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Human MD2 deficiency-an inborn error of immunity with pleiotropic features.
Li Y, Yu Z, Schenk M, Lagovsky I, Illig D, Walz C, Rohlfs M, Conca R, Muise AM, Snapper SB, Uhlig HH, Garty BZ, Klein C, Kotlarz D. Li Y, et al. Among authors: rohlfs m. J Allergy Clin Immunol. 2023 Mar;151(3):791-796.e7. doi: 10.1016/j.jaci.2022.09.033. Epub 2022 Nov 30. J Allergy Clin Immunol. 2023. PMID: 36462957
Recent infection as a risk factor for cerebrovascular ischemia.
Grau AJ, Buggle F, Heindl S, Steichen-Wiehn C, Banerjee T, Maiwald M, Rohlfs M, Suhr H, Fiehn W, Becher H, et al. Grau AJ, et al. Among authors: rohlfs m. Stroke. 1995 Mar;26(3):373-9. doi: 10.1161/01.str.26.3.373. Stroke. 1995. PMID: 7886709 Clinical Trial.
A human immunodeficiency syndrome caused by mutations in CARMIL2.
Schober T, Magg T, Laschinger M, Rohlfs M, Linhares ND, Puchalka J, Weisser T, Fehlner K, Mautner J, Walz C, Hussein K, Jaeger G, Kammer B, Schmid I, Bahia M, Pena SD, Behrends U, Belohradsky BH, Klein C, Hauck F. Schober T, et al. Among authors: rohlfs m. Nat Commun. 2017 Jan 23;8:14209. doi: 10.1038/ncomms14209. Nat Commun. 2017. PMID: 28112205 Free PMC article.
94 results