换一批
换一批
作者：
Claire,Bar [1]
;
Mathieu,Kuchenbuch [2]
;
Giulia,Barcia [1]
;
Amy,Schneider [2]
;
Mélanie,Jennesson [2]
;
Gwenaël,Le Guyader [3]
;
Gaetan,Lesca [4]
;
Cyril,Mignot [5]
;
Martino,Montomoli [6]
;
Elena,Parrini [7]
;
Hervé,Isnard [8]
;
Anne,Rolland [9]
;
Boris,Keren [10]
;
Alexandra,Afenjar [11]
;
Nathalie,Dorison [12]
;
Lynette G,Sadleir [12]
;
Delphine,Breuillard [13]
;
Raphael,Levy [14]
;
Marlène,Rio [11]
;
Sophie,Dupont [15]
;
Susanna,Negrin [16]
;
Alberto,Danieli [17]
;
Emmanuel,Scalais [18]
;
Anne,De Saint Martin [1]
;
Salima,El Chehadeh [2]
;
Jamel,Chelly [19]
;
Alice,Poisson [3]
;
Anne-Sophie,Lebre [20]
;
Anca,Nica [10]
;
Sylvie,Odent [21]
;
Tayeb,Sekhara [22]
;
Vesna,Brankovic [22]
;
Alice,Goldenberg [23]
;
Pascal,Vrielynck [24]
;
Damien,Lederer [25]
;
Hélène,Maurey [25]
;
Gaetano,Terrone [26]
;
Claude,Besmond [27]
;
Laurence,Hubert [28]
;
Patrick,Berquin [29]
;
Thierry,Billette de Villemeur [30]
;
Bertrand,Isidor [31]
;
Jeremy L,Freeman [32]
;
Heather C,Mefford [33]
;
Candace T,Myers [34]
;
Katherine B,Howell [35]
;
Andrés,Rodríguez-Sacristán Cascajo [36]
;
Pierre,Meyer [37]
;
David,Genevieve [38]
;
Agnès,Guët [39]
;
Diane,Doummar [39]
;
Julien,Durigneux [40]
;
Marieke F,van Dooren [17]
;
Marie Claire Y,de Wit [41]
;
Marion,Gerard [42]
;
Isabelle,Marey [43]
;
Arnold,Munnich [44]
;
Renzo,Guerrini [44]
;
Ingrid E,Scheffer [42]
;
Edor,Kabashi [43]
;
Rima,Nabbout [45]
作者单位：
Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Assistance Publique-Hôpitaux de Paris (AP-HP), Necker-Enfants Malades Hospital, Paris, France.
[1]
Imagine Institute, Mixed Unit of Research 1163, University of Paris, Sorbonne University, Paris, France.
[2]
Department of Clinical Genetics, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
[3]
Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
[4]
Department of Pediatrics, American Memorial Hospital, Reims, France.
[5]
Department of Genetics, Poitiers University Hospital Center, Poitiers Cedex, France.
[6]
EA3808-NEUVACOD Neurovascular and Cognitive Disorders Unit, University of Poitiers, Poitiers, France.
[7]
Department of Genetics, Lyon Civil Hospices, Lyon, France.
[8]
NeuroMyoGène Institute, National Center for Scientific Research, Mixed Unit of Research 5310, National Institute of Health and Medical Research U1217, University of Lyon, Claude Bernard Lyon 1 University, Villeurbanne, France.
[9]
National Institute of Health and Medical Research, U1127, National Center for Scientific Research Mixed Unit of Research 7225, Pierre and Marie Curie University Paris 6 Mixed Unit of Research S1127, Brain and Spine Institute, Sorbonne University, Paris, France.
[10]
Department of Genetics, Rare Causes of Intellectual Disability Reference Center, AP-HP, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.
[11]
Pediatric Neurology, Neurogenetics, and Neurobiology Unit and Laboratories, Neuroscience Department, A. Meyer Children's Hospital, University of Florence, Florence, Italy.
[12]
Pediatric Neurologist, Medical Office, Lyon, France.
[13]
Department of Pediatrics, Nantes University Hospital Center, Nantes, France.
[14]
Department of Genetics and Medical Embryology, Reference Center for Malformations and Congenital Diseases of the Cerebellum and Rare Causes of Intellectual Disabilities, Sorbonne University, AP-HP, Trousseau Hospital, Paris, France.
[15]
Pediatric Neurosurgery Department, Rothschild Foundation Hospital, Paris, France.
[16]
Department of Pediatric Neurology, AP-HP, Armand Trousseau Hospital, Sorbonne University, Paris, France.
[17]
Department of Pediatrics and Child Health, University of Otago, Wellington, New Zealand.
[18]
Department of Pediatric Radiology, Necker-Enfants Malades Hospital, Paris, France.
[19]
Laboratory of Developmental Brain Disorders, National Institute of Health and Medical Research Mixed Unit of Research 1163, Imagine Institute, Sorbonne University, Paris, France.
[20]
Epileptology Unit and Rehabilitation Unit, AP-HP, Pitie-Salpêtrière-Charles Foix Hospital, Paris, France.
[21]
Epilepsy and Clinical Neurophysiology Unit, Scientific Institute, IRCCS E. Medea, Treviso, Italy.
[22]
Pediatric Neurology Unit, Luxembourg Hospital Center, Luxembourg City, Luxembourg.
[23]
Department of Pediatric Neurology, Strasbourg University Hospital, Hautepierre Hospital, Strasbourg, France.
[24]
Department of Medical Genetics, Strasbourg University Hospitals, Hautepierre Hospital, Strasbourg, France.
[25]
GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, le Vinatier Hospital Center and EDR-Psy Team (National Center for Scientific Research and Lyon 1 Claude Bernard University), Villeurbanne, France.
[26]
Reims University Hospital Center, Maison Blanche Hospital, Biology Department, Reims, France.
[27]
Neurology Department, Center for Clinical Research (CIC 1414), Rennes University Hospital, Rennes, France.
[28]
Laboratory of Signal Processing, National Institute of Health and Medical Research Mixed Unit of Research 1099, Rennes, France.
[29]
Reference Center for Rare Developmental Abnormalities CLAD-Ouest, Rennes University Hospital Center, Rennes, France.
[30]
National Center for Scientific Research Mixed Unit of Research 6290, Institute of Genetics and Development of Rennes (IGDR), University of Rennes, Rennes, France.
[31]
Department of Pediatric Neurology, C.H.I.R.E.C, Brussels, Belgium.
[32]
Clinic for Child Neurology and Psychiatry, Belgrade, Serbia.
[33]
Reference Center for Developmental Anomalies and Malformation Syndromes, Rouen University Hospital Center, Rouen, France.
[34]
Reference Center for Refractory Epilepsy, Catholic University of Louvain, William Lennox Neurological Hospital, Ottignies, Belgium.
[35]
Human Genetic Center, IPG, Gosselies, Belgium.
[36]
Department of Pediatric Neurology, AP-HP, Bicêtre University Hospital, Kremlin Bicêtre, France.
[37]
Department of Translational Medical Sciences, Section of Pediatrics, Child Neurology Unit, Federico II University, Naples, Italy.
[38]
Translational Genetics, National Institute of Health and Medical Research Mixed Unit of Research 1163, Imagine Institute, University of Paris, Paris, France.
[39]
Department of Pediatric Neurology, Amiens-Picardie University Hospital Center, University of Picardy Jules Verne, Amiens, France.
[40]
Department of Clinical Genetics, Nantes University Hospital Center, Nantes, France.
[41]
Departments of Neurology and Paediatrics, Royal Children's Hospital, University of Melbourne, Melbourne, Victoria, Australia.
[42]
Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
[43]
Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, Washington, United States.
[44]
Pediatric Neurology Unit, Department of Pediatric, Virgen Macarena Hospital, Seville, Spain.
[45]
Department of Pediatrics, School of Medicine, University of Seville, Seville, Spain.
[46]
Department of Pediatric Neurology, Montpellier University Hospital Center, Montpellier, France.
[47]
PhyMedExp, National Institute of Health and Medical Research, U1046, National Center for Scientific Research Mixed Unit of Research 9214, University of Montpellier, Montpellier, France.
[48]
Department of Medical Genetics, Rare Disease, and Personalized Medicine, IRMB, University of Montpellier, National Institute of Health and Medical Research, Montpellier University Hospital Center, Montpellier, France.
[49]
Department of Pediatrics, Louis-Mourier Hospital, Colombes, France.
[50]
Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, the Netherlands.
[51]
Department of Pediatric Neurology and ENCORE Expertise Center, Erasmus University Medical Center, Sophia Children's Hospital, Rotterdam, the Netherlands.
[52]
Clinical Genetics, Côte de Nacre University Hospital Center, Caen, France.
[53]
Florey Institute of Neurosciences and Mental Health, Heidelberg, Victoria, Australia.
[54]
主题词
青少年(Adolescent);成年人(Adult);脑疾病(Brain Diseases);儿童(Child);儿童, 学龄前(Child, Preschool);队列研究(Cohort Studies);脑电描记术(Electroencephalography);癫痫(Epilepsy);女(雌)性(Female);遗传变异(Genetic Variation);人类(Humans);婴儿(Infant);男(雄)性(Male);回顾性研究(Retrospective Studies);Shab钾通道(Shab Potassium Channels);时间因素(Time Factors);治疗结果(Treatment Outcome);青年人(Young Adult)
DOI
10.1111/epi.16679
PMID
32954514
发布时间
2021-02-03
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Epilepsia
Epilepsia
2461-2473页
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