Results 191 to 200 of about 10,294,639 (233)
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Comedonal Darier's disease

British Journal of Dermatology, 1995
Darier's disease is an inherited disorder with well-recognized patterns of presentation. Lesions commonly affect the trunk and flexures. The diagnosis is based on the typical clinical appearance and histology showing acantholytic dyskeratosis. We report two unusual cases with prominent nodular, comedonal lesions on the face and scalp.
E K, Derrick, C R, Darley, S, Burge
openaire   +2 more sources

Cornifying Darier's disease

International Journal of Dermatology, 2000
A 48‐year‐old Caucasian man recounted the onset of keratotic papules on the trunk at the age of 8 years, with subsequent spread to the forearms, scalp, and forehead. His most severe disease was present on the legs. He complained of pain, itching, and noted exacerbations in the summer and with sweating.
R, Katta, J, Reed, J E, Wolf
openaire   +2 more sources

Variable response to low‐dose naltrexone in patients with Darier disease: a case series

Journal of the European Academy of Dermatology and Venereology, 2019
Darier disease is a rare autosomal‐dominant genodermatosis with a loss of function of a Ca2+‐ATPase pump (SERCA2‐pump). Clinically, the disease is characterized by red–brown keratotic papules mainly in seborrhoeic areas and has only limited and ...
D. Boehmer   +4 more
semanticscholar   +1 more source

A case of type 1 segmental Darier disease showing widespread Blaschkoid skin lesions with p.P160L mutation in ATP2A2

Journal of the European Academy of Dermatology and Venereology, 2020
Darier disease is an autosomal dominant skin disease characterized by keratotic greasy papules and plaques, primarily in seborrheic and intertriginous areas. Darier disease is caused by mutations in ATP2A2 that encodes a sarco/endoplasmic reticulum Ca2+ -
A. Agematsu   +11 more
semanticscholar   +1 more source

Darier’s Disease

2015
Darier’s disease (DD) is an autosomal dominant disease induced by haplo-insufficiency with variable expressivity but with complete penetrance in adults. Considerable variation in severity and in clinical manifestation was found between families. Lesions are hyperkeratotic, greasy papules, which are skin colored, yellow, or brown, that may coalesce into
Federico Bardazzi   +2 more
openaire   +1 more source

Pumping the Breaks on Acantholytic Skin Disorders: Targeting Calcium Pumps, Desmosomes, and Downstream Signaling in Darier, Hailey-Hailey, and Grover Disease.

Journal of Investigative Dermatology
Acantholytic skin disorders, by definition, compromise intercellular adhesion between epidermal keratinocytes. The root cause of blistering in these diseases traces back to direct disruption of adhesive cell-cell junctions, exemplified by autoantibody ...
R. Harmon   +5 more
semanticscholar   +1 more source

Darier's Disease

2018
Darier’s disease is an uncommon, autosomal-dominant inherited disorder. It is characterized by greasy, hyperkeratotic, skin-colored, or yellowish-brown papules that show a characteristic dermatoscopic pattern which consists of a central yellowish-brownish area of different morphologies (“star-like,” branched, polygonal, or roundish-oval), generally ...
Enzo Errichetti, Giuseppe Stinco
openaire   +3 more sources

Linear Darier’s Disease

New England Journal of Medicine, 2021
Timothy D, McKinley, Michele, Maroon
openaire   +2 more sources

Darier's Disease

Journal of Cutaneous Pathology, 1975
T G, Soto   +3 more
openaire   +2 more sources

Response of Darier Disease Following Treatment With Baricitinib.

JAMA dermatology, 2022
J. M. Busto Leis   +3 more
semanticscholar   +1 more source

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