Search Results - Van Horn, Patricia

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    Ultra-early tranexamic acid after subarachnoid haemorrhage (ULTRA): a randomised controlled trial by Post, René, Germans, Menno R, Tjerkstra, Maud A, Vergouwen, Mervyn D I, Jellema, Korné, Koot, Radboud W, Kruyt, Nyika D, Willems, Peter W A, Wolfs, Jasper F C, de Beer, Frits C, Kieft, Hans, Nanda, Dharmin, van der Pol, Bram, Roks, Gerwin, de Beer, Frank, Halkes, Patricia H A, Reichman, Loes J A, Brouwers, Paul J A M, van den Berg-Vos, Renske M, Kwa, Vincent I H, van der Ree, Taco C, Bronner, Irene, van de Vlekkert, Janneke, Bienfait, Henri P, Boogaarts, Hieronymus D, Klijn, Catharina J M, van den Berg, René, Coert, Bert A, Horn, Janneke, Majoie, Charles B L M, Rinkel, Gabriël J E, Roos, Yvo B W E M, Vandertop, W Peter, Verbaan, Dagmar, Post, René, Germans, Menno R., Tjerkstra, Maud A., Vergouwen, Mervyn D.I., Jellema, Korné, Koot, Radboud W., Kruyt, Nyika D., Willems, Peter W.A., Wolfs, Jasper F.C., de Beer, Frits C., Kieft, Hans, Nanda, Dharmin, van der Pol, Bram, Roks, Gerwin, de Beer, Frank, Halkes, Patricia H.A., Reichman, Loes J.A., Brouwers, Paul J.A.M., van den Berg-Vos, Renske M., Kwa, Vincent I.H., van der Ree, Taco C., Bronner, Irene, Bienfait, Henri P., Boogaarts, Hieronymus D., Klijn, Catharina J.M., van Bilzen, Martine, Dieks, H.J.G., de Gans, Koen, ten Holter, J.B.M., de Kruijk, Jelle R., Leijzer, Charlie T.J.M., Molenaar, Delmar, van Oostenbrugge, Robbert J., van Pamelen, Jeske, Spaander, Fianne H.M., Vermeer, Sarah E., van de Vlekkert, Janneke, Voorend, J. Manuela, van den Berg, René, Coert, Bert A., Horn, Janneke, Majoie, Charles B.L.M., Rinkel, Gabriël J.E., Roos, Yvo B.W.E.M., Vandertop, W. Peter, Verbaan, Dagmar

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    Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients by Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

    Published in Human mutation
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    The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome by van der Sluijs, Pleuntje J, Jansen, Sandra, Adachi-Fukuda, Miho, Alanay, Yasemin, AlKindy, Adila, Baban, Anwar, Bayat, Allan, Beck-Wödl, Stefanie, Berry, Katherine, Bijlsma, Emilia K, Bok, Levinus A, Brouwer, Alwin F J, van der Burgt, Ineke, Campeau, Philippe M, Canham, Natalie, Chrzanowska, Krystyna, Chu, Yoyo W Y, Chung, Brain H Y, Dahan, Karin, De Rademaeker, Marjan, Destree, Anne, Dudding-Byth, Tracy, Earl, Rachel, Elcioglu, Nursel, Elias, Ellen R, Fagerberg, Christina, Gardham, Alice, Gerkes, Erica H, Grasshoff, Ute, van Haeringen, Arie, den Hollander, Nicolette S, Horn, Denise, Hunt, David, Kant, Sarina G, Kato, Mitsuhiro, Kayserili, Hülya, Kersseboom, Rogier, Kilic, Esra, Krajewska-Walasek, Malgorzata, Lammers, Kylin, Laulund, Lone W, Lederer, Damien, Lees, Melissa, López-González, Vanesa, Maas, Saskia, Mancini, Grazia M S, Marcelis, Carlo, Martinez, Francisco, Maystadt, Isabelle, McGuire, Marianne, McKee, Shane, Mehta, Sarju, Metcalfe, Kay, Milunsky, Jeff, Mizuno, Seiji, Moeschler, John B, Netzer, Christian, Ockeloen, Charlotte W, Oehl-Jaschkowitz, Barbara, Okamoto, Nobuhiko, Olminkhof, Sharon N M, Orellana, Carmen, Pasquier, Laurent, Pottinger, Caroline, Riehmer, Vera, Robertson, Stephen P, Roifman, Maian, Rooryck, Caroline, Ropers, Fabienne G, Rosello, Monica, Ruivenkamp, Claudia A L, Sagiroglu, Mahmut S, Sallevelt, Suzanne C E H, Sanchis Calvo, Amparo, Simsek-Kiper, Pelin O, Soares, Gabriela, Solaeche, Lucia, Sonmez, Fatma Mujgan, Splitt, Miranda, Steenbeek, Duco, Stegmann, Alexander P A, Tanabe, Saori, Uctepe, Eyyup, Utine, G Eda, Veenstra-Knol, Hermine E, Venkateswaran, Sunita, Vilain, Catheline, Vincent-Delorme, Catherine, Vulto-van Silfhout, Anneke T, Wheeler, Patricia, Wilson, Golder N, Wilson, Louise C, Wollnik, Bernd, Kosho, Tomoki, Wieczorek, Dagmar, Eichler, Evan, Pfundt, Rolph, de Vries, Bert B A, Clayton-Smith, Jill, Santen, Gijs W E

    Published in Genetics in medicine
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