Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Sofie, De Schepper"'
Autor:
Nanja van Geel, Liesbeth Delbaere, Laura Mertens, Virginie Vandaele, Lien Depaepe, Jérôme Van Causenbroeck, Sofie De Schepper, Laura Van Coile, Astrid Van Reempts, Ann-Sophie De Vos, Jorien Papeleu, Isabelle Hoorens, Albert Wolkerstorfer, Reinhart Speeckaert
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 9, p 2680 (2024)
Background/Objectives: There is currently no guidance on how to interpret the global degrees of activity (worsening) and repigmentation (improvement) in vitiligo. Stratification into global degrees can be completed for static evaluations (e.g., visib
Externí odkaz:
https://doaj.org/article/16a9f98907884bf999bb3112a3e0f770
Autor:
Yacine Wissam, Laila Belcaid, Ruth Wittoek, Vanessa Smith, Amber Vanhaecke, Sofie De Schepper, Lennart Jans, Daphné t’Kint de Roodenbeke, Andrea Gombos, Sandrine Aspeslagh
Publikováno v:
Journal of Immunotherapy and Precision Oncology, Pp 101-105 (2019)
Immune checkpoint inhibition has revolutionized the treatment for numerous cancer patients; however, the spectrum of immune-related adverse events (irAEs) remains to be fully uncovered. We report a 48-year-old woman who was treated in the Phase III I
Externí odkaz:
https://doaj.org/article/3c963379cc8f4b81aa4a3aafcf0b962f
Autor:
Aude Beyens, Laure Dequeker, Hilde Brems, Sandra Janssens, Hannes Syryn, Anne D’Hooghe, Pascale De Paepe, Lieve Vanwalleghem, Annelies Stockman, Elena Vankwikelberge, Sofie De Schepper, Marleen Goeteyn, Patricia Delbeke, Bert Callewaert
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 4036 (2022)
Mosaic RASopathies are a molecularly heterogeneous group of (neuro)cutaneous syndromes with high phenotypical variability. Postzygotic variants in KRAS have been described in oculoectodermal syndrome (OES), encephalocraniocutaneous lipomatosis (ECCL)
Externí odkaz:
https://doaj.org/article/c8824fda9b56491d8380884d8252d02e
Publikováno v:
Dermatology Practical & Conceptual, Vol 9, Iss 1 (2019)
Externí odkaz:
https://doaj.org/article/9aa5f1003264427d96c3f7457bf7abba
Autor:
Ignace De Decker, Henk Hoeksema, Jozef Verbelen, Petra De Coninck, Marijn Speeckaert, Sofie De Schepper, Phillip Blondeel, Ali Pirayesh, Stan Monstrey, Karel E Y Claes
Publikováno v:
Burns & Trauma. 11
Background Absence of almost the entire reticular dermal layer is inherent to the use of autologous split-thickness skin grafting (STSG) to close full-thickness wounds, often resulting in hypertrophic scars and contractures. Many dermal substitutes h
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 5, p 1040 (2021)
The biologic era has greatly improved the treatment of Crohn’s disease and ulcerative colitis. Biologics can however induce a wide variety of skin eruptions, especially those targeting the TNF-α and Th17 pathway. These include infusion reactions,
Externí odkaz:
https://doaj.org/article/b4c374dd63514fda85d6648471e69fe8
Autor:
Arjen Nikkels, Murielle Sabatiello, Sofie De Schepper, Eve Lebas, Virginie De Schaetzen, Florence Libon
Publikováno v:
Expert Review of Clinical Immunology. 17:947-955
Introduction Psoriasis affects around 2% of children in Europe. The majority of cases is readily managed with topical treatments using corticosteroids without or with calcipotriol. More resistant and extensive moderate-to-severe cases require UVA or
Autor:
Aude Beyens, Kyaran Van Meensel, Lore Pottie, Riet De Rycke, Michiel De Bruyne, Femke Baeke, Piet Hoebeke, Frank Plasschaert, Bart Loeys, Sofie De Schepper, Sofie Symoens, Bert Callewaert
Publikováno v:
Genes, Vol 10, Iss 7, p 528 (2019)
Occipital horn syndrome (OHS) is a rare connective tissue disorder caused by pathogenic variants in ATP7A, encoding a copper transporter. The main clinical features, including cutis laxa, bony exostoses, and bladder diverticula are attributed to a de
Externí odkaz:
https://doaj.org/article/309416e0d3774dffa1e85bbfad332bce
Autor:
Nanja van Geel, Marijn Speeckaert, Ines Chevolet, Sofie De Schepper, Hilde Lapeere, Barbara Boone, Reinhart Speeckaert
Publikováno v:
Journal of Cutaneous and Aesthetic Surgery, Vol 6, Iss 2, Pp 65-72 (2013)
Hypomelanosis of the skin is a frequently encountered problem in childhood, being totally innocent or representing the first sign of a multisystem disorder. Medical history, clinical examination, Wood′s light investigation, histological analysis of
Externí odkaz:
https://doaj.org/article/ac3253d29fee4c178ff55a22a78561cf
Autor:
Ana Karina Alves de Medeiros, Reinhart Speeckaert, Eline Desmet, Mireille Van Gele, Sofie De Schepper, Jo Lambert
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164080 (2016)
The recent interest and elucidation of the JAK/STAT signaling pathway created new targets for the treatment of inflammatory skin diseases (ISDs). JAK inhibitors in oral and topical formulations have shown beneficial results in psoriasis and alopecia
Externí odkaz:
https://doaj.org/article/162c65ec23b14472b44796074549df9b