Inhibition of glucose metabolism abrogates the effector phase of bullous pemphigoid-like epidermolysis bullosa acquisita

2021 ◽  
Author(s):  
Paul Schilf ◽  
Marie Schmitz ◽  
Aleksandra Derenda-Hell ◽  
Markus Thieme ◽  
Tabea Bremer ◽  
...  
Keyword(s):  
Glucose Metabolism ◽  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Acquisita ◽  
Effector Phase

The retinoid-related orphan receptor alpha is essential for the end-stage effector phase of experimental epidermolysis bullosa acquisita

2015 ◽  
Vol 237 (1) ◽  
pp. 111-122 ◽  
Author(s):  
Hengameh Sadeghi ◽  
Yask Gupta ◽  
Steffen Möller ◽  
Unni K Samavedam ◽  
Martina Behnen ◽  
...  
Keyword(s):  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Acquisita ◽  
Orphan Receptor ◽  
Receptor Alpha ◽  
Effector Phase ◽  
End Stage

Epidermolysis bullosa acquisita with Combined Features of Bullous Pemphigoid and Cicatricial Pemphigoid

Dermatology ◽  
1999 ◽  
Vol 198 (3) ◽  
pp. 310-313 ◽  
Author(s):  
N. Wieme ◽  
J. Lambert ◽  
M. Moerman ◽  
M.L. Geerts ◽  
L. Temmerman ◽  
...  
Keyword(s):  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Acquisita ◽  
Cicatricial Pemphigoid ◽  
Combined Features

scholarly journals Bullous Systemic Lupus Erythematosus

2018 ◽  
Vol 19 (2) ◽  
pp. 123-125
Author(s):  
Sk Jakaria Been Sayeed ◽  
Md Mujibur Rahman ◽  
AKM Humayon Kabir ◽  
Md Moniruzzaman ◽  
Uzzal Mallik ◽  
...  
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Lupus Erythematosus ◽  
Dermatitis Herpetiformis ◽  
Epidermolysis Bullosa Acquisita ◽  
Systemic Lupus ◽  
Type Vii Collagen ◽  
Linear Iga Disease ◽  
Distinct Disease

Bullous systemic lupus erythematosus (BSLE) is extremely rare but distinct disease, characterized by vesicobullous skin eruptions in systemic lupus erythematosus (SLE). It can develop either before or after a diagnosis of SLE has been established. BSLE is characterized by a dermatitis herpetiformis-like histology and an autoimmunity to type VII collagen. It must be differentiated from other autoimmune vesicobullous diseases such as epidermolysis bullosa acquisita, dermatitis herpetiformis, linear IgA disease, and bullous pemphigoid. Its important to combine clinical, histological, and immunofluorescence findings to establish a diagnosis of BSLE. We report a case of BSLE to illustrate and emphasize the need for an integrative diagnostic approach.J MEDICINE JUL 2018; 19 (2) : 123-125

Autoantibodies to bullous pemphigoid and epidermolysis bullosa acquisita antigens in an infant

1996 ◽  
Vol 135 (3) ◽  
pp. 443-447 ◽  
Author(s):  
Y. KAWACHI ◽  
M. IKEGAMI ◽  
T. HASHIMOTO ◽  
K. MATSUMURA ◽  
T. TANAKA ◽  
...  
Keyword(s):  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Acquisita

Bullous Pemphigoid and Epidermolysis Bullosa Acquisita: Presentation, Prognosis, and Immunopathology in 11 Children

2009 ◽  
Vol 15 (3) ◽  
pp. 184-190 ◽  
Author(s):  
S. Edwards ◽  
S. H. Wakelin ◽  
F. Wojnarowska ◽  
R. A. Marsden ◽  
G. Kirtschig ◽  
...  
Keyword(s):  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Acquisita
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