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Tilmann Kallinich

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Articles 104
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Recent Articles
11.
Milatz F, Klotsche J, Niewerth M, Sengler C, Windschall D, Kallinich T, et al.
Arthritis Res Ther . 2024 Apr; 26(1):82. PMID: 38600543
Background: Previous studies have shown that growing up with rheumatic conditions can fuel dissatisfaction and psychological distress, which in turn affects disease self-management and treatment adherence. Primary objective of this...
12.
Milatz F, Hansmann S, Klotsche J, Niewerth M, Kallinich T, Dressler F, et al.
Pediatr Rheumatol Online J . 2024 Mar; 22(1):39. PMID: 38509613
Background: Physical active lifestyles are essential throughout growth and maturation and may offer potential preventive and therapeutic benefit in patients with juvenile idiopathic arthritis (JIA). Insufficient physical activity (PA), in...
13.
Kuemmerle-Deschner J, Kallinich T, Henes J, Kortus-Gotze B, Oommen P, Rech J, et al.
RMD Open . 2024 Feb; 10(1). PMID: 38360038
Objective: Interim analysis of the RELIANCE registry, an on-going, non-interventional, open-label, multicentre, prospective study evaluating the long-term safety, dosing regimens and effectiveness of canakinumab in patients with cryopyrin-associated periodic syndromes...
14.
Wolf C, Lim E, Mokhtari M, Kind B, Odainic A, Lara-Villacanas E, et al.
Sci Immunol . 2024 Jan; 9(92):eadi9769. PMID: 38207055
UNC93B1 is critical for trafficking and function of nucleic acid-sensing Toll-like receptors (TLRs) TLR3, TLR7, TLR8, and TLR9, which are essential for antiviral immunity. Overactive TLR7 signaling induced by recognition...
15.
Varga G, Schleifenbaum S, Koenig U, Waldkirch J, Hinze C, Kessel C, et al.
Mol Cell Pediatr . 2023 Dec; 10(1):19. PMID: 38087059
Background: Familial Mediterranean fever (FMF) is a prototypical autoinflammatory syndrome associated with phagocytic cell activation. Pyrin mutations are the genetic basis of this disease, and its expression has been shown...
16.
Sundqvist M, Christenson K, Wekell P, Bjornsdottir H, Dahlstrand Rudin A, Sanchez Klose F, et al.
Front Immunol . 2023 Nov; 14:1233101. PMID: 37954595
We describe a female patient suffering from severe chronic non-bacterial osteomyelitis (CNO) with systemic inflammation and advanced malnutrition and complete deficiency of myeloperoxidase (MPO). CNO is a rare autoinflammatory bone...
17.
Hospach T, Kallinich T, Rietschel C, Hufnagel M, Freudenhammer J, Rucklova K, et al.
Z Rheumatol . 2023 Nov; 83(1):28-33. PMID: 37945990
With the diagnosis and treatment optimization board, the Society for Pediatric and Adolescent Rheumatology (GKJR) has developed a new format for expert-based discussion of rare and complex diseases. So far,...
18.
Knieper A, von Stuckrad A, Minden K, Goetzke C, Kallinich T
Z Rheumatol . 2023 Nov; 83(1):4-14. PMID: 37921883
Monogenic mutations in laccase domain-containing 1 (LACC1) are associated with clinical pictures that mimic severe courses of polyarticular or systemic juvenile idiopathic arthritis. The diseases are characterized by an early...
19.
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...
20.
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...