Genetic and Functional Analysis of Renal Tubular Disorders: from Clinical to Bench Study
博士 === 國防醫學院 === 醫學科學研究所 === 106 === Inherited renal tubular disorders are characterized by muscle weakness, exertional intolerance, polyuria, convulsion, short stature, and rickets during childhood. The main biochemical abnormalities include dysnatremia, dyskalemia, dyscalcemia, metabolic acidosis...
Main Authors: | Tseng, Min-Hua, 曾敏華 |
---|---|
Other Authors: | Lin, Shih-Hua |
Format: | Others |
Language: | en_US |
Published: |
2017
|
Online Access: | http://ndltd.ncl.edu.tw/handle/w98be6 |
Similar Items
-
Renal function in hepatosplenic schistosomiasis--an assessment of renal tubular disorders.
by: Daniella Bezerra Duarte, et al.
Published: (2014-01-01) -
Molecular genetics of renal tubular disorders affecting urate transport
by: Turner, Jeremy J. O.
Published: (2004) -
Clinical, genetic and molecular studies into hereditary renal tubular proteinuria
by: Issler, N.
Published: (2014) -
Clinical and genetic analysis of distal renal tubular acidosis in three Chinese children
by: Jiaojiao Liu, et al.
Published: (2018-10-01) -
Puberty from bench to clinic: Lessons for clinical management of pubertal disorders
by: Subhankar Chowdhury
Published: (2018-01-01)