Tranchant, Christine, 1958-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Christine Tranchant researcher
Tranchant, Christine
VIAF ID: 197798150 (Personal)
Permalink: http://viaf.org/viaf/197798150
Preferred Forms
4xx's: Alternate Name Forms (1)
5xx's: Related Names (2)
- 511 2 _
‡a
Institut de génétique et de biologie moléculaire et cellulaire (Strasbourg)
- 511 2 _
‡a
Université de Strasbourg (2009-....)
Works
| Title | Sources |
|---|---|
| Apport de l'IRM multimodale pour le diagnostic différentiel des syndromes parkinsoniens |
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| Association of Occupational Activities and Exposure to Metals with Two Neurodegenerative Diseases Using the Système National des Données de Santé. |
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| Ataksje móżdżkowe dziedziczone w sposób autosomalny recesywny |
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| Autosomal recessive cerebellar ataxias |
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| Classification phénotypique du tremblement essentiel : étude prospective unicentrique de 57 cas |
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| La crampe des écrivains : étude rétrospective de 42 patients et apport de la tomoscintigraphie par émission monophotonique |
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| Description of the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients. |
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| Le diagnostic génétique des dystrophies musculaires des ceintures : à propos d'une série strasbourgeoise de 79 patients |
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| Effects of drugs affecting noradrenergic neurotransmission in rats with spontaneous petit mal-like seizures |
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| Effects of high-intensity training combined with resistance training on physical capacities and quality of life in multiple sclerosis patients. |
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| Effets de la noradrénaline, de la dopamine et des antidépresseurs sur un modèle d'épilepsie généralisée non convulsivante chez le rat wistar |
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| Effets de l'entraînement à haute intensité associé au renforcement musculaire sur les capacités physiques et la qualité de vie chez les patients atteints de sclérose en plaques |
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| Évaluation de l’efficacité et de la tolérance du traitement par cenobamate : Une étude rétrospective de 81 patients en vie réelle : Thèse présentée pour le diplôme d'État de docteur en médecine. Diplôme d'État D.E.S. de neurologie |
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| Exome sequencing reveals SPG11 mutations causing juvenile ALS |
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| [Foreword] |
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| Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease |
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| Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci. |
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| [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?] |
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| Heterogeneity and frequency of movement disorders in juvenile and adult-onset Niemann-Pick C disease |
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| High insulinlike growth factor I is associated with cognitive decline in Huntington disease. |
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| Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): a potential susceptibility factor for adult-onset lower motor neuron disease |
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| Identification de biomarqueurs et modélisation de la maladie en utilisant des approches multimodales de neuroimagerie dans les maladies polyglutamine. |
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| Impact de la personnalité sur la qualité de vie dans la maladie de Parkinson au stade des fluctuations motrices |
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| Inaugural audiovisual impairment disclosing specific neurological disorders |
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| Intérêt de l'index de synthèse intrathécale anti-Borrelia dans le diagnostic de neuroborréliose |
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| [Internet and amyotrophic lateral sclerosis treatment: what is wrong?] |
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| L'atrophie multisystématisée de type cérébelleux : étude rétrospective et revue de la littérature |
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| Long-term outcomes of CLIPPERS (chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids) in a consecutive series of 12 patients. |
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| Low cancer prevalence in polyglutamine expansion diseases |
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| MALADIE DE PARKINSON ET MITOCHONDRIES |
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| MALADIE DU MOTONEURONE FAMILIALE, DEGENERESCENCE PALLIDO-LUYSO-NIGRIQUE, ET INCLUSIONS RESSEMBLANT A DES CORPS DE LEWY |
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| Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias |
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| Movement disorders in mitochondrial diseases. |
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| MR findings in mannosidosis |
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| Muscle Nogo-A expression is a prognostic marker in lower motor neuron syndromes |
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| Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration. |
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| Myasthénie et thymectomie : à propos de 55 cas |
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| Myoclonus-dystonia: Clinical and electrophysiologic pattern related to SGCE mutations |
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| Neurobehavioral changes following bilateral infarct in the caudate nuclei: a case report with pathological analysis |
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| Neuroendocrine disturbances in Huntington's disease |
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| Neurologie |
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| Neuromuscular symptoms and elevated creatine kinase after statin withdrawal. |
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| Neuropathie trigéminale motrice pure révélée par un syndrome algo-dysfonctionnel de l’appareil manducateur chez une patiente co-infectée par le VIH et le VHC |
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| The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias |
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| New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study. |
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| Next generation sequencing for molecular diagnosis of neuromuscular diseases. |
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| Les nouvelles voies thérapeutiques pharmacologiques non-dopaminergiques dans le traitement de la maladie de Parkinson |
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| Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease |
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| Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects |
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| Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification |
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| Pathologies du mouvement |
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| Pathophysiogical and therapeutic progress in Friedreich ataxia |
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| Peripheral neuropathies associated with hereditary cerebellar ataxias |
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| Personality Impact on Quality of Life in Parkinson's Disease at motor fluctuations stage. |
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| Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression |
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| Platelet functions, alpha 2-adrenergic receptors and cytoplasmic free calcium are normal in the myotonic dystrophy of Steinert. |
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| Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasia |
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| Presence of anti-CSL antibodies in the cerebrospinal fluid of patients: a sensitive and specific test in the diagnosis of multiple sclerosis |
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| Primary brain calcification: an international study reporting novel variants and associated phenotypes |
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| [Prion encephalopathies] |
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| Quality of life in Parkinson's disease improved by apomorphine pump: the OPTIPUMP cohort study |
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| Relevance of corpus callosum splenium versus middle cerebellar peduncle hyperintensity for FXTAS diagnosis in clinical practice |
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| Report from the 58th annual meeting of the American Academy of Neurology |
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| Risk factors of Parkinson's disease in women from the E3N cohort : role of physical activity, adiposity, and diabetes |
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| SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia |
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| Seronegative myasthenia gravis and familial Hodgkin's disease |
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| [Small cell lung cancer and anti-Hu syndrome] |
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| SPG15: a cause of juvenile atypical levodopa responsive parkinsonism |
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| Stimulating effects of prednisolone on acetylcholine receptor expression and myogenesis in primary culture of newborn rat muscle cells |
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| Stimulation à haute fréquence des noyaux sous-thalamiques dans la maladie de Parkinson : expérience strasbourgeoise |
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| [Subthalamic stimulation in a patient with multiple system atrophy: a clinicopathological report] |
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| Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation |
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| Suggestive association between OPRM1 and impulse control disorders in Parkinson's disease. |
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| Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases |
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| Treatment of Myasthenia Gravis Exacerbation With Intravenous Immunoglobulin |
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| Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's disease |
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| Uptake of Abeta 1-40- and Abeta 1-42-coated yeast by microglial cells: a role for LRP. |
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| Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H. |
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| The wide POLG-related spectrum: An integrated view |
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| মুখবন্ধ |
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