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Journal of Pediatric Genetics|September 15, 2016
NephronophthisisShalabh Srivastava, John A Sayer
Frontiers in Pediatrics|January 31, 2018
Many Genes-One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated DisordersShalabh Srivastava, Elisa Molinari, Shreya Raman, et al.
Contemporary Clinical Dentistry|May 9, 2014
Collision tumor of the palate: A rare case reportShoaib R Tippu, Farzan Rahman, Neha Sharma, et al.
BMC Nephrology|October 16, 2020
Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 allelesElisa Molinari, Shalabh Srivastava, Rebecca M Dewhurst, et al.
F1000Research|July 11, 2017
From disease modelling to personalised therapy in patients with CEP290 mutationsElisa Molinari, Shalabh Srivastava, John A Sayer, et al.
Case Reports in Nephrology|November 29, 2017
Large Retroperitoneal Haemorrhage Following Cyst Rupture in a Patient with Autosomal Dominant Polycystic Kidney DiseaseHolly Mabillard, Shalabh Srivastava, Philip Haslam, et al.
Case Reports in Dentistry|January 18, 2013
Van der woude syndrome associated with hypodontia: a rare clinical entityRomesh Soni, Rajul Vivek, Adit Srivastava, et al.
Clinical Kidney Journal|June 13, 2015
Infliximab as long-term maintenance in steroid-resistant and recurrent sarcoidosis in a renal transplant with central nervous system involvementShalabh Srivastava, Ravindra Rajakariar, Neil Ashman, et al.
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