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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Alexandra Durr »
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Alexandra Afenjar < Alexandra Durr < Alexandra Dürr  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
000015 (2015) Isaac M. Adanyeguh [France] ; Pierre-Gilles Henry ; Tra M. Nguyen ; Daisy Rinaldi ; Celine Jauffret ; Romain Valabregue ; Uzay E. Emir ; Dinesh K. Deelchand ; Alexis Brice ; Lynn E. Eberly ; Gülin Öz ; Alexandra Durr ; Fanny MochelIn vivo neurometabolic profiling in patients with spinocerebellar ataxia types 1, 2, 3, and 7.
000132 (2012) Fanny Mochel [France] ; Tra-My N'Guyen [France] ; Dinesh Deelchand [États-Unis] ; Daisy Rinaldi [France] ; Romain Valabregue [France] ; Claire Wary [France] ; Pierre G. Carlier [France] ; Alexandra Durr [France] ; Pierre-Gilles Henry [États-Unis]Abnormal Response to Cortical Activation in Early Stages of Huntington Disease
000155 (2011) Ellis Chan [France] ; Perrine Charles [France] ; Pascale Ribai [France] ; Cyril Goizet [France] ; Cecilia Marelli [France] ; Carlo-Maria Vincitorio [France] ; Alice Le Bayon [France] ; Lucie Guyant-Maréchal [France] ; Nadia Vandenberghe [France] ; Mathieu Anheim [France] ; David Devos [France] ; Leorah Freeman [France] ; Isabelle Le Ber [France] ; Karine N'Guyen [France] ; Maya Tchikviladzé [France] ; Pierre Labauge [France] ; Didier Hannequin [France] ; Alexis Brice [France] ; Alexandra Durr [France] ; Sophie Tezenas Du Montcel [France]Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias
000186 (2011) Tanja Schmitz-Hübsch [Allemagne] ; Mathieu Coudert [France] ; Sophie Tezenas Du Montcel [France] ; Paola Giunti [Royaume-Uni] ; Robyn Labrum [Royaume-Uni] ; Alexandra Durr [France] ; Pascale Ribai [France] ; Perrine Charles [France] ; Christoph Linnemann [Allemagne] ; Ludger Schöls [Allemagne] ; Maryla Rakowicz [Pologne] ; Rafal Rola [Pologne] ; Elszbieta Zdzienicka [Pologne] ; Roberto Fancellu [Italie] ; Caterina Mariotti [Italie] ; Lazlo Baliko [Hongrie] ; Bela Melegh [Hongrie] ; Alessandro Filla [Italie] ; Elena Salvatore [Italie] ; Bart P. C. Van De Warrenburg [Pays-Bas] ; Sandra Szymanski [Allemagne] ; Jon Infante [Espagne] ; Dagmar Timmann [Allemagne] ; Sylvia Boesch [Autriche] ; Chantal Depondt [Belgique] ; Jun-Suk Kang [Allemagne] ; Jörg B. Schulz [Allemagne] ; Thomas Klopstock [Allemagne] ; Nicole Lossnitzer [Allemagne] ; Bernd Löwe ; Caroline Frick ; Daniela Rottl Nder ; Thomas E. Schlaepfer ; Thomas Klockgether [Allemagne]Depression Comorbidity in Spinocerebellar Ataxia
000251 (2009) Diane Doummar [France] ; Fabienne Clot [France] ; Marie Vidailhet [France] ; Alexandra Afenjar [France] ; Alexandra Durr [France] ; Alexis Brice [France] ; Cyril Mignot [France] ; Agnès Guet [France] ; Thierry Billette De Villemeur [France] ; Diana Rodriguez [France]Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
000291 (2008) Christoph Globas [Allemagne] ; Sophie Tezenas Du Montcel [France] ; Laslo Baliko [Hongrie] ; Syliva Boesch [Autriche] ; Chantal Depondt [Belgique] ; Stefano Didonato [Italie] ; Alexandra Durr [France] ; Alessandro Filla [Italie] ; Thomas Klockgether [Allemagne] ; Caterina Mariotti [Italie] ; Bela Melegh [Hongrie] ; Maryla Rakowicz [Pologne] ; Pascale Ribai [France] ; Rafal Rola [Pologne] ; Tanja Schmitz-Hubsch [Allemagne] ; Sandra Szymanski [Allemagne] ; Dagmar Timmann [Allemagne] ; Bart P. Van De Warrenburg [Pays-Bas] ; Peter Bauer [Allemagne] ; Ludger Schols [Allemagne]Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6
000303 (2008) Ebba Lohmann [France] ; Marie-Laure Welter [France] ; Valérie Fraix [France] ; Paul Krack [France] ; Suzanne Lesage [France] ; Sophie Laine [France] ; Marie-Laure Tanguy [France] ; Jean-Luc Houeto [France] ; Valérie Mesnage [France] ; Pierre Pollak [France] ; Alexandra Durr [France] ; Yves Agid [France] ; Alexis Brice [France]Are parkin patients particularly suited for deep‐brain stimulation?
000313 (2007) Claudia Cagnoli [Italie] ; Alessandro Brussino [Italie] ; Eleonora Di Gregorio [Italie] ; Alfredo Brusco [Italie] ; Giovanni Stevanin [France] ; Alexandra Durr [France] ; Alexis Brice [France]The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients
000345 (2007) Lorraine N. Clark [États-Unis] ; Eneli Haamer [Estonie] ; Helen Mejia-Santana [États-Unis] ; Juliette Harris [États-Unis] ; Suzanne Lesage [France] ; Alexandra Durr [France] ; Sabine Janin Bs [France] ; Katja Hedrich [Allemagne] ; Elan D. Louis [États-Unis] ; Lucien J. Cote [États-Unis] ; Howard Andrews [États-Unis] ; Stanley Fahn [États-Unis] ; Cheryl Waters [États-Unis] ; Blair Ford [États-Unis] ; Steven Frucht [États-Unis] ; William Scott [États-Unis] ; Christine Klein [Allemagne] ; Alexis Brice [France] ; Hanno Roomere [Estonie] ; Ruth Ottman [États-Unis] ; Karen Marder [États-Unis]Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

List of associated KwdEn.i

Nombre de
documents		Descripteur
7Humans
6Female
6Nervous system diseases
5Male
4Adult
4DNA Mutational Analysis
4Middle Aged
3Aged
3Spinocerebellar ataxia
2Adolescent
2Follow-Up Studies
2Genetics, Population
2Linear Models
2Mutation
2Parkin
2Parkinson disease
2Spinocerebellar Ataxias (diagnosis)
2Spinocerebellar Ataxias (genetics)
2Ubiquitin-Protein Ligases (genetics)
2Young Adult
2spinocerebellar ataxia
1Adenosine Triphosphate (metabolism)
1Age of onset
1Aged, 80 and over
1Analysis of Variance
1Antiparkinson Agents (adverse effects)
1Antiparkinson Agents (therapeutic use)
1CAG repeat expansion
1Calcium Channels (genetics)
1Case-Control Studies
1Cerebellar ataxia
1Cerebellum
1Cerebellum (pathology)
1Cerebellum (physiopathology)
1Cerebral Cortex (metabolism)
1Cerebral Cortex (physiopathology)
1Cerebral Cortex (radionuclide imaging)
1Chromosome Aberrations
1Chromosome Mapping
1Chromosomes, Human, Pair 16
1Deep Brain Stimulation
1Deep brain stimulation
1Depression
1Disability Evaluation
1Disease Progression
1Dyskinesia, Drug-Induced
1Early stage
1Energy metabolism
1Epidemiology
1Europe
1European Continental Ancestry Group (genetics)
1Evolution
1Family Health
1Gait Disorders, Neurologic (complications)
1Gait disorder
1Gene Expression Profiling (methods)
1Genes, Dominant
1Genetic Testing
1Genotype
1Guanine Nucleotide Exchange Factors (genetics)
1Heterozygote
1Homovanillic Acid (metabolism)
1Homozygote
1Human
1Huntington Disease (pathology)
1Huntington Disease (radionuclide imaging)
1Huntington disease
1Hydroxyindoleacetic Acid (metabolism)
1Infant
1Levodopa (adverse effects)
1Levodopa (therapeutic use)
1Magnetic Resonance Spectroscopy
1Muscle Hypotonia (genetics)
1Muscle Hypotonia (metabolism)
1Muscle Hypotonia (physiopathology)
1Mutation (genetics)
1Nerve Tissue Proteins (genetics)
1Neurology
1Nuclear Proteins (genetics)
1Oligonucleotide Array Sequence Analysis (methods)
1Parkin, Parkinson's disease
1Parkinson Disease (epidemiology)
1Parkinson Disease (genetics)
1Parkinsonian Disorders (genetics)
1Parkinsonian Disorders (therapy)
1Parkinsonism
1Phosphates (metabolism)
1Phosphocreatine (metabolism)
1Phosphorus Isotopes (metabolism)
1Prevalence
1Prognosis
1Repressor Proteins (genetics)
1Reproducibility of Results
1Retrospective Studies
1Sample Size
1Severity of Illness Index
1Sign
1Spectrin (genetics)
1Spectrometry
1Spinocerebellar Ataxias (classification)

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