Renjith Mani
Muscat, MA, Oman
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
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.
Journal: Acta neuropathologica
Published: October 25, 2019
Rituximab Treatment in Myasthaenia Gravis: Report of two paediatric cases.
Journal: Sultan Qaboos University medical journal
Published: November 17, 2017
Longitudinal extensive transverse myelitis (LETM) in children: A twenty-year study from Oman.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: April 19, 2017
Blood Culture Contaminants in a Paediatric Population Retrospective study from a tertiary hospital in Oman.
Journal: Sultan Qaboos University medical journal
Published: August 02, 2016
Rigid Spine Syndrome among Children in Oman.
Journal: Sultan Qaboos University medical journal
Published: November 19, 2014
Magnetic Resonance Imaging Abnormalities in a Child with Acute Cerebellitis.
Journal: Sultan Qaboos University medical journal
Published: November 14, 2014
Eating epilepsy or feeding epilepsy in an infant.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: September 18, 2013
Three-year-old Girl with Sturge-Weber Syndrome without Facial Nevus.
Journal: Sultan Qaboos University medical journal
Published: August 06, 2013
Evolution of Ohtahara syndrome to continuous spikes and waves during slow sleep in an infant.
Journal: The Neurodiagnostic journal
Published: October 02, 2012
One in three: congenital bent bone disease and intermittent hyperthermia in three siblings with stuve-wiedemann syndrome.
Journal: Sultan Qaboos University medical journal
Published: September 02, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026