Results 71 to 80 of about 12,411 (239)
ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis
Veterinary Dermatology, EarlyView.ABSTRACT Background Ichthyosis fetalis (IF), also known as harlequin ichthyosis, is a rare and often fatal autosomal recessive congenital skin disorder. It is characterized by thickened, hard skin plaques and deep skin fissures that limit mobility and cause malformations of the eyes, lips and ears.
Jeanna M. Blake +2 more
wiley +1 more source
Phase II evaluation of VDC-1101 in canine cutaneous T-cell lymphoma. [PDF]
, 2014 BackgroundCanine cutaneous T-cell lymphoma (CTCL) is an uncommon disease for which efficacious therapies are lacking. The novel anticancer nucleotide prodrug VDC-1101 (formerly known as GS-9219) has shown efficacy in dogs with multicentric lymphoma.
Burgess, KE +5 more
core +2 more sources
Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 2, Page 174-184, February 2026.This EBMT Practice Harmonisation and Guidelines Committee consensus provides practical recommendations for the selection, timing and conduct of allogeneic transplantation in advanced‐stage mycosis fungoides and Sézary syndrome, aiming to optimize outcomes through early multidisciplinary collaboration and evidence‐based decision‐making.
Gandhi Damaj +26 more
wiley +1 more source
Boot Camp for Scientists [PDF]
, 2014 An innovative week-long program allows first-year students to explore the sciences at ...
Davis, Laura, Linfield Magazine Staff
core +1 more source
Regional outbreak of staphylococcal scalded skin syndrome in healthy children [PDF]
, 2010 Purpose : Staphylococcal scalded skin syndrome (SSSS) is a relatively uncommon superficial blistering skin disease that is due to Staphylococcus aureus. We had experienced a regional outbreak of SSSS over 3 years in healthy children.
Begier +20 more
core +1 more source
A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis [PDF]
, 2017 Epidermolytic hyperkeratosis (EHK), (bullous congenital ichthyosiform erythroderma), is an autosomal dominant human skin disorder. Recently, we and others have described mutations in keratins 1 and 10 (K1 and K10) in patients with this disease. Structure-
Anton-Lamprecht, Ingrun +7 more
core
Evaluation of Sleep Disorders and Quality of Life in Patients With Mycosis Fungoides
Cancer Reports, Volume 9, Issue 1, January 2026.ABSTRACT Background Mycosis fungoides (MF) is the most common cutaneous T‐cell lymphoma, presenting with variable clinical features that can be pruritic. Pruritus and the overall disease burden may disrupt sleep and diminish quality of life; yet, sleep disturbances in MF remain under‐investigated.
Seyed AmirReza Mohammadi +5 more
wiley +1 more source
Scientific ReportsErythroderma is a severe and heterogeneous inflammatory skin condition with little guidance on the approach to management in cases of unknown etiology.
Hannah L. Cornman +17 more
doaj +1 more source
Cutaneous T-cell lymphoma: Differential diagnostics of erythrodermic conditions
Vestnik Dermatologii i Venerologii, 2019 Erythroderma is a condition damaging at least 80–90 % of the skin surface, characterized by erythema and peeling. This condition may be a manifestation of various diseases of the skin and internal organs, including malignant lymphoproliferative disorders.
A. E. Karamova +3 more
doaj +1 more source
, 2009 This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of seborrheic ...
Kompella, Anu
core +1 more source