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Vrajesh Udani

Showing results (31-40 of 51) with videos related to

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Journal of Clinical Laboratory Analysis|February 13, 2013
Mutational analysis of methyl-CpG binding protein 2 (MECP2) gene in Indian cases of Rett syndromeDhanjit Kumar Das, Vrajesh Udani, Daksha Sanghavi, et al.
Gene|December 25, 2012
Spectrum of MECP2 gene mutations in a cohort of Indian patients with Rett syndrome: report of two novel mutationsDhanjit Kumar Das, Sarbani Raha, Daksha Sanghavi, et al.
Neurology India|September 9, 2022
Correlation of Preoperative Functional Magnetic Resonance Imaging (fMRI) with Intraoperative Cortical Stimulation in Surgeries of Eloquent Brain LesionsPawan Chawla, Basant K Misra, Vrajesh Udani, et al.
Disability and Rehabilitation. Assistive Technology|August 14, 2020
Mobile media exposure and use in children aged zero to five years with diagnosed neurodevelopmental disabilityFranzina Coutinho, Gauri Saxena, Akansha Shah, et al.
Neuromolecular Medicine|December 18, 2012
Novel mutations in cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndromeDhanjit Kumar Das, Bhakti Mehta, Shyla R Menon, et al.
Indian Pediatrics|April 4, 2017
Consensus Statement of the Indian Academy of Pediatrics on Evaluation and Management of Autism Spectrum Disorder, Samir Dalwai, Shabina Ahmed, et al.
Movement Disorders Clinical Practice|May 8, 2019
Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related diseaseBettina Balint, Christopher D Stephen, Vrajesh Udani, et al.
Research in Developmental Disabilities|July 3, 2013
Prenatal, perinatal and neonatal risk factors of Autism Spectrum Disorder: a comprehensive epidemiological assessment from IndiaMadhu Poornima Mamidala, Anupama Polinedi, Praveen Kumar P T V, et al.
Journal of Biosciences|December 4, 2013
Maternal hormonal interventions as a risk factor for Autism Spectrum Disorder: an epidemiological assessment from IndiaMadhu Poornima Mamidala, Anupama Polinedi, P T V Praveen Kumar, et al.
Clinical Genetics|December 5, 2024
Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological DisorderPeriyasamy Radhakrishnan, Neha Quadri, Florian Erger, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Journal of Clinical Laboratory Analysis|February 13, 2013
Mutational analysis of methyl-CpG binding protein 2 (MECP2) gene in Indian cases of Rett syndromeDhanjit Kumar Das, Vrajesh Udani, Daksha Sanghavi, et al.
Gene|December 25, 2012
Spectrum of MECP2 gene mutations in a cohort of Indian patients with Rett syndrome: report of two novel mutationsDhanjit Kumar Das, Sarbani Raha, Daksha Sanghavi, et al.
Neurology India|September 9, 2022
Correlation of Preoperative Functional Magnetic Resonance Imaging (fMRI) with Intraoperative Cortical Stimulation in Surgeries of Eloquent Brain LesionsPawan Chawla, Basant K Misra, Vrajesh Udani, et al.
Disability and Rehabilitation. Assistive Technology|August 14, 2020
Mobile media exposure and use in children aged zero to five years with diagnosed neurodevelopmental disabilityFranzina Coutinho, Gauri Saxena, Akansha Shah, et al.
Neuromolecular Medicine|December 18, 2012
Novel mutations in cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndromeDhanjit Kumar Das, Bhakti Mehta, Shyla R Menon, et al.
Indian Pediatrics|April 4, 2017
Consensus Statement of the Indian Academy of Pediatrics on Evaluation and Management of Autism Spectrum Disorder, Samir Dalwai, Shabina Ahmed, et al.
Movement Disorders Clinical Practice|May 8, 2019
Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related diseaseBettina Balint, Christopher D Stephen, Vrajesh Udani, et al.
Research in Developmental Disabilities|July 3, 2013
Prenatal, perinatal and neonatal risk factors of Autism Spectrum Disorder: a comprehensive epidemiological assessment from IndiaMadhu Poornima Mamidala, Anupama Polinedi, Praveen Kumar P T V, et al.
Journal of Biosciences|December 4, 2013
Maternal hormonal interventions as a risk factor for Autism Spectrum Disorder: an epidemiological assessment from IndiaMadhu Poornima Mamidala, Anupama Polinedi, P T V Praveen Kumar, et al.
Clinical Genetics|December 5, 2024
Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological DisorderPeriyasamy Radhakrishnan, Neha Quadri, Florian Erger, et al.
Pageof 6