Amit K. Satpathy
Bhubaneshwar, OR, India
Last Updated: 09/26/2026
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Found 12 publications
Novel ATP8B1 gene mutation in a family with progressive familial intrahepatic cholestasis.
Journal: BMJ case reports
Published: May 29, 2025
Clinical and Dermoscopic Features of Chronic Lupus Erythematosus Cheilitis: A Prospective Cross-Sectional Study of 35 Patients From a Tertiary Care Hospital in East India.
Journal: Journal of cutaneous medicine and surgery
Published: April 30, 2025
EAST (Epilepsy, Ataxia, Sensorineural Hearing Loss, and Renal Tubulopathy) Syndrome: A Rare Association Between Brain, Ear, and Kidney.
Journal: Cureus
Published: September 07, 2024
From Histoplasmosis to Cryptococcosis: A diagnostic journey of pediatric scalp abscess.
Journal: Indian journal of medical microbiology
Published: August 14, 2024
Correlation of Liver Fibrosis using Noninvasive Transient Elastography with Histological Staging in Infants with Cholestasis - A Prospective Analytical Study.
Journal: Journal of Indian Association of Pediatric Surgeons
Published: July 06, 2024
Spontaneous Resolution of Congenital Intrahepatic Portosystemic Shunt.
Journal: Acta medica Lituanic
Published: January 01, 2024
Osteopetrosis with Arnold Chiari malformation type I.
Journal: BMJ case reports
Published: August 16, 2023
Evaluation of Safety and Efficacy of Add-on Alpha-Lipoic Acid on Migraine Prophylaxis in an Adolescent Population: A Randomized Controlled Trial.
Journal: Journal of clinical pharmacology
Published: February 23, 2023
Secondary Budd-Chiari Syndrome due to Hepatic Tuberculosis in a Pediatric Patient Managed by Left Hepatic Vein Stenting.
Journal: Journal of clinical and experimental hepatology
Published: December 02, 2022
Response to Zoledronic Acid Infusion in Children With Fibrous Dysplasia.
Journal: Frontiers in pediatrics
Published: July 11, 2020
Effect of atorvastatin on dyslipidemia and carotid intima-media thickness in children with refractory nephrotic syndrome: a randomized controlled trial.
Journal: Pediatric nephrology (Berlin, Germany)
Published: April 10, 2018
Chanarin Dorfman syndrome: a case report with novel nonsense mutation.
Journal: Gene
Published: February 08, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026