Maria M. Bujan
B, Argentina
Last Updated: 09/26/2026
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Found 10 publications
Severe atopic dermatitis and growth failure associated with a STAT5B gene mutation in a 7-month-old infant.
Journal: Archivos argentinos de pediatria
Published: August 03, 2026
Eosinophilic cellulitis (Wells' syndrome) in a female pediatric patient.
Journal: Archivos argentinos de pediatria
Published: March 14, 2024
Clinical and genetic characteristics of CARD14-associated papulosquamous eruption in a paediatric case.
Journal: The Australasian journal of dermatology
Published: October 08, 2023
Expanding spectrum, intrafamilial diversity, and therapeutic challenges from 15 patients with heterozygous CARD11-associated diseases: A single center experience.
Journal: Frontiers in immunology
Published: August 16, 2022
Progressive nodular histiocytosis in a 9-year-old boy treated with cobimetinib.
Journal: Pediatric dermatology
Published: December 22, 2021
Cutaneous hyperpigmentation secondary to vitamin B12 deficiency in an infant
Journal: Archivos argentinos de pediatria
Published: August 21, 2019
Iatrogenic Cushing syndrome due to the misuse of topical corticosteroids. Pediatric case report
Journal: Archivos argentinos de pediatria
Published: January 09, 2019
Bazex-Dupré-Christol syndrome: Case series
Journal: Archivos argentinos de pediatria
Published: November 12, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026