Items where Author is "Sinha, Sanjib"

Article

Karan, Kalpita R. ; Satishchandra, Parthasarthy ; Sinha, Sanjib ; Anand, Anuranjan (2018) A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23 Journal of Genetics, 97 (2). pp. 391-398. ISSN 0022-1333

Raju, Praveen K ; Satishchandra, Parthasarathy ; Nayak, Sourav ; Iyer, Vishwanathan ; Sinha, Sanjib ; Anand, Anuranjan (2017) Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy Human Mutation, 38 (7). pp. 816-826. ISSN 10597794

Karan, Kalpita Rashimi ; Satishchandra, P. ; Sinha, Sanjib ; Anand, Anuranjan (2017) Rare SLC1A1 variants in hot water epilepsy Human Genetics, 136 (6). pp. 693-703. ISSN 0340-6717

Sonam, Kothari ; Bindu, Parayil Sankaran ; Srinivas Bharath, M. M. ; Govindaraj, Periyasamy ; Gayathri, Narayanappa ; Arvinda, Hanumanthapura R. ; Chiplunkar, Shwetha ; Nagappa, Madhu ; Sinha, Sanjib ; Khan, Nahid Akhtar ; Nunia, Vandana ; Paramasivam, Arumugam ; Thangaraj, Kumarasamy ; Taly, Arun B. (2017) Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India Mitochondrion, 32 . pp. 42-49. ISSN 1567-7249

Vandana, V. P. ; Bindu, Parayil Sankaran ; Sonam, Kothari ; Govindaraj, Periyasamy ; Taly, Arun B. ; Gayathri, Narayanappa ; Chiplunkar, Shwetha ; Govindaraju, Chikkanna ; Arvinda, H.R. ; Nagappa, Madhu ; Sinha, Sanjib ; Thangaraj, Kumarasamy (2016) Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome Clinical Neurology and Neurosurgery, 148 . pp. 17-21. ISSN 0303-8467

Bindu, Parayil Sankaran ; Govindaraju, Chikanna ; Sonam, Kothari ; Nagappa, Madhu ; Chiplunkar, Shwetha ; Kumar, Rakesh ; Gayathri, Narayanappa ; Bharath, MM Srinivas ; Arvinda, Hanumanthapura R. ; Sinha, Sanjib ; Khan, Nahid Akthar ; Govindaraj, Periyasamy ; Nunia, Vandana ; Paramasivam, Arumugam ; Thangaraj, Kumarasamy ; Taly, Arun B. (2016) Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: a study from South India Mitochondrion, 27 . pp. 1-5. ISSN 1567-7249

Bindu, Parayil Sankaran ; Arvinda, Hanumanthapura ; Taly, Arun B. ; Govindaraju, Chikanna ; Sonam, Kothari ; Chiplunkar, Shwetha ; Kumar, Rakesh ; Gayathri, Narayanappa ; Bharath M. M/, Srinivas ; Nagappa, Madhu ; Sinha, Sanjib ; Khan, Nahid Akthar ; Govindaraj, Periyasamy ; Nunia, Vandana ; Paramasivam, Arumugam ; Thangaraj, Kumarasamy (2015) Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: a study from south India Mitochondrion, 25 . pp. 6-16. ISSN 1567-7249

Sonam, Kothari ; Bindu, P. S. ; Taly, Arun B. ; Govindaraju, Chikkanna ; Gayathri, Narayanappa ; Arvinda, Hanumanthapura R. ; Nagappa, Madhu ; Sinha, Sanjib ; Khan, Nahid Akthar ; Govindaraj, Periyasamy ; Thangaraj, Kumarasamy (2015) Clinical and neuroimaging features in two children with mutations in the mitochondrial ND5 gene Neuropediatrics, 46 (04). pp. 277-281. ISSN 0174-304X

Sonam, Kothari ; Khan, Nahid Akthar ; Bindu, Parayil Sankaran ; Taly, Arun B. ; Gayathri, N. ; Bharath, M. M. Srinivas ; Govindaraju, C. ; Arvinda, H. R. ; Nagappa, Madhu ; Sinha, Sanjib ; Thangaraj, K. (2014) Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations Brain & Development, 36 (9). pp. 807-812. ISSN 0387-7604

Sonam, Kothari ; Bindu, P. S. ; Gayathri, Narayanappa ; Khan, Nahid Akhtar ; Govindaraju, C. ; Arvinda, Hanumanthapura R. ; Nagappa, Madhu ; Sinha, Sanjib ; Thangaraj, K. ; Taly, Arun B. (2014) The “Double Panda” sign in Leigh disease Journal of Child Neurology, 29 (7). pp. 980-982. ISSN 0883-0738

Sinha, Sanjib ; Mathews, Thomas ; Arunodaya, G. R. ; Siddappa, Nagadenahalli B. ; Ranga, Udaykumar ; Desai, A. ; Ravi, V. ; Taly, A. B. (2004) HIV-1 clade-C-associated "ALS"-like disorder: first report from India Journal of the Neurological Sciences, 224 (1-2). pp. 97-100. ISSN 0022-510X