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- [1] WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality riskEPILEPSIA, 2023, 64 (05) : 1351 - 1367Oliver, Karen L.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, Australia Walter & Eliza Hall Inst Med Res, Populat Hlth & Immun Div, Parkville, Vic, Australia Univ Melbourne, Dept Med Biol, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaTrivisano, Marina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Childrens Hosp IRCCS, European Reference Network EpiCARE, Dept Neurosci, Rare & Complex Epilepsy Unit, Rome, Italy Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaMandelstam, Simone A.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia Murdoch Childrens Res Inst, Melbourne, Vic, Australia Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia Royal Childrens Hosp, Dept Radiol, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaDe Dominicis, Angela论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Childrens Hosp IRCCS, European Reference Network EpiCARE, Dept Neurosci, Rare & Complex Epilepsy Unit, Rome, Italy Univ Roma Tor Vergata, Dept Biomed & Prevent, Rome, Italy Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaFrancis, David I.论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaGreen, Timothy E.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaMuir, Alison M.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Seattle, WA USA Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaChowdhary, Apoorva论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Seattle, WA USA Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaHertzberg, Christoph论文数: 0 引用数: 0 h-index: 0机构: Vivantes Hosp Neukoelln, Zent Sozialpadiatr & Neuropadiatr DBZ, Berlin, Germany Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaGoldhahn, Klaus论文数: 0 引用数: 0 h-index: 0机构: DRK Klinikum Westend, Dept Pediat & Neuropediat, Berlin, Germany Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaMetreau, Julia论文数: 0 引用数: 0 h-index: 0机构: Hop Bicetre, Assistance Publ Hop Paris, Dept Pediat Neurol, Le Kremlin Bicetre, France Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaPrager, Christine论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Ctr Chron Sick Children SPZ, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaPinner, Jason论文数: 0 引用数: 0 h-index: 0机构: Sydney Childrens Hosp, Randwick, NSW, Australia Univ New South Wales, Sch Womens & Childrens Hlth, Sydney, NSW, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaCardamone, Michael论文数: 0 引用数: 0 h-index: 0机构: Sydney Childrens Hosp, Randwick, NSW, Australia Univ New South Wales, Sch Womens & Childrens Hlth, Sydney, NSW, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaMyers, Kenneth A.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Dept Pediat, Div Child Neurol, Montreal, PQ, Canada McGill Univ Hlth Ctr, Res Inst, Montreal, PQ, Canada McGill Univ, Montreal Childrens Hosp, Dept Neurol & Neurosurg, Montreal, PQ, Canada Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaLeventer, Richard J.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia Murdoch Childrens Res Inst, Melbourne, Vic, Australia Royal Childrens Hosp, Dept Neurol, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaLesca, Gaetan论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, Australia Univ Claude Bernard Lyon 1, Lyon Univ Hosp, Dept Med Genet, European Reference Network EpiCARE, Lyon, France Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaBahlo, Melanie论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaHildebrand, Michael S.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, Australia Murdoch Childrens Res Inst, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaMefford, Heather C.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Seattle, WA USA St Jude Childrens Res Hosp, Ctr Pediat Neurol Dis Res, Memphis, TN USA Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaKaindl, Angela M.论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Ctr Chron Sick Children SPZ, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Charite Univ Med Berlin, Inst Cell Biol & Neurobiol, Berlin, Germany Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaSpecchio, Nicola论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Childrens Hosp IRCCS, European Reference Network EpiCARE, Dept Neurosci, Rare & Complex Epilepsy Unit, Rome, Italy Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, AustraliaScheffer, Ingrid E.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia Murdoch Childrens Res Inst, Melbourne, Vic, Australia Univ Melbourne, Austin Hlth, Epilepsy Res Ctr, Dept Med, Heidelberg, Vic, Australia
- [2] WWOX-related epileptic encephalopathy caused by a novel mutation in the WWOX gene: a case reportFRONTIERS IN PEDIATRICS, 2024, 12Feng, Dan论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R ChinaLi, Ye论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Hosp 2, Dept Neonatol, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R ChinaZhang, Ya-Ting论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Hosp 2, Dept Neonatol, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R ChinaSong, Yan-Jun论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R ChinaQin, Dong-Yuan论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R ChinaWang, Fan论文数: 0 引用数: 0 h-index: 0机构: Lanzhou Univ, Hosp 2, Dept Neonatol, Lanzhou, Peoples R China Lanzhou Univ, Clin Med Coll 2, Lanzhou, Peoples R China
- [3] West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutationsEPILEPTIC DISORDERS, 2018, 20 (05) : 401 - 412Shaukat, Qudsia论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab Emirates Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab EmiratesHertecant, Jozef论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Div Genet & Metab Disorders, Dept Pediat, Al Ain, U Arab Emirates Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab EmiratesEl-Hattab, Ayman W.论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Div Genet & Metab Disorders, Dept Pediat, Al Ain, U Arab Emirates Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab EmiratesAli, Bassam R.论文数: 0 引用数: 0 h-index: 0机构: UAE Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab EmiratesSuleiman, Jehan论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab Emirates UAE Univ, Coll Med & Hlth Sci, Dept Pediat, Al Ain, U Arab Emirates Tawam Hosp, Dept Pediat, Div Neurol, POB 18258, Al Ain, U Arab Emirates
- [4] Case report: Adult patient with WWOX developmental and epileptic encephalopathy: 40 years of observationFRONTIERS IN GENETICS, 2024, 15Teplyshova, Anna论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Neurol, Moscow, Russia Res Ctr Neurol, Moscow, RussiaSharkov, Artem论文数: 0 引用数: 0 h-index: 0机构: Pirogov Russian Natl Res Med Univ, Veltischev Res & Clin Inst Pediat & Pediat Surg, Moscow, Russia Genomed Ltd, Moscow, Russia Russian Acad Sci, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow, Russia Res Ctr Neurol, Moscow, Russia
- [5] A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delayNEUROGENETICS, 2018, 19 (03) : 151 - 156Johannsen, Jessika论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanyKortuem, Fanny论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanyRosenberger, Georg论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanyBokelmann, Kristin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Clin Pharmacol, Gottingen, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanySchirmer, Markus A.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Clin Radiotherapy & Radiat Oncol, Gottingen, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanyDenecke, Jonas论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, GermanySanter, Rene论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany
- [6] A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delayneurogenetics, 2018, 19 : 151 - 156Jessika Johannsen论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsFanny Kortüm论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsGeorg Rosenberger论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsKristin Bokelmann论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsMarkus A. Schirmer论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsJonas Denecke论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of PediatricsRené Santer论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Hamburg-Eppendorf,Department of Pediatrics
- [7] Epilepsy in patients with WWOX-related epileptic encephalopathy (WOREE) syndromeEPILEPTIC DISORDERS, 2022, 24 (04) : 697 - 712Al Baradie, Raidah论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaMir, Ali论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaAlsaif, Ali论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaAli, Mona论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaAl Ghamdi, Fouad论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaBashir, Shahid论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi ArabiaHowsawi, Yousef论文数: 0 引用数: 0 h-index: 0机构: King Fahad Specialist Hosp, Genet & Metab Dept, Dammam, Saudi Arabia King Fahad Specialist Hosp, Dept Pediat Neurol, Dammam, Saudi Arabia
- [8] Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathyAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (03) : 776 - 785Chong, Shuk Ching论文数: 0 引用数: 0 h-index: 0机构: Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R China Chinese Univ Hong Kong, Joint BCM CUHK Ctr Med Genet, Hong Kong, Peoples R China Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaCao, Ye论文数: 0 引用数: 0 h-index: 0机构: Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R China Chinese Univ Hong Kong, Joint BCM CUHK Ctr Med Genet, Hong Kong, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Obstet & Gynecol, Hong Kong, Peoples R China Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaFung, Eva L. W.论文数: 0 引用数: 0 h-index: 0机构: Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R China Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaKleppe, Soledad论文数: 0 引用数: 0 h-index: 0机构: Hosp Ninos Dr Ricardo Gutierrez, Unidad Metab, Buenos Aires, DF, Argentina Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaGripp, Karen W.论文数: 0 引用数: 0 h-index: 0机构: AI Pont Hosp Children Nemours, Div Med Genet, Delaware, OH USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaHertecant, Jozef论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Dept Pediat, Div Genet & Metab Disorders, Al Ain, U Arab Emirates Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaEl-Hattab, Ayman W.论文数: 0 引用数: 0 h-index: 0机构: Univ Sharjah, Coll Med, Dept Clin Sci, Sharjah, U Arab Emirates Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaSuleiman, Jehan论文数: 0 引用数: 0 h-index: 0机构: Tawam Hosp, Dept Pediat, Div Neurol, Al Ain, U Arab Emirates United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pediat, Al Ain, U Arab Emirates Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaClark, Gary论文数: 0 引用数: 0 h-index: 0机构: Texas Childrens Hosp, Neurol Serv, Baylor Coll Med, Neurol & Dev Neurosci, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R Chinavon Allmen, Gretchen论文数: 0 引用数: 0 h-index: 0机构: McGovern Med Sch, Dept Pediat, Div Child Neurol, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaRodziyevska, Olga论文数: 0 引用数: 0 h-index: 0机构: McGovern Med Sch, Dept Pediat, Div Child Neurol, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaLewis, Richard A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA Texas Childrens Hosp, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaRosenfeld, Jill A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaDong, Jie论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaWang, Xia论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaMiller, Marcus J.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaBi, Weimin论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaLiu, Pengfei论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R ChinaScaglia, Fernando论文数: 0 引用数: 0 h-index: 0机构: Chinese Univ Hong Kong, Joint BCM CUHK Ctr Med Genet, Hong Kong, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Obstet & Gynecol, Hong Kong, Peoples R China Texas Childrens Hosp, Mark Wallace Tower,Suite 1560,6701 Fannin St, Houston, TX 77030 USA Chinese Univ Hong Kong, Dept Paediat, Hong Kong, Peoples R China
- [9] Developmental epileptic encephalopathy caused by homozygosity of a c.172+1G>C variant in the WWOX geneMOLECULAR GENETICS & GENOMIC MEDICINE, 2024, 12 (08):You, Yang论文数: 0 引用数: 0 h-index: 0机构: Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R China Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R ChinaWu, Wenjuan论文数: 0 引用数: 0 h-index: 0机构: Hebei Med Univ, Hebei Childrens Hosp, Dept Neurol, Shijiazhuang, Hebei, Peoples R China Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R ChinaDu, Yakun论文数: 0 引用数: 0 h-index: 0机构: Hebei Med Univ, Hebei Childrens Hosp, Dept Neurol, Shijiazhuang, Hebei, Peoples R China Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R ChinaHu, Jintong论文数: 0 引用数: 0 h-index: 0机构: Hebei Med Univ, Hebei Childrens Hosp, Dept Neurol, Shijiazhuang, Hebei, Peoples R China Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R ChinaLi, Baoguang论文数: 0 引用数: 0 h-index: 0机构: Hebei Med Univ, Hebei Childrens Hosp, Dept Neurol, Shijiazhuang, Hebei, Peoples R China Key Lab Pediat Epilepsy & Neurol Disorders Hebei P, Shijiazhuang, Peoples R China Hebei Med Univ, Hosp 4, Dept Imaging, Shijiazhuang, Hebei, Peoples R China
- [10] WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal periodJournal of Human Genetics, 2015, 60 : 267 - 271Mylène Valduga论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Christophe Philippe论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Laetitia Lambert论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Pascale Bach-Segura论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Emmanuelle Schmitt论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Jean Pierre Masutti论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Bénédicte François论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Patrick Pinaud论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Mireille Vibert论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,Philippe Jonveaux论文数: 0 引用数: 0 h-index: 0机构: Laboratoire de Génétique Médicale,