Zobrazeno 1 - 10 of 236 pro vyhledávání: '"M, Zilbovicius"'
1
Akademický článek
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2
Posterior Fossa Arachnoid Cyst in a Pediatric Population is Associated with Social Perception and Rest Cerebral Blood Flow Abnormalities
Autor: Stéphanie Puget, Hervé Lemaitre, Jennifer Boisgontier, Ludovic Fillion, Ana Saitovitch, Elza Rechtman, Nathalie Boddaert, Jean-Marc Tacchella, M. Zilbovicius, Marie-Laure Cuny
Publikováno v: Cerebellum (London, England). 19(1)
Posterior fossa arachnoid cysts (PFAC) may produce not only neurological symptoms but also other symptoms still poorly understood such as behavioral and learning deficits, awkwardness, and difficulties in social interaction. These subtle social impai
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feb3cb0c1251c367dec1943c8c1e04e4
https://pubmed.ncbi.nlm.nih.gov/31732920
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3
Anatomical and functional abnormalities on MRI in kabuki syndrome
Autor: Ana Saitovitch, Jennifer Boisgontier, Elza Rechtman, Ludovic Fillon, David Grevent, Odile Boute, Elise Schaefer, Elodie Sanchez, Damien Sanlaville, Natacha Lehman, Laurence Faivre, David Geneviève, Vincent Gatinois, Nathalie Boddaert, Jean Marc Tacchella, Kim-Hanh Le Quang Sang, Marlène Rio, M. Zilbovicius, Hervé Lemaitre, Stanislas Lyonnet, Guilaine Boursier, Geneviève Baujat
Publikováno v: Neuroimage-Clinical
Neuroimage-Clinical, Elsevier, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
NeuroImage : Clinical
Neuroimage-Clinical, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
Kabuki syndrome (KS) is a rare congenital disorder (1/32000 births) characterized by distinctive facial features, intellectual disability, short stature, and dermatoglyphic and skeletal abnormalities. In the last decade, mutations in KMT2D and KDM6A
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb98025bcde8087c27465afe3e28b583
https://hal.umontpellier.fr/hal-02573243/file/IRMB_156_main.pdf
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4
Akademický článek
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6
Neuroimaging evidence of brain abnormalities in mastocytosis
Autor: N, Boddaert, A, Salvador, M O, Chandesris, H, Lemaître, D, Grévent, C, Gauthier, O, Naggara, S, Georgin-Lavialle, D S, Moura, F, Munsch, N, Jaafari, M, Zilbovicius, O, Lortholary, R, Gaillard, O, Hermine
Publikováno v: Translational Psychiatry
Mastocytosis is a rare disease in which chronic symptoms are related to mast cell accumulation and activation. Patients can display depression-anxiety-like symptoms and cognitive impairment. The pathophysiology of these symptoms may be associated wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b6e9c77c757ba34e977e572065a53e86
https://pubmed.ncbi.nlm.nih.gov/29743606
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7
Tuning Eye-Gaze Perception by Transitory STS Inhibition
Autor: David Grevent, M. Zilbovicius, Yves Samson, Hervé Lemaitre, Sabine Meunier, Elza Rechtman, Traian Popa, Francis Brunelle, Ana Saitovitch, Nathalie Boddaert, Raphael Calmon, Jean-Charles Lamy
Publikováno v: Cerebral Cortex
Cerebral Cortex, 2016, ⟨10.1093/cercor/bhw045⟩
Cerebral Cortex (New York, NY)
Cerebral Cortex, Oxford University Press (OUP), 2016, ⟨10.1093/cercor/bhw045⟩
Cerebral Cortex, Oxford University Press (OUP), 2016, 〈10.1093/cercor/bhw045〉
International audience; Processing eye-gaze information is a key step to human social interaction. Neuroimaging studies have shown that superior temporal sulcus (STS) is highly implicated in eye-gaze perception. In autism, a lack of preference for th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70525b4925c63db83423f7bd4208582
https://hal.sorbonne-universite.fr/hal-01285650
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8
Imagerie cérébrale dans l’autisme infantile
Autor: Nathalie Boddaert, Ana Saitovitch, M. Zilbovicius, N. Chabane, Francis Brunelle, David Grevent, A Bargiacchi
Publikováno v: Archives de Pédiatrie. 19:547-550
Understanding of brain structural anomalies seen in children with autism has considerably progressed since the apparition of MRI and functional imaging. All the results are converging toward the description of anatomical and functional anomalies in t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0966e97cd935cbeb0c20462b125d9511
https://doi.org/10.1016/j.arcped.2012.02.005
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10
PET Scan Perfusion Imaging in the Prader–Willi Syndrome: New Insights into the Psychiatric and Social Disturbances
Autor: Gwenaelle Diene, Pierre Payoux, Mélanie Glattard, Pierre Celsis, Annick Sevely, Carine Mantoulan, M. Zilbovicius, Bernadette Rogé, Maithé Tauber, Catherine Molinas
Publikováno v: Journal of Cerebral Blood Flow & Metabolism. 31:275-282
The Prader–Willi syndrome (PWS), a rare multisystem genetic disease, leads to severe disabilities, such as morbid obesity, endocrine dysfunctions, psychiatric disorders, and social disturbances. We explored the whole brain of patients with PWS to d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7b6a2f2baba61e85c6556c98d78054
https://doi.org/10.1038/jcbfm.2010.87
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