Zobrazeno 1 - 10
of 156
pro vyhledávání: '"F H, Diercks"'
Publikováno v:
Diagnostics, Vol 14, Iss 15, p 1665 (2024)
The 2018 WHO edition on the classification of cutaneous melanocytic tumors recognizes eight evolutionary pathways of melanoma and describes tumors of uncertain malignant potential for each. When histology and immunohistochemistry do not support a con
Externí odkaz:
https://doaj.org/article/35d226cf111b4d09ab1b4a91fcafb8db
Autor:
Gilles F. H. Diercks, Joost M. Meijer, Maria C. Bolling, Sonja M. H. J. Scholtens-Jaegers, Jeroen Bremer, Barbara Horvath
Publikováno v:
Dermatology Research and Practice, Vol 2024 (2024)
Background. Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare and potentially life-threatening mucocutaneous blistering diseases that clinically can resemble autoimmune bullous diseases. Moreover, it has been shown that a
Externí odkaz:
https://doaj.org/article/2dfc37585baa47bfb19328f2d3de25b9
Autor:
Stephanie Goletz, Federica Giurdanella, Maike M. Holtsche, Miranda Nijenhuis, Barbara Horvath, Gilles F. H. Diercks, Detlef Zillikens, Takashi Hashimoto, Enno Schmidt, Hendri H. Pas
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Anti-laminin 332 mucous membrane pemphigoid (MMP) is an autoimmune blistering disease characterized by predominant mucosal lesions and autoantibodies against laminin 332. The exact diagnosis of anti-laminin 332 MMP is important since nearly 30% of pa
Externí odkaz:
https://doaj.org/article/ababc5e370bd45299b68ae0f420b8693
Autor:
Ellen C. de Heer, Adrienne H. Brouwers, Ronald Boellaard, Wim J. Sluiter, Gilles F. H. Diercks, Geke A. P. Hospers, Elisabeth G. E. de Vries, Mathilde Jalving
Publikováno v:
EJNMMI Research, Vol 8, Iss 1, Pp 1-9 (2018)
Abstract Background Metastatic melanoma patients can have durable responses to systemic therapy and even long-term survival. However, a large subgroup of patients does not benefit. Tumour metabolic alterations may well be involved in the efficacy of
Externí odkaz:
https://doaj.org/article/5086db9bcd3c48ce91148ab49791a9fc
Autor:
Pieter J. Steinkamp, Jasper Vonk, Lydian A. Huisman, Gert-Jan Meersma, Gilles F. H. Diercks, Jan-Luuk Hillebrands, Wouter B. Nagengast, Clark J. Zeebregts, Riemer H. J. A. Slart, Hendrikus H. Boersma, Gooitzen M. van Dam
Publikováno v:
Diagnostics, Vol 11, Iss 7, p 1227 (2021)
Vulnerable atherosclerotic carotid plaques are prone to rupture, resulting in ischemic strokes. In contrast to radiological imaging techniques, molecular imaging techniques have the potential to assess plaque vulnerability by visualizing diseases-spe
Externí odkaz:
https://doaj.org/article/e33eef6a0e1b4b2f836c4d029b67d2a7
Autor:
Gareth Edwards, Gilles F. H. Diercks, Marc A. J. Seelen, Barbara Horvath, Martijn B. A. van Doorn, Jeffrey Damman
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Autoimmune bullous dermatoses (AIBD) are characterized by circulating autoantibodies that are either directed against epidermal antigens or deposited as immune complexes in the basement membrane zone (BMZ). The complement system (CS) can be activated
Externí odkaz:
https://doaj.org/article/8bc250f461d54e45895e811115dcce0f
Autor:
Jenny Giang, Martijn B. A. van Doorn, Gilles F. H. Diercks, Santiago Rodriguez de Cordoba, Thierry P. P. van den Bosch, Marco W. J. Schreurs, Felix Poppelaars, Jeffrey Damman
Publikováno v:
Experimental Dermatology, 32(5), 632-640. Wiley-Blackwell Publishing Ltd
9 p.-2 fig.-2 tab.
Bullous pemphigoid (BP) is characterized by deposition of immunoglobulins and complement along the epidermal basement membrane (BM). In humans, there is a lack of functional studies targeting the complement system (CS). This s
Bullous pemphigoid (BP) is characterized by deposition of immunoglobulins and complement along the epidermal basement membrane (BM). In humans, there is a lack of functional studies targeting the complement system (CS). This s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0427cc8dd3bc33e00969b85904d7c43
https://pure.eur.nl/en/publications/11fe8d25-a9cf-4971-84d4-71c9f8f08399
https://pure.eur.nl/en/publications/11fe8d25-a9cf-4971-84d4-71c9f8f08399
Autor:
Marjolein J. Koldijk, Arjan Diepstra, Gilles F. H. Diercks, Marloes S. van Kester, Larissa E. van Eijk
Publikováno v:
American journal of dermatopathology, 44(2), E19-E22. LIPPINCOTT WILLIAMS & WILKINS
Immunodeficiency-associated lymphoproliferative disorders are associated with latent infection by Epstein-Barr virus (EBV). Most cases of EBV-positive immunodeficiency-associated lymphoproliferative disorders arise from B cells, although some are of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9a4f161b207c9d7860facfdc7545a58
https://hdl.handle.net/11370/3f45a4dc-3bf4-48bb-9eca-3cd1e55bce19
https://hdl.handle.net/11370/3f45a4dc-3bf4-48bb-9eca-3cd1e55bce19
Autor:
Irma van de Beek, Iris E Glykofridis, Jan C Oosterwijk, Peter C van den Akker, Gilles F H Diercks, Maria C Bolling, Quinten Waisfisz, Arjen R Mensenkamp, Jesper A Balk, Rob Zwart, Alex V Postma, Hanne E J Meijers-Heijboer, R Jeroen A van Moorselaar, Rob M F Wolthuis, Arjan C Houweling
Publikováno v:
van de Beek, I, Glykofridis, I E, Oosterwijk, J C, van den Akker, P C, Diercks, G F H, Bolling, M C, Waisfisz, Q, Mensenkamp, A R, Balk, J A, Zwart, R, Postma, A V, Meijers-Heijboer, H E J, van Moorselaar, R J A, Wolthuis, R M F & Houweling, A C 2023, ' PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosis ', Human Molecular Genetics, vol. 32, no. 7, pp. 1223-1235 . https://doi.org/10.1093/hmg/ddac288
Human Molecular Genetics, 32, 1223-1235
Human Molecular Genetics, 32(7), 1223-1235. Oxford University Press
Human molecular genetics, 32(7), 1223-1235. Oxford University Press
Human Molecular Genetics, 32, 7, pp. 1223-1235
Human Molecular Genetics, 32, 1223-1235
Human Molecular Genetics, 32(7), 1223-1235. Oxford University Press
Human molecular genetics, 32(7), 1223-1235. Oxford University Press
Human Molecular Genetics, 32, 7, pp. 1223-1235
Contains fulltext : 291515.pdf (Publisher’s version ) (Open Access) Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant disorder characterized by fibrofolliculomas, pulmonary cysts, pneumothoraces and renal cell carcinomas. Here, we reveal a no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19bee29415900ea2982a28cc3469f7db
https://research.vumc.nl/en/publications/d755d70a-4c1f-4979-ab6b-f902c4942091
https://research.vumc.nl/en/publications/d755d70a-4c1f-4979-ab6b-f902c4942091
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Systemic sclerosis (SSc) is a rare connective tissue disease characterized by autoimmunity, vasculopathy, and progressive fibrosis typically affecting multiple organs including the skin. SSc often is a lethal disorder, because effective disease-modif
Externí odkaz:
https://doaj.org/article/aeab8fc101d24a7c9f51c0102eb3c32a