共 50 条
- [21] SCN8A-related epilepsies: phenotypic overview and correlation with antiepileptic treatmentEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1461 - 1462Johannesen, K. M.论文数: 0 引用数: 0 h-index: 0机构: Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmarkj, Inst Reg Hlth Serv, Odense, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLiu, Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurol & Epileptol, Tubingen, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkTronhjem, C.论文数: 0 引用数: 0 h-index: 0机构: Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkSterbova, K.论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Child Neurol, Fac Med 2, Rague, Czech Republic Univ Hosp Motol, Rague, Czech Republic Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkHoi-Hansen, C.论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Dept Pediat, Copenhagen, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkStriano, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Pediat Neurol & Muscular Dis Unit, Genoa, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark论文数: 引用数: h-index:机构:Verhoeven, J.论文数: 0 引用数: 0 h-index: 0机构: Acad Ctr Epileptol, Heeze, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkOegema, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkHarder, A.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Med Ctr, Dept Neurol, Leiden, Netherlands Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkPendziwiat, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Klinikum Schleswig Holstein, Dept Neuropediat, Campus Kiel, Kiel, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLebon, S.论文数: 0 引用数: 0 h-index: 0机构: Lausanne Univ Hosp, Dept Pediat, Pediat Neurol Unit, Lausanne, Switzerland Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkVaccarezza, M.论文数: 0 引用数: 0 h-index: 0机构: Hosp Italiano Buenos Aires, Dept Neurol, Buenos Aires, Argentina Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkHeine, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig Hosp & Clin, Inst Human Genet, Leipzig, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLemke, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig Hosp & Clin, Inst Human Genet, Leipzig, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLe, N.论文数: 0 引用数: 0 h-index: 0机构: Cleveland Clin, Ctr Pediat Neurol, Cleveland, OH USA Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkChristensen, J.论文数: 0 引用数: 0 h-index: 0机构: Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBerger, A.论文数: 0 引用数: 0 h-index: 0机构: Klinikum Weiden, Dept Neuropediat, Weiden, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkTrivisano, M.论文数: 0 引用数: 0 h-index: 0机构: Osped Pediat Bambino Gesu, Dept Neurosci & Neurorehabil, Rome, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkSpecchio, N.论文数: 0 引用数: 0 h-index: 0机构: Osped Pediat Bambino Gesu, Dept Neurosci & Neurorehabil, Rome, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkHoffman-Zacharska, D.论文数: 0 引用数: 0 h-index: 0机构: Inst Mother & Child Hlth, Dept Med Genet, Warsaw, Poland Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMastrangelo, M.论文数: 0 引用数: 0 h-index: 0机构: ASST Fatebenefratelli Sacco, Vittore Buzzi Hosp, Pediat Neurol Unit, Milan, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBrilstra, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Utrecht, Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkVecchi, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Padua, Dept Womens & Childrens Hlth, Child Neurol & Clin Neurophysiol Unit, Padua, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkVallo, A.论文数: 0 引用数: 0 h-index: 0机构: Ostfold Hosp, Dept Pediat, Graalum, Norway Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMotazacker, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, Amsterdam, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLakeman, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, Amsterdam, Netherlands Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkNizon, M.论文数: 0 引用数: 0 h-index: 0机构: Necker Enfants Malades Hosp, Unit Med Genet, Paris, France Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBetzler, C.论文数: 0 引用数: 0 h-index: 0机构: Schon Klin, Epilepsy Ctr Children & Adolescents, Clin Neuropediat & Neurorehabilitat, Vogtareuth, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMasnada, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Pavia, Dept Brain & Behav Sci, Pavia, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkVegiotti, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, V Buzzi Childrens Hosp, Dept Child Neurol, Milan, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMarini, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Florence, Meyer Childrens Hosp, Pediat Neurol Neurogenet & Neurobiol Unit & Labs, Florence, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkGuerrini, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Florence, Meyer Childrens Hosp, Pediat Neurol Neurogenet & Neurobiol Unit & Labs, Florence, Italy Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkRubboli, G.论文数: 0 引用数: 0 h-index: 0机构: Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLesca, G.论文数: 0 引用数: 0 h-index: 0机构: Malformatifs Ctr Est HCL, Ctr Reference Anomalies Dev & Syndromes, Serv Genet Clin, Lyon, France Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkGardella, E.论文数: 0 引用数: 0 h-index: 0机构: Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLerche, H.论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurol & Epileptol, Tubingen, Germany Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMoller, R. S.论文数: 0 引用数: 0 h-index: 0机构: Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark
- [22] Expanding the genotype-phenotype spectrum in SCN8A-related disordersBMC Neurology, 24Malavika Hebbar论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineNawaf Al-Taweel论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineInderpal Gill论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineCyrus Boelman论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineRichard A. Dean论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineSamuel J. Goodchild论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineJanette Mezeyova论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineNoah Gregory Shuart论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineJ. P. Johnson论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineJames Lee论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineAspasia Michoulas论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineLinda L. Huh论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineLinlea Armstrong论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineMary B. Connolly论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of MedicineMichelle K. Demos论文数: 0 引用数: 0 h-index: 0机构: University of British Columbia,Division of Neurology, Department of Pediatrics, BC Children’s Hospital, Faculty of Medicine
- [23] Phenotypic and genetic spectrum in Chinese children with SCN8A-related disordersSEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2022, 95 : 38 - 49Hu, Chunhui论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R China Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R ChinaLuo, Tian论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R China Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R ChinaWang, Yi论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R China Fudan Univ, Dept Neurol, Childrens Hosp, Shanghai 201102, Peoples R China
- [24] The Power of Delphi and Advocacy: Consensus in SCN8A-Related Epilepsy and Neurodevelopmental DisordersEPILEPSY CURRENTS, 2025, 25 (01) : 32 - 35Joshi, Charuta论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern, Childrens Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA Univ Texas Southwestern, Childrens Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
- [25] A Complex Genomic Rearrangement Resulting in Loss of Function of SCN1A and SCN2A in a Patient with Severe Developmental and Epileptic EncephalopathyINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (21)Orlando, Valeria论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyDi Tommaso, Silvia论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyAlesi, Viola论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyLoddo, Sara论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyGenovese, Silvia论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyCatino, Giorgia论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyMartucci, Licia论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyRoberti, Maria Cristina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyTrivisano, Marina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Dept Neurosci, Rare & Complex Epilepsy Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyDentici, Maria Lisa论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Med Genet Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Genet & Rare Dis Res Div, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalySpecchio, Nicola论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Dept Neurosci, Rare & Complex Epilepsy Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyDallapiccola, Bruno论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Genet & Rare Dis Res Div, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyFerretti, Alessandro论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Dept Neurosci, Rare & Complex Epilepsy Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, ItalyNovelli, Antonio论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy Bambino Gesu Children Hosp, IRCCS, Lab Med Genet, Translat Cytogen Res Unit, I-00146 Rome, Italy
- [26] Phenotypic and genetic spectrum of SCN8A-related disorders, treatment options, and outcomesEPILEPSIA, 2019, 60 : S77 - S85论文数: 引用数: h-index:机构:Moller, Rikke S.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, DK-4293 Dianalund, Denmark Univ Southern Denmark, Inst Reg Hlth Serv, Odense, Denmark Danish Epilepsy Ctr, DK-4293 Dianalund, Denmark
- [27] Electroclinical features of epileptic encephalopathy caused by SCN8A mutationPEDIATRICS INTERNATIONAL, 2015, 57 (04) : 758 - 762Takahashi, Satoru论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, JapanYamamoto, Shiho论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, JapanOkayama, Akie论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, JapanAraki, Akiko论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan论文数: 引用数: h-index:机构:Matsumoto, Naomichi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Human Genet, Grad Sch Med, Yokohama, Kanagawa 232, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, JapanAzuma, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan Asahikawa Med Univ, Dept Pediat, Asahikawa, Hokkaido 0788510, Japan
- [28] Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathyANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2016, 3 (02): : 114 - 123Wagnon, Jacy L.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USABarker, Bryan S.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA USA Univ Virginia Hlth Syst, Grad Program Neurosci, Charlottesville, VA USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAHounshell, James A.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA USA Univ Virginia Hlth Syst, Grad Program Neurosci, Charlottesville, VA USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAHaaxma, Charlotte A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Pediat Neurol, NL-6525 ED Nijmegen, Netherlands Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAShealy, Amy论文数: 0 引用数: 0 h-index: 0机构: Cleveland Clin, Genom Med Inst, Cleveland, OH 44106 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAMoss, Timothy论文数: 0 引用数: 0 h-index: 0机构: Cleveland Clin, Genom Med Inst, Cleveland, OH 44106 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAParikh, Sumit论文数: 0 引用数: 0 h-index: 0机构: Cleveland Clin, Dept Pediat Neurol, Cleveland, OH 44106 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAMesser, Ricka D.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Med Inst, Dept Pediat Neurol, Baltimore, MD 21205 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAPatel, Manoj K.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA USA Univ Virginia Hlth Syst, Grad Program Neurosci, Charlottesville, VA USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USAMeisler, Miriam H.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
- [29] Astrocyte reactivity in a mouse model of SCN8A epileptic encephalopathyEPILEPSIA OPEN, 2022, 7 (02) : 280 - 292Thompson, Jeremy A.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia, Neurosci Grad Program, Charlottesville, VA USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAMiralles, Raquel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia, Neurosci Grad Program, Charlottesville, VA USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAWengert, Eric R.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia, Neurosci Grad Program, Charlottesville, VA USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAWagley, Pravin K.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAYu, Wenxi论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAWenker, Ian C.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USAPatel, Manoj K.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA Univ Virginia, Neurosci Grad Program, Charlottesville, VA USA Univ Virginia Hlth Syst, Dept Anesthesiol, Charlottesville, VA 22903 USA
- [30] TALE of an SCN8A-Associated Epileptic Encephalopathy Mouse ModelEPILEPSY CURRENTS, 2015, 15 (02) : 83 - 84Kearney, Jennifer A.论文数: 0 引用数: 0 h-index: 0