المؤلفون: Elpidorou, Marilena

المساهمون: Johnson, Colin, Sheridan, Eamonn, Poulter, James

مصطلحات موضوعية: 616.8

الوصول الحر: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.800511Test

المؤلفون: Marcuccio, Fabio, Chau, Chalmers C., Tanner, Georgette, Elpidorou, Marilena, Finetti, Martina A., Ajaib, Shoaib, Taylor, Morag, Lascelles, Carolina, Carr, Ian, Macaulay, Iain, Stead, Lucy F., Actis, Paolo

المصدر: Science Advances ; volume 10, issue 10 ; ISSN 2375-2548

الإتاحة: https://doi.org/10.1126/sciadv.adl0515Test

المؤلفون: Elpidorou, Marilena, Poulter, James A, Szymanska, Katarzyna, Baron, Wia, Junger, Katrin, Boldt, Karsten, Ueffing, Marius, Green, Lydia, Livingston, John H, Sheridan, Eammon G, Johnson, Colin A

المصدر: Elpidorou , M , Poulter , J A , Szymanska , K , Baron , W , Junger , K , Boldt , K , Ueffing , M , Green , L , Livingston , J H , Sheridan , E G & Johnson , C A 2022 , ' Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease ' , European journal of human genetics : EJHG , pp. 860-864 . https://doi.org/10.1038/s41431-022-01050-9Test

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/b336891c-ddb4-4acb-83fb-51119eb5538fTest

الإتاحة: https://doi.org/10.1038/s41431-022-01050-9Test
https://hdl.handle.net/11370/b336891c-ddb4-4acb-83fb-51119eb5538fTest
https://research.rug.nl/en/publications/b336891c-ddb4-4acb-83fb-51119eb5538fTest
https://pure.rug.nl/ws/files/237459305/s41431_022_01050_9.pdfTest

المؤلفون: Kyrochristos, Ioannis D., Glantzounis, Georgios K., Goussia, Anna, Eliades, Alexia, Achilleos, Achilleas, Tsangaras, Kyriakos, Hadjidemetriou, Irene, Elpidorou, Marilena, Ioannides, Marios, Koumbaris, George, Mitsis, Michail, Patsalis, Philippos C., Roukos, Dimitrios

المصدر: Frontiers in Oncology ; volume 12 ; ISSN 2234-943X

مصطلحات موضوعية: Cancer Research, Oncology

الإتاحة: https://doi.org/10.3389/fonc.2022.855463Test

المؤلفون: Marcuccio, Fabio, Chau, Chi Cheng, Tanner, Georgette, Elpidorou, Marilena, Finetti, Martina Anna, Ajaib, Shoaib Ali, Taylor, Morag, Lascelles, Carolina, carr, ian, Macaulay, Iain, Stead, Lucy, Actis, Paolo

مصطلحات موضوعية: FOS Medical engineering

وصف الملف: text/plain; application/zip

العلاقة: https://github.com/GliomaGenomics/GBM_NBTest; https://eprints.whiterose.ac.uk/208346Test/; https://dx.doi.org/https://doi.org/10.1126/sciadv.adl0515Test

الإتاحة: https://doi.org/10.5518/1464https://doi.org/10.1126/sciadv.adl0515Test
https://archive.researchdata.leeds.ac.uk/1232Test/

المؤلفون: Dijk, Sas N., Protasoni, Margherita, Elpidorou, Marilena, Kroon, Albert M., Taanman, Jan-Willem

المساهمون: University College London Research Challenges, Royal Free Charity

المصدر: Scientific Reports ; volume 10, issue 1 ; ISSN 2045-2322

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1038/s41598-020-61381-9Test
https://www.nature.com/articles/s41598-020-61381-9.pdfTest
https://www.nature.com/articles/s41598-020-61381-9Test

المؤلفون: Elpidorou, Marilena, Best, Sunayna, Poulter, James A, Hartill, Verity, Hobson, Emma, Sheridan, Eamonn, Johnson, Colin A

المساهمون: British Heart Foundation, Sir Jules Thorn Award for Biomedical Research, Wellcome Trust

المصدر: Journal of Medical Genetics ; volume 58, issue 5, page 334-341 ; ISSN 0022-2593 1468-6244

الإتاحة: https://doi.org/10.1136/jmedgenet-2020-106873Test

المؤلفون: Elpidorou, Marilena, Actis, Paolo, Stead, Lucy

المصدر: Neuro-Oncology ; volume 21, issue Supplement_4, page iv7-iv8 ; ISSN 1522-8517 1523-5866

مصطلحات موضوعية: Cancer Research, Neurology (clinical), Oncology

الإتاحة: https://doi.org/10.1093/neuonc/noz167.031Test
http://academic.oup.com/neuro-oncology/article-pdf/21/Supplement_4/iv7/30627537/noz167.031.pdfTest

المؤلفون: Kara, Eleanna, Tucci, Arianna, Manzoni, Claudia, Lynch, David S., Elpidorou, Marilena, Bettencourt, Conceicao, Chelban, Viorica, Manole, Andreea, Hamed, Sherifa, Haridy, Nourelhoda, Federoff, Monica, Preza, Elisavet, Hughes, Deborah, Pittman, Alan, Jaunmuktane, Zane, Brandner, Sebastian, Xiromerisiou, Georgia, Wiethoff, Sarah, Schottlaender, Lucia, Proukakis, Christos, Morris, Huw, Warner, Tom, Bhatia, Kailash, Korlipara, Prasad, Singleton, Andrew, Hardy, John, Wood, Nicholas, Lewis, Patrick, Houlden, Henry

وصف الملف: text

العلاقة: https://centaur.reading.ac.uk/65702/1/brain.aww111.full.pdfTest; Kara, Eleanna, Tucci, Arianna, Manzoni, Claudia, Lynch, David S., Elpidorou, Marilena, Bettencourt, Conceicao, Chelban, Viorica, Manole, Andreea, Hamed, Sherifa, Haridy, Nourelhoda, Federoff, Monica, Preza, Elisavet, Hughes, Deborah, Pittman, Alan, Jaunmuktane, Zane, Brandner, Sebastian, Xiromerisiou, Georgia, Wiethoff, Sarah, Schottlaender, Lucia, Proukakis, Christos, Morris, Huw, Warner, Tom, Bhatia, Kailash, Korlipara, Prasad, Singleton, Andrew, Hardy, John, Wood, Nicholas, Lewis, Patrick and Houlden, Henry (2016) Genetic and phenotypic characterization of complex hereditary spastic paraplegia. Brain : A Journal of Neurology, 139 (7). pp. 1904-1918. ISSN 1460-2156 doi: https://doi.org/10.1093/brain/aww111Test

الإتاحة: https://doi.org/10.1093/brain/aww111Test
https://centaur.reading.ac.uk/65702Test/
https://centaur.reading.ac.uk/65702/1/brain.aww111.full.pdfTest

المؤلفون: Carr, Ian, Watson, Christopher, Raynor, Morag, Elpidorou, Marilena, Hany, Ummey, Crinnon, Laura, Sheridan, Eamonn, Markham, Alexander, Poulter, James, Bonthron, David

الإتاحة: https://doi.org/10.22541/au.165933904.43435894/v1Test