Zobrazeno 81 - 90
of 126
pro vyhledávání: '"Mei-Chyn Chao"'
Autor:
Yi-Chang Liu, Hui-Hua Hsiao, H H Hsiao, Yi-Hui Hung, Ta-Chih Liu, Shih-Bin Tseng, Yuli Chang, Hui-Jen Tsai, Sheng-Fung Lin, Mei-Chyn Chao
Publikováno v:
International journal of hematology. 80(4)
Chronic lymphocytic leukemia is one of the most common leukemias in the western world and consists of many chromosome aberrations. We report the case of a 74-year-old male patient with chronic lymphocytic leukemia with complex variant translocations
Autor:
Ching-Chia, Li, Mei-Chyn, Chao, Shu-Pin, Huang, Yii-Her, Chou, Chun-Hsiung, Huang, A-Hsiung, Chen, Yi-Ping, Wu
Publikováno v:
The Kaohsiung journal of medical sciences. 18(7)
Kallmann syndrome is a very rare hereditary disease. It is characterized by hypogonadotropic hypogonadism in association with anosmia ot hyposmia, both of which occur as a result of the failure of neuronal migration of the luteinizing hormone releasi
Publikováno v:
Diabetes research and clinical practice. 54(1)
Persistent humoral autoimmunity to the enzyme glutamic acid decarboxylase (GAD) has been described in a substantial proportion of patients with type 1 diabetes mellitus. Higher prevalence of GAD antibody in diabetes patients using a new radioligand-b
Publikováno v:
Pediatrics. 121:S116-S117
INTRODUCTION: Noonan syndrome (NS) is an autosomal-dominant disorder that presents with a characteristic face, short stature, skeletal anomalies, and congenital heart defects. Protein-tyrosine phosphatase nonreceptor-type 11 (PTPN11), encoding SHP-2,
Publikováno v:
Acta Paediatrica. 95:378-379
Publikováno v:
Acta Paediatrica. 95:378-379
Publikováno v:
Archives of Disease in Childhood. 97:A180-A180
Background and Aim Isolated cleft lip with/or cleft palate (CL/P) is a common complex birth defect that varies in prevalence with Asian and Amerindian ancestry having the highest rates. While several genes had significant association to the CL/P, the
Autor:
Kwang-Jen Hsiao, Tso-Ren Wang, Fang-Jong Ko, Kuang-Dong Wuu, Mei-Chyn Chao, Shuan-Yow Li, Jia-Yuh Chen, Pao-Chin Chiu
Publikováno v:
Jinrui idengaku zasshi. The Japanese journal of human genetics. 36(3)
Governmental officials as well as medical scientists in Taiwan have worked hard in recent years to develop and to implement various measures, such as prenatal diagnosis and neonatal screening, to lower the incidence of hereditary diseases and mental
Autor:
Chia-Fang Wu1 960021@ms.kmuh.org.tw, Bai-Hsiun Chen2,3, Shiea, Jentaie4, Chen, Eric K.5, Ching-Kuan Liu6, Mei-Chyn Chao3, Chi-Kung Ho1, Jiunn-Ren Wu3, Ming-Tsang Wu1,7,8
Publikováno v:
Environmental Science & Technology. 12/3/2013, Vol. 47 Issue 23, p13754-13762. 9p.
Autor:
Chia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, Chih-Ping Chen, Shuan-Pei Lin, Mei-Chyn Chao, Shyh-Shin Chiou, Yi-Ning Su
Publikováno v:
BMC Medical Genetics; 2011, Vol. 12 Issue 1, p76-80, 5p