Roesler J - Search Results

1

Hyper-IgE and Carcinoma in CADINS Disease.

Pietzsch L, Körholz J, Boschann F, Sergon M, Dorjbal B, Yee D, Gilly V, Kämmerer E, Paul D, Kastl C, Laass MW, Berner R, Jacobsen EM, Roesler J, Aust D, Lee-Kirsch MA, Snow AL, Schuetz C. Pietzsch L, et al. Among authors: roesler j. Front Immunol. 2022 May 16;13:878989. doi: 10.3389/fimmu.2022.878989. eCollection 2022. Front Immunol. 2022. PMID: 35651609 Free PMC article.

2

Novel mutation and expanding phenotype in IRF2BP2 deficiency.

Körholz J, Gabrielyan A, Sczakiel HL, Schulze L, Rejzek M, Laass MW, Leuchten N, Tiebel O, Aust D, Conrad K, Röber N, Jacobsen EM, Ehmke N, Berner R, Lucas N, Lee-Kirsch MA, Wiedemuth R, Roesler J, Roers A, Amendt T, Schuetz C. Körholz J, et al. Among authors: roesler j. Rheumatology (Oxford). 2023 Apr 3;62(4):1699-1705. doi: 10.1093/rheumatology/keac575. Rheumatology (Oxford). 2023. PMID: 36193988

3

Meningoencephalitis caused by varicella-zoster virus reactivation in a child with dominant partial interferon-gamma receptor-1 deficiency.

Roesler J, Hedrich C, Laass MW, Heyne K, Rösen-Wolff A. Roesler J, et al. Pediatr Infect Dis J. 2011 Mar;30(3):265-6. doi: 10.1097/INF.0b013e3181f6f78a. Pediatr Infect Dis J. 2011. PMID: 20842068

4

More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation.

Bienias M, Gabrielyan A, Geberzahn L, Rösen-Wolff A, Huebner A, Jacobsen EM, Toepfner N, Fang M, Lee-Kirsch MA, Roesler J, Schuetz C. Bienias M, et al. Among authors: roesler j. Pediatr Allergy Immunol. 2021 May;32(4):793-797. doi: 10.1111/pai.13441. Epub 2021 Jan 19. Pediatr Allergy Immunol. 2021. PMID: 33369776 No abstract available.

5

Complement C2 deficiency disarranging innate and adaptive humoral immune responses in a pediatric patient: treatment with rituximab.

Hauck F, Lee-kirsch MA, Aust D, Roesler J, Pessler F. Hauck F, et al. Among authors: roesler j. Arthritis Care Res (Hoboken). 2011 Mar;63(3):454-9. doi: 10.1002/acr.20361. Arthritis Care Res (Hoboken). 2011. PMID: 20890976 Free article. No abstract available.

6

A case of recurrent herpes simplex 2 encephalitis, VZV reactivations, and dominant partial interferon-gamma-receptor-1 deficiency supports relevance of IFNgamma for antiviral defense in humans.

Körholz J, Richter N, Schäfer J, Schuetz C, Roesler J. Körholz J, et al. Among authors: roesler j. Mol Cell Pediatr. 2020 Oct 14;7(1):14. doi: 10.1186/s40348-020-00106-4. Mol Cell Pediatr. 2020. PMID: 33051801 Free PMC article.

7

Schuetz C, Hoenig M, Schulz A, Lee-Kirsch MA, Roesler J, Friedrich W, von Bernuth H. Schuetz C, et al. Among authors: roesler j. Eur J Pediatr. 2007 Aug;166(8):785-8. doi: 10.1007/s00431-006-0317-7. Epub 2006 Nov 14. Eur J Pediatr. 2007. PMID: 17103189

8

Influence of CARD15 mutations on disease activity and response to therapy in 65 pediatric Crohn patients from Saxony, Germany.

Roesler J, Thürigen A, Sun L, Koch R, Winkler U, Laass MW, Gahr M, Rösen-Wolff A, Henker J. Roesler J, et al. J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):27-32. doi: 10.1097/01.mpg.0000165017.00562.27. J Pediatr Gastroenterol Nutr. 2005. PMID: 15990626

9

Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma.

Hauck F, Magg T, Krolo A, Bilic I, Hirschmugl T, Laass M, Rösen-Wolff A, Luksch H, Boztug K, Roesler J. Hauck F, et al. Among authors: roesler j. Klin Padiatr. 2017 May;229(3):113-117. doi: 10.1055/s-0043-104218. Epub 2017 May 30. Klin Padiatr. 2017. PMID: 28561224 English.

10

[Chronic Granulomatous Disease: A Rare Differential Diagnosis in Recurrent Pulmonary Infections in Adults].

Kleymann J, Schütz C, Körholz J, Taube F, Vogler M, Halank M, Kolditz M, Langner S, Geberzahn L, Holotiuk O, Roesler J, Koschel D. Kleymann J, et al. Among authors: roesler j. Pneumologie. 2020 Oct;74(10):678-683. doi: 10.1055/a-1175-4122. Epub 2020 Jul 8. Pneumologie. 2020. PMID: 32643764 Free article. German.

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