Results 71 to 80 of about 12,561 (235)
Acquired Haemophilia A Associated with Bullous Pemphigoid
, 2023 We would like to submit this manuscript for an image report entitled ‘Acquired haemophilia A associated with bullous pemphigoid’. We present the case of an 81-year-old female first investigated for a blistering dermatosis and diagnosed with bullous ...
Wainman, Hannah +2 more
core +1 more source
Bullous pemphigoid evolving into cicatricial pemphigoid?
, 1997 We describe three patients who initially presented with both clinical and immunological findings to support a diagnosis of bullous pemphigoid but whose subsequent course has been that of cicatricial pemphigoid.
Papadavid, E +5 more
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Study of Clinical Characteristics of Desquamative Gingivitis in 60 Patients in the North of Spain
International Journal of Dental Hygiene, EarlyView.ABSTRACT Objectives The aim of this study is to know the clinical characteristics of desquamative gingivitis (DG) in a Spanish population in order to make an early diagnosis of this sign and, therefore, the underlying systemic disease. Methods A cross‐sectional study was conducted.
Valeria Sanmartín‐Barragáns +7 more
wiley +1 more source
Perfil clinicopatológico dos pacientes com doença bolhosa auto-imune atendidos no ambulatório de dermatoses bolhosas do Hospital Universitário- UFSC no período de janeiro a agosto de 2009 [PDF]
, 2009 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Vieira, Adriana
core
, 1997 The cornified envelope is a layer of transglutaminase cross-linked protein that is assembled under the plasma membrane of keratinocytes in the outermost layers of the epidermis.
Christiana Ruhrberg +7 more
core +1 more source
Bullous pemphigoid: therapeutic algrorithm and practical management
, 2013 Introduction: Bullous pemphigoid (BP) is the most common autoimmune subepidermal blistering disease of the skin and mucosae. BP typically affects the elderly and manifests with severe itch, localised or generalised eczematous, urticated and/or bullous ...
Borradori, Luca +2 more
core +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 +31 more
wiley +1 more source
Ticlopidine Induced Bullous Pemphigoid [PDF]
, 2009 Bullous pemphigoid (BP) is an acquired autoimmune disease that`s characterized by subepidermal vesicles and bullae. The etiology for BP is mostly idiopathic, but numerous observations have suggested the role of certain drugs in the occurrence of bullous ...
김수찬
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Interventions for bullous pemphigoid [PDF]
Cochrane Database of Systematic Reviews, 2003 Bullous pemphigoid (BP) is the most common autoimmune blistering disease in the West. Oral steroids are the standard treatment.This is an update of the review published in 2005.To assess treatments for bullous pemphigoid.In August 2010 we updated our searches of the Cochrane Skin Group Specialised Register, the Cochrane Central Register of Controlled ...
Khumalo, N. +5 more
openaire +7 more sources