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Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants.
Rösner S, Pardo LM, Bertoli-Avella AM, Skrahina V, Engel P, Schröder S, Zielske S, Bonke V, Kreth J, Westphal G, Reder F, Skobalj S, Zielke S, Bogdanovic X, Grieger P, Rennecke J, Skripuletz T, Patten M, Aßmus B, Hahn K, Rolfs A, Bauer P; TRAM study. Rösner S, et al. Among authors: skripuletz t. J Clin Med. 2024 Oct 17;13(20):6197. doi: 10.3390/jcm13206197. J Clin Med. 2024. PMID: 39458146 Free PMC article.
Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology.
Skrahina V, Grittner U, Beetz C, Skripuletz T, Juenemann M, Krämer HH, Hahn K, Rieth A, Schaechinger V, Patten M, Tanislav C, Achenbach S, Assmus B, Knebel F, Gingele S, Skrahin A, Hartkamp J, Förster TM, Roesner S, Pereira C, Rolfs A. Skrahina V, et al. Among authors: skripuletz t. Ann Med. 2021 Dec;53(1):1787-1796. doi: 10.1080/07853890.2021.1988696. Ann Med. 2021. PMID: 34658264 Free PMC article.
Multimodal Assessment and Characterization of Sicca Syndrome.
Kramer E, Seeliger T, Skripuletz T, Gödecke V, Beider S, Jablonka A, Witte T, Ernst D. Kramer E, et al. Among authors: skripuletz t. Front Med (Lausanne). 2021 Dec 15;8:777599. doi: 10.3389/fmed.2021.777599. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34977077 Free PMC article.
Phenotyping of congenic dipeptidyl peptidase 4 (DP4) deficient Dark Agouti (DA) rats suggests involvement of DP4 in neuro-, endocrine, and immune functions.
Frerker N, Raber K, Bode F, Skripuletz T, Nave H, Klemann C, Pabst R, Stephan M, Schade J, Brabant G, Wedekind D, Jacobs R, Jörns A, Forssmann U, Straub RH, Johannes S, Hoffmann T, Wagner L, Demuth HU, von Hörsten S. Frerker N, et al. Among authors: skripuletz t. Clin Chem Lab Med. 2009;47(3):275-87. doi: 10.1515/CCLM.2009.064. Clin Chem Lab Med. 2009. PMID: 19327106
226 results