Results 51 to 60 of about 2,889 (186)

Announcement [PDF]

, 1993
En la reestructuración del capitalismo que se produjo en los años 70, las nuevas tecnologías de la información y la comunicación tuvieron un papel fundamental permitiendo una utilización intensiva del conocimiento, papel que podemos rastrear en su ...
Moreno Gálvez, Francisco Javier
core   +2 more sources

Neutrophil-specific deletion of the CARD9 gene expression regulator suppresses autoantibody-induced inflammation in vivo [PDF]

, 2016
Neutrophils are terminally differentiated cells with limited transcriptional activity. The biological function of their gene expression changes is poorly understood.
A Drewniak, A Franke, A Mantovani, A Mócsai, A Mócsai, A Mócsai, A Mócsai, A Mócsai, A Mócsai, A Zhernakova, AS Korganow, BG Yipp, BT Wipke, C Jiang, C Sitaru, CA Lowell, CL Abram, D Wang, DM Evans, DP McGovern, E Passegue, EO Glocker, ER Elliott, FW Farley, H Hara, J Ruland, JE Bakema, JJ Pointon, K Csorba, K Futosi, K Kiryluk, KN Lai, L Li, M Blonska, M Kovács, MA Rivas, MJ Robinson, MT Chiriac, O Gross, P Scapini, P Scapini, PA Monach, R Arya, RC Chou, S LeibundGut-Landmann, S Roth, S Roth, T Németh, T Németh, TS Heng, V Cremasco, V Kouskoff, VW Chan, WC Skarnes, Z Jakus, Z Jakus, Z Jakus, Z Kertész, Z Liu   +58 more
core   +2 more sources

Childhood epidermolysis bullosa acquisita: Confirmation of diagnosis by skin deficient in Type VII Collagen, enzyme-linked immunosorbent assay, and immunoblotting

Indian Journal of Dermatology, 2016
Epidermolysis bullosa acquisita (EBA) is an acquired subepidermal bullous disorder characterized by autoantibodies against Type VII collagen. It usually affects adults; childhood EBA is rare. We describe a 10-year-old girl presenting with recurrent tense
Nupur Goyal, Raghavendra Rao, C Balachandran, Sathish Pai, Balbir S Bhogal, Enno Schmidt, Detlef Zillikens   +6 more
doaj   +1 more source

Periodontitis and Periodontal Conditions in Systemically Healthy Children and Adolescents

Journal of Clinical Periodontology, EarlyView.
ABSTRACT Objective To answer the PICoS question ‘in systemically healthy children and adolescents (Population), what are the main features of periodontitis, necrotising periodontal diseases (NPD) and other periodontal conditions (periodontal abscesses, endo‐periodontal lesions, traumatic occlusal forces, prosthesis‐ and tooth‐related factors ...
Inbar Eshkol‐Yogev, Nagore Ambrosio, Cheryl Somani, Elena Figuero, Lior Shapira, Janet Davies   +5 more
wiley   +1 more source

Necrotizing fasciitis – a complication of autoimmune skin blistering diseases?

Journal of Infection in Developing Countries, 2023
Introduction: Autoimmune bullous diseases (AIBD) are organ-specific skin blistering diseases clinically manifesting as bullae and vesicles of the skin and mucous membranes.
Milana Jurišić, Gorana Nikolić, Maja Nikolić Živanović, Milan Stojičić   +3 more
doaj   +1 more source

Epidermolysis bullosa acquisita: current diagnosis and therapy

Dermatology Reports, 2011
Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune subepidermal blistering disease with an approximate prevalence of 0,2/million people. The hallmark of EBA is the presence of autoantibodies (mainly IgG class) to anchoring fibril collagen ...
Christine R. Mehren, Robert Gniadecki
doaj   +1 more source

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda, B. Tedbirt, C. Bodemer, M. C. Bolling, M. El Hachem, M. Nikolić, E. Benton, M. Caproni, D. De, D. Didona, K. Drenovska, M. Goebeler, M. Hertl, B. Horváth, M. Kasperkiewicz, D. Kiritsi, M. Larralde, A. V. Marzano, J. Meijer, D. F. Murrell, J. Powell, E. Sprecher, N. S. Chandran, M. M. Tomayko, S. Uzun, N. van Beek, H. Ott, A. Patsatsi, A. Torrelo, A. Welfringer‐Morin, E. Schmidt, P. Joly   +31 more
wiley   +1 more source

A case of porphyria cutanea tarda in the setting of hepatitis C infection and tobacco usage [PDF]

, 2019
Porphyria cutanea tarda (PCT) is the most common type of porphyria, presenting in middle-aged patients with a photodistributed vesiculobullous eruption, milia, and scars.
Brinster, NK, Chen, L, Lederhandler, M, Meehan, SA, Neimann, A   +4 more
core  

Acquired Epidermolysis Bullosa and Linear Immunoglobulin A Bullous Dermatosis [PDF]

, 2017
Acquired epidermolysis bullosa is a rare subepidermal bullous disease characterized by autoantibodies to type VII collagen, the major component of anchoring fibrils. Although the exact pathophysiologic mechanism remains unclear, reduction or perturbation
Atay, Seda, Çelik, Gökçen
core   +1 more source

Epidermolysis Bullosa Acquisita

Vestnik dermatologii i venerologii, 2015
Epidermolysis bullosa acquisita (EBA) is a form of pemphigoid which may come with scarring that looks like dystrophic epidermolysis bullosa hereditaria. This subtype with scarring is named mechanobullous EBA, because blisters are evoked by sudden mechanical trauma, such as hitting the back of the hand to the edge of a table.
Catherine Prost-Squarcioni, Frédéric Caux   +1 more
  +6 more sources