孙良忠,主任医师,博士研究生导师。 1993年中山医科大学临床医学专业毕业后一直在中山大学附属第一医院儿科工作;先后获得硕士,博士学位。英国谢菲尔德大学肾脏所访问学者。擅长小儿肾脏病、风湿免疫疾病的诊治。熟练掌握小儿肾穿刺活检术,小儿透析治疗和管理,小儿肾移植前处理。 学术兼职:中国医师协会儿科风湿免疫专业委员会委员,广东省医学会免疫学组副组长,广东省医学会肾脏病分会第八届中青年委员,广东省医学会儿科分会第十五届中青年委员及第十四、十五届儿科肾脏学组秘书,《The Application of Clinical Genetics》,《Renal Failure》, 《中华肾脏病杂志》和《中华临床医师杂志》审稿专家。 获奖情况: 曾两度获得中山大学附属第一医院优秀带教老师。两篇论著分别获中华医学会儿科分会《中华儿科杂志》优秀论文一等奖,中华医学会儿科分会第三次全国中青年儿科医师优秀论文三等奖。 论著 第一作者/通讯作者在国内外核心期刊共发表论文40余篇,其中SCI 10 篇。 承担了包括国家自然科学基金面上项目2项和广东省自然科学基金等9项科研项目。 SCI收录论著 1. Novel compound mutations of SMARCAL1 associated with severe Schimke immuno- osseous dysplasia in a Chinese patient. Nephrology Dialysis Transplantation, 2010, 25(5): 1697-702. 2. The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome. Plos One. 2015, 10 (8): e0135648. 3. Clinical and pathological features of microscopic polyangiitis in 20 children [J]. The Journal of Rheumatology, 2014, 41(8): 1712-19. 4. Clinical and pathological characteristics of 5 children with HBV surface antigen (HBsAg)-negative hepatitis B virus-associated glomerulonephritis. J Clin Virol. 2015 May; 66:1-5. 5. A high mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients. Nephrology (Carlton). 2015 Jul 17. 6. Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome [J]. Asian Journal Andrology, 2014, 16(4): 647-49. 7. Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Loken syndrome [J]. Nephrology (Carlton), 2013, 18(12): 838-42. 8. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children [J]. Renal Failure, 2011, 33(9): 910-14. 9. Novel Mutation of OCRL1 in Lowe Syndrome. Indian J Pediatr. 2014 10. 10. Analysis of pathogenesis and clinical features of nephrotic syndrome in the first year of life. Pediatr Nephrol. 2013, 28: 1582 11. WT1 mutation-associated nephropathy: a single-center experience. ......
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