Reduced parietal activation in cervical dystonia after parietal TMS interleaved with fMRI von de Vries, Paulien M, de Jong, Bauke M, Bohning, Daryl E, Hinson, Vanessa K, George, Mark S, Leenders, Klaus L

Volltext

Structural white matter abnormalities in patients with idiopathic dystonia von Bonilha, Leonardo, de Vries, Paulien M., Vincent, Diana J., Rorden, Chris, Morgan, Paul S., Hurd, Mark W., Besenski, Nada, Bergmann, Kenneth J., Hinson, Vanessa K.

Volltext

Changes in cerebral activations during movement execution and imagery after parietal cortex TMS interleaved with 3T MRI von de Vries, Paulien M, de Jong, Bauke M, Bohning, Daryl E, Walker, John A, George, Mark S, Leenders, Klaus L

Volltext

Changed patterns of cerebral activation related to clinically normal hand movement in cervical dystonia von de Vries, Paulien M, Johnson, Kevin A, de Jong, Bauke M, Gieteling, Esther W, Bohning, Daryl E, George, Mark S, Leenders, Klaus L

Volltext

Disrupted thalamic prefrontal pathways in patients with idiopathic dystonia von Bonilha, Leonardo, de Vries, Paulien M, Hurd, Mark W, Rorden, Chris, Morgan, Paul S, Besenski, Nada, Bergmann, Kenneth J, Hinson, Vanessa K

Volltext

Cerebral activation patterns related to initiation and inhibition of hand movement von Toxopeus, Carolien M, de Vries, Paulien M, de Jong, Bauke M, Johnson, Kevin A, George, Mark S, Bohning, Daryl E, Walker, John, Leenders, Klaus L

Volltext

Functional Interaction between β-Catenin and FOXO in Oxidative Stress Signaling von Marieke A. G. Essers, Lydia M. M. de Vries-Smits, Barker, Nick, Polderman, Paulien E., Boudewijn M. T. Burgering, Korswagen, Hendrik C.

Volltext

Social Media and Body Dissatisfaction: Investigating the Attenuating Role of Positive Parent–Adolescent Relationships von de Vries, Dian A., Vossen, Helen G. M., van der Kolk – van der Boom, Paulien

Volltext

Low-molecular-weight heparin and recurrent placenta-mediated pregnancy complications: a meta-analysis of individual patient data from randomised controlled trials von Rodger, Marc A, Prof, Gris, Jean-Christophe, Prof, de Vries, Johanna I P, Prof, Martinelli, Ida, MD, Rey, Évelyne, MD, Schleussner, Ekkehard, Prof, Middeldorp, Saskia, Prof, Kaaja, Risto, Prof, Langlois, Nicole J, MSc, Ramsay, Timothy, PhD, Mallick, Ranjeeta, PhD, Bates, Shannon M, Prof, Abheiden, Carolien N H, MD, Perna, Annalisa, MSc, Petroff, David, PhD, de Jong, Paulien, MD, van Hoorn, Marion E, MD, Bezemer, P Dick, PhD, Mayhew, Alain D, MSc

Volltext

Multimodal imaging of the disease progression of birdshot chorioretinopathy von Teussink, Michel M., Huis in het Veld, Paulien I., Vries, Lieuwe A. M., Hoyng, Carel B., Klevering, B. Jeroen, Theelen, Thomas

Volltext

TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility von Engwerda, Aafke, Leenders, Erika K S M, Frentz, Barbara, Terhal, Paulien A, Löhner, Katharina, de Vries, Bert B A, Dijkhuizen, Trijnie, Vos, Yvonne J, Rinne, Tuula, van den Berg, Maarten P, Roofthooft, Marc T R, Deelen, Patrick, van Ravenswaaij-Arts, Conny M A, Kerstjens-Frederikse, Wilhelmina S

Volltext

Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability von Monroe, Glen R., Frederix, Gerardus W., Savelberg, Sanne M. C., de Vries, Tamar I., Duran, Karen J., van der Smagt, Jasper J., Terhal, Paulien A., van Hasselt, Peter M., Kroes, Hester Y., Verhoeven-Duif, Nanda M., Nijman, Isaäc J., Carbo, Ellen C., van Gassen, Koen L., Knoers, Nine V., Hövels, Anke M., van Haelst, Mieke M., Visser, Gepke, van Haaften, Gijs

Volltext

De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders von Reynhout, Sara, Jansen, Sandra, Haesen, Dorien, van Belle, Siska, de Munnik, Sonja A., Bongers, Ernie M.H.F., Schieving, Jolanda H., Marcelis, Carlo, Amiel, Jeanne, Rio, Marlène, Mclaughlin, Heather, Ladda, Roger, Sell, Susan, Kriek, Marjolein, Peeters-Scholte, Cacha M.P.C.D., Terhal, Paulien A., van Gassen, Koen L., Verbeek, Nienke, Henry, Sonja, Scott Schwoerer, Jessica, Malik, Saleem, Revencu, Nicole, Ferreira, Carlos R., Macnamara, Ellen, Braakman, Hilde M.H., Brimble, Elise, Ruzhnikov, Maura R.Z., Wagner, Matias, Harrer, Philip, Wieczorek, Dagmar, Kuechler, Alma, Tziperman, Barak, Barel, Ortal, de Vries, Bert B.A., Gordon, Christopher T., Janssens, Veerle, Vissers, Lisenka E.L.M.

Volltext

ALIFE2 study: low-molecular-weight heparin for women with recurrent miscarriage and inherited thrombophilia--study protocol for a randomized controlled trial von de Jong, Paulien G, Quenby, Siobhan, Bloemenkamp, Kitty W M, Braams-Lisman, Babette A M, de Bruin, Jan Peter, Coomarasamy, Arri, David, Michele, DeSancho, Maria T, van der Heijden, Olivier W H, Hoek, Annemieke, Hutten, Barbara A, Jochmans, Kristin, Koks, Carolien A M, Kuchenbecker, Walter K M, Mol, Ben Willem J, Torrance, Helen L, Scheepers, Hubertina C J, Stephenson, Mary D, Verhoeve, Harold R, Visser, Jantien, de Vries, Johanna I P, Goddijn, Mariëtte, Middeldorp, Saskia

Volltext

De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders von Reynhout, Sara, Jansen, Sandra, Haesen, Dorien, van Belle, Siska, de Munnik, Sonja A., Bongers, Ernie M.H.F., Schieving, Jolanda H., Marcelis, Carlo, Amiel, Jeanne, Rio, Marlène, Mclaughlin, Heather, Ladda, Roger, Sell, Susan, Kriek, Marjolein, Peeters-Scholte, Cacha M.P.C.D., Terhal, Paulien A., van Gassen, Koen L., Verbeek, Nienke, Henry, Sonja, Schwoerer, Jessica Scott, Malik, Saleem, Revencu, Nicole, Ferreira, Carlos R., Macnamara, Ellen, Braakman, Hilde M.H., Brimble, Elise, Ruzhnikov, Maura R.Z., Wagner, Matias, Harrer, Philip, Wieczorek, Dagmar, Kuechler, Alma, Tziperman, Barak, Barel, Ortal, de Vries, Bert B.A., Gordon, Christopher T., Janssens, Veerle, Vissers, Lisenka E.L.M.

Volltext

Thromboprophylaxis after Knee Arthroscopy and Lower-Leg Casting von van Adrichem, Raymond A, Nemeth, Banne, Algra, Ale, le Cessie, Saskia, Rosendaal, Frits R, Schipper, Inger B, Nelissen, Rob G.H.H, Cannegieter, Suzanne C

Volltext

Social Media and Body Dissatisfaction: Investigating the Attenuating Role of Positive Parent–Adolescent Relationships von De Vries, Dian A, Vossen, Helen G. M, Van Der Kolk – Van Der Boom, Paulien

Volltext

Dexamethasone for the Prevention of a Pain Flare After Palliative Radiation Therapy for Painful Bone Metastases: The Multicenter Double-Blind Placebo-Controlled 3-Armed Randomized... von van der Linden, Yvette M, Westhoff, Paulien G, Stellato, Rebecca K, van Baardwijk, Angela, de Vries, Kim, Ong, Francisca, Wiggenraad, Ruud, Bakri, Bonnie, Wester, Gerda, de Pree, Ilse, van Veelen, Lieneke, Budiharto, Tom, Schippers, Maaike, Reyners, Anna K.L, de Graeff, Alexander

Volltext

Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations von Fergelot, Patricia, Van Belzen, Martine, Van Gils, Julien, Afenjar, Alexandra, Armour, Christine M., Arveiler, Benoit, Beets, Lex, Burglen, Lydie, Busa, Tiffany, Collet, Marie, Deforges, Julie, de Vries, Bert B. A., Dominguez Garrido, Elena, Dorison, Nathalie, Dupont, Juliette, Francannet, Christine, Garciá-Minaúr, Sixto, Gabau Vila, Elisabeth, Gebre-Medhin, Samuel, Gener Querol, Blanca, Geneviève, David, Gérard, Marion, Gervasini, Cristina Giovanna, Goldenberg, Alice, Josifova, Dragana, Lachlan, Katherine, Maas, Saskia, Maranda, Bruno, Moilanen, Jukka S., Nordgren, Ann, Parent, Philippe, Rankin, Julia, Reardon, Willie, Rio, Marlène, Roume, Joëlle, Shaw, Adam, Smigiel, Robert, Sojo, Amaia, Solomon, Benjamin, Stembalska, Agnieszka, Stumpel, Constance, Suarez, Francisco, Terhal, Paulien, Thomas, Simon, Touraine, Renaud, Verloes, Alain, Vincent-Delorme, Catherine, Wincent, Josephine, Peters, Dorien J. M., Bartsch, Oliver, Larizza, Lidia, Lacombe, Didier, Hennekam, Raoul C.

Volltext

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder von Reijnders, Margot R.F., Miller, Kerry A., Alvi, Mohsan, Goos, Jacqueline A.C., Lees, Melissa M., de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A., Isidor, Bertrand, Kerr, Bronwyn, Marcelis, Carlo, Schluth-Bolard, Caroline, Deshpande, Charu, Ruivenkamp, Claudia A.L., Wieczorek, Dagmar, Baralle, Diana, Blair, Edward M., Engels, Hartmut, Lüdecke, Hermann-Josef, Eason, Jacqueline, Santen, Gijs W.E., Clayton-Smith, Jill, Chandler, Kate, Tatton-Brown, Katrina, Payne, Katelyn, Helbig, Katherine, Radtke, Kelly, Nugent, Kimberly M., Cremer, Kirsten, Strom, Tim M., Bird, Lynne M., Sinnema, Margje, Bitner-Glindzicz, Maria, van Dooren, Marieke F., Alders, Marielle, Koopmans, Marije, Brick, Lauren, Kozenko, Mariya, Harline, Megan L., Klaassens, Merel, Steinraths, Michelle, Cooper, Nicola S., Edery, Patrick, Yap, Patrick, Terhal, Paulien A., van der Spek, Peter J., Lakeman, Phillis, Taylor, Rachel L., Littlejohn, Rebecca O., Pfundt, Rolph, Mercimek-Andrews, Saadet, Stegmann, Alexander P.A., Kant, Sarina G., McLean, Scott, Joss, Shelagh, Swagemakers, Sigrid M.A., Douzgou, Sofia, Wall, Steven A., Küry, Sébastien, Calpena, Eduardo, Koelling, Nils, McGowan, Simon J., Twigg, Stephen R.F., Mathijssen, Irene M.J., Nellaker, Christoffer, Brunner, Han G., Wilkie, Andrew O.M.

Volltext