About: Vincent des Portes

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Portes, Vincent des (19..-....) Portes, Vincent des (19..-....)
alternative label	De la Fosse, Vincent des portes Des Portes de la Fosse, Vincent
Life Event	http://www.idref.fr/077492307/birth
preferred label	Portes, Vincent des (19..-....)
name	Vincent des Portes
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
Given name	Vincent des
familyName	Portes
has biographical i...tion (Deprecated)	Neuro-pédiatre. Centre hospitalier Lyon Sud Directeur d'une thèse en Neuropsychologie soutenue à Lyon 2 (en 2010)
gender	male
is sameAs of	Portes, Vincent des (19..-....) Portes, Vincent des (19..-....) Portes, Vincent des (19..-....) Portes, Vincent des (19..-....)
is Thesis advisor of	http://www.sudoc.fr/172640229/id http://www.sudoc.fr/189469498/id http://www.sudoc.fr/160778360/id http://www.sudoc.fr/176735135/id http://www.sudoc.fr/069474192/id http://www.sudoc.fr/133779912/id http://www.sudoc.fr/149289499/id http://www.sudoc.fr/157436942/id http://www.sudoc.fr/225048493/id http://www.sudoc.fr/113760388/id Étude des réseaux neuronaux et des mécanismes cognitifs impliqués dans les déficiences intellectuelles liées au chromosome X
is Contributor of	Neuropsychological assessment of inhibition disorder in ADHD:From theory to pratice Episodic dysmnesia: about a first case http://hub.abes.fr/cairn/periodical/lae/2014/issue_lae142/D33DAC211B954C2EE053120B220A7CD3/w http://hub.abes.fr/cairn/periodical/rne/2011/issue_rne033/D33A400B9D812F5FE053120B220A4740/w
is Praeses of	http://www.sudoc.fr/257446575/id http://www.sudoc.fr/268405891/id http://www.sudoc.fr/279233213/id
is Author of	http://www.sudoc.fr/053772989/id MECP2 is highly mutated in X-linked mental retardation The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males. Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal data. Type I hyperprolinemia: genotype/phenotype correlations Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndrome. The three stages of epilepsy in patients with CDKL5 mutations. Implicit procedural learning in fragile X and Down syndrome. Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF1 + ADHD) and ADHD Per Se Simultaneous action execution and observation optimise grasping actions. Psychomotor development in infants and children - Part 1 / Normal and pathological aspects ( sleep, diet, sphincter controls, psychomotricity) GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Localisation de gènes impliqués dans les retards mentaux liés au chromosome X et identification du gène doublecortine, impliqué dans les hétérotopies sous corticales et les lissencéphalies liées au chromosome X https://archive-ouverte.unige.ch/unige:42359#id The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia. Stratégie d'exploration d'une déficience intellectuelle inexpliquée POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome. High frequency of creatine deficiency syndromes in patients with unexplained mental retardation. Approche développementale des fonctions exécutives : du bébé à l’adolescence Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping? http://www.sudoc.fr/259550582/id Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056 Motor resonance facilitates movement execution: an ERP and kinematic study LIS1-Related Isolated Lissencephaly MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression. Ring 14 chromosome presenting as early-onset isolated partial epilepsy. New insight in ARX-mutated patients' language specific impairment and underlying FOXP1 dysregulation https://serval.unil.ch/notice/serval:BIB_A32BBFA25741#id GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Le TDAH à l’école : de la rééducation aux aménagements pédagogiques https://serval.unil.ch/notice/serval:BIB_08C9E1B19BCA#id http://id.erudit.org/iderudit/1021269ar#id Outcome of isolated agenesis of the corpus callosum: A population-based prospective study [MRI morphometry, an insight into brain function]. Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability https://sonar.ch/global/documents/304836#id https://serval.unil.ch/notice/serval:BIB_2B2D264EDE75#id Prenatal diagnosis of 'isolated' Dandy-Walker malformation: imaging findings and prenatal counselling. Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with SLC 16A2 mutations X-linked mental deficiency. Etude clinique et génétique chez 80 patients atteints de syndrome de Joubert Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia. Neural correlates of non-verbal social interactions: a dual-EEG study. Dispositif d'évaluation des capacités cognitives d'un patient Psychomotor development in infants and children - Part 2 / Normal and pathological aspects (language, intelligence). https://serval.unil.ch/notice/serval:BIB_945CB8727509#id Anti-tumor necrosis factor alpha therapy (adalimumab) in Rasmussen's encephalitis: An open pilot study Deleterious mutations in exon 1 of MECP2 in Rett syndrome. A Novel Analog Reasoning Paradigm: New Insights in Intellectually Disabled Patients Relevance of different cellular models in determining the effects of mutations on SLC16A2/MCT8 thyroid hormone transporter function and genotype-phenotype correlation. Nouvelles perspectives dans l'atteinte spécifique du langage présentée par les patients ARX et la dysrégulation sous-jacente de FOXP1 Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features Creatine and guanidinoacetate reference values in a French population Prenatal diagnosis of cerebellar cortical dysplasia associated with abnormalities of foliation. Evaluation de la prise en charge rééducative des fonctions exécutives chez l’enfant : l’inhibition dans les troubles neurodéveloppementaux Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient. Prenatal Imaging Features and Postnatal Outcome of Short Corpus Callosum: A Series of 42 Cases Chromosome 6p25 deletion syndrome: report of a case with optic disc coloboma and review of published ophthalmic findings. Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification. Nouvel éclairage sur les hypoplasies pontocérébelleuses : apports des nouveaux gènes dans l'arbre décisionnel de diagnostic Atypical hemispheric asymmetries for the processing of phonological features in children with rolandic epilepsy. Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects. Stroke by carotid artery complete occlusion in Kawasaki disease: case report and review of literature.

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