المؤلفون: P. Hengeveld, M. van der Klift, P. M. Kolijn, F. Davi, F. Kavelaars, E. de Jonge, S. Robrecht, J. Assmann, L. van der Straten, M. Ritgen, P. Westerweel, K. Fischer, V. Goede, M. Hallek, M.-D. Levin, A. Langerak

المصدر: HemaSphere, Vol 6, Pp 550-551 (2022)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: http://journals.lww.com/10.1097/01.HS9.0000845492.79622.ef; https://doaj.org/toc/2572-9241

URL الوصول: https://doaj.org/article/8ec2e1f167de46c895017e0b7885b87e

المؤلفون: K. Groen, M. Seefat, K. Nasserinejad, C. A. Stege, E. van der Spek, Y. M. Bilgin, A. Kentos, M. Sohne, R. J. van Kampen, I. Ludwig, N. Thielen, N. Durdu-Rayman, N. C. de Graauw, N. W. van de Donk, E. G. de Waal, M.-C. Vekemans, G. J. Timmers, M. van der Klift, S. Soechit, P. A. Geerts, M. H. Silbermann, M. Oosterveld, I. Nijhof, P. Sonneveld, S. K. Klein, M.-D. Levin, S. Zweegman

المصدر: HemaSphere, Vol 6, Pp 797-798 (2022)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: http://journals.lww.com/10.1097/01.HS9.0000846496.51905.dd; https://doaj.org/toc/2572-9241

URL الوصول: https://doaj.org/article/de7b33949bb645c785d0c3c2f76a5ff0

المؤلفون: Shala Ghaderi Berntsson, Hans Matsson, Anna Kristoffersson, Valter Niemelä, Hermine A. van Duyvenvoorde, Cindy Richel-van Assenbergh, Heleen M. van der Klift, Olivera Casar-Borota, Carina Frykholm, Anne-Marie Landtblom

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: Becker muscular dystrophy, genetics, MLPA, mRNA, RNA sequencing, intronic variant, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1226766/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/6fcf8f8bf0e6479fb4c92c4215f6da52

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تسجيل الدخول للوصول الكامل.

المؤلفون: Tamara T. Koopmann, Yalda Jamshidi, Mohammad Naghibi-Sistani, Heleen M. van der Klift, Hassan Birjandi, Zuhair Al-Hassnan, Abdullah Alwadai, Giovanni Zifarelli, Ehsan G. Karimiani, Sahar Sedighzadeh, Amir Bahreini, Nayereh Nouri, Merlene Peter, Kyoko Watanabe, Hermine A. van Duyvenvoorde, Claudia A. L. Ruivenkamp, Aalbertine K. K. Teunissen, Arend D. J. Ten Harkel, Sjoerd G. van Duinen, Monique C. Haak, Carlos E. Prada, Gijs W. E. Santen, Reza Maroofian

المصدر: European Journal of Human Genetics, 31, 97-104. SPRINGERNATURE

مصطلحات موضوعية: Genetics, Genetics (clinical)

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af3fd1cb260d1f202ffaee8cd0bfa728
https://pubmed.ncbi.nlm.nih.gov/36253531

المؤلفون: Débora, ArrudaSoares, Miriam F, van Oostwaard, Eveline M, van der Klift

المصدر: Nederlands tijdschrift voor geneeskunde. 166

مصطلحات موضوعية: Adult, Pharmacovigilance, Vaginal Discharge, Drug-Related Side Effects and Adverse Reactions, Burns, Chemical, Vagina, Humans, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::aa93d8b45b3d091fdb100ea832628b69
https://pubmed.ncbi.nlm.nih.gov/35138699

المؤلفون: Erin E. Salo-Mullen, Liying Zhang, David J. Gallagher, Vikas Rai, Magan Trottier, Yirong Li, Michael P. Farrell, Zsofia K. Stadler, Heleen M. van der Klift, Ciyu Yang

المصدر: Genes, chromosomescancerREFERENCES. 60(8)

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Retrotransposon, Minisatellite Repeats, Biology, Germline, 03 medical and health sciences, Exon, 0302 clinical medicine, Germline mutation, Alu Elements, Genetics, medicine, Humans, Gene, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Lynch syndrome, MutS Homolog 2 Protein, MSH2, 030220 oncology & carcinogenesis, DNA mismatch repair

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336aeed32d02ba3909796c22d78bd823
https://pubmed.ncbi.nlm.nih.gov/33822432

المؤلفون: David J. Gallagher, Vikas Rai, Michael P. Farrell, Yirong Li, Magan Trottier, Erin E. Salo-Mullen, Liying Zhang, Heleen M. van der Klift, Zsofia K. Stadler, Ciyu Yang

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Retrotransposon, Biology, medicine.disease, digestive system diseases, Lynch syndrome, Antisense Orientation, Exon, Germline mutation, MSH2, medicine, DNA mismatch repair, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2d29f3503f918e1486ee203c7639f133
https://doi.org/10.22541/au.160619405.59308303/v1

المؤلفون: Inbal Kedar, Christi J. van Asperen, Jeanine J. Houwing-Duistermaat, Laurence Brugières, Sergey Nikolaev, Michael Farrell, Anja Wagner, D. Gareth Evans, Lone Sunde, Yael Goldberg, Mar Rodríguez-Girondo, Jessica I. Hoell, Katharina Wimmer, Karl Heinimann, Stefan Aretz, Maartje Nielsen, Heleen M. van der Klift, Maria Grazia Tibiletti, Tim Ripperger, Leigha Senter, Sanne W. ten Broeke, Wenche Sjursen, Encarna B. Gomez-Garcia, Stefanie Y. Zimmermann, Daniel Rueda, Marjolijn C.J. Jongmans, Noémie Lavoine, Ingrid Winship, Christina Therkildsen, Gabriel Capellá Munar, Chrystelle Colas, Alison H. Trainer, Kory Jasperson, Maurizio Genuardi, Theo A. M. van Os, Yvonne J. Vos, Mitul Modi, Hans F. A. Vasen, Manon Suerink

المساهمون: Suerink M., Rodriguez-Girondo M., van der Klift H.M., Colas C., Brugieres L., Lavoine N., Jongmans M., Munar G.C., Evans D.G., Farrell M.P., Genuardi M., Goldberg Y., Gomez-Garcia E., Heinimann K., Hoell J.I., Aretz S., Jasperson K.W., Kedar I., Modi M.B., Nikolaev S., van Os T.A.M., Ripperger T., Rueda D., Senter L., Sjursen W., Sunde L., Therkildsen C., Tibiletti M.G., Trainer A.H., Vos Y.J., Wagner A., Winship I., Wimmer K., Zimmermann S.Y., Vasen H.F., van Asperen C.J., Houwing-Duistermaat J.J., ten Broeke S.W., Nielsen M., Human Genetics, Clinical Genetics, Klinische Genetica, MUMC+: DA KG Polikliniek (9), RS: GROW - R4 - Reproductive and Perinatal Medicine

المصدر: Suerink, M, Rodríguez-Girondo, M, van der Klift, H M, Colas, C, Brugieres, L, Lavoine, N, Jongmans, M, Munar, G C, Evans, D G, Farrell, M P, Genuardi, M, Goldberg, Y, Gomez-Garcia, E, Heinimann, K, Hoell, J I, Aretz, S, Jasperson, K W, Kedar, I, Modi, M B, Nikolaev, S, van Os, T A M, Ripperger, T, Rueda, D, Senter, L, Sjursen, W, Sunde, L, Therkildsen, C, Tibiletti, M G, Trainer, A H, Vos, Y J, Wagner, A, Winship, I, Wimmer, K, Zimmermann, S Y, Vasen, H F, van Asperen, C J, Houwing-Duistermaat, J J, Ten Broeke, S W & Nielsen, M 2019, ' An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome ', Genetics in Medicine, vol. 21, no. 12, pp. 2706-2712 . https://doi.org/10.1038/s41436-019-0577-z
Evans, D G & et al. 2019, ' An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0577-z
Genetics in Medicine
Genetics in Medicine, 21, 2706. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Nature Publishing Group
Genetics in medicine. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Lippincott Williams & Wilkins
Genetics in Medicine, 21(12), 2706-2712

مصطلحات موضوعية: Male, Oncology, MICROSATELLITE INSTABILITY, Settore MED/03 - GENETICA MEDICA, PHENOTYPE, FAMILIES, Cohort Studies, Risk Factors, PMS2, CRITERIA, Genetics(clinical), Genetics (clinical), Mismatch Repair Endonuclease PMS2, Incidence, Incidence (epidemiology), DNA MISMATCH REPAIR, GERMLINE MUTATIONS, Middle Aged, Lynch syndrome, DNA-Binding Proteins, Cohort, colon cancer risk, Female, Colorectal Neoplasms, bMMRD, Cohort study, Adult, medicine.medical_specialty, HNPCC, colorectal cancer, FREQUENCY, Risk Assessment, BREAST, AGE, SDG 3 - Good Health and Well-being, Internal medicine, SURVEILLANCE, medicine, Humans, Genetic Predisposition to Disease, Germ-Line Mutation, Aged, business.industry, Microsatellite instability, MSH6, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Confidence interval, Mutation, business

وصف الملف: image/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; text/plain; ELETTRONICO; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77776c64c226d28d2628f88134704b43
https://pure.au.dk/portal/da/publications/an-alternative-approach-to-establishing-unbiased-colorectal-cancer-risk-estimation-in-lynch-syndrome(44d3cbe1-e2d3-43cf-a924-6d04a2831e62).html

المؤلفون: G J, Ossenkoppele, D A, Breems, G, Stuessi, Y, van Norden, M, Bargetzi, B J, Biemond, P, A von dem Borne, Y, Chalandon, J, Cloos, D, Deeren, M, Fehr, B, Gjertsen, C, Graux, G, Huls, J J J W, Janssen, A, Jaspers, M, Jongen-Lavrencic, E, de Jongh, S K, Klein, M, van der Klift, M, van Marwijk Kooy, J, Maertens, L, Michaux, M W M, van der Poel, A, van Rhenen, L, Tick, P, Valk, M C, Vekemans, W J F M, van der Velden, O, de Weerdt, T, Pabst, M, Manz, B, Löwenberg, M, Van Marwijk Kooy

المصدر: Leukemia. 34(7)

مصطلحات موضوعية: Aged, 80 and over, Male, Remission Induction, Cytarabine, Induction Chemotherapy, Prognosis, Survival Rate, Leukemia, Myeloid, Acute, Myelodysplastic Syndromes, Antineoplastic Combined Chemotherapy Protocols, Humans, Female, Lenalidomide, Aged, Follow-Up Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::da184de984c87878475706a1b6cbe670
https://pubmed.ncbi.nlm.nih.gov/32733013