共 15 条
- [1] PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian FamilyMOVEMENT DISORDERS, 2016, 31 (05) : 765 - 767Quadri, Marialuisa论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsOlgiati, Simone论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsSensi, Mariachiara论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Arcispedale S Anna, Dept Neurol & Rehabil, Ferrara, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsGualandi, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna, Dept Reprod & Growth, UOL Med Genet, Ferrara, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsGroppo, Elisabetta论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Arcispedale S Anna, Dept Biomed & Specialist Surg Sci, Ferrara, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsRispoli, Vittorio论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Arcispedale S Anna, Dept Biomed & Specialist Surg Sci, Ferrara, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsGraafland, Josja论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsBreedveld, Guido J.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsFabbrini, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, Dept Neurol & Psychiat, Pozzilli, Italy IRCSS Neuromed, Pozzilli, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsBerardelli, Alfredo论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, Dept Neurol & Psychiat, Pozzilli, Italy IRCSS Neuromed, Pozzilli, Italy Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, NetherlandsBonifati, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands Erasmus MC, Dept Clin Genet, POB 2040, NL-3000 CA Rotterdam, Netherlands
- [2] A heterozygous frameshift mutation in the PRKRA (DYT16) gene associated with generalized dystonia in a German patientMOVEMENT DISORDERS, 2008, 23 (01) : S32 - S32Djarmati, A.论文数: 0 引用数: 0 h-index: 0Seibler, P.论文数: 0 引用数: 0 h-index: 0Langpap, B.论文数: 0 引用数: 0 h-index: 0Hagenah, J.论文数: 0 引用数: 0 h-index: 0Schmidt, A.论文数: 0 引用数: 0 h-index: 0Brueggemann, N.论文数: 0 引用数: 0 h-index: 0Siebner, H.论文数: 0 引用数: 0 h-index: 0Jabusch, H. -C.论文数: 0 引用数: 0 h-index: 0Altenmueller, E.论文数: 0 引用数: 0 h-index: 0Muenchau, A.论文数: 0 引用数: 0 h-index: 0Lohmann, K.论文数: 0 引用数: 0 h-index: 0Klein, C.论文数: 0 引用数: 0 h-index: 0
- [3] DYT16 Revisited: Exome Sequencing Identifies PRKRA Mutations in a European Dystonia FamilyMOVEMENT DISORDERS, 2014, 29 (12) : 1504 - 1510Zech, Michael论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Helmholtz Zentrum Munchen, Inst Humangenet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyCastrop, Florian论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanySchormair, Barbara论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Helmholtz Zentrum Munchen, Inst Humangenet, Munich, Germany Tech Univ Munich, Inst Humangenet, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyJochim, Angela论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyWieland, Thomas论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Humangenet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyGross, Nadine论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyLichtner, Peter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, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyPeters, Annette论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Epidemiol 2, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyGieger, Christian论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Zentrum Munchen, Inst Genet Epidemiol, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyMeitinger, Thomas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, D-80290 Munich, Germany SyNergy, Munich Cluster Syst Neurol, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 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, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyOexle, Konrad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, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, GermanyHaslinger, Bernhard论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Neurol Klin & Poliklin, D-80290 Munich, Germany论文数: 引用数: h-index:机构:
- [4] A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patientLANCET NEUROLOGY, 2008, 7 (05): : 380 - 381论文数: 引用数: h-index:机构:Djarmati, Ana论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyLangpap, Brigitte论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyHagenah, Johann论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanySchmidt, Alexander论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyBrueggemann, Norbert论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanySiebner, Hartwig论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyJabusch, Hans-Christian论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyAltenmueller, Eckart论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyMuenchau, Alexander论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyLohmann, Katja论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, GermanyKlein, Christine论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany Med Univ Lubeck, Dept Neurol, D-23538 Lubeck, Germany
- [5] A case of dystonia-parkinsonism associated with a heterozygous PRKRA (DYT16) gene mutationMOVEMENT DISORDERS, 2021, 36 : S274 - S274Wu, J.论文数: 0 引用数: 0 h-index: 0Christie, M.论文数: 0 引用数: 0 h-index: 0Schiess, M.论文数: 0 引用数: 0 h-index: 0
- [6] DYT30 due to VPS16 mutation: An etiology of childhood-onset generalized dystoniaANNALS OF INDIAN ACADEMY OF NEUROLOGY, 2023, 26 (03) : 286 - 288Shashi, Sridhar论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaNashi, Saraswati论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaArunachal, Gautham论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Human Genet, Bengaluru, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaVenkatachalam, N.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaPadmanabha, Hansashree论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaMailankody, Pooja论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaMenon, Deepak论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaArshad, Faheem论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaAlladi, Suvarna论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaMathuranath, Pavagada论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, IndiaMahale, Rohan R.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru 560029, Karnataka, India
- [7] DYT16, a novel young-onset dystonia-parkinson ism disorder:: identification of a segregating mutation in the stress-response protein PRKRALANCET NEUROLOGY, 2008, 7 (03): : 207 - 215Camargos, Sarah论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Univ Fed Minas Gerais, Fac Med, Dept Internal Med, Belo Horizonte, MG, Brazil Hosp Clin, Neurol Serv, Movement Disorders Clin, Belo Horizonte, MG, Brazil NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAScholz, Sonja论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USASimon-Sanchez, Javier论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAPaisan-Ruiz, Coro论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USALewis, Patrick论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAHernandez, Dena论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USADing, Jinhui论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAGibbs, J. Raphael论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USACookson, Mark R.论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USABras, Jose论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Univ Coimbra, Ctr Neurosci & Cell Biol, Coimbra, Portugal NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAGuerreiro, Rita论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Univ Coimbra, Ctr Neurosci & Cell Biol, Coimbra, Portugal NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAOliveira, Catarina Resende论文数: 0 引用数: 0 h-index: 0机构: Univ Coimbra, Ctr Neurosci & Cell Biol, Coimbra, Portugal NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USALees, Andrew论文数: 0 引用数: 0 h-index: 0机构: Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USAHardy, John论文数: 0 引用数: 0 h-index: 0机构: Inst Neurol, London WC1N 3BG, England NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USACardoso, Francisco论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Minas Gerais, Fac Med, Dept Internal Med, Belo Horizonte, MG, Brazil Hosp Clin, Neurol Serv, Movement Disorders Clin, Belo Horizonte, MG, Brazil NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USASingleton, Andrew B.论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
- [8] HOMOZYGOUS GNAL MUTATION ASSOCIATED WITH FAMILIAL CHILDHOOD-ONSET GENERALIZED DYSTONIANEUROLOGY-GENETICS, 2016, 2 (03)Masuho, Ikuo论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, Dept Neurosci, Jupiter, FL USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USAFang, Mingyan论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Key Lab Neurogen, Shenzhen, Peoples R China BGI Shenzhen, Shenzhen, Peoples R China Scripps Res Inst, Dept Neurosci, Jupiter, FL USAGeng, Chunyu论文数: 0 引用数: 0 h-index: 0机构: BGI Shenzhen, Shenzhen, Peoples R China Scripps Res Inst, Dept Neurosci, Jupiter, FL USAZhang, Jianguo论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Key Lab Neurogen, Shenzhen, Peoples R China BGI Shenzhen, Shenzhen, Peoples R China Scripps Res Inst, Dept Neurosci, Jupiter, FL USAJiang, Hui论文数: 0 引用数: 0 h-index: 0机构: BGI Shenzhen, Shenzhen, Peoples R China Scripps Res Inst, Dept Neurosci, Jupiter, FL USAOzgul, Riza Koksal论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Inst Child Hlth, Dept Pediat Metab, Ankara, Turkey Scripps Res Inst, Dept Neurosci, Jupiter, FL USAYilmaz, Didem Yucel论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Inst Child Hlth, Dept Pediat Metab, Ankara, Turkey Scripps Res Inst, Dept Neurosci, Jupiter, FL USAYalnizoglu, Dilek论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Pediat Neurol, Ankara, Turkey Scripps Res Inst, Dept Neurosci, Jupiter, FL USAYuksel, Deniz论文数: 0 引用数: 0 h-index: 0机构: Minist Hlth, Dr Sami Ulus Matern & Childrens Res & Training Ho, Dept Pediat Neurol, Ankara, Turkey Scripps Res Inst, Dept Neurosci, Jupiter, FL USAYarrow, Anna论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hlth Res Ctr, Sioux Falls, SD USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USAMyers, Angela论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hlth Res Ctr, Sioux Falls, SD USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USABurn, Sabrina C.论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hlth Res Ctr, Sioux Falls, SD USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USACrotwell, Patricia L.论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hlth Res Ctr, Sioux Falls, SD USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USAPadilla-Lopez, Sergio论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Coll Med, Dept Child Hlth, Phoenix, AZ 85004 USA Phoenix Childrens Hosp, Barrow Neurol Inst, Movement Disorders Ctr & Neurogen Res Program, Phoenix, AZ 85016 USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USA论文数: 引用数: h-index:机构:Martemyanov, Kirill A.论文数: 0 引用数: 0 h-index: 0机构: Scripps Res Inst, Dept Neurosci, Jupiter, FL USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USAKruer, Michael C.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Coll Med, Dept Child Hlth, Phoenix, AZ 85004 USA Phoenix Childrens Hosp, Barrow Neurol Inst, Movement Disorders Ctr & Neurogen Res Program, Phoenix, AZ 85016 USA Arizona State Univ, Program Neurosci, Tempe, AZ 85287 USA Scripps Res Inst, Dept Neurosci, Jupiter, FL USA
- [9] The Spectrum of GNAO1 Mutation Can Include Childhood-Onset Isolated Generalized DystoniaMOVEMENT DISORDERS CLINICAL PRACTICE, 2024,Chowdhury, Sampurna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, IndiaPriya, Shikha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, Divyani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, IndiaAgarwal, Ayush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 Neuroimaging & Intervent Radiol, New Delhi, India All India Inst Med Sci, Dept Neurol, New Delhi, IndiaSrivastava, Achal Kumar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, India
- [10] Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 MutationJOURNAL OF MOVEMENT DISORDERS, 2019, 12 (03) : 190 - 191Yoo, Dallah论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South Korea Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South KoreaKim, Han-Joon论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South Korea Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South KoreaChae, Jong-Hee论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Childrens Hosp, Pediat Clin Neurosci Ctr, Dept Pediat,Coll Med, Seoul, South Korea Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South KoreaPaek, Sun Ha论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst, Dept Neurosurg,Movement Disorder Ctr,Coll Med, Seoul, South Korea Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South KoreaJeon, Beomseok论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South Korea Seoul Natl Univ, Seoul Natl Univ Hosp, Neurosci Res Inst,Coll Med, Dept Neurol,Movement Disorder Ctr,Parkinson Study, Seoul, South Korea