Results 241 to 250 of about 2,878,066 (285)

Clinical characteristics of three patients with UV^S syndrome, a photosensitive disorder with defective DNA repair

British Journal of Dermatology, 1996
Recently, we established a new category of photosensitive disorder termed UVs syndrome. Cells from patients with UVs syndrome have a similar UV sensitivity as xeroderma pigmentosum (XP) cells, but have a normal level of unscheduled DNA synthesis (UDS) unlike XP.
T Matsui, M. Ichihashi, M Hiro-Oka, Tomomichi Ono, M Matsuno, M. Yamaizumi, T. Itoh   +6 more
  +5 more sources

[Photosensitive disorders--focusing on photosensitive genetic diseases].

Nihon rinsho. Japanese journal of clinical medicine, 2010
Among various photosensitive disorders, photosensitive genetic diseases are noticeable in that physicians play a key role in early diagnosis. Xeroderma pigmentosum (XP) and erythropoetic protoporphyria (EPP) are focused on this issue as photosensitive genetic diseases.
Chikako Nishigori
openaire   +2 more sources

A candidate gene analysis of three related photosensitivity disorders: cutaneous lupus erythematosus, polymorphic light eruption and actinic prurigo

British Journal of Dermatology, 2001
Thomas P. Millard, E. Kondeatis, Angela Cox, A. G. Wilson, Sophie Grabczynska, B. Sean Carey, Cathryn M. Lewis, Munther A. Khamashta, G.W. Duff, G. R. V. Hughes, J.L.M. Hawk, Robert W. Vaughan, J.M. McGregor   +12 more
openalex   +2 more sources

Photosensitivity Disorders

, 2016
Won-An Kwon
openaire   +2 more sources

Photosensitive Disorders

, 2018
James E. Fitzpatrick, Whitney A. High, W. Lamar Kyle   +2 more
openaire   +2 more sources

Some of the next articles are maybe not open access.

Related searches:

Circulating levels of hypoxia-inducible factor-1α and miR-210 are associated with photosensitivity in systemic lupus erythematosus patients.

Current molecular medicine, 2022
BACKGROUND miR-210, a key HypoxamiR, regulates the hypoxia and inflammation-linked hypoxia. Systemic lupus erythematosus (SLE), a chronic autoimmune disease, responsible for many pathological disorders, including photosensitivity.
A. Gamal-Eldeen, C. Fahmy, B. Raafat, Fayez Althobaiti, I. Bassyouni, R. Talaat   +5 more
semanticscholar   +1 more source

The Smith Lemli Opitz syndrome: A newly recognised inherited photosensitivity disorder

Journal of Dermatological Science, 1998
C. R. Charman, A. Ryan, Alexander Vincent Anstey, Anthony D. Pearse   +3 more
openaire   +3 more sources

Inherited skin disorders presenting with poikiloderma

International Journal of Dermatology, 2021
Poikiloderma is a skin condition that combines atrophy, telangiectasia, and macular pigment changes (hypo‐ as well as hyperpigmentation). It is often mistaken for mottled pigmentation by general practitioners or nondermatology specialists.
T. Rayinda, M. V. van Steensel, Retno Danarti   +2 more
semanticscholar   +1 more source

Photosensitive disorders of the skin with ocular involvement

Clinics in Dermatology, 2015
Patients with photosensitive disorders of the skin may present with ocular manifestations that are evident at birth or may be manifested later with progression of the disorder. Dermatologists should be able to recognize these and appropriately refer patients for further management.
Mark S Juzych, Henry W. Lim, Frank S. Hwang, Jennifer Brescoll, Pranita V. Rambhatla   +4 more
openaire   +3 more sources

P.3.007 Photosensitivity and affective disorders: Relationship with anxiety symptomatology

European Neuropsychopharmacology, 2003
Paolo Castrogiovanni, M. Martinucci, K. Paolini, A. De Capua, Letizia Bossini   +4 more
openaire   +3 more sources