Results 51 to 60 of about 61,675,345 (173)

Treatment of diseases associated with cicatricial alopecia

open access: yesPrzegląd Dermatologiczny, 2022
Cicatricial (scarring) alopecia may result from perifollicular inflammation that destroys hair follicles and replaces them with connective tissue (primary cicatricial alopecia) or from damage done to follicles by other pathology that is not primarily ...
Lidia Rudnicka   +4 more
doaj   +1 more source

A Complex Inflammatory Triad: A Rare Case of Parry‐Romberg Syndrome With Systemic Lupus Erythematosus and Thyroiditis

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Parry‐Romberg Syndrome (PRS) is a rare disorder characterized by progressive unilateral facial atrophy, traditionally viewed as a localized scleroderma variant. Its rare coexistence with systemic lupus erythematosus (SLE) and autoimmune thyroiditis (AIT) suggests a broader inflammatory etiology, challenging the notion of PRS as a purely ...
Sakib Abrar   +4 more
wiley   +1 more source

La communication comme levier du dénouement de la crise pré-électorale de 2016 en RD Congo [PDF]

open access: yesMouvements et Enjeux Sociaux, 2023
Alors que les observateurs craignaient que le combat communicationnel entre le régime Kabila et les opposants face à l’impératif de l’alternance démocratique à la tête du pays en 2016 génère un Etat de siège, un coup d’Etat ou une guerre civile, celle-ci
Jenny MPUTU MBO BOLELA
doaj  

Upsurging cases of en coup de sabre: Distinctive clinical manifestations in a series of 41 patients

open access: yes, 2023
Background En coupe de sabre is not uncommon connective tissue disorder of children and adult and often end with marked deep scarring that starts very early and ending with scarring of the skin and scarring alopecia of scalp. Objective The aim of current
Khalifa E. Sharquie   +2 more
core   +1 more source

Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side
Jimmy Girgis William Abdelnour   +3 more
doaj   +1 more source

Sclerosing diseases of the skin

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari   +4 more
wiley   +1 more source

Les Elemens De L'Histoire Ou Ce qu'il faut savoir De Chronologie, De Geographie, De Blazon, De L'Histoire Universelle, De L'Eglise De L'Ancien Testament, Des Monarchies Anciennes, De L'Eglise Du Nouveau Testament, & Des Monarchies Nouvelles : Avant que de lire l'Histoire particuliere

open access: yes
Titelbl. in Rot- und Schwarzdr.Vorlageform des Erscheinungsvermerks: A Amsterdam, Chez Pierre De Coup, Libraire dans le Kalverstraat, à l'Enseigne de Ciceron. M.DCCXIV.Frontisp. (Kupferst.
Le Lorrain de Vallemont, Pierre
core   +3 more sources

Sklerosierende Erkrankungen der Haut

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1303, October 2025.
Zusammenfassung Sklerosierende Hautkrankheiten sind eine Gruppe unterschiedlicher dermatologischer Erkrankungen, die durch fibrotische Veränderungen gekennzeichnet sind und die Lebensqualität der Patienten stark einschränken können. Diese Erkrankungen treten häufig mit kutanen Manifestationen auf und können in bestimmten Fällen auch extrakutanes Gewebe
Yasamin Kalantari   +4 more
wiley   +1 more source

Twardzina linijna en coup de sabre [PDF]

open access: yes, 2019
W pracy przedstawiono opis przypadku 14-letniej dziewczynki leczonej z powodu twardziny linijnej typu en coup de sabre. W leczeniu zastosowano pulsoterapię metyloprednizolonem, natomiast w terapii podtrzymującej — metotreksat i średnie dawki prednizonu ...
Reich, Adam, Stępień, Katarzyna
core  

Dentofacial features of ‘en coup de sabre’ – a case report

open access: yes, 2017
‘En coup de sabre’ or morphea, is a linear scleroderma that typically affects the frontoparietal region of patients resulting in a band-like scar that looks like a sword cut across the face.
Sarah J Merrett   +2 more
core   +1 more source

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