Jurgen Brunner
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Explore the profile of Jurgen Brunner including associated specialties, affiliations and a list of published articles.
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45
Citations
1189
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Recent Articles
1.
Hospach T, Blankenburg F, Heinkele A, Rucklova K, Muller-Abt P, Weller-Heinemann F, et al.
ACR Open Rheumatol
. 2025 Jan;
7(1):e11799.
PMID: 39876070
Objective: Pulmonary involvement in chronic nonbacterial osteomyelitis (CNO) is rare. Limited awareness results in diagnostic challenges, especially because malignancy or infection needs to be considered. Methods: Based on a survey...
2.
Lohrmann F, Doenhardt M, Diffloth N, Jakob A, Hospach A, Schneider D, et al.
J Pediatr
. 2024 Nov;
278:114419.
PMID: 39603520
Objective: To elucidate how the clinical presentation of Pediatric Inflammatory Multisystem Syndrome temporally associated with Severe Acute Respiratory Syndrome-related Coronavirus 2 (PIMS-TS) was influenced by the successive variants of concern...
3.
Weidler S, Koss S, Wolf C, Lucas N, Brunner J, Lee-Kirsch M
Pediatr Rheumatol Online J
. 2024 Jan;
22(1):9.
PMID: 38178067
Background: STING-associated vasculopathy with onset in infancy (SAVI) is a rare type I interferonopathy caused by heterozygous variants in the STING gene. In SAVI, STING variants confer a gain-of-function which...
4.
Mayerhofer T, Perschinka F, Klein S, Peer A, Lehner G, Bellmann R, et al.
J Nephrol
. 2023 Oct;
36(9):2531-2540.
PMID: 37837501
Introduction: Acute kidney injury is a frequent complication in critically ill patients with and without COVID-19. The aim of this study was to evaluate the incidence of, and risk factors...
5.
Ehlers L, Rolfes E, Lieber M, Muller D, Lainka E, Gohar F, et al.
Pediatr Rheumatol Online J
. 2023 Sep;
21(1):108.
PMID: 37752496
Background: The objective of this initiative was to develop a treat-to-target (T2T) approach for the management of patients with Familial Mediterranean Fever (FMF), including the definition of a complex treatment...
6.
Klotsche J, Torok K, Kasapcopur O, Adrovic A, Terreri M, Sakamoto A, et al.
J Scleroderma Relat Disord
. 2023 Sep;
8(3):183-191.
PMID: 37744052
Objectives: Juvenile systemic sclerosis is a rare childhood disease. Three disease activity indices have been published for adult patients with systemic sclerosis: the European Scleroderma Study Group Index, a modified...
7.
Berner J, van de Wetering C, Heredia R, Rashkova C, Ferdinandusse S, Koster J, et al.
J Allergy Clin Immunol
. 2023 Jun;
152(4):1025-1031.e2.
PMID: 37364720
Background: In the isoprenoid biosynthesis pathway, mevalonate is phosphorylated in 2 subsequent enzyme steps by MVK and PMVK to generate mevalonate pyrophosphate that is further metabolized to produce sterol and...
8.
Foeldvari I, Klotsche J, Kasapcopur O, Adrovic A, Terreri M, Sakamoto A, et al.
J Scleroderma Relat Disord
. 2023 Jun;
8(2):120-130.
PMID: 37287945
Objective: To compare organ involvement and disease severity between male and female patients with juvenile onset systemic sclerosis. Methods: Demographics, organ involvement, laboratory evaluation, patient-reported outcomes and physician assessment variables...
9.
Fiegl A, Dirnhofer S, Juskevicius D, Zagrapan B, Dertinger S, Bosl A, et al.
Pathol Res Pract
. 2023 May;
247:154548.
PMID: 37216748
Background: Rosai-Dorfman disease (RDD), a rare form of non-Langerhans cell histiocytosis with heterogenous clinical features, arises from precursor cells that give rise to cells of the histiocytic and monocytic lineages....
10.
van Straalen J, Baas L, Giancane G, Grebenkina L, Brunner J, Vega-Cornejo G, et al.
Pediatr Rheumatol Online J
. 2023 Feb;
21(1):19.
PMID: 36810111
Background: Little is known about the association between juvenile idiopathic arthritis (JIA) and autoimmune thyroid disease (AITD) and therefore there are no indications for AITD screening in this population, which...