Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare “Unpredictable” Event

por Becocci, Andrea, Felice-Civitillo, Cristina, Laurent, Méryle, Boehlen, Françoise, De Luca, Roberta, Fluss, Joel
Publicado 2018

MCF2 is linked to a complex perisylvian syndrome and affects cortical lamination

por Molinard‐Chenu, Aude, Fluss, Joël, Laurent, Sacha, Laurent, Méryle, Guipponi, Michel, Dayer, Alexandre G.
Publicado 2019

Decompressive hemicraniectomy in pediatric malignant arterial ischemic stroke: a case-based review

por Carlhan-Ledermann, Audrey, Bartoli, Andrea, Gebistorf, Fabienne, Beghetti, Maurice, Sologashvili, Tornike, Rebollo Polo, Monica, Fluss, Joel
Publicado 2023

Gait stability in ambulant children with cerebral palsy during dual tasks

por Wist, Sophie, Carcreff, Lena, Bruijn, Sjoerd M., Allali, Gilles, Newman, Christopher J., Fluss, Joel, Armand, Stéphane
Publicado 2022

The Influence of Socioeconomic Status on Children’s Brain Structure

por Jednoróg, Katarzyna, Altarelli, Irene, Monzalvo, Karla, Fluss, Joel, Dubois, Jessica, Billard, Catherine, Dehaene-Lambertz, Ghislaine, Ramus, Franck
Publicado 2012

Correction: The Influence of Socioeconomic Status on Children’s Brain Structure

por Jednoróg, Katarzyna, Altarelli, Irene, Monzalvo, Karla, Fluss, Joel, Dubois, Jessica, Billard, Catherine, Dehaene-Lambertz, Ghislaine, Ramus, Franck
Publicado 2012

Acute cortical deafness in a child with MELAS syndrome

por Pittet, Marie P., Idan, Roni B., Kern, Ilse, Guinand, Nils, Van, Hélène Cao, Toso, Seema, Fluss, Joël
Publicado 2016

Herpes simplex encephalitis as a complication of neurosurgical procedures: report of 3 cases and review of the literature

por Jaques, David A., Bagetakou, Spyridoula, L’Huillier, Arnaud G., Bartoli, Andrea, Vargas, Maria-Isabel, Fluss, Joel, Kaiser, Laurent
Publicado 2016

Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms

por Blanchard-Rohner, Geraldine, Peirolo, Anna, Coulon, Ludivine, Korff, Christian, Horvath, Judit, Burkhard, Pierre R., Gumy-Pause, Fabienne, Ranza, Emmanuelle, Jandus, Peter, Dibra, Harpreet, Taylor, Alexander Malcolm R., Fluss, Joel
Publicado 2022

Bi‐allelic loss of ERGIC1 causes relatively mild arthrogryposis

por Marconi, Caterina, Lemmens, Laure, Masclaux, Frédéric, Mattioli, Francesca, Fluss, Joël, Extermann, Philippe, Mendez, Purificacion, Leuchter, Russia Ha‐Vinh, Stathaki, Elissavet, Laurent, Sacha, Hammar, Eva, Vannier, Anne, Varvagiannis, Konstantinos, Guipponi, Michel, Sloan‐Bena, Frédérique, Blouin, Jean‐Louis, Abramowicz, Marc, Fokstuen, Siv
Publicado 2021

EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations

por Eggens, Veerle RC, Barth, Peter G, Niermeijer, Jikke-Mien F, Berg, Jonathan N, Darin, Niklas, Dixit, Abhijit, Fluss, Joel, Foulds, Nicola, Fowler, Darren, Hortobágyi, Tibor, Jacques, Thomas, King, Mary D, Makrythanasis, Periklis, Máté, Adrienn, Nicoll, James AR, O’Rourke, Declan, Price, Sue, Williams, Andrew N, Wilson, Louise, Suri, Mohnish, Sztriha, Laszlo, Dijns-de Wissel, Marit B, van Meegen, Mia T, van Ruissen, Fred, Aronica, Eleonora, Troost, Dirk, Majoie, Charles BLM, Marquering, Henk A, Poll-Thé, Bwee Tien, Baas, Frank
Publicado 2014

SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum

por Serpieri, Valentina, D’Abrusco, Fulvio, Dempsey, Jennifer C, Cheng, Yong-Han Hank, Arrigoni, Filippo, Baker, Janice, Battini, Roberta, Bertini, Enrico Silvio, Borgatti, Renato, Christman, Angela K, Curry, Cynthia, D'Arrigo, Stefano, Fluss, Joel, Freilinger, Michael, Gana, Simone, Ishak, Gisele E, Leuzzi, Vincenzo, Loucks, Hailey, Manti, Filippo, Mendelsohn, Nancy, Merlini, Laura, Miller, Caitlin V, Muhammad, Ansar, Nuovo, Sara, Romaniello, Romina, Schmidt, Wolfgang, Signorini, Sabrina, Siliquini, Sabrina, Szczałuba, Krzysztof, Vasco, Gessica, Wilson, Meredith, Zanni, Ginevra, Boltshauser, Eugen, Doherty, Dan, Valente, Enza Maria
Publicado 2022

Making sense of missense variants in TTN-related congenital myopathies

por Rees, Martin, Nikoopour, Roksana, Fukuzawa, Atsushi, Kho, Ay Lin, Fernandez-Garcia, Miguel A., Wraige, Elizabeth, Bodi, Istvan, Deshpande, Charu, Özdemir, Özkan, Daimagüler, Hülya-Sevcan, Pfuhl, Mark, Holt, Mark, Brandmeier, Birgit, Grover, Sarah, Fluss, Joël, Longman, Cheryl, Farrugia, Maria Elena, Matthews, Emma, Hanna, Michael, Muntoni, Francesco, Sarkozy, Anna, Phadke, Rahul, Quinlivan, Ros, Oates, Emily C., Schröder, Rolf, Thiel, Christian, Reimann, Jens, Voermans, Nicol, Erasmus, Corrie, Kamsteeg, Erik-Jan, Konersman, Chaminda, Grosmann, Carla, McKee, Shane, Tirupathi, Sandya, Moore, Steven A., Wilichowski, Ekkehard, Hobbiebrunken, Elke, Dekomien, Gabriele, Richard, Isabelle, Van den Bergh, Peter, Domínguez-González, Cristina, Cirak, Sebahattin, Ferreiro, Ana, Jungbluth, Heinz, Gautel, Mathias
Publicado 2021