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- [1] Comparison of methylation episignatures in KMT2B- and KMT2D-related human disordersEPIGENOMICS, 2022, 14 (09) : 537 - 547Lee, Sunwoo论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandOchoa, Eguzkine论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandBarwick, Katy论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London WC1N 1DZ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandCif, Laura论文数: 0 引用数: 0 h-index: 0机构: Hop Gui De Chauliac, Unite Pathol Cerebrales Resistantes, Ctr Hosp Reg Montpellier, Dept Neurochirurg,Unite Rech Sur Comportements &, Montpellier, France Univ Montpellier, Fac Med, Montpellier, France Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandRodger, Fay论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Stratified Med Core Lab NGS Hub, Cambridge Biomed Campus, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandDocquier, France论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Stratified Med Core Lab NGS Hub, Cambridge Biomed Campus, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandPerez-Duenas, Belen论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London WC1N 1DZ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England论文数: 引用数: h-index:机构:Martin, Ezequiel论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Stratified Med Core Lab NGS Hub, Cambridge Biomed Campus, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandBanka, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biol Sci, Fac Biol Med & Hlth, Div Evolut Infect & Genom, Manchester, Lancs, England Manchester Univ Fdn NHS Trust, Manchester Ctr Genom Med, Hlth Innovat Manchester, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandKurian, Manju A.论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London WC1N 1DZ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, EnglandMaher, Eamonn R.论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med Genet, Cambridge CB2 0QQ, England
- [2] Genotypic and phenotypic characterization of Romanian patients with KMT2D-related disordersEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 217 - 217Plaiasu, Vasilica论文数: 0 引用数: 0 h-index: 0机构: IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, RomaniaOzunu, Diana论文数: 0 引用数: 0 h-index: 0机构: INSMC Alessandrescu Rusescu, Genet Lab, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, RomaniaMotei, Gabriela论文数: 0 引用数: 0 h-index: 0机构: INSMC Alessandrescu Rusescu, Genet Lab, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, RomaniaIvan, Mihaela论文数: 0 引用数: 0 h-index: 0机构: IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, RomaniaGhita, Lucica论文数: 0 引用数: 0 h-index: 0机构: INSMC Alessandrescu Rusescu, Dept Neurol, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, RomaniaTrutescu, Carmen论文数: 0 引用数: 0 h-index: 0机构: INSMC Alessandrescu Rusescu, Psychiat Dept, Bucharest, Romania IINSMC Alessandrescu Rusescu, Clin Genet, Bucharest, Romania
- [3] Neuroimaging in Kabuki syndrome and another KMT2D-related disorderAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (12) : 3770 - 3783Stadelmaier, Rachel T.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAKenna, Margaret A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Dept Otolaryngol & Commun Enhancement, Boston, MA USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USABarrett, Devon论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Atlanta, GA 30322 USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAMullen, Thomas E.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst & Harvard, Ctr Mendelian Gen, Cambridge, MA USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USABodamer, Olaf论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAAgrawal, Pankaj B.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Genet & Genom, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USARobson, Caroline D.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Dept Radiol, Boston, MA USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAWojcik, Monica H.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Genet & Genom, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA
- [4] Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (05) : 1053 - 1065Baldridge, Dustin论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USASpillmann, Rebecca C.论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Pediat, Div Med Genet, Durham, NC 27710 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAWegner, Daniel J.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAWambach, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAWhite, Frances, V论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USASisco, Kathleen论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAToler, Tomi L.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USADickson, Patricia, I论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USACole, F. Sessions论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAShashi, Vandana论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Pediat, Div Med Genet, Durham, NC 27710 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USAGrange, Dorothy K.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA Washington Univ, Dept Pediat, Sch Med, St Louis, MO 63110 USA
- [5] Kmt2b hits prime time in the germlineDEVELOPMENT, 2018, 145 (23):Tomizawa, Shin-ichi论文数: 0 引用数: 0 h-index: 0Kobayashi, Yuki论文数: 0 引用数: 0 h-index: 0Shirakawa, Takayuki论文数: 0 引用数: 0 h-index: 0Watanabe, Kumiko论文数: 0 引用数: 0 h-index: 0Mizoguchi, Keita论文数: 0 引用数: 0 h-index: 0Hoshi, Ikue论文数: 0 引用数: 0 h-index: 0Nakajima, Kuniko论文数: 0 引用数: 0 h-index: 0Nakabayashi, Jun论文数: 0 引用数: 0 h-index: 0Singh, Sukhdeep论文数: 0 引用数: 0 h-index: 0Dahl, Andreas论文数: 0 引用数: 0 h-index: 0Alexopoulou, Dimitra论文数: 0 引用数: 0 h-index: 0Seki, Masahide论文数: 0 引用数: 0 h-index: 0Suzuki, Yutaka论文数: 0 引用数: 0 h-index: 0Royo, Helene论文数: 0 引用数: 0 h-index: 0Peters, Antoine H. F. M.论文数: 0 引用数: 0 h-index: 0Anastassiadis, Konstantinos论文数: 0 引用数: 0 h-index: 0Stewart, A. Francis论文数: 0 引用数: 0 h-index: 0Ohbo, Kazuyuki论文数: 0 引用数: 0 h-index: 0
- [6] KMT2A and KMT2B Mediate Memory Function by Affecting Distinct Genomic RegionsCELL REPORTS, 2017, 20 (03): : 538 - 548Kerimoglu, Cemil论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanySakib, M. Sadman论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyJain, Gaurav论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyBenito, Eva论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyBurkhardt, Susanne论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyCapece, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyKaurani, Lalit论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, Germany论文数: 引用数: h-index:机构:Carlos Agis-Balboa, Roberto论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Complexo Hosp Univ Vigo CHUVI, SERGAS, CIBERSAM, Galicia Hlth Res Inst,Psychiat Dis Res Grp, Vigo 36201, Spain Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyStilling, Roman论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany German Primate Ctr, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyUrbanke, Hendrik论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyKranz, Andrea论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Biotechnol Ctr, D-01069 Dresden, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyStewart, A. Francis论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Biotechnol Ctr, D-01069 Dresden, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, GermanyFischer, Andre论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, German Ctr Neurodegenerat Dis Epigenet & Syst Med, D-37075 Gottingen, Germany Univ Med Ctr Goettingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, Germany
- [7] KMT2B: A New Twist in Dystonia GeneticsMOVEMENT DISORDERS, 2017, 32 (04) : 529 - 529Balint, Bettina论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, Queen Sq, London, England Univ Heidelberg Hosp, Dept Neurol, Heidelberg, Germany UCL Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, Queen Sq, London, England论文数: 引用数: h-index:机构:
- [8] Novel missense variants in KMT2B in segmental dystoniaMOVEMENT DISORDERS, 2018, 33 : S58 - S58Ma, J.论文数: 0 引用数: 0 h-index: 0Wan, X. H.论文数: 0 引用数: 0 h-index: 0
- [9] KMT2B Rare Missense Variants in Generalized DystoniaMOVEMENT DISORDERS, 2017, 32 (07) : 1087 - 1091Zech, Michael论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Klin & Poliklin Neurol, Munich, Germany Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyJech, Robert论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyHavrankova, Petra论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyFecikova, Anna论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyBerutti, Riccardo论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Humangenet, Munich, Germany Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyUrgosik, Dusan论文数: 0 引用数: 0 h-index: 0机构: Na Homolce Hosp, Dept Stereotact Neurosurg & Radiosurg, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyKemlink, David论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyStrom, Tim M.论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Humangenet, Munich, Germany Tech Univ Munich, Inst Humangenet, Munich, Germany Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyRoth, Jan论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyRuzicka, Evzen论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic Helmholtz Zentrum Munchen, Inst Neurogen, Munich, GermanyWinkelmann, Juliane论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Klin & Poliklin Neurol, Munich, Germany Tech Univ Munich, Inst Humangenet, Munich, Germany SyNergy, Munich Cluster Syst Neurol, Munich, Germany Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany
- [10] Pallidal Deep Brain Stimulation for KMT2B Related Dystonia in An Indian PatientANNALS OF INDIAN ACADEMY OF NEUROLOGY, 2021, 24 (04) : 586 - 588Rajan, Roopa论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaGarg, Kanwaljeet论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurosurg, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSaini, Arti论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaKumar, Mukesh论文数: 0 引用数: 0 h-index: 0机构: Inst Genom & Integrat Biol, CSIR, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaBinukumar, B. K.论文数: 0 引用数: 0 h-index: 0机构: Inst Genom & Integrat Biol, CSIR, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaScaria, Vinod论文数: 0 引用数: 0 h-index: 0机构: Inst Genom & Integrat Biol, CSIR, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaAggarwal, Rajeev论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaGupta, Anu论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaVishnu, V. Y.论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaGarg, Ajay论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neuroradiol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSingh, Mamta Bhushan论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaBhatia, Rohit论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSrivastava, Achal K.论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSrivastava, M. V. Padma论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSingh, Manmohan论文数: 0 引用数: 0 h-index: 0机构: All India Inst Med Sci, Dept Neurosurg, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, India