Results 101 to 110 of about 14,871 (251)
Darier’s Disease: Report of a Case with Facial Involvement
Darier’s disease is a relatively rare autosomal dominant genodermatosis with a defect in the desmosomal attachment due to a mutation in the ATP2A2 gene.
Chaninan Kositkuljorn +1 more
doaj +1 more source
Spectrum of features in Darier’s disease: A case report with emphasis on differential diagnosis
Oral genodermatoses includes a spectrum of inherited dermatological disorders with varying oral mucosal manifestations. Darier’s disease is an autosomal dominant disorder with defect in desmosomal attachment.
Shwetha V +6 more
doaj +1 more source
Laser Treatment of Darier Disease: Report of Two Cases and Systematic Review of the Literature [PDF]
Introduction: Darier Disease (DD) is a chronic disease with high morbidity and limited treatment options. Laser efficacy in the treatment of DD remains understudied.Methods: A literature search conducted between 07/21/2017 and 05/05/2018 identified all ...
DeKlotz, Cynthia Marie Carver +3 more
core +1 more source
Treatment of erythromelanosis follicularis faciei et colli with a 595‐nm pulsed dye laser
Journal of Cosmetic Dermatology, Volume 23, Issue 3, Page 1104-1106, March 2024.
Zuhong Wang, Qiao Ling, Yanxi Li
wiley +1 more source
Cicatricial alopecia represents a group of disorders sharing a final pathway of destruction followed by replacement with fibrous tissue of the hair follicle unit. Cicatricial alopecia is classified into two categories, namely primary cicatricial alopecia,
Dou, Wenjie +7 more
core +2 more sources
Identification of drug-specific pathways based on gene expression data: application to drug induced lung injury [PDF]
Identification of signaling pathways that are functional in a specific biological context is a major challenge in systems biology, and could be instrumental to the study of complex diseases and various aspects of drug discovery.
Alexopoulos, Leonidas G. +7 more
core +1 more source
Genodermatoses are an inherited disorder, present with multisystem involvement. Help us to identify regular mutations and appalling skin diseases with recessive inheritance.
N Aravindha Babu +3 more
doaj +1 more source
Erythromelanosis follicularis faciei et colli - A cross-sectional, descriptive study
Background: Erythromelanosis follicularis faciei et colli (EFFC) has always been reported as a rare disorder, and more data are needed to define its etiology and epidemiology.
Shagufta Rather +2 more
doaj +1 more source
การศึกษาประสิทธิภาพของคลื่นวิทยุ ชนิดเข็มขนาดเล็กที่มีฉนวน ในการรักษาโรคขนคุด [PDF]
MASTER OF SCIENCE (M.Sc.)วิทยาศาสตรมหาบัณฑิต (วท.ม.)Keratosis pilaris is the most common follicular disorder in children. Several treatments have been used, such as topical moisturizers, exfoliants, anti‐inflammatory agents and topical corticosteroids ...
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