Hacohen, Yael, Rahul Singh, Bethan Lang, Cheryl Hemingway, Ming Lim, and Angela Vincent. "Clinical relevance of VGKC-complex antibodies in children (P6. 253)." Neurology 84, no. 14 Supplement (2015): P6-253.
Kariyawasam, Sanduni, Rahul R. Singh, Jonathan Gadian, Daniel E. Lumsden, Jean-Pierre Lin, Ata Siddiqui, Yael Hacohen, Michael Absoud, and Ming Lim. "Clinical and radiological features of recurrent demyelination following acute disseminated encephalomyelitis (ADEM)." Multiple Sclerosis and Related Disorders 4, no. 5 (2015): 451-456.
Singh RR, S.Jayapal, Heinz Jungbluth, Sushma Goyal, Karine Lascelles . Early Onset movement disorder and epileptic encephalopathy due to de novo dominant SCN8A mutation. Seizure- European Journal of epilepsy 2015 (published online).
Alobeidi, Farah, Baba PD Inusa, Rahul Raman Singh, Jean Marie U-King-Im, and Ming Lim. "Cerebral microhaemorrhages secondary to fat embolus syndrome in sickle cell disease." Postgraduate medical journal 91, no. 1071 (2015): 55-56.
Singh, RR., Sagar Sedani, Ming Lim, Evangeline Wassmer, and Michael Absoud. "RANBP2 mutation and acute necrotizing encephalopathy: 2 cases and a literature review of the expanding clinico-radiological phenotype." European Journal of Paediatric Neurology (2014).
Singh, RR. S. Veronica Tan, Michael G. Hanna, Stephanie A. Robb, Antonia Clarke, and Heinz Jungbluth. "Mutations in SCN4A: A Rare but Treatable Cause of Recurrent LifeThreatening Laryngospasm." Pediatrics 134, no. 5 (2014): e1447-e1450.
Singh, RR., and Ming Lim. "Idiopathic intracranial hypertension: new insights, new definitions but same old problems." Developmental Medicine & Child Neurology (2014).
Hacohen, Yael, Rahul Singh, Vhari Forsyth, Michael Absoud, and Ming Lim. "CSF albumin and immunoglobulin analyses in childhood neurologic disorders." NeurologyNeuroimmunology Neuroinflammation 1, no. 1 (2014): e10.
Singh, RR., Nurdan Ozyilmaz, Simon Waller, U. Jean-Marie, Ming Lim, Ata Siddiqui, and Manish D. Sinha. "A study on clinical and radiological features and outcome in patients with posterior reversible encephalopathy syndrome (PRES)." European journal of pediatrics (2014): 1-7.
Tang SS, Fernandez D, Lazarou LP, Singh R, Fallon P.”MECP2 triplication in 3 Brothers - a rarely described cause of familial neurological regression in Boys”. Eur J Paediatric Neurol. 2012 Mar; 16(2):209-12. doi:10.1016/j.ejpn.2011.07.011. Pub 2011 Aug 6.