Sushil Razdan - Publications

Effectiveness and safety of clobazam as add-on therapy in children after the failure of first antiseizure medicine: a sub-analysis of the ADD-ON study.

Journal: Epilepsy & behavior : E&B

Published: June 06, 2025

Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, India.

Journal: Scientific reports

Published: May 18, 2022

Evaluation of one-year effectiveness of clobazam as an add-on therapy to anticonvulsant monotherapy in participants with epilepsy having uncontrolled seizure episodes: An Indian experience.

Journal: Epilepsy & behavior : E&B

Published: December 09, 2021

Finding the Hidden-cerebellopontine Angle Neurocysticercosis.

Journal: The Journal of the Association of Physicians of India

Published: April 03, 2019

A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications.

Journal: Mitochondrion

Published: January 08, 2018

LoCa LoPa myelopathy: is prevention better than cure?

Journal: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases

Published: July 26, 2017

A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - India.

Journal: Scientific reports

Published: January 09, 2017

Celiac Neuropathy: A Case Report from Kashmir (India).

Journal: The Journal of the Association of Physicians of India

Published: November 03, 2016

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.

Journal: Scientific reports

Published: January 12, 2016

"Peripheral neuropathy crippling bronchial asthma": two rare case reports of churg-strauss syndrome.

Journal: Case reports in pulmonology

Published: June 23, 2014

"Excess gooD can be Dangerous". A case series of iatrogenic symptomatic hypercalcemia due to hypervitaminosis D.

Journal: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases

Published: October 23, 2012

Inbreeding as a cause for deafness: Dadhkai study.

Journal: Indian journal of human genetics

Published: July 04, 2012