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Krüger, Lisa [Author]; Klein, Julian [Author]; Tobian, Frank [Author]; Gaeddert, Mary [Author]; Lainati, Federica [Author]; Klemm, Sarah [Author]; Schnitzler, Paul [Author]; Bartenschlager, Ralf [Author]; Cerikan, Berati [Author]; Neufeldt, Christopher [Author]; Nikolai, Olga [Author]; Lindner, Andreas K. [Author]; Mockenhaupt, Frank Peter [Author]; Seybold, Joachim [Author]; Jones, Terry C. [Author]; Corman, Victor M. [Author]; Pollock, Nira R. [Author]; Knorr, Britta [Author]; Welker, Andreas [Author]; De Vos, Margaretha [Author]; Sacks, Jilian A. [Author]; Denkinger, Claudia M. [Author]; Assaad, K. [Author]; Fuhs, A. [Author]; [...]

Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx : an antigen-detecting point-of-care device for SARS-CoV-2

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https://link.springer.com/10.1007/s15010-021-01681-y

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2022

Published in: Infection ; 50(2022), 2, Seite 395-406
Dürr, Valerie; Wohlfart, Sabrina; Eisenzapf, Tom; Mier, Walter; Fricker, Gert; Uhl, Philipp

Oral Delivery of mRNA by Liposomes Functionalized with Cell-Penetrating Peptides

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MDPI AG, 2023

Published in: Applied Nano
Justo, Damian; Charles, Perrine; Daunizeau, Jean; Delmaire, Christine; Gargiulo, Marcela; Hahn-Barma, Valérie; Naccache, Lionel; Durr, Alexandra

Is non-recognition of choreic movements in Huntington disease always pathological?

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Elsevier BV, 2013

Published in: Neuropsychologia
Bodenmann, Sereina; Rusterholz, Thomas; Dürr, Roland; Stoll, Claudia; Bachmann, Valérie; Geissler, Eva; Jaggi-Schwarz, Karin; Landolt, Hans-Peter

The Functional Val158Met Polymorphism ofCOMTPredicts Interindividual Differences in Brain α Oscillations in Young Men

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Society for Neuroscience, 2009

Published in: The Journal of Neuroscience
Ribaï, Pascale; Depienne, Christel; Fedirko, Estelle; Jothy, Anne-Catherine; Viveweger, Caterine; Hahn-Barma, Valérie; Brice, Alexis; Durr, Alexandra

Mental deficiency in three families with SPG4 spastic paraplegia

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Springer Science and Business Media LLC, 2008

Published in: European Journal of Human Genetics
Ribaï, Pascale; Nguyen, Karine; Hahn-Barma, Valérie; Gourfinkel-An, Isabelle; Vidailhet, Marie; Legout, Antoine; Dodé, Catherine; Brice, Alexis; Dürr, Alexandra

Psychiatric and Cognitive Difficulties as Indicators of Juvenile Huntington Disease Onset in 29 Patients

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American Medical Association (AMA), 2007

Published in: Archives of Neurology
Colin, Emilie; Régulier, Etienne; Perrin, Valérie; Dürr, Alexandra; Brice, Alexis; Aebischer, Patrick; Déglon, Nicole; Humbert, Sandrine; Saudou, Frédéric

Akt is altered in an animal model of Huntington's disease and in patients

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Wiley, 2005

Published in: European Journal of Neuroscience
Heinzmann, Anna; Sayah, Sabrina; Lejeune, François‐Xavier; Hahn, Valérie; Teichmann, Marc; Monin, Marie‐Lorraine; Marchionni, Enrica; Gérard, Fleur; Charles, Perrine; Pariente, Jérémie; Durr, Alexandra

Huntington's Disease with Small CAG Repeat Expansions

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Wiley, 2023

Published in: Movement Disorders
Berges, Alexandra J.; Callanan, Megan; Zawicki, Valerie; Shi, Richard; Athey, Thomas; Ayyappan, Vinay; Metzger, Schuyler; Farrell, Alanna; Manbachi, Amir; Harvey, Susan; Durr, Nicholas J.

A Novel Intermediate Attachment to Reduce Contamination in Reusable Core Needle Biopsy Devices

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ASME International, 2020

Published in: Journal of Medical Devices
Sayah, Sabrina; Rotgé, Jean-Yves; Francisque, Hélène; Gargiulo, Marcela; Czernecki, Virginie; Justo, Damian; Lahlou-Laforet, Khadija; Hahn, Valérie; Pandolfo, Massimo; Pelissolo, Antoine; Fossati, Philippe; Durr, Alexandra

Personality and Neuropsychological Profiles in Friedreich Ataxia

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Springer Science and Business Media LLC, 2018

Published in: The Cerebellum
Biancalana, Valérie; Toft, Mathias; Le Ber, Isabelle; Tison, François; Scherrer, Elisabeth; Thibodeau, Stephen; Mandel, Jean Louis; Brice, Alexis; Farrer, Matthew J.; Dürr, Alexandra

FMR1 Premutations Associated With Fragile X–Associated Tremor/Ataxia Syndrome in Multiple System Atrophy

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American Medical Association (AMA), 2005

Published in: Archives of Neurology
Stevanin, Giovanni; Hahn, Valérie; Lohmann, Ebba; Bouslam, Naima; Gouttard, Michel; Soumphonphakdy, Caroline; Welter, Marie-Laure; Ollagnon-Roman, Elisabeth; Lemainque, Arnaud; Ruberg, Merle; Brice, Alexis; Durr, Alexandra

Mutation in the Catalytic Domain of Protein Kinase C γ and Extension of the Phenotype Associated With Spinocerebellar Ataxia Type 14

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American Medical Association (AMA), 2004

Published in: Archives of Neurology
Tallaksen, Chantal M. E.; Guichart-Gomez, Elodie; Verpillat, Patrice; Hahn-Barma, Valérie; Ruberg, Merle; Fontaine, Bertrand; Brice, Alexis; Dubois, Bruno; Dürr, Alexandra

Subtle Cognitive Impairment but No Dementia in Patients With Spastin Mutations

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American Medical Association (AMA), 2003

Published in: Archives of Neurology
Lohmann, Ebba; Welter, Marie‐Laure; Fraix, Valérie; Krack, Paul; Lesage, Suzanne; Laine, Sophie; Tanguy, Marie‐Laure; Houeto, Jean‐Luc; Mesnage, Valérie; Pollak, Pierre; Alexandra Durr; Agid, Yves; Brice, Alexis

Are parkin patients particularly suited for deep‐brain stimulation?

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Wiley, 2008

Published in: Movement Disorders
Ando, Kunie; Ferlini, Lorenzo; Suain, Valérie; Yilmaz, Zehra; Mansour, Salwa; Le Ber, Isabelle; Bouchard, Cécile; Leroy, Karelle; Durr, Alexandra; Clot, Fabienne; Sarazin, Marie; Bier, Jean-Christophe; Brion, Jean-Pierre

de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia

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Springer Science and Business Media LLC, 2020

Published in: Acta Neuropathologica Communications
Thion, Morgane Sonia; Tézenas du Montcel, Sophie; Golmard, Jean-Louis; Vacher, Sophie; Barjhoux, Laure; Sornin, Valérie; Cazeneuve, Cécile; Bièche, Ivan; Sinilnikova, Olga; Stoppa-Lyonnet, Dominique; Durr, Alexandra; Humbert, Sandrine

CAG repeat size in Huntingtin alleles is associated with cancer prognosis

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Springer Science and Business Media LLC, 2016

Published in: European Journal of Human Genetics
Mariani, Louise-Laure; Tesson, Christelle; Charles, Perrine; Cazeneuve, Cécile; Hahn, Valérie; Youssov, Katia; Freeman, Leorah; Grabli, David; Roze, Emmanuel; Noël, Sandrine; Peuvion, Jean-Noel; Bachoud-Levi, Anne-Catherine; Brice, Alexis; Stevanin, Giovanni; Durr, Alexandra

Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach

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American Medical Association (AMA), 2016

Published in: JAMA Neurology
Klebe, Stephan; Durr, Alexandra; Rentschler, Alexander; Hahn‐Barma, Valerie; Abele, Michael; Bouslam, Naima; Schöls, Ludger; Jedynak, Pierre; Forlani, Sylvie; Denis, Elodie; Dussert, Christel; Agid, Yves; Bauer, Peter; Globas, Christoph; Wüllner, Ullrich; Brice, Alexis; Riess, Olaf; Stevanin, Giovanni

New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

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Wiley, 2005

Published in: Annals of Neurology
Seilhean, Danielle; Takahashi, Junko; El Hachimi, Khalid Hamid; Fujigasaki, Hiroto; Lebre, Anne-Sophie; Biancalana, Valérie; Dürr, Alexandra; Salachas, François; Hogenhuis, Jean; de Thé, Hugues; Hauw, Jean-Jacques; Meininger, Vincent; Brice, Alexis; Duyckaerts, Charles

Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions

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Springer Science and Business Media LLC, 2004

Published in: Acta Neuropathologica
Periquet, Magali; Latouche, Morwena; Lohmann, Ebba; Rawal, Nina; De Michele, Giuseppe; Ricard, Sylvain; Teive, Hélio; Fraix, Valérie; Vidailhet, Marie; Nicholl, David; Barone, Paolo; Wood, Nick W.; Raskin, Salmo; Deleuze, Jean‐François; Agid, Yves; Dürr, Alexandra; Brice, Alexis

Parkin mutations are frequent in patients with isolated early‐onset parkinsonism

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Oxford University Press (OUP), 2003

Published in: Brain

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