About Doctor
Royal College of Phycians and Surgeons, Glasgow UK
Testimonials
The Testimonials provided by Dr Swayam Prakash
CURRENT AFFILIATION
Director Neurology, Balaji Healthcare, Siliguri, India
Sr. Consultant-Neurology, KINS HEALTH, Siliguri, India
Founder Director, Ang Centre of Neurosciences, Bhagalpur, India
RESEARCH INTERESTS
My research interests are exploring Autoimmune Neurological Disorders involving various neuraxis with a special focus on cognitive and behavioral manifestations and their early and effective management.
CURRENT STATUS
Citizen of India.
EDUCATION
Fellow-Indian College of Physicians, India
FICP (India) 2023
Fellow-Royal College of Physicians, London, UK
FRCP (London) 2021
Fellow-Royal College of Physicians and Surgeons, Glasgow UK
FRCP (Glasg) February 2020
UEMS – EBN Europe
Fellow- European Board of Neurology June 2019
Federation of Royal Colleges of Physicians – UK (RCP-UK) the United Kingdom
& Association of British Neurologists
SCE – Neurology June 2018
Sawai Man Singh Medical College and Hospital (SMSMCH) Jaipur, India
D.M. (Neurology) July 2014
Patna Medical College and Hospital (PMCH) Patna, India
M.D. (Medicine) Nov 2006
Jawaharlal Nehru Medical College and Hospital (JLNMCH) Bhagalpur, India
MBBS Dec 1998
Dr. Swayam's Publications
Nagapal K, Sharma B, Prakash S, Panagariva A. GFPT1 gene related congenital myasthenic syndrome: A treatable disorder mimicking limb girdle muscular dystrophy.
Nagpal K, Prakash S. Artificial Intelligence and Medical Ethics: Unresolved Issues. Austin J Surg – Volume 7 Issue 1 – 2020
Need a Neurologist for Check-up?
JUST MAKE AN APPOINTMENT & YOU'RE DONE!
Scanning of Brain
Brain scans offer a way for your neurologist to “see inside” your skull without having to do surgery. As a diagnostic and monitoring tool, a brain scan can be an invaluable part of your doctor’s treatment process.
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Migraine & Headache
Publications
1. Nagapal K, Sharma B, Prakash S, Panagariva A. GFPT1 gene related congenital myasthenic syndrome: A
treatable disorder mimicking limb girdle muscular dystrophy. Neurol Neurol Sci Open Access. 2020; 3(1): 1012.