Results 131 to 140 of about 7,109,345 (167)
Some of the next articles are maybe not open access.
Journal of Dermatological Science, 1994
Pemphigus foliaceus (PF) sera react with a 150 kDa antigen, desmoglein (DG), while pemphigus vulgaris (PV) sera react with a 130 kDa PV antigen. Recent molecular cloning studies have revealed that both DG and PV antigen are members of the cadherin family of cell adhesion molecules and that PV antigen shows very high homology to DG.
K, Hashimoto +5 more
openaire +2 more sources
Pemphigus foliaceus (PF) sera react with a 150 kDa antigen, desmoglein (DG), while pemphigus vulgaris (PV) sera react with a 130 kDa PV antigen. Recent molecular cloning studies have revealed that both DG and PV antigen are members of the cadherin family of cell adhesion molecules and that PV antigen shows very high homology to DG.
K, Hashimoto +5 more
openaire +2 more sources
Sudden vegetation of the mouth. Pemphigus vegetans of the mouth (Hallopeau type).
Archives of dermatology, 1992---
VIRGILI, Anna +2 more
openaire +2 more sources
Ultrastructural studies in epidermolysis bullosa hereditaria
Archives of Dermatological Research, 1976Ultrastructural examination was performed in 42 biopsy specimens from 22 patients with the Hallopeau-Siemens types or with the inverse type of epidermolysis bullosa dystrophica recessiva. The patient group consists of 8 cases of the localized Hallopeua-Siemens type, 9 of the generalized Hallopeau-Siemens type and 5 of the inverse type.
I, Hashimoto +4 more
openaire +2 more sources
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1987
We report the case of a 25-year-old woman with bullous lesions diagnosed as the rare pustular type of pemphigus described by Hallopeau. Direct immunofluorescence studies revealed deposits of IgG and C3 in the intercellular spaces of the epidermis; the indirect immunofluorescence technique revealed circulating antiepithelial IgG antibodies.
M, Gerharz, R, Stadler
openaire +1 more source
We report the case of a 25-year-old woman with bullous lesions diagnosed as the rare pustular type of pemphigus described by Hallopeau. Direct immunofluorescence studies revealed deposits of IgG and C3 in the intercellular spaces of the epidermis; the indirect immunofluorescence technique revealed circulating antiepithelial IgG antibodies.
M, Gerharz, R, Stadler
openaire +1 more source
Angiosarcoma complicating Hallopeau–Siemens‐type hereditary epidermolysis bullosa
British Journal of Dermatology, 1998null Schmutz +4 more
openaire +1 more source
Zeitschrift fur Hautkrankheiten, 1983
In epidermolysis bullosa dystrophica recessiva Hallopeau-Siemens, blister formation is due to an excessive synthesis and secretion of a genetically altered collagenase which, under mechanical trauma, becomes activated out of its pro-enzyme and leads to the destruction of collagen in the papillary dermis. There is evidence that phenytoin can inhibit the
H, Wirth +3 more
openaire +1 more source
In epidermolysis bullosa dystrophica recessiva Hallopeau-Siemens, blister formation is due to an excessive synthesis and secretion of a genetically altered collagenase which, under mechanical trauma, becomes activated out of its pro-enzyme and leads to the destruction of collagen in the papillary dermis. There is evidence that phenytoin can inhibit the
H, Wirth +3 more
openaire +1 more source
Treatment of Acrodermatitis Continua of Hallopeau With Ixekizumab
Journal of Dermatological Treatment, 2021Austinn C Miller
exaly
Acrodermatitis Continua of Hallopeau Successfully Treated With Bimekizumab: A Case Report
SAGE Open Medical Case Reports, 2023Katrina Cirone
exaly
Journal of the European Academy of Dermatology and Venereology, 2022
Takuya Kawamura +11 more
openaire +1 more source
Takuya Kawamura +11 more
openaire +1 more source