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Common pre-diagnostic features in individuals with different rare diseases represent a key for diagnostic support with computerized pattern recognition?
PLoS One. 2019 Oct 10;14(10):e0222637. doi: 10.1371/journal.pone.0222637. eCollection 2019.
PLoS One. 2019.
PMID: 31600214
Free PMC article.
Künstliche Intelligenz zur diagnostischen Unterstützung ausgewählter seltener lysosomaler Speichererkrankungen: Ergebnisse einer Pilotstudie.
Sieg AL, Martin Das A, Maria Muschol N, Köhn A, Lampe C, Kortum X, Mehmecke S, Blöß S, Lechner W, Klawonn F, Grigull L.
Sieg AL, et al. Among authors: kortum x.
Klin Padiatr. 2019 Mar;231(2):60-66. doi: 10.1055/a-0816-5681. Epub 2019 Jan 10.
Klin Padiatr. 2019.
PMID: 30630212
German.
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Patient's Experience in Pediatric Primary Immunodeficiency Disorders: Computerized Classification of Questionnaires.
Mücke U, Klemann C, Baumann U, Meyer-Bahlburg A, Kortum X, Klawonn F, Lechner WM, Grigull L.
Mücke U, et al. Among authors: kortum x.
Front Immunol. 2017 Apr 5;8:384. doi: 10.3389/fimmu.2017.00384. eCollection 2017.
Front Immunol. 2017.
PMID: 28424699
Free PMC article.
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Diagnostic needs for rare diseases and shared prediagnostic phenomena: Results of a German-wide expert Delphi survey.
Blöß S, Klemann C, Rother AK, Mehmecke S, Schumacher U, Mücke U, Mücke M, Stieber C, Klawonn F, Kortum X, Lechner W, Grigull L.
Blöß S, et al. Among authors: kortum x.
PLoS One. 2017 Feb 24;12(2):e0172532. doi: 10.1371/journal.pone.0172532. eCollection 2017.
PLoS One. 2017.
PMID: 28234950
Free PMC article.
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Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial.
Grigull L, Lechner W, Petri S, Kollewe K, Dengler R, Mehmecke S, Schumacher U, Lücke T, Schneider-Gold C, Köhler C, Güttsches AK, Kortum X, Klawonn F.
Grigull L, et al. Among authors: kortum x.
BMC Med Inform Decis Mak. 2016 Mar 8;16:31. doi: 10.1186/s12911-016-0268-5.
BMC Med Inform Decis Mak. 2016.
PMID: 26957320
Free PMC article.
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