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- [1] Novel phenotype associated with OPA1 mutations?MITOCHONDRION, 2012, 12 (05) : 559 - 559Tesarova, Marketa论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicTesarova, Marketa论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicStranecky, Viktor论文数: 0 引用数: 0 h-index: 0机构: Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicKratochvilova, Hana论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicHajkova, Zuzana论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Hansikova, Hana论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicHonzik, Tomas论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicHartmannova, Hana论文数: 0 引用数: 0 h-index: 0机构: Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicNoskova, Lenka论文数: 0 引用数: 0 h-index: 0机构: Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicPiherova, Lenka论文数: 0 引用数: 0 h-index: 0机构: Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic论文数: 引用数: h-index:机构:Majewski, Jacek论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Ctr Hlth, Dept Human Genet, Montreal, PQ, Canada Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicKmoch, Stanislav论文数: 0 引用数: 0 h-index: 0机构: Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech RepublicZeman, Jiri论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic Gen Univ Hosp Prague, Prague, Czech Republic Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic
- [2] MUTATIONS IN OPA1 EXPAND THE CLINICAL PHENOTYPE OF MITOCHONDRIAL DISEASEJOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (11): : E32 - E33论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Amati-Bonneau, P.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, EnglandYu-Wai-Man, P.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England论文数: 引用数: h-index:机构:Duffey, P.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England论文数: 引用数: h-index:机构:Zeviani, M.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, EnglandHorvath, R.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, EnglandMiller, J.论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Carlo Besta, Milan, Italy Univ Angers, Angers, France Newcastle Univ, York Hosp, Newcastle Hosp NHS Trust, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
- [3] Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutationsMOLECULAR GENETICS AND METABOLISM, 2011, 103 (04) : 383 - 387Schaaf, Christian P.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABlazo, Maria论文数: 0 引用数: 0 h-index: 0机构: Scott & White Hosp, Div Med Genet, Temple, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USALewis, Richard Alan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATonini, Ross E.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Otolaryngol, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATakei, Hidehiro论文数: 0 引用数: 0 h-index: 0机构: Methodist Hosp, Dept Pathol, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWang, Jing论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWong, Lee-Jun论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAScaglia, Fernando论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [4] Syndromic parkinsonism and dementia associated with OPA1 missense mutationsANNALS OF NEUROLOGY, 2015, 78 (01) : 21 - 38Carelli, Valerio论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyMusumeci, Olimpia论文数: 0 引用数: 0 h-index: 0机构: Univ Messina, Dept Neurosci, Messina, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyCaporali, Leonardo论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyZanna, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy论文数: 引用数: h-index:机构:Del Dotto, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy论文数: 引用数: h-index:机构:Rugolo, Michela论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyValentino, Maria Lucia论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyIommarini, Luisa论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyMaresca, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyBarboni, Piero论文数: 0 引用数: 0 h-index: 0机构: Studio Oculist DAzeglio, Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyCarbonelli, Michele论文数: 0 引用数: 0 h-index: 0机构: Studio Oculist DAzeglio, Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyTrombetta, Costantino论文数: 0 引用数: 0 h-index: 0机构: Univ Messina, Ophthalmol Clin, Messina, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyValente, Enza Maria论文数: 0 引用数: 0 h-index: 0机构: San Giovanni Rotondo, IRCCS Casa Sollievo Sofferenza, Mendel Lab, Foggia, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyPatergnani, Simone论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Dept Morphol Surg & Expt Med, I-44100 Ferrara, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy论文数: 引用数: h-index:机构:Pinton, Paolo论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Dept Morphol Surg & Expt Med, I-44100 Ferrara, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyRizzo, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Avoni, Patrizia论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyLiguori, Rocco论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyBaruzzi, Agostino论文数: 0 引用数: 0 h-index: 0机构: Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy Univ Bologna, Dept Biomed & Neuromotor Sci, Neurol Unit, I-40139 Bologna, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyToscano, Antonio论文数: 0 引用数: 0 h-index: 0机构: Univ Messina, Dept Neurosci, Messina, Italy Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, ItalyZeviani, Massimo论文数: 0 引用数: 0 h-index: 0机构: MRC, Mitochondrial Biol Unit, Cambridge, England Bellaria Hosp, IRCCS Inst Neurol Sci Bologna, Bologna, Italy
- [5] OPA1 mutations and clinical phenotype in Japanese patients with dominant optic atrophyINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U943 - U943Hewitt, AW论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Sch Med, Nagoya, 43131, JapanFitzgerald, LM论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Sch Med, Nagoya, 43131, JapanMcKay, J论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Sch Med, Nagoya, 43131, JapanMulhall, L论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Sch Med, Nagoya, 43131, JapanMackey, DA论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Sch Med, Nagoya, 43131, Japan
- [6] Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophyOPHTHALMOLOGY, 2006, 113 (03) : 483 - 488Nakamura, M论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanLin, J论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanUeno, S论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanAsaoka, R论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanHirai, T论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanHotta, Y论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanMiyake, Y论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, JapanTerasaki, H论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Ophthalmol, Showa Ku, Nagoya, Aichi 4668550, Japan
- [7] Novel OPA1 mutations identified in Japanese pedigrees with optic atrophyMOLECULAR VISION, 2006, 12 (56-58): : 485 - 491Qin, Minghui论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanKondo, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, Japan Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanUno, Hideaki论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanFujiwara, Eriko论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanUchio, Eiichi论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanTahira, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, JapanHayashi, Kenshi论文数: 0 引用数: 0 h-index: 0机构: Fukuoka Univ, Sch Med, Dept Ophthalmol, Fukuoka 81401, Japan
- [8] Novel OPA1 gene mutations in Japanese patients with optic atrophyINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2019, 60 (09)Sato, Shigeru论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Suita, Osaka, Japan Osaka Univ, Suita, Osaka, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Hotta, Kikuko论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Suita, Osaka, Japan Osaka Univ, Suita, Osaka, JapanFujikado, Takashi论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Suita, Osaka, Japan Osaka Univ, Suita, Osaka, JapanNishida, Kohji论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Suita, Osaka, Japan Osaka Univ, Suita, Osaka, Japan
- [9] Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutationsHUMAN MOLECULAR GENETICS, 2020, 29 (22) : 3631 - 3645Aleo, Serena J.论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyDel Dotto, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Biomed & NeuroMotor Sci DIBINEM, Unit Neurol, I-40139 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyFogazza, Mario论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyMaresca, Alessandra论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, I-40139 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyLodi, Tiziana论文数: 0 引用数: 0 h-index: 0机构: Univ Parma, Dept Chem Life Sci & Environm Sustainabil, I-43124 Parma, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy论文数: 引用数: h-index:机构:Ghelli, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyRugolo, Michela论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyCarelli, Valerio论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Biomed & NeuroMotor Sci DIBINEM, Unit Neurol, I-40139 Bologna, Italy IRCCS Ist Sci Neurol Bologna, I-40139 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyBaruffini, Enrico论文数: 0 引用数: 0 h-index: 0机构: Univ Parma, Dept Chem Life Sci & Environm Sustainabil, I-43124 Parma, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, ItalyZanna, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy Univ Bologna, Dept Pharm & Biotechnol FABIT, Via Selmi 3, I-40126 Bologna, Italy
- [10] Temporal, spatial and chromatic sensitivity losses associated with OPA1 mutationsINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (12)Majander, Anna论文数: 0 引用数: 0 h-index: 0机构: UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, England UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, EnglandYu-Wai-Man, Patrick论文数: 0 引用数: 0 h-index: 0机构: UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, England Newcastle Univ, Wellcome Trust Ctr Mitochondrial Res, Newcastle Upon Tyne, Tyne & Wear, England Royal Victoria Infirm, Newcastle Eye Ctr, Newcastle Upon Tyne, Tyne & Wear, England UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, EnglandJoao, Catarina论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London, England UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, EnglandVotruba, Marcela论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Optometry & Vis Sci, Cardiff, S Glam, Wales Univ Wales Hosp, Cardiff Eye Unit, Cardiff, S Glam, Wales UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, EnglandMoore, Anthony T.论文数: 0 引用数: 0 h-index: 0机构: UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, England UCSF Sch Med, Dept Ophthalmol, San Francisco, CA USA UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, EnglandStockman, Andrew论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London, England UCL, Moorfields Eye Hosp, Inst Ophthalmol, London, England