KOELEAPPARAT TIL STOERKNING AF VAESKER SAASOM ANGAR I PETRISKAALE von PLOMP R W

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Unveiling contextual realities by microscopically entangling a neutron von Shen, J., Kuhn, S. J., Dalgliesh, R. M., de Haan, V. O., Geerits, N., Irfan, A. A. M., Li, F., Lu, S., Parnell, S. R., Plomp, J., van Well, A. A., Washington, A., Baxter, D. V., Ortiz, G., Snow, W. M., Pynn, R.

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A short-term evaluation of a thermoplastic polyurethane implant for osteochondral defect repair in an equine model von Korthagen, N.M., Brommer, H., Hermsen, G., Plomp, S.G.M., Melsom, G., Coeleveld, K., Mastbergen, S.C., Weinans, H., van Buul, W., van Weeren, P.R.

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Muscle-specific kinase myasthenia gravis IgG4 autoantibodies cause severe neuromuscular junction dysfunction in mice von KLOOSTER, Rinse, PLOMP, Jaap J, MARTINEZ-MARTINEZ, Pilar, DE BAETS, Marc H, DER MAAREL, Silvère M. Van, VERSCHUUREN, Jan J, HUIJBERS, Maartje G, NIKS, Erik H, STRAASHEIJM, Kirsten R, DETMERS, Frank J, HERMANS, Pim W, SLEIJPEN, Kevin, VERRIPS, Aad, LOSEN, Mario

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The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants von Runhart, Esmee H, Sangermano, Riccardo, Cornelis, Stéphanie S, Verheij, Joke B G M, Plomp, Astrid S, Boon, Camiel J F, Lugtenberg, Dorien, Roosing, Susanne, Bax, Nathalie M, Blokland, Ellen A W, Jacobs-Camps, Marlie H M, van der Velde-Visser, Saskia D, Pott, Jan-Willem R, Rohrschneider, Klaus, Thiadens, Alberta A H J, Klaver, Caroline C W, van den Born, L Ingeborgh, Hoyng, Carel B, Cremers, Frans P M

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Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders von Levy, Michael A., Relator, Raissa, McConkey, Haley, Pranckeviciene, Erinija, Kerkhof, Jennifer, Barat‐Houari, Mouna, Bargiacchi, Sara, Biamino, Elisa, Palomares Bralo, María, Cappuccio, Gerarda, Ciolfi, Andrea, Clarke, Angus, DuPont, Barbara R., Elting, Mariet W., Faivre, Laurence, Fee, Timothy, Ferilli, Marco, Fletcher, Robin S., Cherick, Florian, Foroutan, Aidin, Friez, Michael J., Gervasini, Cristina, Haghshenas, Sadegheh, Hilton, Benjamin A., Jenkins, Zandra, Kaur, Simranpreet, Lewis, Suzanne, Louie, Raymond J., Maitz, Silvia, Milani, Donatella, Morgan, Angela T., Oegema, Renske, Østergaard, Elsebet, Pallares, Nathalie R., Piccione, Maria, Plomp, Astrid S., Poulton, Cathryn, Reilly, Jack, Rius, Rocio, Robertson, Stephen, Rooney, Kathleen, Rousseau, Justine, Santen, Gijs W. E., Santos‐Simarro, Fernando, Schijns, Josephine, Squeo, Gabriella M., John, Miya St, Thauvin‐Robinet, Christel, Traficante, Giovanna, Sluijs, Pleuntje J., Vergano, Samantha A., Vos, Niels, Walden, Kellie K., Azmanov, Dimitar, Balci, Tugce B., Banka, Siddharth, Gecz, Jozef, Henneman, Peter, Lee, Jennifer A., Mannens, Marcel M. A. M., Roscioli, Tony, Siu, Victoria, Amor, David J., Baynam, Gareth, Bend, Eric G., Boycott, Kym, Brunetti‐Pierri, Nicola, Campeau, Philippe M., Campion, Dominique, Christodoulou, John, Dyment, David, Esber, Natacha, Fahrner, Jill A., Fleming, Mark D., Genevieve, David, Heron, Delphine, Husson, Thomas, Kernohan, Kristin D., McNeill, Alisdair, Menke, Leonie A., Merla, Giuseppe, Prontera, Paolo, Rockman‐Greenberg, Cheryl, Schwartz, Charles, Skinner, Steven A., Stevenson, Roger E., Vincent, Marie, Vitobello, Antonio, Tartaglia, Marco, Alders, Marielle, Tedder, Matthew L., Sadikovic, Bekim

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Search for exotic spin-dependent couplings of the neutron with matter using spin-echo based neutron interferometry von Parnell, S. R., van Well, A. A., Plomp, J., Dalgliesh, R. M., Steinke, N.-J., Cooper, J. F. K., Geerits, N., Steffen, K. E., Snow, W. M., de Haan, V. O.

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Timing of revascularization in patients with transient ST-segment elevation myocardial infarction: a randomized clinical trial von Lemkes, Jorrit S, Janssens, Gladys N, van der Hoeven, Nina W, van de Ven, Peter M, Marques, Koen M J, Nap, Alexander, van Leeuwen, Maarten A H, Appelman, Yolande E A, Knaapen, Paul, Verouden, Niels J W, Allaart, Cornelis P, Brinckman, Stijn L, Saraber, Colette E, Plomp, Koos J, Timmer, Jorik R, Kedhi, Elvin, Hermanides, Renicus S, Meuwissen, Martijn, Schaap, Jeroen, van der Weerdt, Arno P, van Rossum, Albert C, Nijveldt, Robin, van Royen, Niels

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Diagnostic exome sequencing in 266 Dutch patients with visual impairment von Haer-Wigman, Lonneke, van Zelst-Stams, Wendy Ag, Pfundt, Rolph, van den Born, L Ingeborgh, Klaver, Caroline Cw, Verheij, Joke Bgm, Hoyng, Carel B, Breuning, Martijn H, Boon, Camiel Jf, Kievit, Anneke J, Verhoeven, Virginie Jm, Pott, Jan Wr, Sallevelt, Suzanne Ceh, van Hagen, Johanna M, Plomp, Astrid S, Kroes, Hester Y, Lelieveld, Stefan H, Hehir-Kwa, Jayne Y, Castelein, Steven, Nelen, Marcel, Scheffer, Hans, Lugtenberg, Dorien, Cremers, Frans Pm, Hoefsloot, Lies, Yntema, Helger G

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Extracellular vesicles in synovial fluid from juvenile horses: No age-related changes in the quantitative profile von Boere, J., van de Lest, C.H.A., de Grauw, J.C., Plomp, S.G.M., Libregts, S.F.W.M., Arkesteijn, G.J.A., Malda, J., Wauben, M.H.M., van Weeren, P.R.

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Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium von Heutinck, Pam A T, van den Born, L Ingeborgh, Vermeer, Maikel, Iglesias Gonzales, Adriana I, Hoyng, Carel B, Pott, Jan Willem R, Kroes, Hester Y, van Schooneveld, Mary J, Boon, Camiel J F, van Genderen, Maria M, Plomp, Astrid S, de Jong-Hesse, Yvonne, van Egmond-Ebbeling, Michelle B, Hoefsloot, Lies H, A Bergen, Arthur, Klaver, Caroline C W, Meester-Smoor, Magda A, Thiadens, Alberta A H J, Verhoeven, Virginie J M

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Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolv... von Velde, Hedwig M., Vaseghi-Shanjani, Maryam, Smits, Jeroen J., Ramakrishnan, Gayatri, Oostrik, Jaap, Wesdorp, Mieke, Astuti, Galuh, Yntema, Helger G., Hoefsloot, Lies, Lanting, Cris P., Huynen, Martijn A., Lehman, Anna, Turvey, Stuart E., Pennings, Ronald J. E., Kremer, Hannie

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Colchicine in Patients With Chronic Coronary Disease in Relation to Prior Acute Coronary Syndrome von Opstal, Tjerk S.J., Fiolet, Aernoud T.L., van Broekhoven, Amber, Mosterd, Arend, Eikelboom, John W., Nidorf, Stefan M., Thompson, Peter L., Duyvendak, Michiel, van Eck, J.W. Martijn, van Beek, Eugène A., den Hartog, Frank, Budgeon, Charley A., Bax, Willem A., Tijssen, Jan G.P., El Messaoudi, Saloua, Cornel, Jan H., Nidorf, S.M., Xu, X.F., Ireland, M.A., Latchem, D., Whelan, A., Hendriks, R., Salkani, P., Tan, I.W., Thompson, A.G., Morton, A.M., Hockings, B.E., Thompson, P.L., King, B., Cornel, J.H., Bakker-Lohmeijer, H., Mosterd, A., Bunschoten, P., The, S.H.K., van der Kooi, S., Lenderink, T., Lardinois, R.G.J.L., Hoogslag, P.A.M., de Vos, A., Jerzewski, A., Jansen, S., Nierop, P.R., van der Knaap, M., Swart, H.P., Kingma, R., Schaap, J., Blom, L.B., Kuijper, A.F.M., Bayraktar-Verver, E., van Hessen, M.W.J., Engelen, W.C.T.C., van Eck, J.W.M., van der Ven-Elzebroek, N., van Hal, J.M.C., Drost, I.M.J., den Hartog, F.R., van Wijk, D., van Beek, E., van der Horst, C., Bartels, G.L., Hendriks, M., de Nooijer, C., Welten, C., Ronner, E., Dijkshoorn, A., Prins, F.J., Rutten, R.N.A., Beele, D.P.W., Hendriks, I., van der Sluis, A., Badings, E.A., Westendorp, I.C.D., Melein, A., Römer, Tj.J., Bruines, P., van de Wal, R., Leenders - van Lieshout, I., Hemels, M.E.W., Meinen-Werner, K., de Groot, M.R., Post, G., Mulder, M.W.C., Stuij, S., van Nes, E., Luyten, P., Plomp, J., Veldmeijer, S.V., Asselman, M.J., Scholtus, P.A.

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Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq von Koster, R., Brandão, R. D., Tserpelis, D., van Roozendaal, C. E. P., van Oosterhoud, C. N., Claes, K. B. M., Paulussen, A. D. C., Sinnema, M., Vreeburg, M., van der Schoot, V., Stumpel, C. T. R. M., Broen, M. P. G., Spruijt, L., Jongmans, M. C. J., Lesnik Oberstein, S. A. J., Plomp, A. S., Misra-Isrie, M., Duijkers, F. A., Louwers, M. J., Szklarczyk, R., Derks, K. W. J., Brunner, H. G., van den Wijngaard, A., van Geel, M., Blok, M. J.

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1-Year Outcomes of Delayed Versus Immediate Intervention in Patients With Transient ST-Segment Elevation Myocardial Infarction von Janssens, Gladys N., van der Hoeven, Nina W., Lemkes, Jorrit S., Everaars, Henk, van de Ven, Peter M., Marques, Koen M.J., Nap, Alexander, van Leeuwen, Maarten A.H., Appelman, Yolande, Knaapen, Paul, Verouden, Niels J.W., Allaart, Cornelis P., Brinckman, Stijn L., Saraber, Colette E., Plomp, Koos J., Timmer, Jorik R., Kedhi, Elvin, Hermanides, Renicus S., Meuwissen, Martijn, Schaap, Jeroen, van der Weerdt, Arno P., van Rossum, Albert C., Nijveldt, Robin, van Royen, Niels

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Development, behaviour and sensory processing in Marshall–Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes von Mulder, P. A., Balkom, I. D. C., Landlust, A. M., Priolo, M., Menke, L. A., Acero, I. H., Alkuraya, F. S., Arias, P., Bernardini, L., Bijlsma, E. K., Cole, T., Coubes, C., Dapia, I., Davies, S., Di Donato, N., Elcioglu, N. H., Fahrner, J. A., Foster, A., González, N. G., Huber, I., Iascone, M., Kaiser, A.‐S., Kamath, A., Kooblall, K., Lapunzina, P., Liebelt, J., Lynch, S. A., Maas, S. M., Mammì, C., Mathijssen, I. B., McKee, S., Mirzaa, G. M., Montgomery, T., Neubauer, D., Neumann, T. E., Pintomalli, L., Pisanti, M. A., Plomp, A. S., Price, S., Salter, C., Santos‐Simarro, F., Sarda, P., Schanze, D., Segovia, M., Shaw‐Smith, C., Smithson, S., Suri, M., Tatton‐Brown, K., Tenorio, J., Thakker, R. V., Valdez, R. M., Van Haeringen, A., Van Hagen, J. M., Zenker, M., Zollino, M., Dunn, W. W., Piening, S., Hennekam, R. C.

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Development of Refractive Errors—What Can We Learn From Inherited Retinal Dystrophies? von Hendriks, Michelle, Verhoeven, Virginie J.M., Buitendijk, Gabriëlle H.S., Polling, Jan Roelof, Meester-Smoor, Magda A., Hofman, Albert, van Huet, Ramon A., Klevering, B. Jeroen, Bax, Nathalie M., Lambertus, Stanley, Klaver, Caroline C.W., Hoyng, Carel B., Oomen, Clasien J., van Zelst-Stams, Wendy A., Cremers, Frans P., Plomp, Astrid S., van Schooneveld, Mary J., van Genderen, Mies M., Schuil, José, Boonstra, F. Nienke, Schlingemann, Reinier O., Bergen, Arthur A., Pierrache, Laurence, Meester-Smoor, Magda, van den Born, L. Ingeborgh, Boon, Camiel J., Pott, Jan W.R., van Leeuwen, Redmer, Kroes, Hester Y, de Jong-Hesse, Yvonne, Kamermans, Maarten, Ingeborgh van den Born, L., Klaver, Caroline C.W.

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Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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Applying Resonant Spin Flippers with Poleshoes and Longitudinal Radio Frequency Fields to Time of Flight MIEZE von Geerits, N., Parnell, S.R., Thijs, M.A., Bouwman, W.G., Plomp, J.

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A novel lamin A/C mutation in a Dutch family with premature atherosclerosis von Weterings, A.A.W, van Rijsingen, I.A.W, Plomp, A.S, Zwinderman, A.H, Lekanne Deprez, R.H, Mannens, M.M, van den Bergh Weerman, M.A, van der Wal, A.C, Pinto-Sietsma, S.J

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