Juvenile and adult vulvar pemphigoid, an under recognized entity: Case series of fourteen patients

Autor: Hanan Rashid, MD, J. Marja Oldhoff, MD, PhD, Martha Esajas, MD, Gilles F.H. Diercks, MD, PhD, Hendri H. Pas, PhD, Maria C. Bolling, MD, PhD, Barbara Horváth, MD, PhD

Publikováno v: JAAD Case Reports, Vol 13, Iss , Pp 75-80 (2021)

Externí odkaz: https://doaj.org/article/163499c3074f43d9bb665afb3bd37594

Direct Evidence of Endothelial Dysfunction and Glycocalyx Loss in Dermal Biopsies of Patients With Chronic Kidney Disease and Their Association With Markers of Volume Overload

Autor: Josephine Koch, Ryanne S. Hijmans, Manuela Ossa Builes, Wendy A. Dam, Robert A. Pol, Stephan J. L. Bakker, Hendri H. Pas, Casper F. M. Franssen, Jacob van den Born

Publikováno v: Frontiers in Cell and Developmental Biology, Vol 9 (2021)

Cardiovascular morbidity is a major problem in patients with chronic kidney disease (CKD) and endothelial dysfunction (ED) is involved in its development. The luminal side of the vascular endothelium is covered by a protective endothelial glycocalyx

Externí odkaz: https://doaj.org/article/2c22efec536f4b079312ebfec65313ef

Is skin autofluorescence (SAF) representative of dermal advanced glycation endproducts (AGEs) in dark skin? A pilot study

Autor: Isabella M. Atzeni, Jeltje Boersema, Hendri H. Pas, Gilles F.H. Diercks, Jean L.J.M. Scheijen, Casper G. Schalkwijk, Douwe J. Mulder, Piet van der Zee, Andries J. Smit

Publikováno v: Heliyon, Vol 6, Iss 11, Pp e05364- (2020)

Aims: Non-invasively assessed skin autofluorescence (SAF) measures advanced glycation endproducts (AGEs) in the dermis. SAF correlates with dermal AGEs in Caucasians and Asians, but studies in dark-skinned subjects are lacking. In this pilot we aimed

Externí odkaz: https://doaj.org/article/63716b8e7a8e45cb8164b96bc7a2254f

Differences in IgG autoantibody Fab glycosylation across autoimmune diseases

Autor: Jana Koers, Rocco Sciarrillo, Ninotska I.L. Derksen, Esther M. Vletter, Yvonne E. Fillié-Grijpma, Elisabeth Raveling-Eelsing, Nuno A.G. Graça, Thiemo Leijser, Hendri H. Pas, L. Laura van Nijen-Vos, Maaike V.J. Braham, Anne-Marie Buisman, Jan de Jong, Angela I. Schriek, Anne P. Tio-Gillen, Y.K. Onno Teng, Maurice Steenhuis, Francis H. Swaneveld, Steven W. de Taeye, Marit J. van Gils, Jan J.G.M. Verschuuren, Bram Rutgers, Peter Heeringa, Barbara Horváth, Bart C. Jacobs, Karina de Leeuw, Casper F.M. Franssen, Agnès Veyradier, Paul Coppo, Kyra A. Gelderman, S. Marieke van Ham, Cécile A.C.M. van Els, Diane van der Woude, Ruth Huizinga, Maartje G. Huijbers, Taco W. Kuijpers, Rene E.M. Toes, Nicolaas A. Bos, Theo Rispens

Publikováno v: Journal of Allergy and Clinical Immunology, 151(6), 1646-1654. MOSBY-ELSEVIER
Journal of Allergy and Clinical Immunology, 151(6), 1646-1654. Mosby Inc.
Journal of allergy and clinical immunology, 151(6), 1646-1654. Mosby Inc.
T2B Consortium 2023, ' Differences in IgG autoantibody Fab glycosylation across autoimmune diseases ', Journal of Allergy and Clinical Immunology, vol. 151, no. 6, pp. 1646-1654 . https://doi.org/10.1016/j.jaci.2022.10.035

Background: Increased prevalence of autoantibody Fab glycosylation has been demonstrated for several autoimmune diseases. Objectives: To study whether elevated Fab glycosylation is a common feature of autoimmunity, this study investigated Fab glycosy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5813e3dc93eee892ef693f3c417e2f1
https://research.rug.nl/en/publications/53202de0-8a76-4930-ae74-692d30576434

Reduced Skin Blistering in Experimental Epidermolysis Bullosa Acquisita After Anti-TNF Treatment

Autor: Misa Hirose, Anika Kasprick, Foteini Beltsiou, Katharina Schulze Dieckhoff, Franziska Sophie Schulze, Unni K J S R L Samavedam, Jennifer E Hundt, Hendri H Pas, Marcel F Jonkman, Enno Schmidt, Kathrin Kalies, Detlef Zillikens, Ralf J Ludwig, Katja Bieber

Publikováno v: Molecular Medicine, Vol 22, Iss 1, Pp 918-926 (2016)

Abstract Epidermolysis bullosa acquisita (EBA) is a difficult-to-treat subepidermal autoimmune blistering skin disease (AIBD) with circulating and tissue-bound anti-type VII collagen antibodies. Different reports have indicated increased concentratio

Externí odkaz: https://doaj.org/article/cad7ed1862314f8189795dfa12ef02bb