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Sunita Bijarnia-Mahay

Showing results (1-10 of 63) with videos related to

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Indian Pediatrics|October 23, 2019
Testing Modalities for Inborn Errors of Metabolism - What a Clinician Needs to Know?Sunita Bijarnia-Mahay, Seema Kapoor
JIMD Reports|May 13, 2020
Tyrosine hydroxylase deficiency-Clinical insights and a novel deletion in <i>TH</i> gene in an Indian patientSunita Bijarnia-Mahay, Vivek Jain, Beat Thöny
Methods in Molecular Biology (Clifton, N.J.)|May 1, 2017
Prenatal Diagnosis of Lysosomal Storage Disorders Using Chorionic VilliJyotsna Verma, Sunita Bijarnia-Mahay, Ishwar C Verma
Molecular Syndromology|January 29, 2021
Eyes See what the Mind Knows: Clues to Pattern Recognition in Single Enzyme Deficiency-Related Peroxisomal DisordersVeronica Arora, Sunita Bijarnia-Mahay, Sudhisha Dubey, et al.
Journal of Human Reproductive Sciences|April 26, 2024
Decoding the Genetics of Recurrent Molar PregnancySumita Mehta, Sunita Bijarnia Mahay, Abhishek Satapathy, et al.
Indian Pediatrics|August 18, 2014
Mitochondrial DNA depletion syndrome causing liver failureSunita Bijarnia-Mahay, Neelam Mohan, Deepak Goyal, et al.
Indian Journal of Pediatrics|December 9, 2014
Newborn screening: need of the hour in IndiaIshwar C Verma, Sunita Bijarnia-Mahay, Geetu Jhingan, et al.
Neurology India|December 21, 2020
Familial Prion Disease: First Indian Kindred with Gerstmann-Sträussler-Scheinker SyndromeSameer Bhatia, Sunita Bijarnia-Mahay, Sudisha Dubey, et al.
American Journal of Medical Genetics. Part A|March 5, 2020
Expanding the phenotypic and genotypic spectrum of Wiedemann-Steiner syndrome: First patient from IndiaVeronica Arora, Ratna D Puri, Sunita Bijarnia-Mahay, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase DeficiencyVinu Narayan, Sunita Bijarnia Mahay, Ishwar Chander Verma, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Indian Pediatrics|October 23, 2019
Testing Modalities for Inborn Errors of Metabolism - What a Clinician Needs to Know?Sunita Bijarnia-Mahay, Seema Kapoor
JIMD Reports|May 13, 2020
Tyrosine hydroxylase deficiency-Clinical insights and a novel deletion in <i>TH</i> gene in an Indian patientSunita Bijarnia-Mahay, Vivek Jain, Beat Thöny
Methods in Molecular Biology (Clifton, N.J.)|May 1, 2017
Prenatal Diagnosis of Lysosomal Storage Disorders Using Chorionic VilliJyotsna Verma, Sunita Bijarnia-Mahay, Ishwar C Verma
Molecular Syndromology|January 29, 2021
Eyes See what the Mind Knows: Clues to Pattern Recognition in Single Enzyme Deficiency-Related Peroxisomal DisordersVeronica Arora, Sunita Bijarnia-Mahay, Sudhisha Dubey, et al.
Journal of Human Reproductive Sciences|April 26, 2024
Decoding the Genetics of Recurrent Molar PregnancySumita Mehta, Sunita Bijarnia Mahay, Abhishek Satapathy, et al.
Indian Pediatrics|August 18, 2014
Mitochondrial DNA depletion syndrome causing liver failureSunita Bijarnia-Mahay, Neelam Mohan, Deepak Goyal, et al.
Indian Journal of Pediatrics|December 9, 2014
Newborn screening: need of the hour in IndiaIshwar C Verma, Sunita Bijarnia-Mahay, Geetu Jhingan, et al.
Neurology India|December 21, 2020
Familial Prion Disease: First Indian Kindred with Gerstmann-Sträussler-Scheinker SyndromeSameer Bhatia, Sunita Bijarnia-Mahay, Sudisha Dubey, et al.
American Journal of Medical Genetics. Part A|March 5, 2020
Expanding the phenotypic and genotypic spectrum of Wiedemann-Steiner syndrome: First patient from IndiaVeronica Arora, Ratna D Puri, Sunita Bijarnia-Mahay, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase DeficiencyVinu Narayan, Sunita Bijarnia Mahay, Ishwar Chander Verma, et al.
Pageof 7