Results 41 to 50 of about 9,158,896 (219)

Increased caries risk in a Xerostomic patient with Darier disease: a case report of incipient and advanced carious lesions. [PDF]

Oxf Med Case Reports
Giannakopoulos K, Lambrou P, Kaklamanos EG, Christodoulou MN.   +3 more
europepmc   +2 more sources

The first report of Tocilizumab for Darier disease with summer exacerbations. [PDF]

An Bras Dermatol
Chen L, Wang W, Zhou S, Li Z.
europepmc   +2 more sources

Author Correction: Microbial imbalance in Darier disease: Dominance of various staphylococcal species and absence of Cutibacteria. [PDF]

Sci Rep
Plázár D, Metyovinyi Z, Kiss N, Bánvölgyi A, Makra N, Dunai Z, Mayer B, Holló P, Medvecz M, Ostorházi E.   +9 more
europepmc   +2 more sources

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

Biomedicines
Frustaci A, De Luca A, Verardo R, Guida V, Alfarano M, Calvieri C, Sansone L, Russo MA, Chimenti C.   +8 more
europepmc   +3 more sources

Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease

Human Mutation, 2016
R.G.L. Nellen, Peter M. Steijlen, Maurice A. M. Van Steensel, Maaike Vreeburg, Jorge Frank, Michel van Geel   +5 more
openalex   +2 more sources

Carbon dioxide laser treatment for Darier disease [PDF]

JAAD International
Hasina Maredia, MD, Christian Baum, MD, Randall Roenigk, MD, Addison Demer, MD   +3 more
doaj   +2 more sources

A compendium of late-onset darier with an unusual report

Clinical Dermatology Review, 2023
Darier disease is an autosomal dominant inherited skin disorder with complete penetrance and variable expressivity due to mutation in the ATP 2A2 gene. It usually develops from childhood and persists through adolescence. Late onset of this genodermatosis
Bhavni Oberoi, Suhasini Chand, Divya Shelly, Reetu Agarwal   +3 more
doaj   +1 more source

Dissection of the Functional Differences between Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA) 1 and 2 Isoforms and Characterization of Darier Disease (SERCA2) Mutants by Steady-state and Transient Kinetic Analyses [PDF]

Journal of Biological Chemistry, 2003
Jens Peter Andersen, Alain Hovnanian
exaly   +2 more sources

Naltrexone, a therapeutic alternative in Darier disease

Revista Médica del Hospital General de México, 2021
Darier disease is a clinically variable rare disease with autosomal dominant inheritance caused by mutations in ATP2A2 gene. It affects skin, mucous membranes, and nails.
Dennise L. Smith-Pellegrin, María R. Rivera-Vega, Jorge R. Cazarín-Barrientos, Aralí Melgarejo-Gómez, Olga M. Messina-Baas, Sergio Cuevas-Covarrubias   +5 more
doaj   +1 more source

Impaired calcium signalling and neuropsychiatric disorders in Darier disease: An exploratory review

Experimental Dermatology, 2022
Darier (Darier‐White) disease (DD) is an autosomal dominant skin disorder caused by pathogenic mutations in the ATP2A2 gene which encodes a calcium ATPase in the sarco‐endoplasmic reticulum (SERCA2). Defects in the SERCA2 protein lead to an impairment of
Austin B. Ambur, A. Zaidi, Charles Dunn, Rajiv Nathoo   +3 more
semanticscholar   +1 more source