醫(yī)生介紹
徐浩，醫(yī)學博士，同濟醫(yī)院泌尿外科主治醫(yī)師，中華醫(yī)學會男科學分會生殖內分泌學組委員。長期從事男性孤立性低促性腺激素性性腺功能減退癥/卡爾曼綜合征的臨床診療及基礎與臨床研究工作，以第一、第二作者在國際知名雜志發(fā)表相關研究論文數(shù)篇，相關成果多次于國內、國際學術會議發(fā)言。目前主持國家自然科學基金青年項目一項，參與學術專著《男性性腺功能減退癥》、《中國遲發(fā)性性腺功能減退癥診療手冊》、《實用性醫(yī)學》、《產(chǎn)后壓力性尿失禁康復指南》、《男性健康系列科普叢書-雄風再起：老年男性如何走出更年期》等醫(yī)學專著的編寫。
社會任職
中華醫(yī)學會男科學分會生殖內分泌學組委員
科研成果
Xu H, Niu Y, Wang T, Liu S, Xu H, Wang S, Liu J*. Novel FGFR1 and KISS1R Mutations in Chinese Kallmann Syndrome Males with Cleft Lip/Palate. BIOMED RES INT. 2015; 2015:1-9.（第一作者）Xu H, Li Z, Wang T, Wang S, Liu J*, Wang DW*. Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family. ANDROLOGIA. 2015-12-01; 47（10）: 1160-5. （第一作者）Wang X, Xu H, Jiang H, Wang L, Lu C, Wei X, Liu J, Xu S. Clinical features and outcomes of discharged coronavirus disease 2019 patients: a prospective cohort study. QJM. 2020;113（9）:657-665.（共同第一作者，IF：2.529）Xu H, Li Z, Sun T, Chen Y, Wang D, Wang T, Wang S, Liu J. An isolated hypogonadotropic hypogonadism male with a novel de novoFGFR1 mutation fathered a normal son evidenced by prenatal genetic diagnosis. Andrologia. 2020;52（11）:e13821.（共同第一作者，IF 1.951）Chen Y, Sun T, Niu Y, Wang D, Xiong Z, Li C, Liu K, Qiu Y, Sun Y, Gong J, Wang T, Wang S, Xu H, Liu J. Correlations Among Genotype and Outcome in Chinese Male Patients With Congenital Hypogonadotropic Hypogonadism Under HCG Treatment. J Sex Med. 2020;17（4）:645-657. （共同通訊，IF 3.293）Chen Y, Sun T, Niu Y, Wang D, Liu K, Wang T, Wang S, Xu H, Liu J. Cell adhesion molecule L1 like plays a role in the pathogenesis of idiopathic hypogonadotropic hypogonadism. J Endocrinol Invest. 2021. Epub ahead of print.（共同通訊，IF 3.397）Xu H, Ma J, Chen Z*, Yang J, Yuan H, Wang T, Liu J, Yang W, Ye Z. Safety and Efficacy of En Bloc Transurethral Resection Wi
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