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Neerja Gupta

Showing results (191-200 of 238) with videos related to

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Indian Pediatrics|January 16, 2020
Newborn Screening and Diagnosis of Infants with Congenital Adrenal HyperplasiaPallavi Vats, Aashima Dabas, Vandana Jain, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7Ramesh Reddy, Elie Akoury, Ngoc Minh Phuong Nguyen, et al.
European Heart Journal. Cardiovascular Imaging|October 20, 2019
Clarifying the anatomy of common arterial trunk: a clinical study of 70 patientsSaurabh Kumar Gupta, Abhinav Aggarwal, Manish Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Prenatal diagnosis in India is not limited to sex selectionAshwin B Dalal, Prajnya Ranganath, Shubha R Phadke, et al.
Indian Journal of Pediatrics|July 5, 2026
Impact of Enzyme Replacement Therapy on Patients with Late Onset Pompe Disease - Real World Data from a Developing CountrySwasti Pal, Sunita Bijarnia-Mahay, Sheela Nampoothiri, et al.
Indian Pediatrics|February 23, 2023
Consensus Statement of the Neurodevelopmental Pediatrics Chapter of Indian Academy of Pediatrics (IAP) on the Management of Children With Down SyndromeShaji Thomas John, Kizhanipurath Gayathri, Shabina Ahmed, et al.
Clinical Genetics|November 6, 2018
Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndromePuneeth H Somashekar, Katta M Girisha, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part A|November 26, 2015
Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathyGandham SriLakshmi Bhavani, Hitesh Shah, Anju Shukla, et al.
Journal of the Neurological Sciences|December 21, 2010
Molecular and structural analysis of metachromatic leukodystrophy patients in Indian populationPallavi Shukla, Suman Vasisht, Ranjana Srivastava, et al.
Indian Journal of Pediatrics|January 27, 2026
Molecular Landscape of Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency in IndiaSudhisha Dubey, Renu Saxena, Sudha Kohli, et al.
Pageof 24

Showing results (191-200 of 238) with videos related to

Sort By:
Pageof 24
Indian Pediatrics|January 16, 2020
Newborn Screening and Diagnosis of Infants with Congenital Adrenal HyperplasiaPallavi Vats, Aashima Dabas, Vandana Jain, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7Ramesh Reddy, Elie Akoury, Ngoc Minh Phuong Nguyen, et al.
European Heart Journal. Cardiovascular Imaging|October 20, 2019
Clarifying the anatomy of common arterial trunk: a clinical study of 70 patientsSaurabh Kumar Gupta, Abhinav Aggarwal, Manish Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Prenatal diagnosis in India is not limited to sex selectionAshwin B Dalal, Prajnya Ranganath, Shubha R Phadke, et al.
Indian Journal of Pediatrics|July 5, 2026
Impact of Enzyme Replacement Therapy on Patients with Late Onset Pompe Disease - Real World Data from a Developing CountrySwasti Pal, Sunita Bijarnia-Mahay, Sheela Nampoothiri, et al.
Indian Pediatrics|February 23, 2023
Consensus Statement of the Neurodevelopmental Pediatrics Chapter of Indian Academy of Pediatrics (IAP) on the Management of Children With Down SyndromeShaji Thomas John, Kizhanipurath Gayathri, Shabina Ahmed, et al.
Clinical Genetics|November 6, 2018
Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndromePuneeth H Somashekar, Katta M Girisha, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part A|November 26, 2015
Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathyGandham SriLakshmi Bhavani, Hitesh Shah, Anju Shukla, et al.
Journal of the Neurological Sciences|December 21, 2010
Molecular and structural analysis of metachromatic leukodystrophy patients in Indian populationPallavi Shukla, Suman Vasisht, Ranjana Srivastava, et al.
Indian Journal of Pediatrics|January 27, 2026
Molecular Landscape of Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency in IndiaSudhisha Dubey, Renu Saxena, Sudha Kohli, et al.
Pageof 24