Zobrazeno 1 - 10
of 2 425
pro vyhledávání: '"Dimitri M"'
Autor:
Steffan P. Jones, Nathanael O'Neill, Jenna C. Carpenter, Sharon Muggeo, Gaia Colasante, Dimitri M. Kullmann, Gabriele Lignani
Publikováno v:
Neurobiology of Disease, Vol 201, Iss , Pp 106688- (2024)
Dravet Syndrome (DS) is most often caused by heterozygous loss-of-function mutations in the voltage-gated sodium channel gene SCN1A (Nav1.1), resulting in severe epilepsy and neurodevelopmental impairment thought to be cause by reduced interneuron ex
Externí odkaz:
https://doaj.org/article/1ccb07d314b2457881d3f817618dbcda
Autor:
Dimitri M. Drekonja, Peyton Smith
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology, Vol 4 (2024)
Externí odkaz:
https://doaj.org/article/7308c20a65264c7e8e6313bc85ba87bc
Autor:
Jennifer M. Becker, Dimitri M. L. Van Ryckeghem, Stefaan Van Damme, Geert Crombez, Yalou Schoot, Reinout W. H. J. Wiers, Ralph C. A. Rippe, Antoinette I. M. van Laarhoven
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionItch is unpleasant and induces the urge to scratch. This is adaptive to remove the itch-inducing stimulus from the skin. Accordingly, itch draws attention to protect our bodily integrity. Recent studies investigated whether attention is p
Externí odkaz:
https://doaj.org/article/2dd1db0dafca4cfb9bd320e7bb51beee
Autor:
Shannon L. Andrews, Amy A. Gravely, Amanda Beaudoin, Meghan K. Rothenberger, Dimitri M. Drekonja
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology, Vol 3 (2023)
Among 37 internal-medicine resident physicians assigned to our outpatient clinic at Minneapolis Veterans’ Affairs Health Care System (MVAHCS) on July 1, 2017, we designed a pre- and postintervention observational study. Our results show that in-per
Externí odkaz:
https://doaj.org/article/aa518a6e2a4e46bc87bc991d36f4afe5
The emptiness formation problem is addressed for a one-dimensional quantum polytropic gas characterized by an arbitrary polytropic index $\gamma$, which defines the equation of state $P \sim \rho^\gamma$, where $P$ is the pressure and $\rho$ is the d
Externí odkaz:
http://arxiv.org/abs/2412.11686
Publikováno v:
Cells, Vol 12, Iss 10, p 1382 (2023)
Dominantly inherited missense mutations of the KCNA1 gene, which encodes the KV1.1 potassium channel subunit, cause Episodic Ataxia type 1 (EA1). Although the cerebellar incoordination is thought to arise from abnormal Purkinje cell output, the under
Externí odkaz:
https://doaj.org/article/acf6debb9ffe4877a37e882c3796453f
Publikováno v:
JMIR Research Protocols, Vol 11, Iss 1, p e32359 (2022)
BackgroundTo date, research has found variable success in using attentional bias modification training (ABMT) procedures in pain samples. Several factors could contribute to these mixed findings, including boredom and low motivation. Indeed, training
Externí odkaz:
https://doaj.org/article/153c4b0eaf02445aa1494f5240121c61
Autor:
Jennifer M Becker, Henning Holle, Dimitri M L van Ryckeghem, Stefaan Van Damme, Geert Crombez, Dieuwke S Veldhuijzen, Andrea W M Evers, Ralph C A Rippe, Antoinette I M van Laarhoven
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0273581 (2022)
Rapidly attending towards potentially harmful stimuli to prevent possible damage to the body is a critical component of adaptive behavior. Research suggests that individuals display an attentional bias, i.e., preferential allocation of attention, for
Externí odkaz:
https://doaj.org/article/c89307b24cbd4f66850afb51e0fb3232
Autor:
Maité Van Alboom, Fleur Baert, Aline Wauters, Melanie Beeckman, Sarah Maes, Ama Kissi, Elke Veirman, Dimitri M. L. Van Ryckeghem, Annick De Paepe, Louise Poppe
Publikováno v:
Psychologica Belgica, Vol 61, Iss 1 (2021)
To limit the spread of COVID-19, many countries, including Belgium, have installed physical distancing measures. Yet, adherence to these newly installed behavioral measures has been described as challenging and effortful. Based on the Health Action P
Externí odkaz:
https://doaj.org/article/0eefb8485a0e4af8b96666c2722e5b08
Autor:
Vincenzo Salpietro, Christine L. Dixon, Hui Guo, Oscar D. Bello, Jana Vandrovcova, Stephanie Efthymiou, Reza Maroofian, Gali Heimer, Lydie Burglen, Stephanie Valence, Erin Torti, Moritz Hacke, Julia Rankin, Huma Tariq, Estelle Colin, Vincent Procaccio, Pasquale Striano, Kshitij Mankad, Andreas Lieb, Sharon Chen, Laura Pisani, Conceicao Bettencourt, Roope Männikkö, Andreea Manole, Alfredo Brusco, Enrico Grosso, Giovanni Battista Ferrero, Judith Armstrong-Moron, Sophie Gueden, Omer Bar-Yosef, Michal Tzadok, Kristin G. Monaghan, Teresa Santiago-Sim, Richard E. Person, Megan T. Cho, Rebecca Willaert, Yongjin Yoo, Jong-Hee Chae, Yingting Quan, Huidan Wu, Tianyun Wang, Raphael A. Bernier, Kun Xia, Alyssa Blesson, Mahim Jain, Mohammad M. Motazacker, Bregje Jaeger, Amy L. Schneider, Katja Boysen, Alison M. Muir, Candace T. Myers, Ralitza H. Gavrilova, Lauren Gunderson, Laura Schultz-Rogers, Eric W. Klee, David Dyment, Matthew Osmond, Mara Parellada, Cloe Llorente, Javier Gonzalez-Peñas, Angel Carracedo, Arie Van Haeringen, Claudia Ruivenkamp, Caroline Nava, Delphine Heron, Rosaria Nardello, Michele Iacomino, Carlo Minetti, Aldo Skabar, Antonella Fabretto, SYNAPS Study Group, Miquel Raspall-Chaure, Michael Chez, Anne Tsai, Emily Fassi, Marwan Shinawi, John N. Constantino, Rita De Zorzi, Sara Fortuna, Fernando Kok, Boris Keren, Dominique Bonneau, Murim Choi, Bruria Benzeev, Federico Zara, Heather C. Mefford, Ingrid E. Scheffer, Jill Clayton-Smith, Alfons Macaya, James E. Rothman, Evan E. Eichler, Dimitri M. Kullmann, Henry Houlden
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-16 (2019)
Genetic variants in ionotropic glutamate receptors have been implicated in neurodevelopmental disorders. Here, the authors report heterozygous de novo mutations in the GRIA2 gene in 28 individuals with intellectual disability and neurodevelopmental a
Externí odkaz:
https://doaj.org/article/67fdcf82e84544e095b6c7c81e0bd8ff