Architecture of an Expert System to Support Diagnostic Decisions for Hereditary Diseases
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Publisher
Springer Nature Switzerland
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https://link.springer.com/content/pdf/10.1007/978-3-031-50381-8_14
Reference11 articles.
1. Semschikova, Y.P., Kozlov, Y.A., Yakovlev, A.B., Shinkareva, V.M., Barzunova, T.V., Manjkova, N.I., Balakirev, E.A.: Rare case of morquio syndrome (mucopolysaccharidosis type IVA): difficulties of diagnostic search and management. Pediatr. Pharmacol. 19(1), 39–44 (2022)
2. Shashel, V.A., Firsova, V.N., Trubilina, M.M., Podporina, L.A., Firsov, N.A.: Orphan diseases and associated problems. Med. Herald South Russia 12(2), 28–35 (2021)
3. Gorbunova, V.N.: Congenital metabolic diseases Lysosomal storage diseases. Pediatrician 12(2), 73–83 (2021)
4. Kobrinskii, B.A., Blagosklonov, N.A., Gribova, V.V., Shalfeeva, E.A.: Expert system for the diagnosis of orphan diseases. In: Kovalev, S., Sukhanov, A., Akperov, I., Ozdemir, S. (eds.) Proceedings of the Sixth International Scientific Conference “Intelligent Information Technologies for Industry” (IITI’22). IITI 2022. Lecture Notes in Networks and Systems, Vol. 566. Springer, Cham (2023). https://doi.org/10.1007/978-3-031-19620-1_24
5. Platt, F.M., D’Azzo, A., Davidson, B.L., Neufeld, E.F., Tifft, C.J.: Lysosomal storage diseases. Nat. Rev. Dis. Primers. 4, 27 (2018). https://doi.org/10.1038/s41572-018-0025-4
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