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- [1] 47 patients with FLNA associated periventricular nodular heterotopiaORPHANET JOURNAL OF RARE DISEASES, 2015, 10Lange, Max论文数: 0 引用数: 0 h-index: 0机构: Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyKasper, Burkhard论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Med Ctr, Epilepsy Ctr, Dept Neurol, Erlangen, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyBohring, Axel论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Human Genet, Munster, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyRutsch, Frank论文数: 0 引用数: 0 h-index: 0机构: Muenster Univ Childrens Hosp, Dept Gen Pediat, Munster, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyKluger, Gerhard论文数: 0 引用数: 0 h-index: 0机构: Schon Klin Vogtareuth, Neuropediat, Vogtareuth, Germany Paracelsus Med Univ, Salzburg, Austria Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyHoffjan, Sabine论文数: 0 引用数: 0 h-index: 0机构: Ruhr Univ Bochum, Dept Human Genet, Bochum, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanySpranger, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Klinikum Bremen Mitte, Praxis Humangenet, Bremen, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyBehnecke, Anne论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Univ, Inst Human Genet, Heidelberg, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyFerbert, Andreas论文数: 0 引用数: 0 h-index: 0机构: Klinikum Kassel, Klin Neurol, Kassel, Germany Sch Med, Kassel, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyHahn, Andreas论文数: 0 引用数: 0 h-index: 0机构: Univ Giessen, Dept Neuropediat, D-35390 Giessen, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyOehl-Jaschkowitz, Barbara论文数: 0 引用数: 0 h-index: 0机构: Praxis Humangenet, Homburg, Saar, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyGraul-Neumann, Luitgard论文数: 0 引用数: 0 h-index: 0机构: Univ Med, Ambulantes Gesundheitszentrum, Charite Humangenet, Berlin, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyDiepold, Katharina论文数: 0 引用数: 0 h-index: 0机构: Klinikum Kassel, Dept Neuropediat, Kassel, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanySchreyer, Isolde论文数: 0 引用数: 0 h-index: 0机构: Uni Jena, Inst Humangenet, Jena, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyBernhard, Matthias K.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Med Ctr, Dept Pediat, D-04109 Leipzig, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyMueller, Franziska论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Regensburg, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanySiebers-Renelt, Ulrike论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Human Genet, Munster, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyBeleza-Meireles, Ana论文数: 0 引用数: 0 h-index: 0机构: Guys & St Thomas NHS Fdn Trust, Genet Clin, London, England Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyUyanik, Goekhan论文数: 0 引用数: 0 h-index: 0机构: Hanusch Krankenhaus Wiener Gebietskrankenkasse, Zentrum Med Genet, Vienna, Austria Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyJanssens, Sandra论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Ctr Med Genet, Ghent, Belgium Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyBoltshauser, Eugen论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Zurich, Div Neuropediat, Zurich, Switzerland Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyWinkler, Juergen论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Univ Hosp, Div Mol Neurol, D-91054 Erlangen, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanySchuierer, Gerhard论文数: 0 引用数: 0 h-index: 0机构: Univ Regensburg, Med Ctr, Dept Neuroradiol, D-93053 Regensburg, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, GermanyHehr, Ute论文数: 0 引用数: 0 h-index: 0机构: Univ Regensburg, Med Ctr, Dept Human Genet, D-93053 Regensburg, Germany Univ Regensburg, Med Ctr, Dept Neurosurg, D-93053 Regensburg, Germany
- [2] Three Generations of FLNA-Associated Periventricular Nodular HeterotopiaCASE REPORTS IN NEUROLOGY, 2021, 13 (03) : 776 - 780Eisenbiegler, Grace E.论文数: 0 引用数: 0 h-index: 0机构: Univ Vermont, Larner Coll Med, Burlington, VT 05405 USA Univ Vermont, Larner Coll Med, Burlington, VT 05405 USABrown, Stephen A.论文数: 0 引用数: 0 h-index: 0机构: Univ Vermont, Larner Coll Med, Burlington, VT 05405 USA Univ Vermont, Med Ctr, Dept Obstet & Gynecol, Burlington, VT 05405 USA Univ Vermont, Larner Coll Med, Burlington, VT 05405 USA
- [3] Lung disease associated with periventricular nodular heterotopia and an FLNA mutationEUROPEAN JOURNAL OF MEDICAL GENETICS, 2011, 54 (01) : 25 - 28Masurel-Paulet, Alice论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, Ctr Genet, F-21034 Dijon, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceHaan, Eric论文数: 0 引用数: 0 h-index: 0机构: Womens & Childrens Hosp, SA Pathol, S Australian Clin Genet Serv, Adelaide, SA, Australia Univ Adelaide, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceThompson, Elizabeth M.论文数: 0 引用数: 0 h-index: 0机构: Womens & Childrens Hosp, SA Pathol, S Australian Clin Genet Serv, Adelaide, SA, Australia Univ Adelaide, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceGoizet, Cyril论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, Ctr Genet, F-21034 Dijon, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceTai, Andrew论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Adelaide, SA, Australia Womens & Childrens Hosp, Dept Pulm Med, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceKennedy, Declan论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Adelaide, SA, Australia Womens & Childrens Hosp, Dept Pulm Med, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceSmith, Greg论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Adelaide, SA, Australia Womens & Childrens Hosp, Dept Pulm Med, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceKhong, Teck Yee论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Adelaide, SA, Australia Womens & Childrens Hosp, SA Pathol, Dept Surg Pathol, Adelaide, SA, Australia Hop Enfants, Ctr Genet, F-21034 Dijon, FranceSole, Guilhem论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceGuerineau, Elodie论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceCoupry, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux 2, Lab Genet Humaine, F-33076 Bordeaux, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceHuet, Frederic论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, Ctr Genet, F-21034 Dijon, France Hop Enfants, Ctr Genet, F-21034 Dijon, FranceRobertson, Stephen论文数: 0 引用数: 0 h-index: 0机构: Univ Otago, Dept Paediat, Dunedin, New Zealand Hop Enfants, Ctr Genet, F-21034 Dijon, FranceFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, Ctr Genet, F-21034 Dijon, France Hop Enfants, Ctr Genet, F-21034 Dijon, France
- [4] Hemizygous FLNA variant in West syndrome without periventricular nodular heterotopiaHUMAN GENOME VARIATION, 2020, 7 (01)Hiromoto, Yoshitaka论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, JapanAzuma, Yoshiteru论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, JapanSuzuki, Yuichi论文数: 0 引用数: 0 h-index: 0机构: Fukushima Med Univ, Dept Pediat, Sch Med, Fukushima 9601295, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, JapanHoshina, Megumi论文数: 0 引用数: 0 h-index: 0机构: Ohara Gen Hosp, Dept Pediat, Fukushima 9608611, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, JapanUchiyama, Yuri论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan Yokohama City Univ, Dept Oncol, Grad Sch Med, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Kato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Dept Pediat, Sch Med, Tokyo 1428555, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, JapanMatsumoto, Naomichi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan Yokohama City Univ, Dept Human Genet, Grad Sch Med, 3-9 Fukuura, Kanazawa, Ishikawa 2360004, Japan
- [5] Filamin A Gene Associated Periventricular Nodular Heterotopia and Epilepsy in a Cohort of Chinese PatientsCHINESE MEDICAL JOURNAL, 2017, 130 (20) : 2506 - 2507Liu, Wen-Yu论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, West China Hosp, Dept Neurol, 37 GuoXue Alley, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, West China Hosp, Dept Neurol, 37 GuoXue Alley, Chengdu 610041, Sichuan, Peoples R ChinaZhou, Dong论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, West China Hosp, Dept Neurol, 37 GuoXue Alley, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, West China Hosp, Dept Neurol, 37 GuoXue Alley, Chengdu 610041, Sichuan, Peoples R China
- [6] Filamin A Gene Associated Periventricular Nodular Heterotopia and Epilepsy in a Cohort of Chinese Patients中华医学杂志英文版, 2017, 130 (20) : 2506 - 2507Liu Wen-Yu论文数: 0 引用数: 0 h-index: 0机构: ChengduZhou Dong论文数: 0 引用数: 0 h-index: 0机构: Chengdu
- [7] A Case of Prenatally Diagnosed Periventricular Nodular Heterotopia in a Surviving Male Patient with FLNA MutationJOURNAL OF PEDIATRIC NEUROLOGY, 2022, 20 (01) : 57 - 59Tencer, Jaclyn论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USAVirupakshaiah, Akash论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USACampbell, Ian M.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USAZackai, Elaine H.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USAZarnow, Deborah论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Radiol, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USAAgarwal, Sonika论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Neurol, Dept Pediat, Philadelphia, PA USA
- [8] Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsyEPILEPSY & BEHAVIOR, 2015, 51 : 321 - 327Fallil, Zianka论文数: 0 引用数: 0 h-index: 0机构: NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAPardoe, Heath论文数: 0 引用数: 0 h-index: 0机构: NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USABachman, Robert论文数: 0 引用数: 0 h-index: 0机构: NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USACunningham, Benjamin论文数: 0 引用数: 0 h-index: 0机构: NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAParulkar, Isha论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Neurol, Epilepsy Genet Program,Boston Childrens Hosp, Boston, MA 02115 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAShain, Catherine论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Neurol, Epilepsy Genet Program,Boston Childrens Hosp, Boston, MA 02115 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAPoduri, Annapurna论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Neurol, Epilepsy Genet Program,Boston Childrens Hosp, Boston, MA 02115 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAKnowlton, Robert论文数: 0 引用数: 0 h-index: 0机构: UCSF, Epilepsy Ctr, San Francisco, CA USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USAKuzniecky, Ruben论文数: 0 引用数: 0 h-index: 0机构: NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA NYU, Epilepsy Ctr, Langone Med Ctr, New York, NY 10016 USA
- [9] Atypical male and female presentations of FLNA-related periventricular nodular heterotopiaEUROPEAN JOURNAL OF MEDICAL GENETICS, 2012, 55 (05) : 313 - 318Fergelot, Patricia论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceCoupry, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceDeforges, Julie论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceMaurat, Elise论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceSole, Guilhem论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France CHU Bordeaux, Pessac, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceBoute, Odile论文数: 0 引用数: 0 h-index: 0机构: CHRU, Clin Genet Guy Fontaine, Hop Jeanne Flandre, Lille, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceDieux-Coeslier, Anne论文数: 0 引用数: 0 h-index: 0机构: CHRU, Clin Genet Guy Fontaine, Hop Jeanne Flandre, Lille, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceDavid, Albert论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, F-44035 Nantes 01, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceMarchal, Cecile论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceThambo, Jean-Benoit论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Unite Cardiol Pediat, Pessac, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceLacombe, Didier论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceArveiler, Benoit论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, FranceGoizet, Cyril论文数: 0 引用数: 0 h-index: 0机构: Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France Univ Bordeaux, Lab Malad Rares Genet & Metab MRGM, EA4576, Bordeaux, France Hop Pellegrin, CHU Bordeaux, Ctr Reference Anomalies Dev Embryonnaire, Serv Genet Med, F-33076 Bordeaux, France
- [10] Treatment of Epilepsy Associated with Periventricular Nodular HeterotopiaCURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2020, 20 (12)Khoo, Hui Ming论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Neurosurg, 2-2 Yamada Oka, Suita, Osaka 5650871, Japan Osaka Univ, Grad Sch Med, Dept Neurosurg, 2-2 Yamada Oka, Suita, Osaka 5650871, JapanGotman, Jean论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Dept Neurol & Neurosurg, 3801 Univ St, Montreal, PQ H3A 2B4, Canada Osaka Univ, Grad Sch Med, Dept Neurosurg, 2-2 Yamada Oka, Suita, Osaka 5650871, JapanHall, Jeffery A.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Dept Neurol & Neurosurg, 3801 Univ St, Montreal, PQ H3A 2B4, Canada Osaka Univ, Grad Sch Med, Dept Neurosurg, 2-2 Yamada Oka, Suita, Osaka 5650871, JapanDubeau, Francois论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Dept Neurol & Neurosurg, 3801 Univ St, Montreal, PQ H3A 2B4, Canada Osaka Univ, Grad Sch Med, Dept Neurosurg, 2-2 Yamada Oka, Suita, Osaka 5650871, Japan