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Dr. SHEN Ming

Shen Ming graduated from the Department of Medicine of Sun Yat-Sen University in 1984 as a master of medicine. She is now the member of Editorial board of International Journal of Pediatrics and Journal of Chinese Clinical Medicine and Senior Reviewer of Chinese Journal of Medical Genetics. She won many prizes and took part in many researches such as the Ministerial-level Project of "new development of the treatment of PKU".
Titles: Senior doctor
Education: Bachelor , Peking Union Medical College , 1997;
Master of Medicine, Department of Medicine of Sun Yat-Sen University, 1984.
Experience: Working in China-Japan Friendship Hospital, 1984.8-present;
Years of Treating experience of PKU and BH4D patients, 2005.4-present;
Forty prenatal gene diagnoses for PKU families to avoid the second fetus with genetic disease.
Specialty: inherited metabolic diseases such as chondrodysplasia, inherited dwarfism and inherited hyperphenylalaninemia (phenylketonuria, tetrahydrobiopterin deficiency).
Positions: Member of Editorial board of International Journal of Pediatrics and Journal of Chinese Clinical Medicine;
Senior Reviewer of Chinese Journal of Medical Genetics;
Disease filtration expert of newborns in Beijing;
Member of the review board of medical negligence in Chaoyang district, Beijing.
Honors: First Prize of Advanced technology award  by China-Japan Friendship Hospital in 1997;
Third Prize of Advanced technology award  by China-Japan Friendship Hospital in 1999;
The title of Excellent Teacher in 2000 by China-Japan Friendship Hospital;
The title of Excellent Member of Communist Party in 2001 and 2008 by China-Japan Friendship Hospital;
The title of Honorable Individual in 2009 by the health ministry of Beijing.
Research: In Charge of a state-level training program of Continuing Medical Education on the diagnosis and treatment of inherited hyperphenylalaninemia by conducting several theory and clinical research on PKU and BH4D;
Pioneer engaged in the diagnosis and treatment the diseases arising from the gene of inherited dwarfism such as chondrodysplasia by analyzing the Point mutation of the gene of FGFR3 patient with advanced molecular technique;
Ministerial-level Project of "new development of the treatment of PKU" ;
Two institutional-level projects of “Research on the Deficiency of BH4 Reactive PAH” and “The Imaging and Nerve Assessment of PKU”.
Publications: Author of Over 30 papers;
Editor of 4 Famous Chinese medical books.
Activities: Addressed and exchanged posters in many international conferences in Europe and America