Results 61 to 70 of about 7,109,345 (167)

Ustekinumab for the treatment of acrodermatitis continua of Hallopeau refractory to anti-TNF agents

open access: yes, 2017
Acrodermatitis continua of Hallopeau (ACH) is a variant of pustular psoriasis that is often very difficult to treat. Almost all anti-psoriatic agents have been used in the treatment of ACH. Ustekinumab, a fully human monoclonal antibody of the IgG1 class,
Temel, BERKAY   +3 more
core   +1 more source

Epidermolysis bullosa. Report and discussion of two clinical cases

open access: yes, 1995
The authors present two clinical cases of epydermolisis bullosa (Hallopeau-Siemens type), to underline characteristic mucous and dental diseases of these types of genodermatosis; they analyze mean diferentiative criteria and the diagnostic possibilities;
S.Menni, BRUNO, EUGENIO, L. Paini
core   +1 more source

Crusted scabies mimicking an acrodermatitis continua of Hallopeau

open access: yes, 2020
Introducción: La escabiasis costrosa (EC) es una variante poco común de sarcoptiosis clásica, altamente contagiosa. Las lesiones poseen una elevada concentración del ácaro Sarcoptes scabiei var hominis, lo que conlleva a un cuadro clínico más extenso que
Roldán Franco, María S.   +2 more
core   +1 more source

A Case of Acrodermatitis Continua of Hallopeau Treated with Etanercept. [PDF]

open access: yes, 2012
Acrodermatitis continua of Hallopeau (ACH) is a rare form of acropustular eruption characterized by a presence of aseptic pustules on inflammatory periungual or subungual regions.
박창욱, 이윤선, 이광훈
core  

Uso della tomografia a coerenza ottica nella valutazione dell’efficacia del trattamento in paziente con acrodermatite di Hallopeau [PDF]

open access: yes, 2017
Si presenta il caso di una donna di 75 anni affetta da una grave forma di acrodermatite di Hallopeau delle mani trattata con 40 mg di adalimumab ogni 2 settimane e 25 mg di prednisone al giorno.
BIGI, Laura   +4 more
core  

Autoantibodies in anti-p200 pemphigoid stain skin lacking laminin 5 and type VII collagen

open access: yes, 2000
We report the case of a patient with a widespread bullous skin disease and linear deposits of IgG and C3 at the dermal-epidermal junction using direct immunofluorescence microscopy.
Chimanovitch, I   +6 more
core   +1 more source

Pemphigus Vegetans masquerading as Cutis Verticis Gyrata

open access: yes, 2013
Pemphigus vegetans a variant of pemphigus vulgaris divided  into  Neumann  type,  which  begins  and  ends  as  Pemphigus  vulgaris,  and Hallopeau  type,  which  is  relatively  benign,  having  pustules  as primary  lesions  instead of  bullae ...
Gupta, Nishant; Govt. Stanley medical college hospital   +4 more
core   +3 more sources

A -96C-T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolys bullosa

open access: yes, 2000
Hereditary dystrophic epidermolysis bullosa (DEB) refers to a group of clinically heterogeneous skin blistering diseases due to mutations in the collagen type VII gene (COL7A1). We report two novel mutations found in a patient affected by the most severe
ZOPPI, Nicoletta   +4 more
core   +1 more source

Caractérisation d\u27une insertion CG dans le gène du collagène VII chez un patient atteint d\u27épidermolyse bulleuse dystrophique récessive de Hallopeau-Siemens [PDF]

open access: yes, 1997
L\u27épidermolyse bulleuse dystrophique récessive généralisée mutilante de Hallopeau-Siemens (EBDR-HS) est une génodermatose grave, caractérisée par une fragilité cutanéo-muqueuse extrême associée à une forte diminution, voire une absence des fibres d ...
Hilal, L.   +2 more
core  

Dermatoses neutrofílicas: parte II

open access: yes, 2011
Neste artigo são abordadas as dermatoses neutrofílicas, complementando o artigo anterior (parte I). São apresentadas e comentadas as seguintes dermatoses: pustulose subcórnea de Sneddon-Wilkinson, dermatite crural pustulosa e atrófica, pustulose ...
Fernanda Razera   +2 more
core   +1 more source

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