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Kuntal Sen

Showing results (1-10 of 31) with videos related to

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BMJ Case Reports|April 7, 2018
More than meets the eye: infant presenting with hypoxic ischaemic encephalopathyKuntal Sen, Rajkumar Agarwal
Journal of Neurology|July 6, 2020
Bi-allelic variants in PNPLA6 possibly associated with Parkinsonian features in addition to spastic paraplegia phenotypeKuntal Sen, Melesilika Finau, Pritha Ghosh
International Journal of Neonatal Screening|November 29, 2021
Select Ethical Aspects of Next-Generation Sequencing Tests for Newborn Screening and Diagnostic Evaluation of Critically Ill NewbornsKuntal Sen, Jennifer Harmon, Andrea L Gropman
The Yale Journal of Biology and Medicine|December 31, 2021
Neuromonitoring in Rare Disorders of MetabolismCarlos Castillo-Pinto, Kuntal Sen, Andrea Gropman
Journal of Pediatric Genetics|February 8, 2021
Expanding Role of Proton Magnetic Resonance Spectroscopy: Timely Diagnosis and Treatment Initiation in Partial Ornithine Transcarbamylase DeficiencyKuntal Sen, Carlos Castillo Pinto, Andrea L Gropman
Neuropediatrics|November 26, 2019
Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) DeficiencyBrian Pfeiffer, Kuntal Sen, Shagun Kaur, et al.
Neuropediatrics|May 26, 2022
Haploinsufficiency of PRRT2 Leading to Familial Hemiplegic Migraine in Chromosome 16p11.2 Deletion SyndromeKuntal Sen, Ilyse Genser, Marc DiFazio, et al.
Translational Science of Rare Diseases|December 21, 2020
Multimodal imaging in urea cycle-related neurological disease - What can imaging after hyperammonemia teach us?Kuntal Sen, Matthew T Whitehead, Andrea L Gropman
Neurology India|December 21, 2019
Differential DNA Methylation Patterns in Patients with Epilepsy due to Malformations of Cortical Development: A Pilot StudyKuntal Sen, Rupali Gadkari, Rajkumar Agarwal, et al.
Pediatric Neurology|June 1, 2025
A National Survey on the Neurogenetics Workforce: Practice Models, Evolving Challenges, and Future DirectionsAlexa Taylor, Rebecca J Levy, Radhika Dhamija, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
BMJ Case Reports|April 7, 2018
More than meets the eye: infant presenting with hypoxic ischaemic encephalopathyKuntal Sen, Rajkumar Agarwal
Journal of Neurology|July 6, 2020
Bi-allelic variants in PNPLA6 possibly associated with Parkinsonian features in addition to spastic paraplegia phenotypeKuntal Sen, Melesilika Finau, Pritha Ghosh
International Journal of Neonatal Screening|November 29, 2021
Select Ethical Aspects of Next-Generation Sequencing Tests for Newborn Screening and Diagnostic Evaluation of Critically Ill NewbornsKuntal Sen, Jennifer Harmon, Andrea L Gropman
The Yale Journal of Biology and Medicine|December 31, 2021
Neuromonitoring in Rare Disorders of MetabolismCarlos Castillo-Pinto, Kuntal Sen, Andrea Gropman
Journal of Pediatric Genetics|February 8, 2021
Expanding Role of Proton Magnetic Resonance Spectroscopy: Timely Diagnosis and Treatment Initiation in Partial Ornithine Transcarbamylase DeficiencyKuntal Sen, Carlos Castillo Pinto, Andrea L Gropman
Neuropediatrics|November 26, 2019
Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) DeficiencyBrian Pfeiffer, Kuntal Sen, Shagun Kaur, et al.
Neuropediatrics|May 26, 2022
Haploinsufficiency of PRRT2 Leading to Familial Hemiplegic Migraine in Chromosome 16p11.2 Deletion SyndromeKuntal Sen, Ilyse Genser, Marc DiFazio, et al.
Translational Science of Rare Diseases|December 21, 2020
Multimodal imaging in urea cycle-related neurological disease - What can imaging after hyperammonemia teach us?Kuntal Sen, Matthew T Whitehead, Andrea L Gropman
Neurology India|December 21, 2019
Differential DNA Methylation Patterns in Patients with Epilepsy due to Malformations of Cortical Development: A Pilot StudyKuntal Sen, Rupali Gadkari, Rajkumar Agarwal, et al.
Pediatric Neurology|June 1, 2025
A National Survey on the Neurogenetics Workforce: Practice Models, Evolving Challenges, and Future DirectionsAlexa Taylor, Rebecca J Levy, Radhika Dhamija, et al.
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