Resultados de búsqueda - Joël Fluss
- Mostrando 1 - 16 Resultados de 16
-
1
Cognitive and academic profiles in children with cerebral palsy: A narrative review por Joël Fluss, Karen Lidzba
Publicado 2020Revisão -
2
-
3
A Functionally Guided Approach to the Morphometry of Occipitotemporal Regions in Developmental Dyslexia: Evidence for Differential Effects in Boys and Girls por Irène Altarelli, Karla Monzalvo, Stéphanie Iannuzzi, Joël Fluss, C. Billard, Franck Ramus, Ghislaine Dehaene‐Lambertz
Publicado 2013Artigo -
4
-
5
-
6
From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand? por Stéphane Chabrier, Margaux Pouyfaucon, Alain Chatelin, Yannick Bleyenheuft, Joël Fluss, V. Gautheron, Christopher J. Newman, Guillaume Sébire, Patrick Van Bogaert, Carole Vuillerot, Sylvain Brochard, M. Dinomais
Publicado 2019Artigo -
7
Feasibility, safety, and outcome of recanalization treatment in childhood stroke por Sandra Bigi, Andrea Dulcey, Jan Gralla, Corrado Bernasconi, Amber Melliger, Alexandre Datta, Marcel Arnold, Johannes Kaesmacher, Joël Fluss, Annette Hackenberg, Oliver Maier, Johannes Weber, Claudia Poloni, Urs Fischer, Maja Steinlin
Publicado 2018Artigo -
8
Cerebral sinus venous thrombosis in Swiss children por Sebastian Grunt, Kevin Wingeier, E Wehrli, Eugen Boltshauser, Andrea Capone, Joël Fluss, Danielle Gubser-Mercati, Pierre‐Yves Jeannet, Elmar Keller, J. Marcoz, Thomas Schmitt‐Mechelke, Christian Weber, M Weissert, Maja Steinlin
Publicado 2010Artigo -
9
Factors affecting cognitive outcome in early pediatric stroke por Martina Studer, Eugen Boltshauser, Andrea Mori, Alexandre Datta, Joël Fluss, Danielle Mercati, Annette Hackenberg, Elmar Keller, Oliver Maier, Jean‐Pierre Marcoz, Gianpaolo Ramelli, Claudia Poloni, Regula Schmid, Thomas Schmitt‐Mechelke, E Wehrli, Theda Heinks, Maja Steinlin
Publicado 2014Artigo -
10
Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic Stroke por Stéphane Chabrier, Emeline Peyric, Laure Drutel, J Deron, Manoëlle Kossorotoff, M. Dinomais, Leïla Lazaro, Jérémie Lefranc, Guillaume Thébault, Gérard Dray, Joël Fluss, Cyrille Renaud, Sylvie Nguyen The Tich, Stéphane Darteyre, C. Degano, Matthieu Delion, Samuel Groeschel, Lucie Hertz‐Pannier, B. Husson, Émilie Presles, Magaly Ravel, Carole Vuillerot
Publicado 2016Artigo -
11
Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders por Halie May, Jae‐Hoon Jeong, Anya Revah‐Politi, Julie S. Cohen, Anna Chassevent, Júlia Baptista, Evan H. Baugh, Louise Bier, Armand Bottani, Maria resa Te Carminho A. Rodrigues, Charles Conlon, Joël Fluss, Michel Guipponi, Chong Ae Kim, Naomichi Matsumoto, Richard Person, Michelle Primiano, Julia Rankin, Marwan Shinawi, Constance Smith‐Hicks, Aida Telegrafi, Samantha Toy, Yuri Uchiyama, Vimla S. Aggarwal, David B. Goldstein, Katherine W. Roche, Kwame Anyane‐Yeboa
Publicado 2021Artigo -
12
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects por Roberta De Mori, Marta Romani, Stefano D’Arrigo, Maha S. Zaki, Elisa Lorefice, Silvia Tardivo, Tommaso Biagini, Valentina Stanley, Damir Musaev, Joël Fluss, Alessia Micalizzi, Sara Nuovo, Barbara Illi, Luisa Chiapparini, Lucia Di Marcotullio, Mahmoud Y. Issa, Danila Anello, Antonella Casella, Monia Ginevrino, Autumn Sa’na Leggins, Susanne Roosing, Romina Alfonsi, Jessica Rosati, Rachel Schot, Grazia M.S. Mancini, Enrico Bertini, William B. Dobyns, Tommaso Mazza, Joseph G. Gleeson, Enza Maria Valente
Publicado 2017Artigo -
13
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations por Veerle Rc Eggens, P. G. Barth, Jikke-Mien F. Niermeijer, Jonathan Berg, Niklas Darín, Abhijit Dixit, Joël Fluss, Nicola Foulds, Darren Fowler, Tibor Hortobágyi, Thomas S. Jacques, Mary D. King, Periklis Makrythanasis, Adrienn Máté, James A. R. Nicoll, Declan O’Rourke, Sue Price, Andrew N. Williams, Louise C. Wilson, Mohnish Suri, László Sztriha, Marit B Dijns-de Wissel, Mia T van Meegen, Fred van Ruissen, Eleonora Aronica, Dirk Troost, Charles B.L.M. Majoie, Henk A. Marquering, Bwee Tien Poll‐The, Frank Baas
Publicado 2014Artigo -
14
Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy por Gabrielle Rudolf, Gaëtan Lesca, Mana M. Mehrjouy, Audrey Labalme, Manal Salmi, Iben Bache, Nadine Bruneau, Manuela Pendziwiat, Joël Fluss, Julitta de Bellescize, Julia Scholly, Rikke S. Møller, Dana Craiu, Niels Tommerup, Maria Paola Valenti‐Hirsch, Caroline Schluth–Bolard, Frédérique Sloan‐Béna, Katherine L. Helbig, Sarah Weckhuysen, Patrick Edery, Safia Coulbaut, Mohamed Abbas, Ingrid E. Scheffer, Sha Tang, Candace T. Myers, Hannah Stamberger, Gemma L. Carvill, Deepali N. Shinde, Heather C. Mefford, Elena Neagu, Robert Huether, Hsiao‐Mei Lu, Alice Dica, Julie S. Cohen, Catrinel Iliescu, Cristina Pomeran, James L. Rubenstein, Ingo Helbig, Damien Sanlaville, Édouard Hirsch, Pierre Szepetowski
Publicado 2016Artigo -
15
Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections por Benson Ogunjimi, Shen‐Ying Zhang, Katrine B. Sørensen, Kristian Alsbjerg Skipper, Madalina E. Carter-Timofte, Gaspard Kerner, Stefanie Luecke, Thaneas Prabakaran, Yujia Cai, Josephina Meester, Esther Bartholomeus, Nikhita Bolar, Geert Vandeweyer, Charlotte Claes, Yasmine Sillis, Lazaro Lorenzo, Raffaele A. Fiorenza, Soraya Boucherit, Charlotte Dielman, Steven Heynderickx, George Elias, Andrea Kurotova, Ann Vander Auwera, Lieve Verstraete, Lieven Lagae, Hélène Verhelst, Anna Jansen, José Ramet, Arvid Suls, Evelien Smits, Berten Ceulemans, Lut Van Laer, Genevieve Plat Wilson, Jonas H Kreth, Capucine Pïcard, Horst von Bernuth, Joël Fluss, Stéphane Chabrier, Laurent Abel, Geert Mortier, Sébastien Fribourg, Jacob Giehm Mikkelsen, Jean‐Laurent Casanova, Søren R. Paludan, Trine H. Mogensen
Publicado 2017Artigo -
16
Making sense of missense variants in TTN-related congenital myopathies por Martin Rees, Roksana Nikoopour, Atsushi Fukuzawa, Ay Lin Kho, Miguel A. Fernandez-Garcia, Elizabeth Wraige, István Bódi, Charu Deshpande, Özkan Özdemir, Hülya‐Sevcan Daimagüler, Mark Pfuhl, Mark Holt, Birgit Brandmeier, Sarah A. Grover, Joël Fluss, Cheryl Longman, Maria Elena Farrugia, Emma Matthews, Michael G. Hanna, Francesco Muntoni, Anna Sárközy, Rahul Phadke, Rosaline C. M. Quinlivan, Emily C. Oates, Rolf Schröder, Christian T. Thiel, Jens Reimann, Nicol C. Voermans, Corrie E. Erasmus, Erik‐Jan Kamsteeg, Chaminda Konersman, Carla Grosmann, Shane McKee, Sandya Tirupathi, Steven A. Moore, Ekkehard Wilichowski, Elke Hobbiebrunken, Gabriele Dekomien, Isabelle Richard, Peter Van den Bergh, Cristina Domínguez‐González, Sebahattin Çırak, Ana Ferreiro, Heinz Jungbluth, Mathias Gautel
Publicado 2021Artigo
Herramientas de búsqueda:
Materias Relacionadas
Medicine
Biology
Gene
Genetics
Psychology
Pediatrics
Psychiatry
Cognition
Internal medicine
Neuroscience
Phenotype
Population
Stroke (engine)
Audiology
Cerebral palsy
Developmental psychology
Engineering
Environmental health
Mechanical engineering
Missense mutation
Neuropsychology
Physical medicine and rehabilitation
Arterial Ischemic Stroke
Disease
Effects of sleep deprivation on cognitive performance
Epilepsy
Intellectual disability
Ischemia
Law
Mutation