Glutaric aciduria type-I: A potentially treatable and easily diagnosable neurometabolic disorder by Mahesh Kamate

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

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Clinico-investigative profile of hereditary spastic paraplegia in children by Mahesh Kamate, Mayank Detroja

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Isolated and asymmetric basal ganglia involvement in early subacute sclerosing panencephalitis by Mahesh Kamate, Mayank Detroja

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A case of hereditary sensory autonomic neuropathy type IV by G P Prashanth, Mahesh Kamate

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Rubinstein Taybi syndrome: Broad thumbs - Hallux syndrome by Mahesh Kamate, N S Mahantshetti, Anshul Mehra

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Attention-deficit hyperactivity disorder in children with idiopathic epilepsy: A cross-sectional study by Joel Philip, Nanasaheb M Patil, Mahesh Kamate

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KCNQ2 encephalopathy and effect of early treatment on the clinical phenotype by Mahesh Kamate, Anuraag N Reddy, Mayank Detroja

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Cerebral visual impairment and effect of phase-wise stimulation strategies—An interim analysis by K S Smitha, Bhagyajyothi Kurbet, Mahesh Kamate, Samvedya Veenish

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Neuronal ceroid lipofuscinoses in children by Mahesh Kamate, Narendranadha Reddy, Mayank Detroja, Virupaxi Hattiholi

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Acute encephalopathy: A novel presentation of mineralizing microangiopathy of childhood by Mahesh Kamate, Mukul Malhotra, D H Gangamma, Virupaxi Hattiholi

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Cardiofaciocutaneous syndrome by Ranjan Modi, Pournima Patil, Veerappa A Kothiwale, Mahesh Kamate

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Iron and zinc deficiency in children with febrile convulsions aged 6‒60 months ‒ A 1-year hospital-based case‒control study by Jyothirmai Mallela, Tanmaya Metgud, Mahesh Kamate, Deepti M Kadeangadi

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Authors′ reply by Mahesh Kamate, Vivek Chetal, Venkatesh Tonape, Niranjana Mahantshetti, Virupaxi Hattiholi

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Glutaric aciduria type I: A treatable neurometabolic disorder by Mahesh Kamate, Vishwanath Patil, Vivek Chetal, Pavan Darak, Virupaxi Hattiholi

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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 by Muntaj Shaik, Mahesh Kamate, T P Kruthika-Vinod, Anakala Basappa Vedamurthy

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Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease by Jayesh Sheth, Mehul Mistri, Chaitanya Datar, Umesh Kalane, Shekhar Patil, Mahesh Kamate, Harshuti Shah, Sheela Nampoothiri, Sarita Gupta, Frenny Sheth

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Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patients by Jayesh Sheth, Mehul Mistri, Riddhi Bhavsar, Dhairya Pancholi, Mahesh Kamate, Neerja Gupta, Madhulika Kabra, Sanjiv Mehta, Sheela Nampoothiri, Arpita Thakker, Vivek Jain, Raju Shah, Frenny Sheth

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Effect of Maternal Docosahexaenoic Acid (DHA) Supplementation on Offspring Neurodevelopment at 12 Months in India: A Randomized Controlled Trial by Shweta Khandelwal, Dimple Kondal, Monica Chaudhry, Kamal Patil, Mallaiah Kenchaveeraiah Swamy, Deepa Metgud, Sandesh Jogalekar, Mahesh Kamate, Gauri Divan, Ruby Gupta, Dorairaj Prabhakaran, Nikhil Tandon, Usha Ramakrishnan, Aryeh D. Stein

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The impact of DocosaHexaenoic Acid supplementation during pregnancy and lactation on Neurodevelopment of the offspring in India (DHANI): trial protocol by Shweta Khandelwal, M. K. Swamy, Kamal Patil, Dimple Kondal, Monica Chaudhry, Ruby Gupta, Gauri Divan, Mahesh Kamate, Lakshmy Ramakrishnan, Mrutyunjaya B. Bellad, Anita Gan, Bhalchandra S. Kodkany, Reynaldo Martorell, K. Srinath Reddy, Dorairaj Prabhakaran, Usha Ramakrishnan, Nikhil Tandon, Aryeh D. Stein

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