Clinical aspects of neuroregression: our experience on batten disease

by Kamate, Mahesh
Published 2014

A case of hereditary sensory autonomic neuropathy type IV

by Prashanth, G. P., Kamate, Mahesh
Published 2012

Authors’ reply

by Kamate, Mahesh, Chetal, Vivek, Tonape, Venkatesh, Mahantshetti, Niranjana, Hattiholi, Virupaxi
Published 2011

Glutaric aciduria type I: A treatable neurometabolic disorder

by Kamate, Mahesh, Patil, Vishwanath, Chetal, Vivek, Darak, Pavan, Hattiholi, Virupaxi
Published 2012

Acute encephalopathy: A novel presentation of mineralizing microangiopathy of childhood

by Kamate, Mahesh, Malhotra, Mukul, Gangamma, DH, Hattiholi, Virupaxi
Published 2016

Protein structure prediction for novel mutations in Arylsulfatase-A gene

by Divya, M, Jain, S Jamal Md Nurul, Phadke, SR, Kishore, Ratna, Kamate, Mahesh, Gupta, Neerja, Dalal, Ashwin
Published 2014

Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease

by Sheth, Jayesh, Mistri, Mehul, Datar, Chaitanya, Kalane, Umesh, Patil, Shekhar, Kamate, Mahesh, Shah, Harshuti, Nampoothiri, Sheela, Gupta, Sarita, Sheth, Frenny
Published 2014

Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing

by Kumar, Kishore R, Wali, G.M., Kamate, Mahesh, Wali, Gautam, Minoche, André E, Puttick, Clare, Pinese, Mark, Gayevskiy, Velimir, Dinger, Marcel E, Roscioli, Tony, Sue, Carolyn M., Cowley, Mark J
Published 2016