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- [31] FEBRILE ATAXIA AND MYOKYMIA BROADEN THE SPG26 HEREDITARY SPASTIC PARAPLEGIA PHENOTYPENEUROLOGY-GENETICS, 2017, 3 (03)Dad, Rubina论文数: 0 引用数: 0 h-index: 0机构: Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, Pakistan Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanWalker, Susan论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Paediat, Toronto, ON, Canada Hosp Sick Children, Ctr Appl Genom Genet & Genome Biol, Toronto, ON, Canada Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanScherer, Stephen W.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Paediat, Toronto, ON, Canada Hosp Sick Children, Ctr Appl Genom Genet & Genome Biol, Toronto, ON, Canada Univ Toronto, Dept Mol Genet, Toronto, ON, Canada Univ Toronto, McLaughlin Ctr, Toronto, ON, Canada Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanHassan, Muhammad Jawad论文数: 0 引用数: 0 h-index: 0机构: Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, Pakistan Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanAlghamdi, Mohammad Domaia论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Aramco Healthcare, Div Neurol, Dept Pediat, Dhahran, Saudi Arabia Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanMinassian, Berge A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada Hosp Sick Children, Div Neurol, Toronto, ON, Canada Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, PakistanAlkhater, Reem A.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Aramco Healthcare, Div Neurol, Dept Pediat, Dhahran, Saudi Arabia Natl Univ Sci & Technol NUST, Atta Ur Rahman Sch Appl Biosci, Islamabad, Pakistan
- [32] ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegiaAMERICAN JOURNAL OF HUMAN GENETICS, 2006, 79 (02) : 351 - 357Mannan, Ashraf U.论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyKrawen, Philip论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanySauter, Simone M.论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyBoehm, Johann论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyChronowska, Agnieszka论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyPaulus, Walter论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyNeesen, Juergen论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, GermanyEngel, Wolfgang论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Inst Human Genet, D-37073 Gottingen, Germany
- [33] A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal SystemPLOS GENETICS, 2013, 9 (12):Khundadze, Mukhran论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyKollmann, Katrin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Childrens Hosp, Dept Biochem, Hamburg, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyKoch, Nicole论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Inst Biochem 1, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyBiskup, Christoph论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Dept Biomol Photon, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyNietzsche, Sandor论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Electron Microscopy Ctr, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany论文数: 引用数: h-index:机构:Hennings, J. Christopher论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyHuebner, Antje K.论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanySymmank, Judit论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyJahic, Amir论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Inst Clin Chem, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyIlina, Elena I.论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurol, Tubingen, Germany Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyKarle, Kathrin论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurol, Tubingen, Germany Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis DZNE, Tubingen, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanySchoels, Ludger论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurol, Tubingen, Germany Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis DZNE, Tubingen, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyKessels, Michael论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Inst Biochem 1, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyBraulke, Thomas论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Childrens Hosp, Dept Biochem, Hamburg, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyQualmann, Britta论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Inst Biochem 1, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyKurth, Ingo论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyBeetz, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Jena Univ Hosp, Inst Clin Chem, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, GermanyHuebner, Christian A.论文数: 0 引用数: 0 h-index: 0机构: Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany Univ Jena, Inst Human Genet, Jena Univ Hosp, Jena, Germany
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- [36] SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in BrazilCLINICAL GENETICS, 2014, 86 (02) : 194 - 196Franca, M. C., Jr.论文数: 0 引用数: 0 h-index: 0机构: Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilDogini, D. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Campinas UNICAMP, Sch Med Sci, BR-13083887 Campinas, SP, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilD'Abreu, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilTeive, H. A. G.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilMunhoz, R. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilRaskin, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilMoro, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilMelo, C. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilGomes, A. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Parana, Hosp Clin, Neurol Serv, Movement Disorders Unit, BR-80060000 Curitiba, Parana, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilSaute, J. A. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Med Genet Serv, Porto Alegre, RS, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilJardim, L. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Med Genet Serv, Porto Alegre, RS, Brazil Univ Fed Rio Grande do Sul, Dept Internal Med, Porto Alegre, RS, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, BrazilLopes-Cendes, I.论文数: 0 引用数: 0 h-index: 0机构: Univ Campinas UNICAMP, Sch Med Sci, BR-13083887 Campinas, SP, Brazil Univ Campinas UNICAMP, Dept Neurol, BR-13083887 Campinas, SP, Brazil
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- [39] SPG3A mutations are associated with pure and complex forms of Hereditary Spastic ParaplegiaNEUROMUSCULAR DISORDERS, 2006, 16 : S63 - S63Claeys, Kristl论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumIvanova, Nevyana论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumDeconinck, Tine论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumLitvinenko, Ivan论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumJordanova, Albena论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumLoefgren, Ann论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumNelis, Eva论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumMercelis, Rudy论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumAuer-Grumbach, Michaela论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumPriller, Josef论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumCeulemans, Berten论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumSereda, Michael论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumKremensky, Ivo论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumMitev, Vanio论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumDe Jonghe, Peter论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium
- [40] Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutationNEUROLOGY, 2000, 55 (05) : 702 - 705Santorelli, FM论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyPatrono, C论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyFortini, D论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyTessa, A论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyComanducci, G论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyBertini, E论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyPierallini, A论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyAmabile, GA论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, ItalyCasali, C论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Osped Bambino Gesu, I-00165 Rome, Italy