About: Emmanuel Roze

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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	Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue)
alternative label	Flamand-Roze, Emmanuel
Life Event	http://www.idref.fr/075067889/birth
preferred label	Roze, Emmanuel (1971-.... ; neurologue)
name	Emmanuel Roze
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/eng http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000358677121
Given name	Emmanuel
familyName	Roze
has biographical i...tion (Deprecated)	Thèse de doctorat en Neurosciences soutenue en 2007 à l'Université de Paris 6 Neurologue. Professeur des universités, directeur de recherche et praticien hospitalier à Sorbonne Université, GH Pitié Salpêtrière, Paris (en 2023)
gender	male
ORCID iD	0000-0001-9727-3459
ISI Researcher ID	EVS-1253-2022 FUJ-4996-2022
Scopus ID	15726060000
is sameAs of	Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue) Roze, Emmanuel (1971-.... ; neurologue)
is Thesis advisor of	http://www.sudoc.fr/197599133/id http://www.sudoc.fr/121814289/id http://www.sudoc.fr/19386696X/id http://www.sudoc.fr/25911619X/id http://www.sudoc.fr/268815763/id http://www.sudoc.fr/272959006/id
is Praeses of	http://www.sudoc.fr/25996784X/id
is Author of	http://www.sudoc.fr/122754786/id Neurologie http://www.sudoc.fr/127911847/id http://www.sudoc.fr/219944067/id http://www.sudoc.fr/075071622/id http://www.sudoc.fr/15551511X/id http://www.sudoc.fr/197173446/id http://www.sudoc.fr/112584462/id Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification COVID-19-related anosmia is associated with viral persistence and inflammation in human olfactory epithelium and brain infection in hamsters Treatable Hyperkinetic Movement Disorders Not to Be Missed http://www.sudoc.fr/247058122/id Rôle de la protéine Mitogen and Stress Activated protein Kinase-1 dans l'altération de la réponse nucléosomale et la mort neuronale dans la maladie de Huntington Head tremor in Parkinson's disease Caractérisation des formes autosomiques récessives de la maladie de Parkinson dans une large cohorte multi-centrique Structural and functional abnormalities within sensori-motor and limbic networks underpin intermittent explosive symptoms in Tourette disorder Multivariate classification provides a neural signature of Tourette disorder https://archive-ouverte.unige.ch/unige:32814#id Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia http://www.sudoc.fr/264403452/id Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein The adolescent and adult form of cobalamin C disease: clinical and molecular spectrum. Abnormal cerebellar processing of the neck proprioceptive information drives dysfunctions in cervical dystonia Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype Targeted versus untargeted omics — the CAFSA story Parkinson's disease polygenic risk score is not associated with impulse control disorders: A longitudinal study http://hub.abes.fr/cairn/periodical/rsi/2018/issue_rsi133/D33B19F5ACDC3606E053120B220A0F4F/w Increased diagnostic yield in complex dystonia through exome sequencing Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect Long-term Outcome in Neurozika: When Biological Diagnosis Matters MRI of neurodegeneration with brain iron accumulation Predominant cortical dysfunction in Guadeloupean parkinsonism The “Neurological Hat Game”: A fun way to learn the neurological semiology The microbiome–nose–brain axis in health and disease Impact of recommendations on the initial therapy of Parkinson's disease: a population-based study in France. Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum De novo mutations in HCN1 cause early infantile epileptic encephalopathy Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression. Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency Quality of life in Parkinson’s disease improved by apomorphine pump: the OPTIPUMP cohort study http://www.sudoc.fr/263286401/id Risk factors for spinal cord lesions in dystonic cerebral palsy and generalised dystonia. Neuromimetic model of saccades for localizing deficits in an atypical eye-movement pathology. Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to ε-sarcoglycan mutations: a pilot study. Explicit Agency in Patients with Cervical Dystonia: Altered Recognition of Temporal Discrepancies between Motor Actions and Their Feedback Head tremor in Parkinson's disease. Haloperidol protects striatal neurons from dysfunction induced by mutated huntingtin in vivo. Oromandibular Dystonia: A Clinical Examination of 2,020 Cases Dystonia and parkinsonism in GM1 type 3 gangliosidosis. Role of the ERK/MSK1 signalling pathway in chromatin remodelling and brain responses to drugs of abuse. https://archive-ouverte.unige.ch/unige:19747#id Restoration of normal motor control in Parkinson's disease during REM sleep Dissociation in reactive and proactive inhibitory control in Myoclonus dystonia Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements Long-term effect of apomorphine infusion in advanced Parkinson’s disease: a real-life study https://hal.archives-ouvertes.fr/hal-03361375#id Long-term outcome in neuroZika 29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance Invalidation of Parkinson's disease diagnosis after years of follow-up based on clinical, radiological and neurophysiological examination Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. Suggestive association between OPRM1 and impulse control disorders in Parkinson's disease PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia https://hal.archives-ouvertes.fr/hal-02945241#id

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