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Page 1
Treat-to-target strategies for the management of familial Mediterranean Fever in children.
Ehlers L, Rolfes E, Lieber M, Müller D, Lainka E, Gohar F, Klaus G, Girschick H, Hörstermann J, Kümmerle-Deschner J, Brunner J, Palm-Beden K, Tenbrock K, von Wrangel L, Faßhauer M, Blank N, Trauzeddel R, von Stuckrad ASL, Higgins S, Welzel T, Lutz T, Hentgen V, Foell D, Wittkowski H, Kallinich T. Ehlers L, et al. Among authors: kallinich t. Pediatr Rheumatol Online J. 2023 Sep 26;21(1):108. doi: 10.1186/s12969-023-00875-y. Pediatr Rheumatol Online J. 2023. PMID: 37752496 Free PMC article.
Human procaspase-1 variants with decreased enzymatic activity are associated with febrile episodes and may contribute to inflammation via RIP2 and NF-κB signaling.
Heymann MC, Winkler S, Luksch H, Flecks S, Franke M, Ruß S, Ozen S, Yilmaz E, Klein C, Kallinich T, Lindemann D, Brenner S, Ganser G, Roesler J, Rösen-Wolff A, Hofmann SR. Heymann MC, et al. Among authors: kallinich t. J Immunol. 2014 May 1;192(9):4379-85. doi: 10.4049/jimmunol.1203524. Epub 2014 Apr 4. J Immunol. 2014. PMID: 24706726
LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages.
Omarjee O, Mathieu AL, Quiniou G, Moreews M, Ainouze M, Frachette C, Melki I, Dumaine C, Gerfaud-Valentin M, Duquesne A, Kallinich T, Tahir Turanli E, Malcus C, Viel S, Pescarmona R, Georgin-Lavialle S, Jamilloux Y, Larbre JP, Sarrabay G, Magnotti F, Rice GI, Bleicher F, Reboulet J, Merabet S, Henry T, Crow YJ, Faure M, Walzer T, Belot A. Omarjee O, et al. Among authors: kallinich t. J Exp Med. 2021 Mar 1;218(3):e20201006. doi: 10.1084/jem.20201006. J Exp Med. 2021. PMID: 33606008 Free PMC article.
Are diffuse and limited juvenile systemic sclerosis different in clinical presentation? Clinical characteristics of a juvenile systemic sclerosis cohort.
Foeldvari I, Klotsche J, Torok KS, Kasapcopur O, Adrovic A, Stanevicha V, Terreri MT, Alexeeva E, Katsicas M, Cimaz R, Kostik M, Lehman T, Sifuentes-Giraldo WA, Smith V, Sztajnbok F, Avcin T, Jose Santos M, Moll M, Nemcova D, Battagliotti C, Eleftheriou D, Janarthanan M, Kallinich T, Anton J, Minden K, Nielsen S, Uziel Y, Helmus N. Foeldvari I, et al. Among authors: kallinich t. J Scleroderma Relat Disord. 2019 Feb;4(1):49-61. doi: 10.1177/2397198318790494. Epub 2018 Aug 7. J Scleroderma Relat Disord. 2019. PMID: 35382144 Free PMC article.
An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing.
Mackenroth L, Fischer-Zirnsak B, Egerer J, Hecht J, Kallinich T, Stenzel W, Spors B, von Moers A, Mundlos S, Kornak U, Gerhold K, Horn D. Mackenroth L, et al. Among authors: kallinich t. Am J Med Genet A. 2016 Apr;170A(4):1080-5. doi: 10.1002/ajmg.a.37547. Epub 2016 Jan 22. Am J Med Genet A. 2016. PMID: 26799614
143 results