Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Nathalie Angeard"'
Autor:
Martine Frischmann, Marie-Lise Babonneau, Christian Réveillère, Marcela Gargiulo, Marie Meunier, Nathalie Angeard, Sabrina Sayah, Bettina Beaujard, Ariane Herson, Nayla Debs, Claire-Cécile Michon
Publikováno v:
Contraste. :219-235
Depuis le mois de mars 2020, nous vivons une crise sanitaire qui a conduit a une transformation profonde de nos pratiques professionnelles. Cet article, ecrit a plusieurs mains, a comme objectif de rendre compte de l’essentiel de notre experience d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dc894959b5b90964c3deb0aeecbe967
https://doi.org/10.3917/cont.053.0219
https://doi.org/10.3917/cont.053.0219
Publikováno v:
Canadian Psychology / Psychologie canadienne. 61:215-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bff2931100abb6b9a5de5327448d4d2
https://doi.org/10.1037/cap0000185
https://doi.org/10.1037/cap0000185
Autor:
Joana Garmendia, Garazi Labayru, Jone Aliri, Stefan Winblad, Nathalie Angeard, Adolfo López de Munain, Andone Sistiaga
Publikováno v:
Neuromuscular disorders : NMD. 32(9)
Currently, no rapid and specific instrument is available to briefly estimate intelligence in patients with myotonic dystrophy type 1 (DM1), a multisystemic disease that involves the CNS and is associated with cognitive deficits and low intellectual f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c6b9ed4110858ef2c13d28c4d7387c
https://pubmed.ncbi.nlm.nih.gov/35868899
https://pubmed.ncbi.nlm.nih.gov/35868899
Autor:
Tina Duong, Kiera Berggren, Craig Campbell, Tetsuo Ashizawa, Leah Hellerstein, Chiara Marini-Bettolo, Anne Berit Ekström, Nicholas E. Johnson, Nathalie Angeard, Valeria A. Sansone, Eugenio Zapata Aldana, Cuixia Tian
Publikováno v:
Paediatrics Publications
Neurology: Clinical Practice
Neurology: Clinical Practice
Purpose of reviewMyotonic dystrophy type 1 is a multisystemic disorder caused by a noncoding triplet repeat. The age of onset is variable across the lifespan, but in its most severe form, the symptoms appear at birth (congenital myotonic dystrophy) o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::095c68871835bfcc1ad0741783dc3da6
https://doi.org/10.1212/cpj.0000000000000646
https://doi.org/10.1212/cpj.0000000000000646
Autor:
Alexandre Morin, Aurelie Funkiewiez, Alexandre Routier, Raphael Le Bouc, Nicolas Borderies, Damien Galanaud, Richard Levy, Mathias Pessiglione, Bruno Dubois, Bruno Eymard, Claire-Cecile Michon, Nathalie Angeard, Anthony Behin, Pascal Laforet, Tanya Stojkovic, Carole Azuar
Publikováno v:
Brain communications. 4(3)
Myotonic dystrophy type 1 is an autosomal dominant multisystemic disorder affecting muscular and extra muscular systems, including the central nervous system. Cerebral involvement in myotonic dystrophy type 1 is associated with subtle cognitive and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8d837b82e1486c9c03eaff14404e6bf
https://pubmed.ncbi.nlm.nih.gov/35611304
https://pubmed.ncbi.nlm.nih.gov/35611304
Autor:
Laurent Servais, A. Jacquette, Nathalie Angeard, Marcela Gargiulo, Bruno Eymard, David Cohen, Delphine Héron, E. Huerta, Jean Xavier
Myotonic dystrophy type 1 (DM1) is a multisystemic disorder with neuromuscular symptoms and brain dysfunctions. Depending on the phenotypic expression, the degree of cognitive impairment remains heterogeneous, ranging from moderate to severe intellec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9323569dc5aecbaf7c79851b84260370
https://doi.org/10.1016/j.nmd.2017.12.006
https://doi.org/10.1016/j.nmd.2017.12.006
Autor:
Marcela Gargiulo, Nathalie Angeard, Guillaume Bassez, Bettina Beaujard, Anthony Behin, Ariane Herson, Sarah Louis, Marion Masingue, Sandra Misdrahi, Sabrina Sayah, Tanya Stojkovic, Bruno Eymard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0807844bb47453b52c4d623d18224d23
https://doi.org/10.3917/eres.boiss.2019.01.0145
https://doi.org/10.3917/eres.boiss.2019.01.0145
Autor:
Charlotte Mennetrey, Nathalie Angeard
Publikováno v:
Cognitive Development. 48:125-134
The Dimensional Change Card-Sorting task (DCCS) is frequently used to assess preschool-children’s executive abilities. Children are asked to sort bidimensional cards (a blue boat) first according to one dimension (color) and then according to the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8457baf5f4556aa86aab7e663bf6e245
https://doi.org/10.1016/j.cogdev.2018.08.004
https://doi.org/10.1016/j.cogdev.2018.08.004
Autor:
Nathalie Angeard
Publikováno v:
Developmental medicine and child neurologyReferences. 61(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bff65bff9d9c16ba8c32747eaa94e34
https://pubmed.ncbi.nlm.nih.gov/30706460
https://pubmed.ncbi.nlm.nih.gov/30706460
Autor:
Valeria A. Sansone, Marla B. Ferschl, Elisa De Mattia, John W. Day, Anne-Berit Ekström, Gordon F. Tomaselli, James E. Hilbert, Todd Goodglick, Tetsuo Ashizawa, Laurie Gutmann, Ericka Simpson, Nicholas E. Johnson, Linda Nguyen, S. H. Subramony, Laurie Sterling, Nathalie Angeard, Marie Kierkegaard, Belen Esparis, Careniña Trujillo, Baziel G.M. van Engelen, Benedikt Schoser, William J. Groh, Tina Duong, Edith H. C. Cup, Elisabetta Roma, Wilma J. Koopman, Shannon L. Venance, Venessa Holland, Kiera Berggren, Janice L.B. Byrne, Ann Broderick, Guillaume Bassez, Daphne Maas, Saman Nazarian, Kari Lane, Chad Heatwole, Peg Nopoulos, Giovanni Meola, Jacinda B. Sampson, Cuixia Tian, Aparajitha Verma, Louis Richer, Marco Bozzali, Subha Raman, Richard T. Moxley, Jack Puymirat, Shahinaz M. Gadalla, Cynthia Gagnon, Katherine D. Mathews, Stefan Winblad, Katy Eichinger, Craig Campbell, Benjamin Gallais, Jeffrey Statland, Richard E. Petty, David J. Moser, Deepak Bhakta, Shree Pandya, Denis Duboc, Chris Turner, Ami Mankodi, Janel Phetteplace, Darren G. Monckton, Molly White, Bruno Eymard, Mark T. Rogers
Publikováno v:
Paediatrics Publications
Neurology. Clinical Practice, 8, 6, pp. 507-520
Neurology: Clinical Practice
Neurology: Clinical Practice, 2018, 8 (6), pp.507-520. ⟨10.1212/CPJ.0000000000000531⟩
Neurology. Clinical Practice, 8, 507-520
Neurology. Clinical Practice, 8, 6, pp. 507-520
Neurology: Clinical Practice
Neurology: Clinical Practice, 2018, 8 (6), pp.507-520. ⟨10.1212/CPJ.0000000000000531⟩
Neurology. Clinical Practice, 8, 507-520
Purpose of review: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No evidence-based guideline exists to inform the care of these patients, and most do not have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee3d1ad9bb57439767406ba7ad93787
https://ir.lib.uwo.ca/paedpub/202
https://ir.lib.uwo.ca/paedpub/202