Gérald Bussy

Gérald Bussy

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Gérald Bussy

Gérald Bussy

Publications by authors named "Gérald Bussy"

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Basal ganglia involvement in patients: The reason for patients very specific grasping?

Neuroimage Clin 2018 5;19:454-465. Epub 2018 Apr 5.

Psychiatric Neuroimaging Program, Department of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA; Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

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http://dx.doi.org/10.1016/j.nicl.2018.04.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029499PMC
January 2019

Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant.

Psychiatr Genet 2017 06;27(3):105-109

aClaude Bernard Lyon 1 University bInstitute of Cognitive Science, CNRS UMR 5304 cFrench National Reference Center for Rare Diseases with Intellectual Disability dReference Center on Learning Disabilities, Pediatric Functional Rehabilitation Department, Escale, Women Mothers and Children Hospital eDepartment of Child Psychiatry, Neurological Hospital fDepartment of Medical Genetics, Lyon University Hospital gCNRS UMR 5292, INSERM U1028, CNRL hDepartment of Child Psychiatry, Saint Jean de Dieu Hospital, Lyon, France.

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http://dx.doi.org/10.1097/YPG.0000000000000165DOI Listing
June 2017

Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation.

Am J Med Genet A 2013 Dec 16;161A(12):3063-71. Epub 2013 Aug 16.

Service de Génétique and Centre de Référence des Anomalies du Développement, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France; INSERM U1028, CNRS, UMR5292, Lyon Neuroscience Research Center, TIGER Team, University Claude Bernard Lyon 1, Université de Lyon, Lyon, France.

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http://dx.doi.org/10.1002/ajmg.a.36162DOI Listing
December 2013

Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndrome.

Eur J Med Genet 2012 Jun 28;55(6-7):433-6. Epub 2012 Mar 28.

Hospices Civils de Lyon, HFME, Centre de Référence, Déficiences Intellectuelles de Causes Rares, 59 Boulevard Pinel, Bron, France.

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http://dx.doi.org/10.1016/j.ejmg.2012.03.008DOI Listing
June 2012

Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiency.

Eur J Med Genet 2009 Jan-Feb;52(1):6-13. Epub 2008 Sep 25.

Institut des Sciences Cognitives, CNRS UMR5230, Université Claude Bernard Lyon 1 and Hospices Civils de Lyon, Lyon, France.

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http://dx.doi.org/10.1016/j.ejmg.2008.09.003DOI Listing
April 2009

Reactivity to visual signals and the cerebellar vermis: Evidence from a rare case with rhombencephalosynapsis.

Behav Neurosci 2009 Feb;123(1):86-96

Université Lumière-Lyon 2, Laboratoire d'Etude des Mécanismes Cognitifs, Département de Psychologie Cognitive Expérimentale & Neuropsychologie, Bron Cedex, France.

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http://doi.apa.org/getdoi.cfm?doi=10.1037/a0013726
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http://dx.doi.org/10.1037/a0013726DOI Listing
February 2009