Results 61 to 70 of about 23,288 (156)

MORPHOLOGICAL CHARACTERISTICS OF CORONARY AND CAROTID ATHEROSCLEROTIC PLAQUES IN PATIENTS WITH MYOCARDIAL INFARCTION

open access: yesНаука и инновации в медицине, 2017
Aim - to study the correlation between the thickness of the fibrous cap and collagen in the coronary and carotid plaques in patients with myocardial infarction. Materials and methods.
LN N Slatova   +4 more
doaj   +1 more source

An Exceedingly Rare Case of Mechanobullous Epidermolysis Bullosa Acquisita in a Prepubertal Child: A Review of the Clinical and Laboratory Considerations

open access: yesAntibodies
Introduction: Epidermolysis bullosa acquisita (EBA) is a rare autoimmune disease causing subepithelial blistering due to autoantibodies against type VII collagen.
Aleksandra Wiktoria Bratborska   +3 more
doaj   +1 more source

Unusual presentation of childhood Systemic Lupus Erythematosus

open access: yesPediatric Rheumatology Online Journal, 2007
Bullous systemic lupus erythematosus is a rare blistering condition with a distinctive combination of clinical, histological and immunopathologic features that together constitute a unique bullous disease phenotype.
Agarwal Indira, Kumar Sathish
doaj   +1 more source

Hemidesmosomes, Collagen VII, and Intermediate Filaments in Basal Cell Carcinoma

open access: yesJournal of Investigative Dermatology, 1989
We have undertaken an analysis of hemidesmosomes (HD) and their associated structures, intermediate filaments (IF) and anchoring fibrils (AF), in various types of basal cell carcinoma (BCC). Using a combination of electron microscopy and immunofluorescence microscopy we show that there is a correlation between the loss of HD and tumor type (i.e., in ...
Jones, Jonathan C.R.   +2 more
openaire   +2 more sources

Drug‐induced linear IgA disease with antibodies to collagen VII

open access: yesBritish Journal of Dermatology, 1998
Linear IgA disease (LAD) is characterized by circulating and tissue-bound IgA antibodies against heterogeneous antigens in the cutaneous basement membrane zone. In most cases the cause is unknown, but a minority of cases has been drug induced. We report a 76-year-old man who developed an acute blistering eruption following high-dose penicillin ...
Wakelin, S   +3 more
openaire   +3 more sources

A Novel COL7A1 Mutation in a Patient With Dystrophic Epidermolysis Bullosa. Successful Treatment With Upadacitinib

open access: yesClinical, Cosmetic and Investigational Dermatology
Shuqin Lai,* Chunli Lin,* Zimeng Guo, Yun Lai, Ling Xie, Chunlei Wan, Tao Yang, Longnian Li Department of Dermatology, Candidate Branch of National Clinical Research Centre for Skin and Immune Diseases, First Affiliated Hospital of Gannan Medical
Lai S   +7 more
doaj  

First Report of Homozygous COL7A1 c.5756delG Mutation Causing Recessive Dystrophic Epidermolysis Bullosa in a Non‐Consanguineous Japanese Family

open access: yesJEADV Clinical Practice
Severe recessive dystrophic epidermolysis bullosa (RDEB) is usually caused by biallelic loss‐of‐function mutations in COL7A1. While the c.5756delG variant has been previously reported in heterozygous form, its clinical impact in homozygosity has not been
Nozomi Kohama   +6 more
doaj   +1 more source

Combinatorial Omics Analysis Reveals Perturbed Lysosomal Homeostasis in Collagen VII-deficient Keratinocytes. [PDF]

open access: yesMol Cell Proteomics, 2018
Thriene K   +13 more
europepmc   +1 more source

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