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- [1] Genetic Risk Score Analysis in Early-Onset Bipolar Disorder[J]. JOURNAL OF CLINICAL PSYCHIATRY, 2017, 78 (09) : 1337 - 1343Croarkin, Paul E.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Psychiat, Rochester, MN USA Mayo Clin, Dept Psychol, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USALuby, Joan L.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA Mayo Clin, Dept Psychiat, Rochester, MN USACercy, Kelly论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Div Biomed Stat & Informat, Dept Hlth Sci Res, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USAGeske, Jennifer R.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Div Biomed Stat & Informat, Dept Hlth Sci Res, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USAVeldic, Marin论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Psychiat, Rochester, MN USA Mayo Clin, Dept Psychol, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USASimonson, Matthew论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Div Biomed Stat & Informat, Dept Hlth Sci Res, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USAJoshi, Paramjit T.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Dept Psychiat & Behav Sci, Washington, DC 20010 USA Mayo Clin, Dept Psychiat, Rochester, MN USAWagner, Karen Dineen论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Med Branch, Dept Psychiat & Behav Sci, Galveston, TX 77555 USA Mayo Clin, Dept Psychiat, Rochester, MN USAWalkup, John T.论文数: 0 引用数: 0 h-index: 0机构: Weill Cornell Med Coll, Dept Psychiat, New York, NY USA Mayo Clin, Dept Psychiat, Rochester, MN USANassan, Malik M.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Psychiat, Rochester, MN USA Mayo Clin, Dept Psychol, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USACuellar-Barboza, Alfredo B.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, San Nicolas De Los Garza, Mexico Mayo Clin, Dept Psychiat, Rochester, MN USACasuto, Leah论文数: 0 引用数: 0 h-index: 0机构: Lindner Ctr HOPE, Mason, OH USA Mayo Clin, Dept Psychiat, Rochester, MN USAMcElroy, Susan L.论文数: 0 引用数: 0 h-index: 0机构: Lindner Ctr HOPE, Mason, OH USA Mayo Clin, Dept Psychiat, Rochester, MN USAJensen, Peter S.论文数: 0 引用数: 0 h-index: 0机构: REACH Inst, New York, NY USA Mayo Clin, Dept Psychiat, Rochester, MN USAFrye, Mark A.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Psychiat, Rochester, MN USA Mayo Clin, Dept Psychol, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USABiernacka, Joanna M.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Psychiat, Rochester, MN USA Mayo Clin, Dept Psychol, Rochester, MN USA Mayo Clin, Div Biomed Stat & Informat, Dept Hlth Sci Res, Rochester, MN USA Mayo Clin, Dept Psychiat, Rochester, MN USA
- [2] De Novo Mutations in YWHAG Cause Early-Onset Epilepsy[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (02) : 300 - 310Guella, Ilaria论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaMcKenzie, Marna B.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaEvans, Daniel M.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaBuerki, Sarah E.论文数: 0 引用数: 0 h-index: 0机构: Inselspital Bern, Univ Childrens Hosp, Dept Neuropediat Dev & Rehabil, CH-3010 Bern, Switzerland Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaToyota, Eric B.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pediat, Div Neurol, Vancouver, BC V6H 3V4, Canada British Columbia Childrens Hosp, Vancouver, BC V6H 3V4, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaVan Allen, Margot I.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Med Genet, Vancouver, BC V6H 3N1, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaSuri, Mohnish论文数: 0 引用数: 0 h-index: 0机构: Nottingham Univ Hosp NHS Trust, Reg Clin Genet Serv, Nottingham NG5 1PB, England Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaElmslie, Frances论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ Hosp NHS Fdn Trust, South West Thames Reg Genet Serv, London SW17 0QT, England Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaSimon, Marleen E. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Med Genet, NL-3508 AB Utrecht, Netherlands Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canadavan Gassen, Koen L. I.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Med Genet, NL-3508 AB Utrecht, Netherlands Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaHeron, Delphine论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dept Genet, F-75651 Paris, France Hop La Pitie Salpetriere, AP HP, Ctr Reference Deficiences Intellectuelles Causes, F-75651 Paris, France Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaKeren, Boris论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dept Genet, F-75651 Paris, France Hop La Pitie Salpetriere, AP HP, Ctr Reference Deficiences Intellectuelles Causes, F-75651 Paris, France Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaNava, Caroline论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dept Genet, F-75651 Paris, France Hop La Pitie Salpetriere, AP HP, Ctr Reference Deficiences Intellectuelles Causes, F-75651 Paris, France Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaConnolly, Mary B.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pediat, Div Neurol, Vancouver, BC V6H 3V4, Canada British Columbia Childrens Hosp, Vancouver, BC V6H 3V4, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaDemos, Michelle论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Pediat, Div Neurol, Vancouver, BC V6H 3V4, Canada British Columbia Childrens Hosp, Vancouver, BC V6H 3V4, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, CanadaFarrer, Matthew J.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canada Univ British Columbia, Ctr Appl Neurogenet, Vancouver, BC V5R 6H8, Canada
- [3] Functional mutations in CADPS identified in patients with early-onset bipolar disorder[J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2015, 25 : S222 - S223Sitbon, J.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceKappeler, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceNicolas, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceHenrion, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceRhee, J.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Expt Med, Dept Mol Neurobiol, D-37075 Gottingen, Germany Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceLeboyer, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, FranceJamain, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France Hop Henri Mondor, INSERM, ESPRY, Psychiat Translat,IMRB,U955, F-94010 Creteil, France
- [4] Early-onset bipolar disorder and suicide[J]. ASIAN JOURNAL OF PSYCHIATRY, 2020, 47Sher, Leo论文数: 0 引用数: 0 h-index: 0机构: James J Peters Vet Adm Med Ctr, 130 W Kingsbridge Rd, New York, NY 10468 USA Icahn Sch Med Mt Sinai, New York, NY 10029 USA James J Peters Vet Adm Med Ctr, 130 W Kingsbridge Rd, New York, NY 10468 USA
- [5] De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients[J]. NEUROBIOLOGY OF AGING, 2015, 36 (11) : 3117.e1 - 3117.e6Huebers, Annemarie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyJust, Walter论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyRosenbohm, Angela论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyMueller, Kathrin论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyMarroquin, Nicolai论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyGoebel, Ingrid论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyHoegel, Josef论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyThiele, Holger论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, CCG, D-50931 Cologne, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyAltmueller, Janine论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, CCG, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyNuernberg, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, CCG, D-50931 Cologne, Germany Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyWeishaupt, Jochen H.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyKubisch, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyLudolph, Albert C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, GermanyVolk, Alexander E.论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, D-89069 Ulm, Germany Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Hosp Ulm, Dept Neurol, D-89081 Ulm, Germany
- [6] Search for de novo mutations in bipolar disorder[J]. BIPOLAR DISORDERS, 2019, 21 : 40 - 40Nishioka, M.论文数: 0 引用数: 0 h-index: 0机构: RIKEN Ctr Brain Sci, Lab Mol Dynam Mental Disorders, Saitama, Japan RIKEN Ctr Brain Sci, Lab Mol Dynam Mental Disorders, Saitama, Japan
- [7] De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy[J]. JOURNAL OF MEDICAL GENETICS, 2017, 54 (08) : 550 - 557Guey, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceGrangeon, Lou论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceBrunelle, Francis论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Univ, Univ Hosp Necker Enfants Malades, AP HP, Dept Pediat Radiol, Paris, France Paris Descartes Univ, Univ Hosp Necker Enfants malades, Dept Neuroradiol, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France论文数: 引用数: h-index:机构:Amiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades, AP HP, Dept Genet, Paris, France Paris Descartes Univ, Imagine Inst, Sorbonne Paris Cite, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceLyonnet, Stanislas论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades, AP HP, Dept Genet, Paris, France Paris Descartes Univ, Imagine Inst, Sorbonne Paris Cite, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceDelaforge, Audrey论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp St Louis Lariboisiere, AP HP, Ctr Reference Malad Vasc Rares Cerveau & Oeil, Serv Genet Mol Neurovasc, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France论文数: 引用数: h-index:机构:Desnous, Beatrice论文数: 0 引用数: 0 h-index: 0机构: Robert Debre Univ Hosp, AP HP, Dept Pediat Neurol, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceBellesme, Celine论文数: 0 引用数: 0 h-index: 0机构: Bicetre Univ Hosp, AP HP, Dept Pediat Neurol, Le Kremlin Bicetre, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceHerve, Dominique论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France Grp Hosp St Louis Lariboisiere, AP HP, Serv Neurol, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceSchwitalla, Jan C.论文数: 0 引用数: 0 h-index: 0机构: Alfried Krupp Hosp Essen, Dept Neurol, Essen, Germany Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, FranceKraemer, Markus论文数: 0 引用数: 0 h-index: 0机构: Alfried Krupp Hosp Essen, Dept Neurol, Essen, Germany Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France论文数: 引用数: h-index:机构:Kossorotoff, Manoelle论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades, AP HP, French Ctr Pediat Stroke, Paris, France Univ Hosp Necker Enfants Malades, Pediat Neurol Dept, Paris, France Univ Hosp Necker Enfants Malades, French Ctr Pediat Stroke, Paris, France Univ Paris Diderot, Genet & Physiopathol Malad Cerebrovasc, Sorbonne Paris Cite, INSERM UMR S1161, Paris, France
- [8] De novo KCNT1 mutations in early-onset epileptic encephalopathy[J]. EPILEPSIA, 2015, 56 (09) : E121 - E128Ohba, Chihiro论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Dept Clin Neurol & Stroke Med, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTakahashi, Nobuya论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanOsaka, Hitoshi论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Neurol, Clin Res Inst, Yokohama, Kanagawa, Japan Jichi Med Sch, Dept Pediat, Shimotsuke, Tochigi, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanShiihara, Takashi论文数: 0 引用数: 0 h-index: 0机构: Gunma Childrens Med Ctr, Dept Neurol, Shibukawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTohyama, Jun论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Dept Pediat, Epilepsy Ctr, Niigata, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Fujii, Yuji论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ Hosp, Dept Pediat, Hiroshima, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanHara, Munetsugu论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Med Ctr Maternal & Child Hlth, Dept Neonatol, Kurume, Fukuoka, Japan Kurume Univ, Sch Med, Dept Pediat & Child Hlth, Kurume, Fukuoka 830, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTsurusawa, Reimi论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Chikushi Hosp, Dept Pediat, Fukuoka 81401, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanInoue, Takahito论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Chikushi Hosp, Dept Pediat, Fukuoka 81401, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanOgata, Reina论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Childrens Hosp, Dept Pediat Neurol, Fukuoka, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanWatanabe, Yoriko论文数: 0 引用数: 0 h-index: 0机构: Kurume Univ, Sch Med, Dept Pediat & Child Hlth, Kurume, Fukuoka 830, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTogashi, Noriko论文数: 0 引用数: 0 h-index: 0机构: Miyagi Childrens Hosp, Dept Neurol, Sendai, Miyagi, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanKodera, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanNakashima, Mitsuko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTsurusaki, Yoshinori论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanMiyake, Noriko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, JapanTanaka, Fumiaki论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Dept Clin Neurol & Stroke Med, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, 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 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan
- [9] EARLY-ONSET AND LATE-ONSET BIPOLAR AFFECTIVE-DISORDER - GENETIC STUDY[J]. ARCHIVES OF GENERAL PSYCHIATRY, 1977, 34 (06) : 715 - 719JAMES, NM论文数: 0 引用数: 0 h-index: 0机构: ASHBURN HALL PRIVATE PSYCHIAT HOSP,DUNEDIN,NEW ZEALAND ASHBURN HALL PRIVATE PSYCHIAT HOSP,DUNEDIN,NEW ZEALAND
- [10] Psychotic symptoms in early-onset bipolar disorder[J]. BIPOLAR DISORDERS, 2008, 10 : 43 - 43Fu-I, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Dept & Inst Psychiat, Child & Adolescent Psychiat Serv, BR-05508 Sao Paulo, Brazil Univ Sao Paulo, Dept & Inst Psychiat, Child & Adolescent Psychiat Serv, BR-05508 Sao Paulo, BrazilWang, Y. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Dept & Inst Psychiat, Child & Adolescent Psychiat Serv, BR-05508 Sao Paulo, Brazil Univ Santo Amaro, Sch Med, Dept Psychiat, Sao Paulo, Brazil Univ Sao Paulo, Dept & Inst Psychiat, Child & Adolescent Psychiat Serv, BR-05508 Sao Paulo, Brazil