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Journal of Pediatric Genetics|May 9, 2024
Charcot-Marie-Tooth Disease Type 4C and Autosomal Dominant Heterozygous Ichthyosis Vulgaris, with Bilateral Hearing Loss: A Novel Association with Review of LiteratureMonika Chhajed, Pradeep Kumar Gunasekaran, Singanamalla Bhanudeep, et al.
Asian Journal of Psychiatry|May 2, 2022
Isolated psychiatric presentation of cobalamin C type disorder with novel mutation in middle childhood: A case reportMonika Chhajed, Pradeep Kumar Gunasekaran, Lokesh Saini, et al.
Neurology|January 4, 2024
Teaching NeuroImage: Neuroimaging Features of Wilson DiseasePradeep Kumar Gunasekaran, Sarbesh Tiwari, Ashna Kumar, et al.
Journal of Tropical Pediatrics|July 22, 2022
Lyme Neuroborreliosis with Intracranial Hypertension and Erythema Multiforme: A Rare PresentationMonika Chhajed, Amit Jain, Pradeep Kumar Gunasekaran, et al.
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association|May 1, 2023
Predictors of Risk for Cerebral Palsy: A ReviewTanochni Mohanty, Sibi Daniel Joseph, Pradeep Kumar Gunasekaran, et al.
Journal of Tropical Pediatrics|April 5, 2024
Familial hemiplegic migraine in Indian children-a tertiary center experienceLokesh Saini, Pradeep Kumar Gunasekaran, Sarbesh Tiwari, et al.
Tropical Doctor|July 27, 2022
Cutaneous and ocular manifestations in Indian children with neurocutaneous syndromes: A cross-sectional studySwetlana Mukherjee, Pradeep Kumar Gunasekaran, Lokesh Saini, et al.
Pediatric Neurology|January 18, 2023
Paroxysmal Neuropathic Pruritus in Patients With Chiari Malformation Type I: A Rare PhenotypeLokesh Saini, Pradeep Kumar Gunasekaran, Sarbesh Tiwari, et al.
Pediatric Neurology|January 4, 2024
Primary Diffuse Leptomeningeal Melanomatosis in an Indian Child With Review of LiteratureAshna Kumar, Pradeep Kumar Gunasekaran, Divya Aggarwal, et al.
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