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Sunita Bijarnia

Showing results (1-10 of 79) with videos related to

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Indian Journal of Pediatrics|June 10, 2003
Triple A syndrome--diagnostic and management issuesSunita Bijarnia, I C Verma
Indian Pediatrics|October 23, 2019
Testing Modalities for Inborn Errors of Metabolism - What a Clinician Needs to Know?Sunita Bijarnia-Mahay, Seema Kapoor
Indian Journal of Pediatrics|March 29, 2003
Genetic counseling in acrocallosal syndromeSunita Bijarnia, Ashok Baijal, I C Verma
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
Journal of Inherited Metabolic Disease|February 19, 2011
Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second testSunita Bijarnia, Bridget Wilcken, Veronica C Wiley
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
Indian Journal of Pediatrics|January 5, 2005
Gerodermia OsteodysplasticaRitu Paul, Seema Kapoor, Ratna Puri, et al.
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.
Pageof 8

Showing results (1-10 of 79) with videos related to

Sort By:
Pageof 8
Indian Journal of Pediatrics|June 10, 2003
Triple A syndrome--diagnostic and management issuesSunita Bijarnia, I C Verma
Indian Pediatrics|October 23, 2019
Testing Modalities for Inborn Errors of Metabolism - What a Clinician Needs to Know?Sunita Bijarnia-Mahay, Seema Kapoor
Indian Journal of Pediatrics|March 29, 2003
Genetic counseling in acrocallosal syndromeSunita Bijarnia, Ashok Baijal, I C Verma
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
Journal of Inherited Metabolic Disease|February 19, 2011
Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second testSunita Bijarnia, Bridget Wilcken, Veronica C Wiley
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
Indian Journal of Pediatrics|January 5, 2005
Gerodermia OsteodysplasticaRitu Paul, Seema Kapoor, Ratna Puri, et al.
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.
Pageof 8