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VEXAS-Syndrom – Ein Kurzreview

Aktuelle Dermatologie
ZusammenfassungVEXAS (Vakuolen, E1-Enzyme, X-chromosomal, Autoinflammation, Somatisch)-Syndrom, 2020 erstmals beschrieben, ist verursacht durch Mutationen des UBA1-Gens im X-Chromosom, was zu Dysregulation des angeborenen Immunsystems infolge von fehlerhafter Ubiquitinierung führt.
openaire   +1 more source

Acute tubulointerstitial nephritis revealing VEXAS syndrome

Kidney International, 2022
Charles, Ronsin, Laurent, Benard, Amélie, Mourtada, François, Perrin, Zakaria, Boukerroucha   +4 more
openaire   +2 more sources

Clinical and pathological features of cutaneous manifestations in VEXAS syndrome: A multicenter retrospective study of 59 cases

Journal of the American Academy of Dermatology, 2023
Alexis Mathian, Philippe Moguelet
exaly  

VEXAS syndrome: lessons learnt from an early Australian case series

Internal Medicine Journal, 2022
Sadia Islam, Daniel Sumpton, Arvin K Damodaran   +2 more
exaly  

Le syndrome Vexas

La Revue de Médecine Interne, 2023
openaire   +1 more source

A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosis

Blood Cells, Molecules, and Diseases, 2022
Gregory M Vercellotti, Charles J Billington Jr., Sophia Yohe   +2 more
exaly  

Characteristic bone marrow findings in patients with UBA1 somatic mutations and VEXAS syndrome

Seminars in Hematology, 2021
Katherine R Calvo
exaly  

Therapeutic options in VEXAS syndrome: insights from a retrospective series

Blood, 2021
Estelle Bourbon, Maël Heiblig, Thomas Barba   +2 more
exaly  

Clonal hematopoiesis in VEXAS syndrome

Blood, 2023
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Vexas syndrome successfully treated with canakinumab

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2023
Cristina, Collantes-Rodríguez, David, Jiménez-Gallo, Raquel, de la Varga-Martínez, Francisco, Mora-López, Maria Paz, Garrastazul-Sánchez, Mario, Linares-Barrios   +5 more
openaire   +2 more sources