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- [1] Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IINEUROLOGY, 2006, 66 (05) : 748 - 751Coen, K论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumPareyson, D论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumAuer-Grumbach, M论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumBuyse, G论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumGoemans, N论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumClaeys, KG论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumVerpoorten, N论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumLaurà, M论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumScaioli, V论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumSalmhofer, W论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumPieber, TR论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumNelis, E论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumDe Jonghe, P论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, BelgiumTimmerman, V论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Peripheral Neuropathy Grp, Dept Mol Genet, B-2610 Antwerp, Belgium
- [2] MUTATIONS IN THE FLVCR1 GENE CAUSE HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE 2AMERICAN JOURNAL OF HEMATOLOGY, 2016, 91 (03) : E266 - E266Chiabrando, Deborah论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyValperga, Giulio论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyAltruda, Fiorella论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalySilengo, Lorenzo论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyDi Rocco, Maja论文数: 0 引用数: 0 h-index: 0机构: G Gaslini Inst Children, Unit Pediat 2, Genoa, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyCastori, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Roma La Sapienza, San Camillo Forlanini Hosp, Dept Med Genet, Piazzale Aldo Moro 5, I-00185 Rome, Italy San Camillo Forlanin, Rome, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyKurth, Ingo论文数: 0 引用数: 0 h-index: 0机构: Jena Univ Hosp, Inst Human Genet, Jena, Germany Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, ItalyTolosano, Emanuela论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy
- [3] Hereditary sensory autonomic neuropathy type II: Report of two novel mutations in the FAM134B geneJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2019, : 354 - 358Falcao de Campos, Catarina论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, Portugal Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, PortugalVidailhet, Marie论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Neurol, ICM, Paris, France Sorbonne Univ, Paris, France Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, PortugalToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: Univ Tours, Univ Hosp, INSERM, UMR 1253,iBrain,Genet Dept, Tours, France Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, Portugalde Becdelievre, Alix论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Est Creteil, Hop Henri Mondor, AP HP, Dept Med Genet,Inserm,UMR955, Creteil, France Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, Portugal论文数: 引用数: h-index:机构:Bonello-Palot, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Hop La Timone, AP HM, Dept Med Genet, Marseille, France Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, PortugalStojkovic, Tanya论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Ctr Reference Malad Neuromusculaires, Paris, France Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Dept Neurol, Lisbon, Portugal
- [4] The evaluation of autonomic nervous function in a patient with hereditary sensory and autonomic neuropathy type IV with novel mutations of the TRKA geneNEUROPEDIATRICS, 2004, 35 (05) : 274 - 278Ohto, T论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanIwasaki, N论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanFujiwara, J论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanOhkoshi, N论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanKimura, S论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanKawade, K论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanTanaka, R论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, JapanMatsui, A论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, Japan
- [5] A rare case of hereditary sensory and autonomic neuropathy type IICLINICAL CASE REPORTS, 2023, 11 (03):Mamytova, Elmira论文数: 0 引用数: 0 h-index: 0机构: IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, KyrgyzstanJusupova, Asel论文数: 0 引用数: 0 h-index: 0机构: IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, KyrgyzstanToktomametova, Anara论文数: 0 引用数: 0 h-index: 0机构: IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, KyrgyzstanKarbozova, Kunduz论文数: 0 引用数: 0 h-index: 0机构: IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, KyrgyzstanKadyrova, Begimay论文数: 0 引用数: 0 h-index: 0机构: Int Higher Sch Med, Dept Special Clin Disciplines, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan论文数: 引用数: h-index:机构:Tagaev, Tugolbai论文数: 0 引用数: 0 h-index: 0机构: IK Akhunbaev Kyrgyz State Med Acad, Dept Publ Hlth & Healthcare, Bishkek, Kyrgyzstan IK Akhunbaev Kyrgyz State Med Acad, AN Murzaliev Dept Neurol & Clin Genet, Bishkek, Kyrgyzstan
- [6] HSN2 Gene mutation in Hereditary Sensory Autonomic Neuropathy type IINEUROMUSCULAR DISORDERS, 2006, 16 : S69 - S69An, Jae Young论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaPark, Min Soo论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaKim, Byoung Joon论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaChung, Jin Sang论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaSuh, Yeon-Lim论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaCho, Hyun Jung论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South KoreaKi, Chang Seok论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea Sungkyunkwan Univ Sch Med, Samsung Med Ctr, Seoul, South Korea
- [7] Novel Findings in Hereditary Sensory and Autonomic Neuropathy Type IVNEUROLOGY, 2019, 92 (15)Varma-Doyle, Aditi论文数: 0 引用数: 0 h-index: 0机构: LSUHSC, New Orleans, LA USA LSUHSC, New Orleans, LA USAMcbride, Lori论文数: 0 引用数: 0 h-index: 0机构: LSUHSC, New Orleans, LA USA LSUHSC, New Orleans, LA USAMarble, Michael论文数: 0 引用数: 0 h-index: 0机构: LSUHSC, New Orleans, LA USA LSUHSC, New Orleans, LA USATilton, Ann论文数: 0 引用数: 0 h-index: 0机构: LSUHSC, New Orleans, LA USA LSUHSC, New Orleans, LA USA
- [8] A case of hereditary sensory and autonomic neuropathy type II with plantar ulcerationJOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2006, 20 (06) : 753 - 754Ekmekci, TR论文数: 0 引用数: 0 h-index: 0机构: Sisli Etfal Training & Res Hosp, Dept Dermatol, Istanbul, TurkeyKoslu, A论文数: 0 引用数: 0 h-index: 0机构: Sisli Etfal Training & Res Hosp, Dept Dermatol, Istanbul, TurkeyCelik, M论文数: 0 引用数: 0 h-index: 0机构: Sisli Etfal Training & Res Hosp, Dept Dermatol, Istanbul, TurkeyForta, H论文数: 0 引用数: 0 h-index: 0机构: Sisli Etfal Training & Res Hosp, Dept Dermatol, Istanbul, Turkey
- [9] Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type IAMERICAN JOURNAL OF HUMAN GENETICS, 2010, 87 (04) : 513 - 522Rotthier, Annelies论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumAuer-Grumbach, Michaela论文数: 0 引用数: 0 h-index: 0机构: Med Univ Graz, Dept Internal Med, Div Endocrinol & Metab, A-8036 Graz, Austria Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumJanssens, Katrien论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumBaets, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, B-2650 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumPenno, Anke论文数: 0 引用数: 0 h-index: 0机构: Univ Zurich Hosp, Inst Clin Chem, CH-8091 Zurich, Switzerland Competence Ctr Syst Physiol & Metab Dis, CH-8093 Zurich, Switzerland Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumAlmeida-Souza, Leonardo论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumVan Hoof, Kim论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumJacobs, An论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumDe Vriendt, Els论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumSchlotter-Weigel, Beate论文数: 0 引用数: 0 h-index: 0机构: Univ Munich, Friedrich Baur Inst, Dept Neurol, D-80336 Munich, Germany Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumLoscher, Wolfgang论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Neurol, A-6020 Innsbruck, Austria Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumVondracek, Petr论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp & Masaryk Univ, Dept Paediat Neurol, CZ-61300 Brno, Czech Republic Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumSeeman, Pavel论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Sch Med Prague 2, Dept Child Neurol, CZ-15006 Prague, Czech Republic Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumDe Jonghe, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, B-2650 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumVan Dijck, Patrick论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, VIB Dept Mol Microbiol, Mol Cell Biol Lab, B-3001 Louvain, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumJordanova, Albena论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumHornemann, Thorsten论文数: 0 引用数: 0 h-index: 0机构: Univ Zurich Hosp, Inst Clin Chem, CH-8091 Zurich, Switzerland Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland Univ Zurich, Zurich Ctr Integrat Human Physiol ZIHP, CH-8057 Zurich, Switzerland Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, BelgiumTimmerman, Vincent论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2610 Antwerp, Belgium Univ Antwerp, Peripheral Neuropathy Grp, VIB Dept Mol Genet, B-2610 Antwerp, Belgium
- [10] Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV:: demonstration of a founder mutation in the Turkish populationNEUROGENETICS, 2008, 9 (02) : 119 - 125Tuysuz, Beyhan论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Pediat, Div Genet, Cerrahpasa Fac Med, Istanbul, Turkey Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USABayrakli, Fatih论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USADiLuna, Michael L.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USABilguvar, Kaya论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USABayri, Yasar论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAYalcinkaya, Cengiz论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Neurol, Div Child Neurol, Cerrahpasa Fac Med, Istanbul, Turkey Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USABursali, Aysegul论文数: 0 引用数: 0 h-index: 0机构: Baltalimani Metin Sabanci Kemik Hastanesi, Istanbul, Turkey Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAOzdamar, Elif论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Pediat, Div Genet, Cerrahpasa Fac Med, Istanbul, Turkey Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAKorkmaz, Baris论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Neurol, Div Child Neurol, Cerrahpasa Fac Med, Istanbul, Turkey Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAMason, Christopher E.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAOzturk, Ali K.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USALifton, Richard P.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAState, Matthew W.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USAGunel, Murat论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA Yale Univ, Sch Med, Program Neurogenet, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA