Prasad Thomas Oommen
Overview
Explore the profile of Prasad Thomas Oommen including associated specialties, affiliations and a list of published articles.
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14
Citations
63
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Recent Articles
1.
Bruck N, Reiser C, Oommen P, Welzel T
Z Rheumatol
. 2025 Feb;
84(2):140-151.
PMID: 39961862
Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease in children and adolescents. Currently, JIA is classified into seven categories according to the International League of Associations for...
2.
Trojovsky K, Seidl M, Babor F, Ehl S, Lee-Kirsch M, Friedt M, et al.
Front Pediatr
. 2025 Jan;
12():1516017.
PMID: 39840313
Suppressors of cytokine signaling (SOCS) proteins play a critical role in regulating immune signaling pathways. Deficiency of SOCS1 leads to various autoimmune pathologies. We present two unrelated patients with distinct...
3.
Schultheiss C, Paschold L, Mohebiany A, Escher M, Kattimani Y, Muller M, et al.
Sci Adv
. 2024 Aug;
10(34):eadl3975.
PMID: 39167656
Genetic (A20) inactivation is a classical somatic lymphoma lesion and the genomic trait in haploinsufficiency of A20 (HA20). In a cohort of 34 patients with HA20, we show that heterozygous...
4.
Gossling K, Kobbe R, Boetticher B, Soura S, Borkhardt A, Wittkowski H, et al.
Dtsch Arztebl Int
. 2023 Dec;
120(46):795-796.
PMID: 38099603
No abstract available.
5.
Rensing-Ehl A, Lorenz M, Fuhrer M, Willenbacher W, Willenbacher E, Sopper S, et al.
J Allergy Clin Immunol
. 2023 Nov;
153(1):297-308.e12.
PMID: 37979702
Background: Elevated TCRαβCD4CD8 double-negative T cells (DNT) and serum biomarkers help identify FAS mutant patients with autoimmune lymphoproliferative syndrome (ALPS). However, in some patients with clinical features and biomarkers consistent...
6.
Thiele F, Klein A, Klotsche J, Windschall D, Dressler F, Kuemmerle-Deschner J, et al.
Rheumatology (Oxford)
. 2022 Oct;
62(6):2230-2238.
PMID: 36222562
Objective: To investigate the impact of additionally given MTX on biologic treatment of polyarticular JIA in terms of effectiveness, safety and drug survival. Methods: Patients suffering from polyarticular JIA and...
7.
Escherich C, Botticher B, Harmsen S, Homberg M, Schaper J, Lorenz M, et al.
Front Pediatr
. 2022 Jul;
10:885893.
PMID: 35774100
Deficiency of Adenosine Deaminase Type 2 (DADA2) is a rare autosomal recessive inherited disorder with a variable phenotype including generalized or cerebral vasculitis and bone marrow failure. It is caused...
8.
Zeus M, Janssen S, Laws H, Fischer U, Borkhardt A, Oommen P
Z Rheumatol
. 2021 Jul;
82(2):123-133.
PMID: 34196794
Objective: To analyze the composition of the oral microbiome in children and adolescents with chronic nonbacterial osteomyelitis (CNO) with respect to age distribution, gender differences, effects of medication, disease activity...
9.
Lainka E, Baehr M, Raszka B, Haas J, Hugle B, Fischer N, et al.
Pediatr Rheumatol Online J
. 2021 Mar;
19(1):38.
PMID: 33752669
Background: Systemic juvenile idiopathic arthritis (sJIA) is a complex disease with dysregulation of the innate immune system driven by cytokines. A major role is ascribed to interleukin-1β (IL-1β), supporting the...
10.
Horn S, Minden K, Speth F, Schwarz T, Dressler F, Grosch N, et al.
Clin Exp Rheumatol
. 2020 Oct;
40(2):433-442.
PMID: 33124555
Objectives: To describe a German cohort of patients with juvenile dermatomyositis (JDM) and to evaluate clinical manifestations, disease course and prognosis in JDM patients with a certain myositis-specific autoantibody. Methods:...