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Neurology India|March 10, 2015
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapyPuneet Jain, Shivaram Shastri, Sheffali Gulati, et al.Fetal Diagnosis and Therapy|July 31, 2026
Posterior Fossa Anomalies: A Detailed Review of Prenatal Findings and Management from a tertiary care centreTanisha Gupta, K Aparna Sharma, Vatsla Dadhwal, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 6, 2011
Molecular analysis of ABCD1 gene in Indian patients with X-linked adrenoleukodystrophyPallavi Shukla, Neerja Gupta, Sheffali Gulati, et al.Pediatric Neurology|January 3, 2021
Association of Sleep Apnea With Development and Behavior in Down Syndrome: A Prospective Clinical and Polysomnographic StudyVaishakh Anand, Garima Shukla, Neerja Gupta, et al.Indian Journal of Pediatrics|July 14, 2012
Prevalence of celiac disease in Indian children with Down syndrome and its clinical and laboratory predictorsAbdus Sami Bhat, Mona K Chaturvedi, Savita Saini, et al.BMC Medical Genetics|October 28, 2019
Decoding of novel missense TSC2 gene variants using in-silico methodsShruthi Sudarshan, Manoj Kumar, Punit Kaur, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 16, 2021
Spectrum of Movement Disorders of Late-Onset Niemann-Pick Disease Type CJasmine Parihar, Deepa Dash, Bhawana Aggarwal, et al.Birth Defects Research|December 13, 2023
Minimally invasive autopsy in the evaluation of fetal malformations and stillbirths: A feasibility studyNeerja Gupta, Nitika Langeh, Aparna Sharma, et al.JIMD Reports|January 18, 2015
Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from IndiaSunita Bijarnia-Mahay, Sireesha Movva, Neerja Gupta, et al.Bone|May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.Pageof 20