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Quoted phrase not found in phrase index: "Abnormal dermoepidermal junction morphology"
Page 1
Bullous systemic lupus erythematosus: a review and update to diagnosis and treatment.
Contestable JJ, Edhegard KD, Meyerle JH. Contestable JJ, et al. Am J Clin Dermatol. 2014 Dec;15(6):517-24. doi: 10.1007/s40257-014-0098-0. Am J Clin Dermatol. 2014. PMID: 25358414 Review.
It is a heterogeneous disease that is caused by autoantibodies to the dermoepidermal junction, mainly type VII collagen. Similarities in histology and immunopathology exist between BSLE and other primary bullous dermatoses, namely dermatitis herpetiformis (DH …
It is a heterogeneous disease that is caused by autoantibodies to the dermoepidermal junction, mainly type VII collagen. Simil …
Immunofluorescence antigen mapping for hereditary epidermolysis bullosa.
Rao R, Mellerio J, Bhogal BS, Groves R. Rao R, et al. Indian J Dermatol Venereol Leprol. 2012 Nov-Dec;78(6):692-7. doi: 10.4103/0378-6323.102358. Indian J Dermatol Venereol Leprol. 2012. PMID: 23075637 Free article. Review.
Epidermolysis bullosa (EB) is a group of inherited, mechanobullous disorders that are caused by mutations in the structural proteins in the epidermis or dermoepidermal junction. Characteristic clinical picture is the presence of blisters at trauma prone areas of the …
Epidermolysis bullosa (EB) is a group of inherited, mechanobullous disorders that are caused by mutations in the structural proteins in the …
Epidermolysis bullosa acquisita in childhood.
Callot-Mellot C, Bodemer C, Caux F, Bourgault-Villada I, Fraitag S, Goudié G, Heller M, de Prost Y, Prost C. Callot-Mellot C, et al. Arch Dermatol. 1997 Sep;133(9):1122-6. Arch Dermatol. 1997. PMID: 9301589 Review.
BACKGROUND: Epidermolysis bullosa acquisita (EBA) is an autoimmune bullous disease characterized by the presence of antitype VII collagen antibodies, leading to the formation of bullae in the dermoepidermal junction. This disease is rare in childhood. OBSERVATIONS: …
BACKGROUND: Epidermolysis bullosa acquisita (EBA) is an autoimmune bullous disease characterized by the presence of antitype VII collagen an …
Epidermolysis bullosa acquisita.
Stein JA, Mikkilineni R. Stein JA, et al. Dermatol Online J. 2007 Jan 27;13(1):15. Dermatol Online J. 2007. PMID: 17511948 Free article.
A direct immunofluorescence test showed a linear deposit of IgG at the dermo-epidermal junction. These findings were consistent with a diagnosis of epidermolysis bullosa acquisita. ...
A direct immunofluorescence test showed a linear deposit of IgG at the dermo-epidermal junction. These findings were consistent with …
Immunofluorescence mapping for the diagnosis of epidermolysis bullosa.
Pohla-Gubo G, Cepeda-Valdes R, Hintner H. Pohla-Gubo G, et al. Dermatol Clin. 2010 Apr;28(2):201-10, vii. doi: 10.1016/j.det.2009.12.005. Dermatol Clin. 2010. PMID: 20447482 Review.
Immunofluorescence mapping is based on the detection of structural proteins of keratinocytes or of the dermo-epidermal junction using specific poly- or monoclonal antibodies. Through this method, the level of split formation can be determined by investigating the location …
Immunofluorescence mapping is based on the detection of structural proteins of keratinocytes or of the dermo-epidermal junction using …
Ultrastructural findings in epidermolysis bullosa.
Smith LT. Smith LT. Arch Dermatol. 1993 Dec;129(12):1578-84. Arch Dermatol. 1993. PMID: 7504435
Changes in the density and structure of anchoring fibrils and the relative amount of type VII collagen detected by immunostaining of the dermoepidermal junction in dystrophic EB have led to sequencing of mutations in the type VII collagen gene. Although mutations in …
Changes in the density and structure of anchoring fibrils and the relative amount of type VII collagen detected by immunostaining of the …
Characterisation of the pathophysiology of neuropathy and sensory dysfunction in a mouse model of recessive dystrophic epidermolysis bullosa.
Schmidt D, Díaz P, Muñoz D, Espinoza F, Nystrom A, Fuentes I, Ezquer M, Bennett DL, Calvo M. Schmidt D, et al. Pain. 2022 Oct 1;163(10):2052-2060. doi: 10.1097/j.pain.0000000000002599. Epub 2022 Jan 28. Pain. 2022. PMID: 35311752
Recessive dystrophic epidermolysis bullosa (RDEB) is a rare genetic condition in which mutations in the type VII collagen gene ( COL7A1 ) lead to decreased expression of this anchoring protein of the skin, causing the loss of stability at the dermo-epidermal junction. Most …
Recessive dystrophic epidermolysis bullosa (RDEB) is a rare genetic condition in which mutations in the type VII collagen gene ( COL7A1 ) le …
The biomolecular and ultrastructural basis of epidermolysis bullosa.
Solovan C, Ciolan M, Olariu L. Solovan C, et al. Acta Dermatovenerol Alp Pannonica Adriat. 2005 Dec;14(4):127-35. Acta Dermatovenerol Alp Pannonica Adriat. 2005. PMID: 16435041 Free article. Review.
Transmission electron microscopy, immunoelectron microscopy, immunofluorescence and antigenic mapping have improved our understanding of the dermo-epidermal junction. We have reviewed some ultrastructural and biomolecular aspects related to the dermo-epidermal junction …
Transmission electron microscopy, immunoelectron microscopy, immunofluorescence and antigenic mapping have improved our understanding of the …
Antigenic features and structural correlates of basement membranes. Relationship to epidermolysis bullosa.
Fine JD. Fine JD. Arch Dermatol. 1988 May;124(5):713-7. Arch Dermatol. 1988. PMID: 2452606 Review.
Numerous antigenic epitopes are present within the dermoepidermal junction of human skin. Using monoclonal antibodies, the distribution of these epitopes in ontogeny, wound healing, and epidermolysis bullosa are being defined. ...
Numerous antigenic epitopes are present within the dermoepidermal junction of human skin. Using monoclonal antibodies, the dis …
Dynamic Optical Coherence Tomography Capillaroscopy: A New Imaging Tool in Autoimmune Connective Tissue Disease.
Ring HC, Themstrup L, Banzhaf CA, Jemec GB, Mogensen M. Ring HC, et al. JAMA Dermatol. 2016 Oct 1;152(10). doi: 10.1001/jamadermatol.2016.2027. JAMA Dermatol. 2016. PMID: 27366896
IMPORTANCE: Vasculopathy characterized by functional and structural abnormalities of the microcirculation plays an important role in systemic sclerosis and dermatomyositis. ...Moreover, cross-sectional OCT images demonstrated a characteristic loss of distinct dermo-epiderm …
IMPORTANCE: Vasculopathy characterized by functional and structural abnormalities of the microcirculation plays an important role in …
38 results