1997 

M.B.B.S. 

PGIMS 

 

2001

D.CH.

PGIMS 

 

2005

F.R.C.P.

MRCPCH, London 

MRCPCH, 2005
Royal College of Paediatrics and Child Health, UK

FRCPCH, 2011
Royal College of Paediatrics and Child Health, UK

CCT - British Board, 2011
Oxford University Hospital, UK 

General Medical Council (GMC), UK

Indian Medical Council & Delhi Medical Council

Royal College of Paediatrics and Child Health (RCPCH), UK

British Paediatric Neurology Association (BPNA), UK

International League Against Epilepsy (ILAE)

Fellow, Royal College of Paediatrics and Child Health (RCPCH), UK

International Child Neurology Association (ICNA), US
Association of Child Neurology, India

International Headache Society, USA. 

-Skeletal Muscle Myopathy Mutations at the Actin-Tropomyosin Interface that Cause Gain Or Loss of Function. Biophysical Journal Jan 2012. 102(3) pp. 231a

Publication: Recurrent apnoeas in an infant with Prader-Willi syndrome. Developmental Medicine and Child Neurology supp.1 January 2013 Vol. 53

Publication: Video EEG (vEEG) outcome on children referred following a single unprovoked afebrile seizure. Developmental Medicine and Child Neurology supp1 January 2012; 54: 67-67

Publication: Hypertonic nemaline myopathy: a novel disease entity (accepted in journal of 'NEUROLOGY'/2011/395210)

Publication: Video EEG (vEEG) outcome on children referred following a single unprovoked afebrile seizure. Arch Dis Child. 2012 Jan; 97(1):90. Epub 2011 Oct 6

Publication: Evaluation of the floppy infant. Journal of Paediatrics and Child Health Nov 2011; 21: 495-500

Publication: Electro-clinical outcome of children referred with suspected absence seizures. Arch Dis Child. 2011 Oct; 96(10): 987-8. Epub 2011 Sep 8

Presentation: Recurrent apnoeas in an infant with Prader-Willi syndrome. Poster presentation, BPNA Annual conference, Edinburgh. Jan 2013

Presentation: Video EEG (vEEG) outcome on children referred following a single unprovoked afebrile seizure. Poster presentation, BPNA Annual conference, London. Jan 2012

Presentation: The EEG in children referred for suspected epileptic absences: How often is it diagnostic. Poster presentation, BPNA Annual conference, Edinburgh. Jan 2011

Presentation: An infantile onset epileptic encephalopathy associated with a homozygous missense variant in the SCN1A gene.

Platform presentation, BPNA (British Paediatric Neurology Association) Annual conference, Edinburgh. Jan 2010

Presentation: Non-organic seizure disorder, Paediatric grand round, JRH, Oxford. Dec 2009
Training for examiners for OSCE, Oxford Dec 2011
Advance Paediatric EEG Workshop (5 day), Birmingham, Oct 2011

Paediatric Neurology master classes, Bristol Sep 2011

Course: Quality and Safety in patient management, NESC course centre, Oxford Sep 2011