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BMJ Case Reports|July 9, 2020
Progressive familial intrahepatic cholestasis type 4 in an Indian child: presentation, initial course and novel compound heterozygous mutationNida Mirza, Ravi Bharadwaj, Smita Malhotra, et al.Journal of Pediatric Genetics|August 1, 2024
Prolonged Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA DeficiencyNida Mirza, Ravi Bharadwaj, Smita Malhotra, et al.The Journal of Neuropsychiatry and Clinical Neurosciences|May 12, 2015
Group Dialectical-Behavior Therapy Skills Training for Conversion Disorder With SeizuresKim D Bullock, Nida Mirza, Craig Forte, et al.Journal of Pediatric Genetics|August 14, 2023
Esophageal Stricture and Dermal Pathology Related to Compound Heterozygous Mutations in the <i>TNXB</i> GeneNida Mirza, Sundeep Upadhyaya, Sagar Mehta, et al.Journal of Indian Association of Pediatric Surgeons|March 13, 2023
Clinical Profile of Acute Pancreatitis in Children and Adolescents from a Single Center in Northern IndiaNida Mirza, Sagar Mehta, Karunesh Kumar, et al.Pageof 1