Results 81 to 90 of about 2,851 (167)

PDE4 Inhibition as Potential Treatment of Epidermolysis Bullosa Acquisita [PDF]

, 2016
Pemphigoid diseases such as epidermolysis bullosa acquisita (EBA) may be difficult to treat. In pemphigoid diseases, mucocutaneous blistering is caused by autoantibodies to hemidesmosomal antigens; in EBA the autoantigen is type VII collagen.
Ghorbanalipoor, Saeedeh, Hashimoto, Takashi, Jonkman, Marcel F., Kasprick, Anika, Koga, Hiroshi, Ludwig, Ralf J., Pas, Hendri H., Recke, Andreas, Tenor, Hermann, Vidarsson, Gestur, Zillikens, Detlef   +10 more
core   +1 more source

Klinisches und immunpathologisches Spektrum des Immunglobulin‐M‐Pemphigoids: eine multizentrische Fallserie

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 12, Page 1555-1565, December 2025.
Zusammenfassung Hintergrund und Zielsetzung Die Pemphigoid‐Erkrankungen werden primär durch IgG‐ oder IgA‐Autoantikörper gegen die kutane Basalmembranzone (BMZ) vermittelt. Obwohl rezente Arbeiten auf die Existenz einer ausschließlich IgM‐vermittelten Pemphigoid‐Erkrankung hindeuten, fehlt bislang eine umfassendere Untersuchung.
Kaan Yilmaz, Stephanie Goletz, Christoph M. Hammers, Katharina Boch, Claudia Zeidler, Henning Wiegmann, Estelle Bergmann, Tina Rastegar Lari, Onur Dikmen, Nina Häring, Robert Strohal, Andreas Kleinheinz, Eva N. Hadaschik, Nina van Beek, Sonja Ständer, Enno Schmidt   +15 more
wiley   +1 more source

Pyostomatitis vegetans : a review of the literature [PDF]

, 2009
Pyostomatitis vegetans (PV) is a rare condition characterized by pustules that affect the oral mucosa. It is a highly specific marker for inflammatory bowel disease and its correct recognition may lead to the diagnosis of ulcerative colitis or Crohn?s ...
Buonaiuto, Curzio, Cirillo, Nicola, Dell?Ermo, Antonio, Femiano, Felice, Lanza, Alessandro, Perillo, Letizia   +5 more
core  

Normal Molecular Weight of Type VII Collagen Produced by Recessive Dystrophic Epidermolysis Bullosa Keratinocytes [PDF]

, 1993
Studies of the recessive dystrophic form of epidermolysis bullosa (RDEB) have suggested that an abnormality in type VII collagen may be involved in the pathogenesis of this disorder.
Fine, Jo-David, Gammon, W. Ray, Jenison, Mark, O&apos   +3 more
core   +2 more sources

A Case of Palmoplantar Vesiculobullous Lesions

JEADV Clinical Practice, Volume 5, Issue 1, Page 315-318, March 2026.
Ali Abid, Kelvin Truong, Jing Jing Li, Artiene Tatian   +3 more
wiley   +1 more source

Mechanobullous form of epidermolysis bullosa acquisita: Insights into disease mechanisms as inferred by response to rituximab, but not to JAK inhibitors

JEADV Clinical Practice
Epidermolysis bullosa acquisita (EBA) is a rare autoimmune blistering disease associated with IgG autoantibodies directed against type VII collagen. Different clinical forms have been described, including the classical mechanobullous variant resembling ...
L. Gueissaz, A. Junge, R. Wolf, C. Schlapbach, L. Feldmeyer, L. Borradori   +5 more
doaj   +1 more source

A viral infection usually seen after feast of sacrifice: Human orf, in this case accompanied with erythema multiforme

Medicine Science, 2018
Orf is an infectious disease caused by an epitheliotrophic double stranded deoxyribonucleic acid parapoxvirus which primarily affects sheep and goats but humans can also be infected by contact with infected animals.
Sezin Ficicioglu
doaj   +1 more source

Diagnosis of pemphigoid diseases [PDF]

, 2018
Itch in elderly due to newly recognized autoimmune diseases pemphigoidWith ageing comes itch, a common and burdensome complaint in elderly people and comparable to chronic pain.
Meijer, Joost Martien
core   +4 more sources

The Risk of Immune‐Mediated Skin Disease Under Dipeptidyl‐Peptidase IV Inhibitor: A Global Population‐Based Study

International Journal of Dermatology, Volume 65, Issue 2, Page 356-358, February 2026.
Noor Mruwat, Noga Givon‐Lavi, Ralf J. Ludwig, Khalaf Kridin   +3 more
wiley   +1 more source

Epidermolysis bullosa acquisita with moderately severe dysphagia due to esophageal strictures

Indian Journal of Dermatology, 2011
Epidermolysis bullosa acquisita (EBA) is a chronic, autoimmune condition involving the skin and mucous membranes. Symptomatic mucosal involvement is rare, but can impact on quality of life, due to esophageal strictures and dysphagia.
Jenny Tu, Prasad W Kumarasinghe
doaj   +1 more source