Tilmann Kallinich
Overview
Explore the profile of Tilmann Kallinich including associated specialties, affiliations and a list of published articles.
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104
Citations
2365
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Recent Articles
1.
Goetzke C, Massoud M, Frischbutter S, Guerra G, Ferreira-Gomes M, Heinrich F, et al.
Nature
. 2025 Mar;
PMID: 40074901
In a subset of children and adolescents, SARS-CoV-2 infection induces a severe acute hyperinflammatory shock termed multisystem inflammatory syndrome in children (MIS-C) at four to eight weeks after infection. MIS-C...
2.
Bjelde A, Leitz D, Goetzke C, von Stuckrad A, Thumfart J, Kallinich T
Klin Padiatr
. 2025 Feb;
237(2):102-105.
PMID: 39900083
No abstract available.
3.
Budzinski L, Kang G, Riedel R, Sempert T, Lietz L, Maier R, et al.
Gut Microbes
. 2025 Jan;
17(1):2452250.
PMID: 39815413
IgA-coated fractions of the intestinal microbiota of Crohn's disease (CD) patients have been shown to contain taxa that hallmark the compositional dysbiosis in CD microbiomes. However, the correlation between other...
4.
Oommen P, Kallinich T, Rech J, Blank N, Weber-Arden J, Kuemmerle-Deschner J
Rheumatol Ther
. 2024 Dec;
12(1):137-155.
PMID: 39724475
Introduction: Interim analysis of the long-term safety and effectiveness of canakinumab, at a patient level, in the mevalonate kinase deficiency/hyperimmunoglobulin-D syndrome (MKD/HIDS) cohort of the RELIANCE registry. Methods: From June...
5.
Budzinski L, Sempert T, Lietz L, Maier R, Kang G, von Stuckrad A, et al.
Mol Cell Pediatr
. 2024 Dec;
11(1):12.
PMID: 39653980
Objective: Juvenile Idiopathic Arthritis (JIA) comprises diverse chronic inflammatory conditions driven by malfunction of the immune system. The intestinal microbiota is considered a crucial environmental factor correlating with chronic inflammatory...
6.
Mevalonate kinase deficiency: an updated clinical overview and revision of the SHARE recommendations
Lengvari L, Takacs K, Lengyel A, Palinkas A, Wouters C, Kone-Paut I, et al.
Front Immunol
. 2024 Nov;
15:1466844.
PMID: 39600705
Mevalonate kinase deficiency (MKD), a rare auto-inflammatory disorder, arises from mutations in the gene, disrupting isoprenoid biosynthesis, and affecting cellular processes. This comprehensive review provides an updated perspective on MKD,...
7.
Elhani I, Backes S, Kallinich T, Amaryan G, Belot A, Berendes R, et al.
RMD Open
. 2024 Nov;
10(4).
PMID: 39581688
Introduction: Familial Mediterranean fever (FMF) is a genetic disease leading to recurrent episodes of inflammation. Two pathogenic variants are required for classical disease, but the disease can occur in heterozygous...
8.
Milatz F, Pedersen M, Klotsche J, Liedmann I, Niewerth M, Hospach A, et al.
Pediatr Rheumatol Online J
. 2024 Oct;
22(1):93.
PMID: 39434096
Background: Regular physical activity (PA) has been proven to help prevent non-communicable diseases and is beneficial for disease management in chronically ill populations. Physical inactivity and recreational screen-based media (SBM)...
9.
Raulien N, Friedrich K, Strobel S, Raps S, Hecker F, Pierer M, et al.
Sci Signal
. 2024 Jul;
17(845):eadd8913.
PMID: 39012939
Hypoxia and low glucose abundance often occur simultaneously at sites of inflammation. In monocytes and macrophages, glucose-oxygen deprivation stimulates the assembly of the NLRP3 inflammasome to generate the proinflammatory cytokine...
10.