المؤلفون: Caruana, M, Baars, MJ, Bashiardes, E, Benke, K, Bjorck, E, Codreanu, A, Rubio, ED, Dumfarth, J, Evangelista, A, Groenink, M, Kallenbach, K, Kempers, M, Keravnou, A, Loeys, B, Muino-Mosquera, L, Nagy, E, Milleron, O, Nistri, S, Pepe, G, Roos-Hesselink, J, Szabolcs, Z, Teixido-Tura, G, Timmermans, J, Van de Laar, I, van Kimmenade, R, Verstraeten, A, Von Kodolitsch, Y, De Backer, J, Jondeau, G

المصدر: European journal of medical genetics. 66(1):104673

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:151610102Test

المؤلفون: Parenti, I., Lehalle, D., Nava, C., Torti, E., Leitão, E., Person, R., Mizuguchi, T., Matsumoto, N., Kato, M., Nakamura, K., De Man, S. A., Cope, H., Shashi, V., Friedman, J., Joset, P., Steindl, K., Rauch, A., Muffels, I., Van Hasselt, P. M., Petit, Florence, Smol, T., Le Guyader, G., Bilan, F., Sorlin, A., Vitobello, A., Philippe, C., Van De Laar, I. M. B. H., Van Slegtenhorst, M. A., Campeau, P. M., Au, P. Y. B., Nakashima, M., Saitsu, H., Yamamoto, T., Nomura, Y., Louie, R. J., Lyons, M. J., Dobson, A., Plomp, A. S., Motazacker, M. M., Kaiser, F. J., Timberlake, A. T., Fuchs, S. A., Depienne, C., Mignot, C.

المساهمون: Université de Lille, CHU Lille, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364, Maladies RAres du DEveloppement embryonnaire et du MEtabolisme : du Phénotype au Génotype et à la Fonction - ULR 7364 RADEME, Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon)

وصف الملف: application/octet-stream; application/rdf+xml; charset=utf-8; application/pdf

العلاقة: Human Genetics; Hum Genet; http://hdl.handle.net/20.500.12210/84176Test

الإتاحة: https://doi.org/20.500.12210/84176Test
https://hdl.handle.net/20.500.12210/84176Test

المؤلفون: Detert Oude Weme, S. E. H., Hulskotte, L. M. G., Vervenne, W. L., Imholz, A. L. T., Cremers, R. G. H. M., Taxis, K., Reyners, A. K. L., van Berlo-van de Laar, I. R. F., Jansman, F. G. A., Benoist, G. E.

المصدر: Clinical Pharmacokinetics ; volume 62, issue 7, page 989-996 ; ISSN 0312-5963 1179-1926

مصطلحات موضوعية: Pharmacology (medical), Pharmacology

الإتاحة: https://doi.org/10.1007/s40262-023-01255-1Test

المؤلفون: Foroutan A., Haghshenas S., Bhai P., Levy M. A., Kerkhof J., McConkey H., Niceta M., Ciolfi A., Pedace L., Miele E., Genevieve D., Heide S., Alders M., Zampino G., Merla G., Fradin M., Bieth E., Bonneau D., Dieterich K., Fergelot P., Schaefer E., Faivre L., Vitobello A., Maitz S., Fischetto R., Gervasini C., Piccione M., van de Laar I., Tartaglia M., Sadikovic B., Lebre A. -S.

المساهمون: Foroutan A., Haghshenas S., Bhai P., Levy M.A., Kerkhof J., McConkey H., Niceta M., Ciolfi A., Pedace L., Miele E., Genevieve D., Heide S., Alders M., Zampino G., Merla G., Fradin M., Bieth E., Bonneau D., Dieterich K., Fergelot P., Schaefer E., Faivre L., Vitobello A., Maitz S., Fischetto R., Gervasini C., Piccione M., van de Laar I., Tartaglia M., Sadikovic B., Lebre A.-S.

مصطلحات موضوعية: Abnormalities, Multiple, Craniofacial Abnormalitie, DNA methylation, Epigenetic, Episignature, Facie, Growth Disorder, Human, Hypertrichosi, Intellectual disability, KMT2A gene, Neurodevelopmental disorder, Phenotype, Wiedemann–Steiner syndrome

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35163737; info:eu-repo/semantics/altIdentifier/wos/WOS:000759997000001; volume:23; issue:3; numberofpages:17; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/10447/547094Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85123938038

الإتاحة: https://doi.org/10.3390/ijms23031815Test
http://hdl.handle.net/10447/547094Test

المؤلفون: Prins-Can, I., van Berlo - van de Laar, I. R.F., Zeeman, M., Vermeij, C. G., van ’t Riet, E., Taxis, K., Jansman, F. G.A.

المصدر: Prins-Can , I , van Berlo - van de Laar , I R F , Zeeman , M , Vermeij , C G , van ’t Riet , E , Taxis , K & Jansman , F G A 2022 , ' Assessing the binding interaction of polystyrene sulfonate with amitriptyline in healthy volunteers : a cross-over design — The BIND study ' , European Journal of Clinical Pharmacology , vol. 78 , no. 5 , pp. 839-845 . https://doi.org/10.1007/s00228-022-03283-5Test

مصطلحات موضوعية: Chronic kidney disease, Drug interactions, Drug safety, Pharmacokinetic-pharmacodynamic, Pharmacotherapy

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/09fd9065-27ae-47b2-b2c6-25089790df25Test

الإتاحة: https://doi.org/10.1007/s00228-022-03283-5Test
https://hdl.handle.net/11370/09fd9065-27ae-47b2-b2c6-25089790df25Test
https://research.rug.nl/en/publications/09fd9065-27ae-47b2-b2c6-25089790df25Test
https://pure.rug.nl/ws/files/662419757/s00228_022_03283_5.pdfTest
http://www.scopus.com/inward/record.url?scp=85124958604&partnerID=8YFLogxKTest

المؤلفون: van Berlo-van de Laar, I R F, Prins-Can, I, Schuiling-Veninga, C C M, Taxis, K, Jansman, F G A

المصدر: van Berlo-van de Laar , I R F , Prins-Can , I , Schuiling-Veninga , C C M , Taxis , K & Jansman , F G A 2022 , ' Exploring co-dispensed drug use in patients on sevelamer or polystyrene sulfonate to identify potential novel binding interactions : a cross sectional in silico study: Potential novel binding interactions with resins ' , International journal of clinical pharmacy , vol. 44 , pp. 389-398 . https://doi.org/10.1007/s11096-021-01355-7Test

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/1e31ae52-4824-48a1-b03f-1877298c47f2Test

الإتاحة: https://doi.org/10.1007/s11096-021-01355-7Test
https://hdl.handle.net/11370/1e31ae52-4824-48a1-b03f-1877298c47f2Test
https://research.rug.nl/en/publications/1e31ae52-4824-48a1-b03f-1877298c47f2Test
https://pure.rug.nl/ws/files/215368040/VanBerloVanDeLaar2022_Article_ExploringCo_dispensedDrugUseIn.pdfTest

المؤلفون: Wong, M., Kampen, R., Braden, R., Alagöz, G., Hildebrand, M., Barnett, C., Barnett, M., Brusco, A., Carli, D., De Vries, B., Dingemans, A., Elmslie, F., Ferrero, G., Jansen, N., Van de Laar, I., Moroni, A., Mowat, D., Murray, L., Novara, F., Peron, A., Scheffer, I., Sirchia, F., Turner, S., Vignoli, A., Vino, A., Weber, S., Chung, W., Gerard, M., López-González, V., Palmer, E., Morgan, A., Van Bon, B., Fisher, S.

المصدر: medRxiv

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/21.11116/0000-000B-304F-7Test; http://hdl.handle.net/21.11116/0000-000B-3051-3Test

الإتاحة: https://doi.org/10.1101/2022.03.04.22271462Test
http://hdl.handle.net/21.11116/0000-000B-304F-7Test
http://hdl.handle.net/21.11116/0000-000B-3051-3Test

المؤلفون: Parenti, I., Lehalle, D., Nava, C., Torti, E., Leitão, E., Person, R., Mizuguchi, T., Matsumoto, N., Kato, M., Nakamura, K., de Man, S. A., Cope, H., Shashi, V., Friedman, J., Joset, P., Steindl, K., Rauch, A., Muffels, I., van Hasselt, P. M., Petit, Florence, Smol, T., Le Guyader, G., Bilan, F., Sorlin, A., Vitobello, A., Philippe, C., van de Laar, I. M. B. H., van Slegtenhorst, M. A., Campeau, P. M., Au, P. Y. B., Nakashima, M., Saitsu, H., Yamamoto, T., Nomura, Y., Louie, R. J., Lyons, M. J., Dobson, A., Plomp, A. S., Motazacker, M. M., Kaiser, F. J., Timberlake, A. T., Fuchs, S. A., Depienne, C., Mignot, C.

المساهمون: Maladies RAres du DEveloppement embryonnaire et du MEtabolisme : du Phénotype au Génotype et à la Fonction - ULR 7364 (RADEME), Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)

المصدر: ISSN: 0340-6717.

مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33944996; hal-04219762; https://hal.univ-lille.fr/hal-04219762Test; https://hal.univ-lille.fr/hal-04219762/documentTest; https://hal.univ-lille.fr/hal-04219762/file/s00439-021-02283-2.pdfTest; PUBMED: 33944996

الإتاحة: https://doi.org/10.1007/s00439-021-02283-2Test
https://hal.univ-lille.fr/hal-04219762Test
https://hal.univ-lille.fr/hal-04219762/documentTest
https://hal.univ-lille.fr/hal-04219762/file/s00439-021-02283-2.pdfTest

المؤلفون: van Berlo-van de Laar, I. R. F., Gedik, A., van't Riet, E., de Meijer, A., Taxis, K., Jansman, F. G. A.

المصدر: van Berlo-van de Laar , I R F , Gedik , A , van't Riet , E , de Meijer , A , Taxis , K & Jansman , F G A 2020 , ' Identifying patients with metformin associated lactic acidosis in the emergency department ' , International Journal of Clinical Pharmacy , vol. 42 , no. 5 , pp. 1286-1292 . https://doi.org/10.1007/s11096-020-01069-2Test

مصطلحات موضوعية: Acidosis, Diagnosis, Lactic, Metformin, Renal insufficiency, Sepsis, CAMPAIGN INTERNATIONAL GUIDELINES, CASE SERIES, MANAGEMENT, LACTATE

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/83e72102-ad82-42b3-94c4-9e2f15bb19c6Test

الإتاحة: https://doi.org/10.1007/s11096-020-01069-2Test
https://hdl.handle.net/11370/83e72102-ad82-42b3-94c4-9e2f15bb19c6Test
https://research.rug.nl/en/publications/83e72102-ad82-42b3-94c4-9e2f15bb19c6Test
https://pure.rug.nl/ws/files/145912394/VanBerlo_vanDeLaar2020_Article_IdentifyingPatientsWithMetform.pdfTest

المؤلفون: Haijes, H, Koster, M, Rehmann, H, Li, D, Hakonarson, H, Cappuccio, G, Hancarova, M, Lehalle, D, Reardon, W, Schaefer, G, Lehman, A, Van De Laar, I, Tesselaar, C, Turner, C, Goldenberg, A, Patrier, S, Thevenon, J, Pinelli, M, Brunetti-Pierri, N, Prchalová, D, Havlovicová, M, Vlckova, M, Sedláček, Z, Lopez, E, Ragoussis, V, Pagnamenta, A, Kini, U, Vos, H, Van Es, R, Van Schaik, R, Van Essen, T, Kibaek, M, Taylor, J, Sullivan, J, Shashi, V, Petrovski, S, Fagerberg, C, Martin, D, Van Gassen, K, Pfundt, R, Falk, M, McCormick, E, Timmers, H, Van Hasselt, P

العلاقة: https://ora.ox.ac.uk/objects/uuid:a38bf334-3015-4933-8183-455bc0548681Test; https://doi.org/10.1016/j.ajhg.2019.06.016Test

الإتاحة: https://doi.org/10.1016/j.ajhg.2019.06.016Test
https://ora.ox.ac.uk/objects/uuid:a38bf334-3015-4933-8183-455bc0548681Test