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- [1] Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformationBRAIN & DEVELOPMENT, 2016, 38 (10): : 950 - 953Kobayashi, Yu论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, JapanMagara, Shinichi论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, JapanOkazaki, Kenichi论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, JapanKomatsubara, Takao论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, 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, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo, Japan Nishi Niigata Chuo Natl Hosp, Dept Child Neurol, Niigata, Japan论文数: 引用数: h-index:机构:
- [2] EML1-associated brain overgrowth syndrome with ribbon-like heterotopiaAMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2019, 181 (04) : 627 - 637Oegema, Renske论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsMcGillivray, George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, Australia Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsLeventer, Richard论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Dept Neurol, Melbourne, Vic, Australia Univ Melbourne, Dept Pediat, Melbourne, Vic, Australia Univ Melbourne, Dept Pediat, Melbourne, Vic, Australia Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsLe Moing, Anne-Gaelle论文数: 0 引用数: 0 h-index: 0机构: CHU Amiens, Dept Child Neurol, Paris, France Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsBahi-Buisson, Nadia论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Sorbonne Paris Cites, Paris, France Inst Imagine INSERM, Embryol & Genet Congenital Malformat, Paris, France Necker Enfants Malades Hosp, AP HP, Pediat Neurol, Paris, France Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsBarnicoat, Angela论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Clin Genet, London, England Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands论文数: 引用数: h-index:机构:Francis, David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, Australia Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsFrancis, Fiona论文数: 0 引用数: 0 h-index: 0机构: INSERM U 1270, Paris, France Sorbonne Univ, UMR S 1270, Paris, France Inst Fer Moulin, Paris, France Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsMancini, Grazia M. S.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC Univ Med Ctr, Dept Clin Genet, Rotterdam, Netherlands Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsSavelberg, Sanne论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlandsvan Haaften, Gijs论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsMankad, Kshitij论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Radiol, London, England Univ Med Ctr Utrecht, Dept Genet, Utrecht, NetherlandsLequin, Maarten H.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Radiol, Utrecht, Netherlands Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands
- [3] A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defectsJOURNAL OF HUMAN GENETICS, 2021, 66 (12) : 1159 - 1167Markus, Fenja论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyKannengiesser, Annika论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyNaeder, Patricia论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyAtigbire, Paul论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyScholten, Alexander论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Div Biochem Biochem Signal Transduct Neurosensory, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyVoesing, Christine论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyBueltmann, Eva论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Inst Diagnost & Intervent Neuroradiol, Hannover, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyKorenke, G. Christoph论文数: 0 引用数: 0 h-index: 0机构: Klinikum Oldenburg, Univ Childrens Hosp, Dept Neuropediat, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, GermanyOwczarek-Lipska, Marta论文数: 0 引用数: 0 h-index: 0机构: Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Human Genet, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Res Ctr Neurosensory Sci, Oldenburg, Germany Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, Fac 6, Jr Res Grp,Genet Childhood Brain Malformat, Oldenburg, Germany论文数: 引用数: h-index:机构:
- [4] A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defectsJournal of Human Genetics, 2021, 66 : 1159 - 1167Fenja Markus论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIAnnika Kannengießer论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIPatricia Näder论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIPaul Atigbire论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIAlexander Scholten论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIChristine Vössing论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIEva Bültmann论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIG. Christoph Korenke论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIMarta Owczarek-Lipska论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VIJohn Neidhardt论文数: 0 引用数: 0 h-index: 0机构: University of Oldenburg,Junior Research Group, Genetics of Childhood Brain Malformations, Faculty VI
- [5] [AEPH2][GeSb2S6]•CH3OH: a thiogermanate-thioantimonate featuring an infinite ribbon-like structure with an unusual {GeSb3S11} unit and exhibiting the ability of photocatalytic degradation of organic dyeCRYSTENGCOMM, 2013, 15 (25): : 5007 - 5011Feng, Mei-Ling论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R ChinaHu, Chun-Li论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R ChinaWang, Kai-Yao论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R ChinaDu, Cheng-Feng论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R ChinaHuang, Xiao-Ying论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China