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Sheffali Gulati

Showing results (261-270 of 368) with videos related to

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Neurology India|September 9, 2022
X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in ChildrenMadhu Rajeshwari, Neena Dhiman, Biswaroop Chakrabarty, et al.
Neurology India|March 5, 2024
Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation - An Error of Glycosylation Masquerading as a Congenital MyopathyAakash Mahesan, Gautam Kamila, Richa Tiwari, et al.
Seizure|May 14, 2018
Clinical spectrum of psychogenic non epileptic seizures in children; an observational studyPriyanka Madaan, Sheffali Gulati, Biswaroop Chakrabarty, et al.
American Journal of Medical Genetics. Part A|March 18, 2025
Correlation Between Neuronal Apoptosis Inhibitory Protein (NAIP), SMN2, and SMA Phenotypes: A Tertiary Care Centre Experience From IndiaSoumalya Chakraborty, Amita Singh, Shama Perveen, et al.
Autism : the International Journal of Research and Practice|January 26, 2023
Attention control in autism: Eye-tracking findings from pre-school children in a low- and middle-income country settingGeorgia Lockwood Estrin, Luke Mason, Rashi Arora, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
The National Medical Journal of India|May 13, 2011
Aetiology of global developmental delay in young children: experience from a tertiary care centre in IndiaAnurag Tikaria, Madhulika Kabra, Neerja Gupta, et al.
Neurology India|July 23, 2024
White Matter Mineralization in an Adolescent Girl with Vanishing White Matter DiseasePuneet K Choudhary, Aakash Mahesan, Gautam Kamila, et al.
BMC Pediatrics|April 6, 2018
A novel homozygous mutation in POLR3A gene causing 4H syndrome: a case reportVishal V Tewari, Ritu Mehta, C M Sreedhar, et al.
Muscle & Nerve|December 2, 2017
Prevalence and predictors of peripheral neuropathy in nondiabetic children with chronic kidney diseaseSangeetha Yoganathan, Arvind Bagga, Sheffali Gulati, et al.
Pageof 37

Showing results (261-270 of 368) with videos related to

Sort By:
Pageof 37
Neurology India|September 9, 2022
X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in ChildrenMadhu Rajeshwari, Neena Dhiman, Biswaroop Chakrabarty, et al.
Neurology India|March 5, 2024
Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation - An Error of Glycosylation Masquerading as a Congenital MyopathyAakash Mahesan, Gautam Kamila, Richa Tiwari, et al.
Seizure|May 14, 2018
Clinical spectrum of psychogenic non epileptic seizures in children; an observational studyPriyanka Madaan, Sheffali Gulati, Biswaroop Chakrabarty, et al.
American Journal of Medical Genetics. Part A|March 18, 2025
Correlation Between Neuronal Apoptosis Inhibitory Protein (NAIP), SMN2, and SMA Phenotypes: A Tertiary Care Centre Experience From IndiaSoumalya Chakraborty, Amita Singh, Shama Perveen, et al.
Autism : the International Journal of Research and Practice|January 26, 2023
Attention control in autism: Eye-tracking findings from pre-school children in a low- and middle-income country settingGeorgia Lockwood Estrin, Luke Mason, Rashi Arora, et al.
Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.
The National Medical Journal of India|May 13, 2011
Aetiology of global developmental delay in young children: experience from a tertiary care centre in IndiaAnurag Tikaria, Madhulika Kabra, Neerja Gupta, et al.
Neurology India|July 23, 2024
White Matter Mineralization in an Adolescent Girl with Vanishing White Matter DiseasePuneet K Choudhary, Aakash Mahesan, Gautam Kamila, et al.
BMC Pediatrics|April 6, 2018
A novel homozygous mutation in POLR3A gene causing 4H syndrome: a case reportVishal V Tewari, Ritu Mehta, C M Sreedhar, et al.
Muscle & Nerve|December 2, 2017
Prevalence and predictors of peripheral neuropathy in nondiabetic children with chronic kidney diseaseSangeetha Yoganathan, Arvind Bagga, Sheffali Gulati, et al.
Pageof 37