Bitte benutzen Sie diese Kennung, um auf die Ressource zu verweisen:
http://dx.doi.org/10.25673/121514Langanzeige der Metadaten
| DC Element | Wert | Sprache |
|---|---|---|
| dc.contributor.author | Hellmann, Fabio | - |
| dc.contributor.author | Ristow, Inka | - |
| dc.contributor.author | Well, Lennart | - |
| dc.contributor.author | Lohse, Swanhild | - |
| dc.contributor.author | Anokhin, Maxim | - |
| dc.contributor.author | Kuhlen, Michaela | - |
| dc.contributor.author | André, Elisabeth | - |
| dc.contributor.author | Harder, Anja | - |
| dc.date.accessioned | 2025-12-01T12:23:20Z | - |
| dc.date.available | 2025-12-01T12:23:20Z | - |
| dc.date.issued | 2025 | - |
| dc.identifier.uri | https://opendata.uni-halle.de//handle/1981185920/123467 | - |
| dc.identifier.uri | http://dx.doi.org/10.25673/121514 | - |
| dc.description.abstract | Modern Artificial Intelligence (AI) has demonstrated its effectiveness by achieving human-level performance in various complex tasks, including the biomedical field. Cancer research, adapting to a fast-changing world, is leveraging AI as a promising framework to better understand tumor development. Moreover, current AI methods can help predict more suitable and personalized treatment strategies for specific types of tumors. We explored AI methods applied to Neurofibromatosis Type 1, focusing on glial tumors. Additionally, we have reviewed all publicly available datasets to date. Discussion of future challenges is highly desirable since Neurofibromatosis Type 1 is one of the most common hereditary tumor syndromes and is associated with an increased rate of glial tumors as well as a reduced life expectancy due to malignancy. | eng |
| dc.language.iso | eng | - |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
| dc.subject.ddc | 610 | - |
| dc.title | Artificial intelligence-based tools for precision diagnosis and treatment of neurofibromatosis type 1 associated peripheral and central glial tumors | eng |
| dc.type | Article | - |
| local.versionType | publishedVersion | - |
| local.bibliographicCitation.journaltitle | Orphanet journal of rare diseases | - |
| local.bibliographicCitation.volume | 20 | - |
| local.bibliographicCitation.publishername | BioMed Central | - |
| local.bibliographicCitation.publisherplace | London | - |
| local.bibliographicCitation.doi | 10.1186/s13023-025-04093-5 | - |
| local.openaccess | true | - |
| dc.identifier.ppn | 1940604044 | - |
| cbs.publication.displayform | 2025 | - |
| local.bibliographicCitation.year | 2025 | - |
| cbs.sru.importDate | 2025-12-01T12:22:59Z | - |
| local.bibliographicCitation | Enthalten in Orphanet journal of rare diseases - London : BioMed Central, 2006 | - |
| local.accessrights.dnb | free | - |
| Enthalten in den Sammlungen: | Open Access Publikationen der MLU | |
Dateien zu dieser Ressource:
| Datei | Beschreibung | Größe | Format | |
|---|---|---|---|---|
| s13023-025-04093-5.pdf | 2.32 MB | Adobe PDF | ![]() Öffnen/Anzeigen |
