S. Mehta

Clinical and molecular characterization of patients with gross hypotonia and impaired lower motor neuron function

F. Sheth, J. Sheth, H. Patel, 2013, Indian Pediatrics.

Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patients

M. Kabra, S. Nampoothiri, N. Gupta, 2018, BMC Neurology.

Splenomegaly, Cardiomegaly, and Osteoporosis in a Child with Gaucher Disease

J. Sheth, M. Mistri, N. Nanavaty, 2011, Case reports in pediatrics.

Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test

F. Sheth, J. Sheth, H. Sheth, 2023, BMC Neurology.

Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India

K. Srivastava, A. Saini, R. Suthar, 2023, Epilepsia open.