Results 161 to 170 of about 9,158,896 (219)

Novel ATP2A2 Gene Mutation c.118G>A Causing Keratinocyte and Cardiomyocyte Disconnection in Darier Disease

open access: green
Andrea Frustaci   +7 more
openalex   +1 more source

Kaposi varicelliform eruption in Darier disease

open access: yesDermatologica Sinica
Yu-Wen Huang   +2 more
doaj   +1 more source

Darier Disease: A Case Report with Psychiatric Involvement

open access: gold
Anusha Rao   +5 more
openalex   +1 more source

Darier disease: first molecular study of a Portuguese family. [PDF]

open access: yesHeliyon, 2019
Almeida A, Lobo ML, Moura C, Rivera I.
europepmc   +1 more source

Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene.

open access: yesJAMA Dermatol
Atzmony L   +9 more
europepmc   +1 more source
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Darier disease

Journal of Dermatology, 2016
AbstractDarier disease (DD) is a type of inherited keratinizing disorder that exhibits autosomal dominant inheritance. DD is caused by the mutations of ATP2A2, which encodes an endoplasmic reticulum calcium pump, sarco/endoplasmic reticulum ATPase type 2 (SERCA2).
Shigaku Ikeda
exaly   +5 more sources

Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects

British Journal of Dermatology, 2016
R. Dodiuk-Gad   +13 more
exaly   +2 more sources

An Update on the Cutaneous Manifestations of Darier Disease

Journal of Cutaneous Medicine and Surgery, 2021
Background Knowledge about the clinical features of Darier disease, an orphan autosomal-dominant genetic disorder, is sparse and has been evaluated only in few studies.
Algit Yeshurun   +11 more
semanticscholar   +1 more source

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