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Indian Journal of Pediatrics|November 28, 2006
Twins with senior-Loken syndromeS Giridhar, R Padmaraj, Prabha SenguttuvanMolecular and Cellular Biochemistry|November 26, 2016
WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndromeAravind Selvin Kumar Ramanathan, Murali Vijayan, Srilakshmi Rajagopal, et al.Journal of Family & Community Medicine|March 2, 2016
Budding adult hypertensives with modifiable risk factors: "Catch them young"Aravind S K Ramanathan, Prabha Senguttuvan, Vel Prakash, et al.The Indian Journal of Medical Research|December 10, 2016
Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndromeAravind Selvin Kumar, R Srilakshmi, Smk Karthickeyan, et al.Journal of Hypertension|March 21, 2013
Efficacy and safety of valsartan in hypertensive children 6 months to 5 years of ageFranz Schaefer, Rosanna Coppo, Arvind Bagga, et al.Indian Pediatrics|March 28, 2008
Management of steroid sensitive nephrotic syndrome: revised guidelines, Arvind Bagga, Uma Ali, et al.Journal of Biomedical Research|October 19, 2018
Effect of angiotensin converting enzyme gene I/D polymorphism in South Indian children with nephrotic syndromeAravind Selvin Kumar Ramanathan, Balakrishnan Karuppiah, Murali Vijayan, et al.Nephrology (Carlton, Vic.)|November 15, 2015
Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndromeAravind Selvin Kumar Ramanathan, Prabha Senguttuvan, Rathika Chinniah, et al.Journal of the American Society of Nephrology : JASN|May 7, 2016
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary TractAsaf Vivante, Daw-Yang Hwang, Stefan Kohl, et al.Human Genetics|June 24, 2019
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humansThomas M Kitzler, Ronen Schneider, Stefan Kohl, et al.Pageof 2