共 50 条
- [41] Autism Spectrum Disorder and Suicide: A Case ReportCUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)Fatani, Abrar N.论文数: 0 引用数: 0 h-index: 0机构: Mental Hlth Hosp, Dept Psychiat, Jeddah, Saudi Arabia Mental Hlth Hosp, Dept Psychiat, Jeddah, Saudi ArabiaAlasiri, Nouf M.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Hosp, Dept Pediat, Jeddah, Saudi Arabia Mental Hlth Hosp, Dept Psychiat, Jeddah, Saudi ArabiaGasem, Osama A.论文数: 0 引用数: 0 h-index: 0机构: Mental Hlth Hosp, Dept Psychiat, Jeddah, Saudi Arabia Mental Hlth Hosp, Dept Psychiat, Jeddah, Saudi Arabia
- [42] Food intake restriction in patient with autism spectrum disorder and Moebius syndrome, a strong association. A case reportEUROPEAN PSYCHIATRY, 2024, 67 : S454 - S454Del Sol Calderon, P.论文数: 0 引用数: 0 h-index: 0机构: Hosp Puerta Hierro, Psychiat, Madrid, Spain Hosp Puerta Hierro, Psychiat, Madrid, SpainIzquierdo de la Puente, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Puerta Hierro, Psychiat, Madrid, Spain Hosp Puerta Hierro, Psychiat, Madrid, SpainFernandez, R.论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Infanta Cristina, Psychiat, Madrid, Spain Hosp Puerta Hierro, Psychiat, Madrid, SpainGarcia Moreno, M.论文数: 0 引用数: 0 h-index: 0机构: Hosp Puerta Hierro, Psychiat, Madrid, Spain Hosp Puerta Hierro, Psychiat, Madrid, SpainErdocia, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Puerta Hierro, Psychiat, Madrid, Spain Hosp Puerta Hierro, Psychiat, Madrid, Spain
- [43] Autism spectrum disorder and Coffin-Siris syndrome-Case reportFRONTIERS IN PSYCHIATRY, 2023, 14Milutinovic, Luka论文数: 0 引用数: 0 h-index: 0机构: Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, Serbia Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, Serbia论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Joksic, Ivana论文数: 0 引用数: 0 h-index: 0机构: Clin Gynecol & Obstet Narodni Front, Belgrade, Serbia Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, SerbiaLjubomirovic, Natasa论文数: 0 引用数: 0 h-index: 0机构: Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, Serbia Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, SerbiaMilovancevic, Milica Pejovic论文数: 0 引用数: 0 h-index: 0机构: Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, Serbia Inst Mental Hlth, Clin Dept Children & Adolescents, Belgrade, Serbia
- [44] Cri du Chat Syndrome Coexistent with Autism Spectrum Disorder: A Case ReportPSYCHIATRY AND BEHAVIORAL SCIENCES, 2018, 8 (02): : 89 - 92Firat, Sumeyra论文数: 0 引用数: 0 h-index: 0机构: Sirnak State Hosp, Sirnak, Turkey Sirnak State Hosp, Sirnak, TurkeySenor, Pinar Uran论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Child & Adolescent Psychiat, Ankara, Turkey Sirnak State Hosp, Sirnak, TurkeyAysev, Fatma Ayla Soykan论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Child & Adolescent Psychiat, Ankara, Turkey Sirnak State Hosp, Sirnak, Turkey
- [45] Williams Syndrome Associated With Autism Spectrum Disorder: Case Report and Review of the LiteratureCUREUS JOURNAL OF MEDICAL SCIENCE, 2020, 12 (08)Carvalho, Max M.论文数: 0 引用数: 0 h-index: 0机构: Univ Brasilia, Fac Med, Brasilia, DF, Brazil Univ Brasilia, Fac Med, Brasilia, DF, BrazilMazza, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Brasilia Univ Hosp, Pediat Neurol & Neurogenet, Brasilia, DF, Brazil Univ Brasilia, Fac Med, Brasilia, DF, Brazil
- [46] A CASE REPORT OF A CAT-EYE SYNDROME PRESENTING WITH AN AUTISM SPECTRUM DISORDEREUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1337 - 1338Barbosa, Sofia论文数: 0 引用数: 0 h-index: 0机构: Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, PortugalLages, Marta论文数: 0 引用数: 0 h-index: 0机构: Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, PortugalBorja-Santos, Nuno论文数: 0 引用数: 0 h-index: 0机构: Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, PortugalGoncalves, Patricia论文数: 0 引用数: 0 h-index: 0机构: Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, PortugalBarreta, Ana论文数: 0 引用数: 0 h-index: 0机构: Joaquim Chaves Saude, Miraflores, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, PortugalMaia, Teresa论文数: 0 引用数: 0 h-index: 0机构: Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal Hosp Prof Doutor Fernando Fonseca EPE, Amadora, Portugal
- [47] Living birth following preimplantation genetic testing for monogenic disorders to prevent low-level germline mosaicism related Nicolaides-Baraitser syndromeFRONTIERS IN GENETICS, 2022, 13Pan, Jiexue论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Shanghai Ji Ai Genet & IVF Inst, Shanghai, Peoples R China Shanghai Key Lab Embryo Original Dis, Shanghai, Peoples R China Chinese Acad Med Sci, Res Units Embryo Original Dis, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R ChinaLi, Jie论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Shanghai Ji Ai Genet & IVF Inst, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R ChinaChen, Songchang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Shanghai Ji Ai Genet & IVF Inst, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R ChinaXu, Chenming论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Shanghai Ji Ai Genet & IVF Inst, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R ChinaHuang, Hefeng论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Shanghai Key Lab Embryo Original Dis, Shanghai, Peoples R China Chinese Acad Med Sci, Res Units Embryo Original Dis, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R ChinaJin, Li论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Shanghai Ji Ai Genet & IVF Inst, Shanghai, Peoples R China Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China
- [48] Report of a Patient With Temple-Baraitser SyndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (03) : 848 - 851Yesil, Gozde论文数: 0 引用数: 0 h-index: 0机构: Bezmialem Vakif Univ Med, Dept Med Genet, Istanbul, Turkey Bezmialem Vakif Univ Med, Dept Med Genet, Istanbul, TurkeyGuler, Serhat论文数: 0 引用数: 0 h-index: 0机构: Bezmialem Vakif Univ Med, Dept Pediat Neurol, Istanbul, Turkey Bezmialem Vakif Univ Med, Dept Med Genet, Istanbul, TurkeyYuksel, Adnan论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Cerrahpasa Med Fac, Dept Med Genet, Istanbul, Turkey Bezmialem Vakif Univ Med, Dept Med Genet, Istanbul, TurkeyAlanay, Yasemin论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ Med, Dept Pediat Genet, Istanbul, Turkey Bezmialem Vakif Univ Med, Dept Med Genet, Istanbul, Turkey
- [49] Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome ( SMARCA2 Mutation)-Due to a POLG1 -Related Effect?NEUROPEDIATRICS, 2020, 51 (01) : 49 - 52Hofmeister, Benedikt论文数: 0 引用数: 0 h-index: 0机构: Ludwig Maximilian Univ Munich, Munich, Germany Munich Hosp Bogenhausen, Hosp Gastroenterol Hepatol & Gastroenterol Oncol, Munich, Germany Ludwig Maximilian Univ Munich, Munich, Germanyvon Stuelpnagel, Celina论文数: 0 引用数: 0 h-index: 0机构: Paracelsus Private Med Univ Salzburg, Inst Transit Rehabil & Palliat, Salzburg, Austria Univ Hosp Munich, Comprehens Epilepsy Program Children, Div Pediat Neurol Dev Med & Social Pediat, LMU Munich,Dept Pediat, Munich, Germany Ludwig Maximilian Univ Munich, Munich, GermanyBerweck, Steffen论文数: 0 引用数: 0 h-index: 0机构: Ludwig Maximilian Univ Munich, Munich, Germany Schoen Klin Vogtareuth, Ctr Epilepsy Children & Adolescents, Hosp Neuropediat & Neurol Rehabil, Vogtareuth, Germany Ludwig Maximilian Univ Munich, Munich, GermanyAbicht, Angela论文数: 0 引用数: 0 h-index: 0机构: MGZ Med Genet Ctr, Munich, Germany Ludwig Maximilian Univ Munich, Munich, GermanyKluger, Gerhard论文数: 0 引用数: 0 h-index: 0机构: Paracelsus Private Med Univ Salzburg, Inst Transit Rehabil & Palliat, Salzburg, Austria Schoen Klin Vogtareuth, Ctr Epilepsy Children & Adolescents, Hosp Neuropediat & Neurol Rehabil, Vogtareuth, Germany Ludwig Maximilian Univ Munich, Munich, GermanyWeber, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Basel, Dept Neuropediat & Dev Pediat, Basel, Switzerland Ludwig Maximilian Univ Munich, Munich, Germany
- [50] De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndromeGENETICS IN MEDICINE, 2020, 22 (11) : 1838 - 1850Cappuccio, Gerarda论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Translat Med, Naples, Italy Telethon Inst Genet & Med, Pozzuoli, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalySayou, Camille论文数: 0 引用数: 0 h-index: 0机构: Univ Grenoble Alpes, Inst Adv Biosci, CNRS UMR 5309, INSERM,U1209, Grenoble, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyLe Tanno, Pauline论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Grenoble Alpes, Dept Genet & Reprod, Grenoble, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyTisserant, Emilie论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:Sa, Joaquim论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp & Univ Rio Coimbra, Hosp Pediat, Med Genet Unit, Coimbra, Portugal Univ Naples Federico II, Dept Translat Med, Naples, ItalyLow, Karen J.论文数: 0 引用数: 0 h-index: 0机构: Univ Bristol, Univ Hosp Bristol NHS Fdn Trust, Bristol, Avon, England Univ Naples Federico II, Dept Translat Med, Naples, ItalyDias, Cristina论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Dept Med & Mol Genet, London, England Francis Crick Inst, London, England Great Ormond St Hosp Children NHS Fdn Trust, Clin Genet, London, England Univ Naples Federico II, Dept Translat Med, Naples, ItalyHavlovicova, Marketa论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Univ Naples Federico II, Dept Translat Med, Naples, ItalyHancarova, Miroslava论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Univ Naples Federico II, Dept Translat Med, Naples, ItalyEichler, Evan E.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Genome Sci, Sch Med, Seattle, WA USA Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA Univ Naples Federico II, Dept Translat Med, Naples, ItalyDevillard, Francoise论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Grenoble Alpes, Dept Genet & Reprod, Grenoble, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: Maison St Protestante Bordeaux Bagatelle, Pole Mere Enfant, CPDPN, Talence, France Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:Dubourg, Christele论文数: 0 引用数: 0 h-index: 0机构: BMT HC Jean Dausset, Serv Genet Mol & Genom, Rennes, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Rennes, Inst Genet & Dev Rennes IGDR UMR 6290, Serv Genet Clin, CHU Rennes, Rennes, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyGerard, Benedicte论文数: 0 引用数: 0 h-index: 0机构: Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyPiton, Amelie论文数: 0 引用数: 0 h-index: 0机构: Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:Okamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Womens & Childrens Hosp, Dept Med Genet, Osaka, Japan Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:Metcalfe, Kay论文数: 0 引用数: 0 h-index: 0机构: Manchester Ctr Genom Med, Manchester, Lancs, England Univ Naples Federico II, Dept Translat Med, Naples, ItalyMoh, Anna论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Dept Genet & Metab, Washington, DC 20010 USA Univ Naples Federico II, Dept Translat Med, Naples, ItalyChapman, Kimberly A.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Dept Genet & Metab, Washington, DC 20010 USA Univ Naples Federico II, Dept Translat Med, Naples, ItalyAref-Eshghi, Erfan论文数: 0 引用数: 0 h-index: 0机构: Victoria Hosp, London Hlth Sci Ctr, Mol Genet Lab, London, ON, Canada Western Univ, Dept Pathol & Lab Med, London, ON, Canada Univ Naples Federico II, Dept Translat Med, Naples, ItalyKerkhof, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Victoria Hosp, London Hlth Sci Ctr, Mol Genet Lab, London, ON, Canada Univ Naples Federico II, Dept Translat Med, Naples, ItalyTorella, Annalaura论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med, Pozzuoli, Italy Univ Campania Luigi Vanvitelli, Dept Precis Med, Naples, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalyNigro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med, Pozzuoli, Italy Univ Campania Luigi Vanvitelli, Dept Precis Med, Naples, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalyPerrin, Laurence论文数: 0 引用数: 0 h-index: 0机构: Robert Debre Hosp, AP HP, Dept Genet, Paris, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyPiard, Juliette论文数: 0 引用数: 0 h-index: 0机构: Univ Franche Comte, Ctr Gent Humaine, Besancon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyLe Guyader, Gwenael论文数: 0 引用数: 0 h-index: 0机构: Univ Poitiers Hosp, Dept Med Genet, Poitiers, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyJouan, Thibaud论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France CHU Dijon, Ctr Reference Deficiences Intellectuelles Causes, Dijon, France CHU Dijon, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyDuffourd, Yannis C.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyGeorge-Abraham, Jaya K.论文数: 0 引用数: 0 h-index: 0机构: Dell Childrens Med Grp, Austin, TX USA Univ Texas Austin, Dell Med Sch, Dept Pediat, Austin, TX 78712 USA Univ Naples Federico II, Dept Translat Med, Naples, ItalyBuchanan, Catherine A.论文数: 0 引用数: 0 h-index: 0机构: Dell Childrens Med Grp, Austin, TX USA Univ Naples Federico II, Dept Translat Med, Naples, ItalyWilliams, Denise论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens NHS Fdn Trust, Birmingham, W Midlands, England Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Sousa, Sergio B.论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp & Univ Rio Coimbra, Hosp Pediat, Med Genet Unit, Coimbra, Portugal Univ Coimbra, Univ Clin Genet, Fac Med, Coimbra, Portugal Univ Naples Federico II, Dept Translat Med, Naples, ItalyHennekam, Raoul C. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Acad Med Ctr, Dept Pediat & Translat Genet, Amsterdam, Netherlands Univ Naples Federico II, Dept Translat Med, Naples, ItalySadikovic, Bekim论文数: 0 引用数: 0 h-index: 0机构: Victoria Hosp, London Hlth Sci Ctr, Mol Genet Lab, London, ON, Canada Western Univ, Dept Pathol & Lab Med, London, ON, Canada Univ Naples Federico II, Dept Translat Med, Naples, ItalyThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Grenoble Alpes, Dept Genet & Reprod, Grenoble, France Univ Naples Federico II, Dept Translat Med, Naples, Italy论文数: 引用数: h-index:机构:Vitobello, Antonio论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comt, FHU TRANSLAD, Genet Dev Disorders, Inserm UMR 1231 GAD, Dijon, France CHU Dijon, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Naples Federico II, Dept Translat Med, Naples, ItalyBrunetti-Pierri, Nicola论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Translat Med, Naples, Italy Telethon Inst Genet & Med, Pozzuoli, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalyCasari, Giorgio论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med, Pozzuoli, Italy Univ Vita Salute San Raffaele, Milan, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalyPinelli, Michele论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med, Pozzuoli, Italy Univ Naples Federico II, Dept Translat Med, Naples, ItalyMusacchia, Francesco论文数: 0 引用数: 0 h-index: 0机构: Telethon Inst Genet & Med, Pozzuoli, Italy Univ Naples Federico II, Dept Translat Med, Naples, Italy