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458 results

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Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.
Buch S, Innes H, Lutz PL, Nischalke HD, Marquardt JU, Fischer J, Weiss KH, Rosendahl J, Marot A, Krawczyk M, Casper M, Lammert F, Eyer F, Vogel A, Marhenke S, von Felden J, Sharma R, Atkinson SR, McQuillin A, Nattermann J, Schafmayer C, Franke A, Strassburg C, Rietschel M, Altmann H, Sulk S, Thangapandi VR, Brosch M, Lackner C, Stauber RE, Canbay A, Link A, Reiberger T, Mandorfer M, Semmler G, Scheiner B, Datz C, Romeo S, Ginanni Corradini S, Irving WL, Morling JR, Guha IN, Barnes E, Ansari MA, Quistrebert J, Valenti L, Müller SA, Morgan MY, Dufour JF, Trebicka J, Berg T, Deltenre P, Mueller S, Hampe J, Stickel F. Buch S, et al. Among authors: muller sa. Gut. 2023 Feb;72(2):381-391. doi: 10.1136/gutjnl-2022-327196. Epub 2022 Jul 4. Gut. 2023. PMID: 35788059 Free PMC article.
Crohn's disease involving the penis.
Slaney G, Muller S, Clay J, Sumathipala AH, Hillenbrand P, Thompson H. Slaney G, et al. Gut. 1986 Mar;27(3):329-33. doi: 10.1136/gut.27.3.329. Gut. 1986. PMID: 3699553 Free PMC article.
Performance of ARVC Risk Calculators in (Likely) Pathogenic Plakophilin-2 Variant Carriers Without Definite ARVC Diagnosis.
Muller SA, Asatryan B, Murray B, Tichnell C, Cox MGPJ, Amin AS, Yap SC, Gasperetti A, Carrick RT, Cadrin-Tourigny J, Oerlemans MIFJ, Calkins H, van Tintelen JP, James CA, Te Riele ASJM. Muller SA, et al. Circ Arrhythm Electrophysiol. 2024 Dec 13:e013144. doi: 10.1161/CIRCEP.124.013144. Online ahead of print. Circ Arrhythm Electrophysiol. 2024. PMID: 39670315 No abstract available.
Myeloid cell-specific loss of NPC1 in mice recapitulates microgliosis and neurodegeneration in patients with Niemann-Pick type C disease.
Dinkel L, Hummel S, Zenatti V, Malara M, Tillmann Y, Colombo A, Monasor LS, Suh JH, Logan T, Roth S, Paeger L, Hoffelner P, Bludau O, Schmidt A, Müller SA, Schifferer M, Nuscher B, Njavro JR, Prestel M, Bartos LM, Wind-Mark K, Slemann L, Hoermann L, Kunte ST, Gnörich J, Lindner S, Simons M, Herms J, Paquet D, Lichtenthaler SF, Bartenstein P, Franzmeier N, Liesz A, Grosche A, Bremova-Ertl T, Catarino C, Beblo S, Bergner C, Schneider SA, Strupp M, Di Paolo G, Brendel M, Tahirovic S. Dinkel L, et al. Among authors: muller sa. Sci Transl Med. 2024 Dec 4;16(776):eadl4616. doi: 10.1126/scitranslmed.adl4616. Epub 2024 Dec 4. Sci Transl Med. 2024. PMID: 39630885
Arrhythmogenic Cardiomyopathy: Towards Genotype Based Diagnoses and Management.
Muller SA, Bertoli G, Wang J, Gasperetti A, Cox MGPJ, Calkins H, Riele ASJMT, Judge DP, Delmar M, Hauer RNW, Boink GJJ, Cerrone M, Tintelen JPV, James CA. Muller SA, et al. J Cardiovasc Electrophysiol. 2024 Dec 2. doi: 10.1111/jce.16519. Online ahead of print. J Cardiovasc Electrophysiol. 2024. PMID: 39623588 Review.
458 results