Diane,Doummar [6]
;
Joel,Fluss [7]
;
Alexandra,Afenjar [8]
;
Patrick,Berquin [9]
;
Anne,De Saint Martin [10]
;
Sophie,Dupont [11]
;
Alice,Goldenberg [12]
;
Damien,Lederer [13]
;
Gaétan,Lesca [14]
;
Hélène,Maurey [15]
;
Pierre,Meyer [16]
;
Cyril,Mignot [17]
;
Anca,Nica [18]
;
Sylvie,Odent [19]
;
Alice,Poisson [20]
;
Emmanuel,Scalais [21]
;
Tayeb,Sekhara [22]
;
Pascal,Vrielynck [23]
;
Giulia,Barcia [24]
;
Rima,Nabbout [25]
作者单位：
APHP, Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Hôpital Necker-Enfants Malades, member of ERN EPICARE, Université de Paris, Paris, France; Laboratory of Translational Research for Neurological Disorders, INSERM UMR 1163, Imagine Institute, Université de Paris, Paris, France.
[1]
Department of Pediatrics, American Memorial Hospital, Reims, France.
[2]
Department of Genetics, CHU de Poitiers, BP 577, 86021 Poitiers Cedex, France; EA3808 - NEUVACOD Unité neurovasculaire et troubles cognitifs, Université de Poitiers, Pôle Biologie Santé, France.
[3]
Pediatric Neurologist, Medical Office 28 rue de la république, Lyon 69002, France.
[4]
Department of Pediatrics, CHU de NANTES, Nantes, France.
[5]
Department of Pediatric Neurology, AP-HP, Hôpital Armand Trousseau, Sorbonne Université, Paris, France.
[6]
Pediatric Neurology Unit, Geneva Children's Hospital, 6 rue Willy-Donzé, 1211 Genève 4, Switzerland.
[7]
Sorbonne Universités, Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, département de génétique et embryologie médicale, Hôpital Trousseau, AP-HP, Paris, France.
[8]
Department of Pediatric Neurology, CHU Amiens-Picardie, Université de Picardie Jules Verne, Amiens France Pediatric Neurology Unit, France.
[9]
Department of Pediatric Neurology, Strasbourg University Hospital, Strasbourg, Hôpital de Hautepierre, Strasbourg, France.
[10]
Epileptology Unit and Rehabilitation Unit AP-HP, GH Pitie-Salpêtrière-Charles Foix, F-75013 Paris, France; Sorbonne University, UPMC Univ. Paris 06, F-75005 Paris, France.
[11]
Centre de Référence Anomalies du Développement et Syndromes Malformatifs, CHU Rouen, Rouen, France.
[12]
Human Genetic Centre, IPG, Gosselies, Belgium.
[13]
Department of Genetics, Hospices Civils de Lyon, 69002 Lyon, France; Institut NeuroMyoGène, CNRS UMR 5310 - INSERM U1217, Université de Lyon, Université Claude Bernard Lyon 1, France.
[14]
Department of Pediatric Neurology, AP-HP, Hôpital Universitaire Bicêtre, Kremlin Bicêtre, France.
[15]
Department of Pediatric Neurology, CHU Montpellier, Montpellier, France; PhyMedExp, U1046 INSERM, UMR9214 CNRS, Université de Montpellier, Montpellier, France.
[16]
INSERM, U 1127, CNRS UMR 7225, Sorbonne Université, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France; APHP, Sorbonne Université, Groupe Hospitalier Pitié-Salpêtrière, Department of Genetics, Centre de Reference Déficience Intellectuelle de Causes Rares.
[17]
Neurology Department, Center for Clinical Research (CIC 1414), Rennes University Hospital, France; Laboratory Of Signal Processing (LTSI), UMR 1099 INSERM, Rennes F-35000, France.
[18]
Service de Génétique clinique, Reference Ccentre for Rare Developmental Abnormalities CLAD-Ouest, member of ERN ITHACA, CHU Rennes, France; CNRS UMR 6290 Institut de Génétique et Développement de Rennes IGDR, Univ Rennes, Rennes, France.
[19]
GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), France.
[20]
Pediatric Neurology Unit, Centre Hospitalier de Luxembourg, Luxembourg.
[21]
Department of Pediatric Neurology, C.H.I.R.E.C, Brussels, Belgium.
[22]
William Lennox Neurological Hospital, Reference Center for Refractory Epilepsy UCLouvain, Ottignies, Belgium.
[23]
Laboratory of Translational Research for Neurological Disorders, INSERM UMR 1163, Imagine Institute, Université de Paris, Paris, France; APHP, Department of Clinical Genetics, Necker-Enfants Malades Hospital, Paris, France.
[24]
APHP, Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Hôpital Necker-Enfants Malades, member of ERN EPICARE, Université de Paris, Paris, France; Laboratory of Translational Research for Neurological Disorders, INSERM UMR 1163, Imagine Institute, Université de Paris, Paris, France. Electronic address: rima.nabbout@aphp.fr.
[25]
主题词
适应, 心理学(Adaptation, Psychological);青少年(Adolescent);成年人(Adult);脑疾病(Brain Diseases);儿童(Child);儿童, 学龄前(Child, Preschool);癫痫(Epilepsy);人类(Humans);Shab钾通道(Shab Potassium Channels);青年人(Young Adult)
DOI
10.1016/j.yebeh.2021.108471
PMID
34915430
发布时间
2022-05-31
- 浏览1
Epilepsy & behavior
108471页
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