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205 results

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Page 1
TLR4 gene variants modify endotoxin effects on asthma.
Werner M, Topp R, Wimmer K, Richter K, Bischof W, Wjst M, Heinrich J. Werner M, et al. Among authors: wimmer k. J Allergy Clin Immunol. 2003 Aug;112(2):323-30. doi: 10.1067/mai.2003.1648. J Allergy Clin Immunol. 2003. PMID: 12897738
Progress and challenges in the elimination of hepatitis C among people who inject drugs in Germany: results of a pilot study for a national monitoring system, 10 years after the first data collection.
Steffen G, Krings A, Guttmann S, Lübke N, Meyer-Schlinkmann K, Tiemann C, Timm J, Walker A, Zimmermann R; DRUCK 2.0-study group. Steffen G, et al. Harm Reduct J. 2024 Dec 20;21(1):222. doi: 10.1186/s12954-024-01119-2. Harm Reduct J. 2024. PMID: 39707505 Free PMC article.
BRCA loss of function including BRCA1 DNA-methylation, but not BRCA-unrelated homologous recombination deficiency, is associated with platinum hypersensitivity in high-grade ovarian cancer.
Fiegl H, Schnaiter S, Reimer DU, Leitner K, Nardelli P, Tsibulak I, Wieser V, Wimmer K, Schamschula E, Marth C, Zeimet AG. Fiegl H, et al. Among authors: wimmer k. Clin Epigenetics. 2024 Nov 27;16(1):171. doi: 10.1186/s13148-024-01781-0. Clin Epigenetics. 2024. PMID: 39605059 Free PMC article.
Nodal Burden and Oncologic Outcomes in Patients With Residual Isolated Tumor Cells After Neoadjuvant Chemotherapy (ypN0i+): The OPBC-05/ICARO Study.
Montagna G, Laws A, Ferrucci M, Mrdutt MM, Sun SX, Bademler S, Balbaloglu H, Balint-Lahat N, Banys-Paluchowski M, Barrio AV, Benson J, Bese N, Boughey JC, Boyle MK, Diego EJ, Eden C, Eller R, Goldschmidt M, Hlavin C, Heidinger M, Jelinska J, Karadeniz Cakmak G, Kesmodel SB, King TA, Kuerer HM, Loesch J, Milardi F, Murawa D, Moo TA, Menes TS, Passeri D, Pastoriza JM, Perhavec A, Pislar N, Polidorio N, Rami A, Ryu JM, Schulz A, Sevilimedu V, Ugurlu MU, Uras C, van Hemert A, Wong SM, Yoo TR, Zhang JQ, Karanlik H, Cabioğlu N, Peeters MV, Morrow M, Weber WP; ICARO Study Group. Montagna G, et al. J Clin Oncol. 2024 Nov 7:JCO2401052. doi: 10.1200/JCO.24.01052. Online ahead of print. J Clin Oncol. 2024. PMID: 39509672
ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management.
Colas C, Guerrini-Rousseau L, Suerink M, Gallon R, Kratz CP, Ayuso É; ERN GENTURIS CMMRD Guideline Group; Brugières L, Wimmer K. Colas C, et al. Among authors: wimmer k. Eur J Hum Genet. 2024 Dec;32(12):1526-1541. doi: 10.1038/s41431-024-01708-6. Epub 2024 Oct 17. Eur J Hum Genet. 2024. PMID: 39420201 Free PMC article. Review.
Comprehensive analysis of constitutional mismatch repair deficiency-associated non-Hodgkin lymphomas in a global cohort.
Rigaud C, Forster VJ, Al-Tarrah H, Attarbaschi A, Bianchi V, Burke A, Burkhardt B, Colas C, Devalck C, Edwards M, Elitzur S, Garthe AK, Goldberg Y, Guerrini-Rousseau L, Horpaopan S, Januszkiewicz-Lewandowska D, Kabíčková E, Kratz CP, Loeffen J, Pérez-Alonso V, Pineda M, Minard-Colin V, Rueda D, Ruiz-Ponte C, Trinquand A, Uyttebroeck A, Wimmer K, Auperin A, Tabori U, Brugieres L. Rigaud C, et al. Among authors: wimmer k. Pediatr Blood Cancer. 2024 Dec;71(12):e31302. doi: 10.1002/pbc.31302. Epub 2024 Sep 19. Pediatr Blood Cancer. 2024. PMID: 39300701
205 results