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Neurology India|November 6, 2023
Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian CohortMadhu Nagappa, Shivani Sharma, Periyasamy Govindaraj, et al.
Muscle & Nerve|September 17, 2020
Ganglioside complex antibodies in an Indian cohort of Guillain-Barré syndromeRahul Wahatule, Debprasad Dutta, Monojit Debnath, et al.
Plos One|May 7, 2019
Genetic analysis of ATP7B in 102 south Indian families with Wilson diseaseNivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah, et al.
Neurology India|March 16, 2018
Sarcoidosis with primary neurological involvementE Ratnavalli, D Nagaraja, V Santosh, et al.
Brain & Development|November 23, 2013
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutationsKothari Sonam, Nahid Akthar Khan, Parayil Sankaran Bindu, et al.
Clinical Neurology and Neurosurgery|July 1, 2016
Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndromeV P Vandana, Parayil Sankaran Bindu, Kothari Sonam, et al.
Metabolic Brain Disease|June 17, 2016
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1Shwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa, et al.
Mitochondrion|August 22, 2021
Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disordersAkshata Huddar, Periyasamy Govindaraj, Shwetha Chiplunkar, et al.
Annals of Indian Academy of Neurology|March 7, 2015
Ictal Generalized EEG Attenuation (IGEA) and hypopnea in a child with occipital type 1 cortical dysplasia - Is it a biomarker for SUDEP?Ganne Chaitanya, N Subbareddy Santosh, Jayabal Velmurugan, et al.
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