Lo, Fu-Sung ,M.D. 
Intitution:Chang Gung Memorial Hospital
Position:
Director/Pediatrician/Associate Professor
Department:
Division of Pediatric Endocrinology & Genetics, Department of Pediatrics 
Address:No.5, Fusing St., Gueishan Township, Taoyuan County 333, Taiwan (R.O.C.)
Tel:+886-3-3281200 Fax:+886-3-3285056
E-mail: lofusu@adm.cgmh.org.tw
Focus of Interest:- Endocrinology & Metabolism
- Pediatrics
Education:
1985-1992 Bachelor of Medicine Diploma, Taipei Medical College, 250 Wu Hsing St., Taipei, Taiwan 105
Employment Records:
◎2012- Associate Professor, Department of Pediatrics, Chang Gung Memorial Hospital
◎2011- Chief, Division of Endocrinology and Genetics, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan
◎2004-2012 Assistant Professor, Chang Gung Memorial Hospital
◎2002-2004 Instructor, Chang Gung Memorial Hospital & Chang Gung University
◎1998-1999 Research Fellow, Department of Endocrinology, Children’s Hospital Boston
◎1997- Attending Pediatrician, Division of Endocrinology, Department of Pediatrics, Chang Gung Children’s Hospital
◎1995-1997 Chief Resident & Fellowship, Division of Endocrinology, Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan
◎1992-1995 Residency, Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan
◎1991-1992 Rotating Internship, Mackay Memory Hospital, Taipei, Taiwan
Selected Main Publications:
- Huang YH, Wai YY, VanYH,Lo FS*. Effect of growth hormone (GH) therapy in Taiwanese children with GH deficiency. J Formos Med Assoc. 2012 Jul;111(7):355-63. Epub 2012 May 23.
- Lo FS, Luo JD, Lee YJ, Shu SG, Kuo MT, Chiou CC*. High resolution melting analysis for mutation detection for PTPN11 gene: Applications of thismethod for diagnosis of Noonan syndrome. ClinicaChimicaActa 2009; 409:75-77.
- Wei HY, Yang CP, Cheng CH, Lo FS*. Fanconi syndrome in a patient with b-thalassemia major after using deferasirox for 27 months. Transfusion 2011 May;51(5):949-54. doi: 10.1111/j.1537-2995.2010.02939.x. Epub 2010 Nov 15.
- Lo FS*, Lin JL, KuoMT, ChiuPC, ShuSG, ChaoMC, LeeYJ,Lin SP. Noonan syndrome caused by germ-line KRAS mutation in Taiwan: two case reports and a Noonan syndrome caused by germ-line. Eur J Pediatr2009 Aug;168(8):919-23. Epub 2008 Oct 29.
- Lo FS*, Kuo MT, Wang CJ, Chang CH, Lee ZL, Van YH. Two novel PHEX mutations in Taiwanese patients with x-linked hypophosphatemic rickets. Nephron Physiology 2006;103:157-163.
Full Publication List