Results 61 to 70 of about 238,615 (114)

Dermoscopic Patterns of Genodermatoses: A Comprehensive Analysis. [PDF]

Biomedicines, 2023
Plázár D, Meznerics FA, Pálla S, Anker P, Farkas K, Bánvölgyi A, Kiss N, Medvecz M.   +7 more
europepmc   +1 more source

Retrospective analysis of nail findings in the National Registry for Ichthyosis and Related Disorders database

Supplemental Figure LegendSupplemental Figure 1. Autosomal recessive congenital ichthyosis (Harlequin ichthyosis, ABCA12 genetic mutation) subject with parrot beak nails and pachyonychia of the fingernails. Supplemental Figure 2.
Curtis, K (via Mendeley Data)
core   +1 more source

Secukinumab for lamellar ichthyosis in an adolescent: a case report. [PDF]

Transl Pediatr
Li L, Wei F.
europepmc   +1 more source

Successful Treatment of Two Rare Pediatric Keratinization Disorders with Secukinumab: Epidermolytic Ichthyosis and PRP-GPP Overlap. [PDF]

Psoriasis (Auckl)
Xu Q, Zhang J.
europepmc   +1 more source

Defining Histological Patterns in Inherited Ichthyoses: Toward a Diagnostic Algorithm Based on 66 Confirmed Cases. [PDF]

Dermatopathology (Basel)
Süßmuth K, Oji V, Bodes J, Jochum I, Muhs F, Komlosi K, Hausser I, Schmuth M, Traupe H, Fischer J, Metze D.   +10 more
europepmc   +1 more source

Congenital ichthyosis in a Maltese dog: A case report. [PDF]

Vet Med (Praha), 2021
Kim TS, Seo JA, Oh TH, Park JK, Jeong KS, Hong IH.   +5 more
europepmc   +1 more source

Desmosomal-Type Acantholysis-A New Histologic Pattern Related to Mutations of Genes for Desmosomal Proteins. [PDF]

Dermatopathology (Basel)
Metze D, Süßmuth K, Metze C, Oji V, Traupe H.   +4 more
europepmc   +1 more source

Staphylococcus aureus bacteremia and infective endocarditis in a patient with epidermolytic hyperkeratosis: A case report. [PDF]

World J Clin Cases, 2022
Chen Y, Chen D, Liu H, Zhang CG, Song LL.   +4 more
europepmc   +1 more source

Vancomycin-Induced Linear IgA Bullous Disease in a Neonate. [PDF]

Indian Dermatol Online J
Gupta A, Rajan R, Telugu RB.
europepmc   +1 more source

Partial Loss of Function ABCA12 Mutations Generate Reduced Deposition of Glucosyl-Ceramide, Leading to Patchy Ichthyosis and Erythrodermia Resembling Erythrokeratodermia Variabilis et Progressiva (EKVP). [PDF]

Int J Mol Sci, 2023
Terrinoni A, Sala G, Bruno E, Pitolli C, Minieri M, Pieri M, Gambacurta A, Campione E, Belardi R, Bernardini S.   +9 more
europepmc   +1 more source