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- [21] PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndromeJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (09): : 5377 - 5381Binder, G论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, Germany Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, GermanyNeuer, K论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, Germany Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, GermanyRanke, MB论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, Germany Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, GermanyWittekindt, NE论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, Germany Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, D-72076 Tubingen, Germany
- [22] Familial Noonan Syndrome due to mutations in PTPN11 and PLOD1 genesHORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 241 - 241Chirayath, Shiga论文数: 0 引用数: 0 h-index: 0机构: Sidra Med, Doha, Qatar Sidra Med, Doha, QatarMohammed, Idris论文数: 0 引用数: 0 h-index: 0机构: Sidra Med, Doha, Qatar Sidra Med, Doha, QatarMohamadsalih, Ghassan论文数: 0 引用数: 0 h-index: 0机构: Sidra Med, Doha, Qatar Sidra Med, Doha, QatarBen-Omran, Tawfeg论文数: 0 引用数: 0 h-index: 0机构: Sidra Med, Doha, Qatar Sidra Med, Doha, QatarHussain, Khalid论文数: 0 引用数: 0 h-index: 0机构: Sidra Med, Doha, Qatar Sidra Med, Doha, Qatar
- [23] Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutationsBMC MEDICAL GENETICS, 2020, 21 (01)Athota, Jeevana Praharsha论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mol Genet, Bengaluru 560100, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaBhat, Meenakshi论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mol Genet, Bengaluru 560100, India Indira Gandhi Inst Child Hlth, Pediat Genet, Bengaluru 560029, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaNampoothiri, Sheela论文数: 0 引用数: 0 h-index: 0机构: Amrita Inst Med Sci & Res Ctr AIMS, Pediat Genet, Kochi 682041, Kerala, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaGowrishankar, Kalpana论文数: 0 引用数: 0 h-index: 0机构: Kanchi Kamakoti CHILDS Trust Hosp, Med Genet, Chennai 600034, Tamil Nadu, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaNarayanachar, Sanjeeva Ghanti论文数: 0 引用数: 0 h-index: 0机构: Indira Gandhi Inst Child Hlth, Pediat Genet, Bengaluru 560029, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaPuttamallesh, Vinuth论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mol Genet, Bengaluru 560100, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaFarooque, Mohammed Oomer论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mol Genet, Bengaluru 560100, India Ctr Human Genet, Mol Genet, Bengaluru 560100, IndiaShetty, Swathi论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mol Genet, Bengaluru 560100, India Ctr Human Genet, Mol Genet, Bengaluru 560100, India
- [24] Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic CardiomyopathyGENES, 2020, 11 (08) : 1 - 6Caiazza, Martina论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyRubino, Marta论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyMonda, Emanuele论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyPassariello, Annalisa论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyFusco, Adelaide论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyCirillo, Annapaola论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyEsposito, Augusto论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyPierno, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Physiol Nutr, I-80138 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyDe Fazio, Federica论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyPacileo, Roberta论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyEvangelista, Eloisa论文数: 0 引用数: 0 h-index: 0机构: Ames Genet Lab, I-80138 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyPacileo, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Monaldi Hosp, Cardiomyopathies & Heart Failure Dept, I-80138 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyRusso, Maria Giovanna论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, ItalyLimongelli, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy UCL, Inst Cardiovascr Sci, London WC1E 6DD, England St Bartholomews Hosp, London WC1E 6DD, England Univ Campania Luigi Vanvitelli, Monaldi Hosp, Dept Translat Med Sci, Inherited & Rare Cardiovasc Dis, I-80131 Naples, Italy
- [25] Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel MutationsThe Indian Journal of Pediatrics, 2016, 83 : 517 - 521Tahir Atik论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineAyca Aykut论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineFiliz Hazan论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineHuseyin Onay论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineDamla Goksen论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineSukran Darcan论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineAjlan Tukun论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of MedicineFerda Ozkinay论文数: 0 引用数: 0 h-index: 0机构: Ege University,Division of Genetics, Department of Pediatrics, School of Medicine
- [26] Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel MutationsINDIAN JOURNAL OF PEDIATRICS, 2016, 83 (06): : 517 - 521Atik, Tahir论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, Turkey论文数: 引用数: h-index:机构:Hazan, Filiz论文数: 0 引用数: 0 h-index: 0机构: Dr Behcet Uz Childrens Hosp, Dept Med Genet, Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, TurkeyOnay, Huseyin论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Sch Med, Dept Med Genet, Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, TurkeyGoksen, Damla论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Sch Med, Dept Pediat, Div Endocrinol, Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, TurkeyDarcan, Sukran论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Sch Med, Dept Pediat, Div Endocrinol, Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, TurkeyTukun, Ajlan论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Genet, Ankara, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, TurkeyOzkinay, Ferda论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, Turkey Ege Univ, Sch Med, Dept Med Genet, Izmir, Turkey Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, Turkey
- [27] PTPN11 mutations in Noonan Syndrome type 1:: Detection of recurrent mutations in Exons 3 and 13HUMAN MUTATION, 2002, 20 (04) : 298 - 304Maheshwari, M论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABelmont, J论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAFernbach, S论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAHo, T论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAMolinari, L论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAYakub, I论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAYu, F论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACombes, A论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATowbin, J论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACraigen, WJ论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGibbs, R论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [28] Variants of the PTPN11 Gene in Mexican Patients with Noonan SyndromeGENES, 2024, 15 (11)Zepeda-Olmos, Paola Montserrat论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico Univ Guadalajara, Ctr Univ Ciencias Salud, Doctorado Genet Humana, Sierra Mojada 950, Guadalajara 44340, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, MexicoEsparza-Garcia, Eduardo论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Hosp Pediat Ctr Med Nacl Occidente, Unidad Med Alta Especialidad, Belisario Dominguez 735, Guadalajara 44360, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, MexicoRobles-Espinoza, Kiabeth论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico Univ Guadalajara, Ctr Univ Ciencias Salud, Doctorado Genet Humana, Sierra Mojada 950, Guadalajara 44340, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, MexicoGonzalez-Garcia, Juan Ramon论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, MexicoGutierrez, Perla Graciela Rodriguez论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, MexicoMagana-Torres, Maria Teresa论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Guadalajara 44360, Jalisco, Mexico
- [29] Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case seriesJOURNAL OF NEUROLOGY, 2024, 271 (03) : 1331 - 1341Pugliese, Alessia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ctr Neurolesi Bonino Pulejo, Messina, Italy Childrens Hosp Eastern Ontario Res Inst, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyDella Marina, Adela论文数: 0 引用数: 0 h-index: 0机构: Univ Duisburg Essen, Ctr Neuromuscular Disorders, Ctr Translat Neuro & Behav Sci, Dept Pediat Neurol, D-45147 Essen, Germany IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyEstephan, Eduardo de Paula论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo FMUSP, Dept Neurol, Fac Med, Sao Paulo, Brazil Sao Jose do Rio Preto State Med Sch, Dept Neurol Sci Psychiat & Med Psychol, Sao Jose Do Rio Preto, SP, Brazil IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyZanoteli, Edmar论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo FMUSP, Dept Neurol, Fac Med, Sao Paulo, Brazil IRCCS Ctr Neurolesi Bonino Pulejo, Messina, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Topf, Ana论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, Translat & Clin Res Inst, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne, England IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyThompson, Rachel论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario Res Inst, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyPolavarapu, Kiran论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario Res Inst, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada IRCCS Ctr Neurolesi Bonino Pulejo, Messina, ItalyLochmueller, Hanns论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario Res Inst, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada Ottawa Hosp, Dept Med, Div Neurol, Ottawa, ON, Canada Univ Ottawa, Brain & Mind Res Inst, Ottawa, ON, Canada Univ Freiburg, Fac Med, Med Ctr, Dept Neuropediat & Muscle Disorders, Freiburg, Germany Ctr Nacl Anal Genom CNAG, Barcelona, Catalonia, Spain IRCCS Ctr Neurolesi Bonino Pulejo, Messina, Italy
- [30] Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case seriesJournal of Neurology, 2024, 271 : 1331 - 1341Alessia Pugliese论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroAdela Della Marina论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroEduardo de Paula Estephan论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroEdmar Zanoteli论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroAndreas Roos论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroUlrike Schara-Schmidt论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroAndreas Hentschel论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroYoshiteru Azuma论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroAna Töpf论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroRachel Thompson论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroKiran Polavarapu论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational NeuroHanns Lochmüller论文数: 0 引用数: 0 h-index: 0机构: IRCCS Centro Neurolesi “Bonino Pulejo”,Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro