Clinical aspects of neuroregression: our experience on batten disease

Yazar: Kamate, Mahesh
Baskı/Yayın Bilgisi 2014

Cysts in White Matter: A Novel Neuroimaging Finding in Infantile GM1 Gangliosidosis

Yazar: Kamate, Mahesh
Yayımlandı Ann Indian Acad Neurol (2018)

Acute Leukoencephalopathy with Restricted Diffusion

Yazar: Kamate, Mahesh
Yayımlandı Indian J Crit Care Med (2018)

Clinico-Investigative Profile of Hereditary Spastic Paraplegia in Children

Yazar: Kamate, Mahesh, Detroja, Mayank
Yayımlandı Ann Indian Acad Neurol (2019)

Isolated and Asymmetric Basal Ganglia Involvement in Early Subacute Sclerosing Panencephalitis

Yazar: Kamate, Mahesh, Detroja, Mayank
Yayımlandı Ann Indian Acad Neurol (2019)

A case of hereditary sensory autonomic neuropathy type IV

Yazar: Prashanth, G. P., Kamate, Mahesh
Baskı/Yayın Bilgisi 2012

Safety of lacosamide in children with refractory partial epilepsy

Yazar: Pasha, Ismail, Kamate, Mahesh, Suresh, D.K.
Yayımlandı Saudi Pharm J (2015)

Giant axonal neuropathy: a rare inherited neuropathy with simple clinical clues

Yazar: Kamate, Mahesh, Ramakrishna, Shashikala, Kambali, Shweta, Mahadevan, Anita
Baskı/Yayın Bilgisi 2014

Fructose-1,6-diphosphatase deficiency: a treatable neurometabolic disorder

Yazar: Kamate, Mahesh, Jambagi, Milind, Gowda, Prashanth, Sonoli, Smita
Baskı/Yayın Bilgisi 2014

Acute encephalopathy: A novel presentation of mineralizing microangiopathy of childhood

Yazar: Kamate, Mahesh, Malhotra, Mukul, Gangamma, DH, Hattiholi, Virupaxi
Yayımlandı Ann Indian Acad Neurol (2016)

Neuronal Ceroid Lipofuscinoses in Children

Yazar: Kamate, Mahesh, Reddy, Narendranadha, Detroja, Mayank, Hattiholi, Virupaxi
Yayımlandı Ann Indian Acad Neurol (2021)

Do All Children With Autoimmune Encephalitis Need Aggressive Immunotherapy?

Yazar: Kamate, Mahesh, Ritesh, B. R., Garg, Divyani, Sharma, Suvasini
Yayımlandı Indian Pediatr (2020)

Central nervous system inflammatory demyelinating disorders of childhood

Yazar: Kamate, Mahesh, Chetal, Vivek, Tonape, Venkatesh, Mahantshetti, Niranjana, Hattiholi, Virupaxi
Baskı/Yayın Bilgisi 2010

Authors’ reply

Yazar: Kamate, Mahesh, Chetal, Vivek, Tonape, Venkatesh, Mahantshetti, Niranjana, Hattiholi, Virupaxi
Baskı/Yayın Bilgisi 2011

Glutaric aciduria type I: A treatable neurometabolic disorder

Yazar: Kamate, Mahesh, Patil, Vishwanath, Chetal, Vivek, Darak, Pavan, Hattiholi, Virupaxi
Baskı/Yayın Bilgisi 2012

A Low-Excretor Biochemical Phenotype of Glutaric Aciduria Type I: Identification of Novel Mutations in the Glutaryl CoA Dehydrogenase Gene and Review of Literature from India

Yazar: Shaik, Muntaj, Kamate, Mahesh, Kruthika-Vinod, T.P., Vedamurthy, Anakala Basappa
Yayımlandı Ann Indian Acad Neurol (2020)

Single Lysis‐Salting Out Method of Genomic DNA Extraction From Dried Blood Spots

Yazar: Shaik, Muntaj, Shivanna, Devaraju Kuramkote, Kamate, Mahesh, AB, Vedamurthy, TP, Kruthika‐Vinod
Yayımlandı J Clin Lab Anal (2016)

Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India

Yazar: Sheth, Jayesh, Mistri, Mehul, Mahadevan, Lakshmi, Mehta, Sanjeev, Solanki, Dhaval, Kamate, Mahesh, Sheth, Frenny
Yayımlandı BMC Med Genet (2018)

Protein structure prediction for novel mutations in Arylsulfatase-A gene

Yazar: Divya, M, Jain, S Jamal Md Nurul, Phadke, SR, Kishore, Ratna, Kamate, Mahesh, Gupta, Neerja, Dalal, Ashwin
Baskı/Yayın Bilgisi 2014

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

Yazar: Sheth, Jayesh, Mistri, Mehul, Datar, Chaitanya, Kalane, Umesh, Patil, Shekhar, Kamate, Mahesh, Shah, Harshuti, Nampoothiri, Sheela, Gupta, Sarita, Sheth, Frenny
Yayımlandı Mol Genet Metab Rep (2014)