Results 171 to 180 of about 3,796 (217)

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

Therapie der Schilddrüsenüberfunktion [PDF]

open access: yes, 1977
Bay, V.   +9 more
core  

Darier′s disease with perifollicular hypopigmentation

open access: yesIndian Journal of Dermatology, 2010
Sornakumar L, Srinivas C
doaj  
Some of the next articles are maybe not open access.

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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   +3 more sources

Darier's disease in Singapore

British Journal of Dermatology, 2005
Darier's disease is a rare, dominantly inherited genodermatosis. Although it has been well studied in caucasians, very little is known about the clinical spectrum of this disorder among Asians.To determine the demographic and clinical profile of Asian patients with Darier's disease.This is a retrospective study of all new cases of Darier's disease seen
B K, Goh, P, Ang, C L, Goh
exaly   +3 more sources

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   +2 more sources

Hemorrhagic Darier's Disease

Archives of Dermatology, 1964
Four cases of Darier's disease (keratosis follicularis) with unusual acral hemorrhagic lesions are presented and discussed. It is suggested that the lesions represent hemorrhage into lacunae secondary to trauma.
W N, JONES, T E, NIX, W H, CLARK
openaire   +2 more sources

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