检索结果 - Annick Vogels

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  1. 1
    Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome

    Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome 由 Annick Vogels

    出版 2003
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    Carta
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  2. 2
    Pfeiffer syndrome

    Pfeiffer syndrome 由 Annick Vogels, Jean‐Pierre Fryns

    出版 2006
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    Revisão
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  3. 3
    Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders

    Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders 由 Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen, Geert Mortier, Koenraad Devriendt, Eric Legius, J P Fryns

    出版 2003
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  4. 4
    Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills

    Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills 由 A Denayer, Hilde Van Esch, Thomy de Ravel, Jean‐Pierre Frijns, Griet Van Buggenhout, Annick Vogels, Koenraad Devriendt, J. Geutjens, Paul Thiry, Ann Swillen

    出版 2012
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  5. 5
    Prevalence and comorbidities of autism among children referred to the outpatient clinics for neurodevelopmental disorders

    Prevalence and comorbidities of autism among children referred to the outpatient clinics for neurodevelopmental disorders 由 Davin Mbeya Mpaka, Daniel Luwa E-Andjafono, Ally Omba Ndjukendi, Adelin N’Situ, Sebastien Yabassi Kinsala, Joachim Ebwel Mukau, Valentin Malanda Ngoma, Esperance Kashala-Abotenes, Samuel Ma-Miezi-Mampunza, Annick Vogels, Jean Steyaert

    出版 2016
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  6. 6
    Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing

    Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing 由 Nathalie Brison, Maria Neofytou, Luc Dehaspe, Baran Bayindir, Kris Van Den Bogaert, Leila Dardour, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch

    出版 2018
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  7. 7
    Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial

    Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial 由 Thijs van der Vaart, Ellen Plasschaert, André B. Rietman, Marleen Renard, Rianne Oostenbrink, Annick Vogels, Marie‐Claire Y. de Wit, Mie‐Jef Descheemaeker, Yvonne Vergouwe, Coriene E. Catsman‐Berrevoets, Eric Legius, Ype Elgersma, Henriëtte A. Moll

    出版 2013
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  8. 8
    Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies

    Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies 由 Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, Jessica M.E. van den Oever, Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch

    出版 2016
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  9. 9
    Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

    Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant 由 Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch

    出版 2008
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  10. 10
    Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor

    Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor 由 Jeroen Breckpot, Marieke Vercruyssen, Eddy Weyts, Sean Vandevoort, Greet D'Haenens, Griet Van Buggenhout, Lore Leempoels, Elise Brischoux‐Boucher, Lionel Van Maldergem, Alessandra Renieri, Maria Antonietta Mencarelli, Carla S. D’Angelo, Verónica Mericq, Mariëtte J.V. Hoffer, Maïthé Tauber, Catherine Molinas, Claudia Castiglioni, Nathalie Brison, Joris Vermeesch, Marina Danckaerts, Pascal Sienaert, Koenraad Devriendt, Annick Vogels

    出版 2016
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  11. 11
    Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

    Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome 由 Jacob Vorstman, Elemi Breetvelt, Sasja N. Duijff, Stéphan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R. Hooper, Eva W.C. Chow, Wai Lun Alan Fung, Nancy J. Butcher, Donald A. Young, Donna M. McDonald‐McGinn, Annick Vogels, Thérèse van Amelsvoort, Doron Gothelf, Ronnie Weinberger, Abraham Weizman, Petra Klaassen, Sanne Koops, Wendy R. Kates, Kevin M. Antshel, Tony J. Simon, Opal Ousley, Ann Swillen, Raquel E. Gur, Carrie E. Bearden, René S. Kahn, Anne S. Bassett

    出版 2015
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  12. 12
    Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2

    Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 由 Erik Boot, Nancy J. Butcher, Sean Udow, Connie Marras, Kin Y. Mok, Satoshi Kaneko, Matthew J. Barrett, Paolo Prontera, Brian D. Berman, Mario Masellis, Boris Dufournet, Karine Nguyen, Perrine Charles, Eugénie Mutez, Téodor Danaila, Aurélia Jacquette, Olivier Colin, Sophie Drapier, Michel Borg, Ania Fiksinski, Elfi Vergaelen, Ann Swillen, Annick Vogels, Annika Plate, Claudia Perandones, Thomas Gasser, Kristien Clerinx, Frédéric Bourdain, K.R. Mills, Nigel Williams, Nicholas Wood, Jan Booij, Anthony E. Lang, Anne S. Bassett, Nicola Tambasco, Gabriela M. Repetto, Rosemarie Fritsch, Barber M Tinselboer, Jacob Vorstman, Luis A. Pellene, Stephen G. Reich, Claudia Schulte, A. Dekker

    出版 2018
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  13. 13
    Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia

    Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia 由 Claire Guissart, Xénia Latypova, Paul Rollier, Tahir Naeem Khan, Hannah Stamberger, Kirsty McWalter, Megan T. Cho, Susanne Kjærgaard, Sarah Weckhuysen, Gaëtan Lesca, Thomas Besnard, Katrin Õunap, Lynn Schema, Andreas G. Chiocchetti, Marie McDonald, Julitta de Bellescize, Marie Vincent, Hilde Van Esch, Shannon G. Sattler, Irman Forghani, Isabelle Thiffault, Christine M. Freitag, Deborah Barbouth, Maxime Cadieux‐Dion, Rebecca Willaert, María J. Guillen Sacoto, Nicole P. Safina, Christèle Dubourg, Lauren Grote, Wilfrid Carré, Carol Saunders, Sander Pajusalu, Emily Farrow, Anne Boland, Danielle Karlowicz, Jean‐François Deleuze, Monica H. Wojcik, Rena Pressman, Bertrand Isidor, Annick Vogels, Wim Van Paesschen, Lihadh Al‐Gazali, Aisha M. Al Shamsi, Mireille Claustres, Aurora Pujol, Stephan Sanders, François Rivier, Nicolas Leboucq, Benjamin Cogné, Souphatta Sasorith, Damien Sanlaville, Kyle Retterer, Sylvie Odent, Nicholas Katsanis, Stéphane Bézieau, M. Kœnig, Erica E. Davis, Laurent Pasquier, Sébastien Küry

    出版 2018
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  14. 14
    Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion 由 Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston, Thomas Monfeuga, Donna M. McDonald‐McGinn, Raquel E. Gur, Bernice E. Morrow, Ann Swillen, Jacob Vorstman, Carrie E. Bearden, Eva W. C. Chow, Marianne B. M. van den Bree, B S Emanuel, Joris Vermeesch, Stephen T. Warren, Michael J. Owen, Pankaj Chopra, David J. Cutler, Richard Duncan, Alex Kotlar, Jennifer G. Mulle, Anna J. Voss, Michael E. Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Salmons, Oanh Tran, Peter Holmans, Antonio F. Pardiñas, James Walters, Wolfram Demaerel, Erik Boot, Nancy J. Butcher, Gregory Costain, Chelsea Lowther, Rens Evers, Thérèse van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koenraad Devriendt, Elfi Vergaelen, Annick Vogels, T. Blaine Crowley, Daniel E. McGinn, Edward Moss, Robert Sharkus, Marta Unolt, Elaine H. Zackai, Monica E. Calkins, Robert S. Gallagher, Ruben C. Gur, Sunny X. Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M. Repetto, Elemi Breetvelt, Sasja N. Duijff, Ania Fiksinski, Hayley Moss, Maria Niarchou, Kieran C. Murphy, Sarah E. Prasad, Eileen Daly, Maria Gudbrandsen, Clodagh M. Murphy, Declan Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Cubells, Opal Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori‐Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider

    出版 2020
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