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The American Journal of Dermatopathology|January 19, 2013
Dyschromia related to severe combined immunodeficiencyPaola Maldonado-Cid, Lucero Noguera-Morel, Ricardo Moreno-Alonso-de-Celada, et al.
Pediatric Dermatology|October 16, 2013
Postvaccination bullous pemphigoid in infancy: report of three new cases and literature reviewSonia de la Fuente, Ángela Hernández-Martín, Raúl de Lucas, et al.
American Journal of Medical Genetics. Part A|October 26, 2022
Keratitis-ichthyosis-deafness syndrome with lethal p.Ala88Val variant and severe hypercalcemiaAna Elísabet López-Sundh, Esperanza Escribano-Palomino, Marta Feito-Rodríguez, et al.
Pediatric Dermatology|June 5, 2007
Perforating neutrophilic and granulomatous dermatitis of the newborn--a clue to immunodeficiencyAntonio Torrelo, Angel Vera, Mar Portugués, et al.
Pediatric Dermatology|December 23, 2017
Identical COL71A1 heterozygous mutations resulting in different dystrophic epidermolysis bullosa phenotypesNicole Knöpfel, Lucero Noguera-Morel, Angela Hernández-Martin, et al.
Orphanet Journal of Rare Diseases|April 24, 2013
Prioritization of therapy uncertainties in Dystrophic Epidermolysis Bullosa: where should research direct to? an example of priority setting partnership in very rare disordersPaula Davila-Seijo, Angela Hernández-Martín, Evanina Morcillo-Makow, et al.
Clinical and Experimental Dermatology|March 26, 2026
Upadacitinib in children under 12 years with dupilumab-refractory severe atopic dermatitis: a real-world case seriesAndrés Vidal González, Sergio López Alcázar, Rafael Escudero Tornero, et al.
Pediatric Dermatology|December 10, 2015
Two Cases of Autosomal Recessive Congenital Ichthyosis due to CYP4F22 Mutations: Expanding the Genotype of Self-Healing Collodion BabyLucero Noguera-Morel, Marta Feito-Rodríguez, Paola Maldonado-Cid, et al.
Pediatric Dermatology|June 14, 2020
Staphylococcal toxic shock syndrome in a child with interleukin-17 inhibitor treatment for psoriasisMaría Sánchez Martín, Irene Amores Hernández, David Argumánez García, et al.
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