孫良忠

孫良忠，主任醫(yī)師，博士研究生導(dǎo)師。 1993年中山醫(yī)科大學(xué)臨床醫(yī)學(xué)專業(yè)畢業(yè)后一直在中山大學(xué)附屬第一醫(yī)院兒科工作；先后獲得碩士，博士學(xué)位。英國謝菲爾德大學(xué)腎臟所訪問學(xué)者。擅長小兒腎臟病、風(fēng)濕免疫疾病的診治。熟練掌握小兒腎穿刺活檢術(shù)，小兒透析治療和管理，小兒腎移植前處理。 學(xué)術(shù)兼職：中國醫(yī)師協(xié)會(huì)兒科風(fēng)濕免疫專業(yè)委員會(huì)委員，廣東省醫(yī)學(xué)會(huì)免疫學(xué)組副組長，廣東省醫(yī)學(xué)會(huì)腎臟病分會(huì)第八屆中青年委員，廣東省醫(yī)學(xué)會(huì)兒科分會(huì)第十五屆中青年委員及第十四、十五屆兒科腎臟學(xué)組秘書，《The Application of Clinical Genetics》，《Renal Failure》, 《中華腎臟病雜志》和《中華臨床醫(yī)師雜志》審稿專家。 獲獎(jiǎng)情況： 曾兩度獲得中山大學(xué)附屬第一醫(yī)院優(yōu)秀帶教老師。兩篇論著分別獲中華醫(yī)學(xué)會(huì)兒科分會(huì)《中華兒科雜志》優(yōu)秀論文一等獎(jiǎng)，中華醫(yī)學(xué)會(huì)兒科分會(huì)第三次全國中青年兒科醫(yī)師優(yōu)秀論文三等獎(jiǎng)。 論著 第一作者/通訊作者在國內(nèi)外核心期刊共發(fā)表論文40余篇，其中SCI 10 篇。 承擔(dān)了包括國家自然科學(xué)基金面上項(xiàng)目2項(xiàng)和廣東省自然科學(xué)基金等9項(xiàng)科研項(xiàng)目。 SCI收錄論著 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. ...

兒童腎臟病和風(fēng)濕免疫疾病。包括兒童血尿、蛋白尿、腎病綜合征，急、慢性腎炎，腎衰竭；系統(tǒng)性紅斑狼瘡、過敏性紫癜、溶血尿毒綜合征；多囊腎，海面腎，腎單位腎癆，腎結(jié)石，腎小管酸中毒，Dent病，巴特綜合征，遺尿；遺傳性腎病，Alport綜合征，家族性血尿等。