Lee-Kirsch MA - Search Results

1

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. 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.

2

Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34-->q35 by radiation hybrid mapping.

Lee-Kirsch MA, Engel K, Paditz E, Rösen-Wolff A, Lee YA, Gahr M. Lee-Kirsch MA, et al. Cytogenet Cell Genet. 2001;92(3-4):358. doi: 10.1159/000056933. Cytogenet Cell Genet. 2001. PMID: 11435718 No abstract available.

3

Schuetz C, Hoenig M, Schulz A, Lee-Kirsch MA, Roesler J, Friedrich W, von Bernuth H. Schuetz C, et al. 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

4

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. 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.

5

[Genetic methods for analysis of autoinflammatory diseases].

Bienias M, König N, Wolf C, Kretschmer S, Rösen-Wolff A, Berner R, Tüngler V, Lee-Kirsch MA. Bienias M, et al. Z Rheumatol. 2017 May;76(4):295-302. doi: 10.1007/s00393-017-0300-x. Z Rheumatol. 2017. PMID: 28378116 Review. German.

6

Therapeutic Approaches to Type I Interferonopathies.

Bienias M, Brück N, Griep C, Wolf C, Kretschmer S, Kind B, Tüngler V, Berner R, Lee-Kirsch MA. Bienias M, et al. Curr Rheumatol Rep. 2018 Apr 20;20(6):32. doi: 10.1007/s11926-018-0743-3. Curr Rheumatol Rep. 2018. PMID: 29679241 Review.

7

Janus kinase inhibition in complement component 1 deficiency.

Wolf C, Brück N, Koss S, Griep C, Kirschfink M, Palm-Beden K, Fang M, Röber N, Winkler S, Berner R, Latz E, Günther C, Lee-Kirsch MA. Wolf C, et al. J Allergy Clin Immunol. 2020 Dec;146(6):1439-1442.e5. doi: 10.1016/j.jaci.2020.04.002. Epub 2020 Apr 20. J Allergy Clin Immunol. 2020. PMID: 32325142 Free article. No abstract available.

8

Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?

Heinen A, Schnabel A, Brück N, Smitka M, Wolf C, Lucas N, Dollinger S, Hahn G, Günther C, Berner R, Lee-Kirsch MA, Schuetz C. Heinen A, et al. Rheumatology (Oxford). 2021 Apr 6;60(4):e136-e138. doi: 10.1093/rheumatology/keaa657. Rheumatology (Oxford). 2021. PMID: 33200187 No abstract available.

9

Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation.

Körholz J, Lucas N, Boiti F, Althaus K, Tiebel O, Fang M, Berner R, Lee-Kirsch MA, Knöfler R. Körholz J, et al. TH Open. 2020 Dec 25;4(4):e413-e416. doi: 10.1055/s-0040-1718910. eCollection 2020 Oct. TH Open. 2020. PMID: 33376940 Free PMC article.

10

[How Often is Rare Really Rare? A Survey on the Frequency of Rare Diseases at a University Hospital].

Kretschmer T, Danker A, Müller O, Rösen-Wolff A, Lee-Kirsch MA, Berner R. Kretschmer T, et al. Gesundheitswesen. 2022 Jun;84(6):526-531. doi: 10.1055/a-1388-7095. Epub 2021 Apr 15. Gesundheitswesen. 2022. PMID: 33860487 German.

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