Renjith Mani

Anti-CD20 monoclonal antibody in acute life threatening haemolytic anaemia complicating childhood onset SLE

R. Mani, R. Abdwani, Renjith Mani, 2009, Lupus.

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

K. Kandaswamy, E. Aronica, P. Bauer, 2019, bioRxiv.

Evolution of Ohtahara Syndrome to Continuous Spikes and Waves during Slow Sleep in an Infant

R. Koul, Rajesh Poothrikovil, Amna Al Futaisi, 2012, The Neurodiagnostic journal.

Rituximab Treatment in Myasthaenia Gravis: Report of two paediatric cases.

A. Al-Asmi, R. Koul, A. Al-Futaisi, 2018, Sultan Qaboos University medical journal.

One in three: congenital bent bone disease and intermittent hyperthermia in three siblings with stuve-wiedemann syndrome.

R. Koul, A. Al-Futaisi, A. Al-Kindy, 2013, Sultan Qaboos University medical journal.

Blood Culture Contaminants in a Paediatric Population Retrospective study from a tertiary hospital in Oman.

R. Abdwani, Rana A Abdelrahim, Z. Al-Muharrmi, 2017, Sultan Qaboos University medical journal.