Výsledky vyhledávání - Katrin Bürk
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Cognitive deficits in spinocerebellar ataxia 2 Autor Katrin Bürk
Vydáno 1999Artigo -
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Friedreich Ataxia: current status and future prospects Autor Katrin Bürk
Vydáno 2017Revisão -
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Autosomal dominant cerebellar ataxia type I Clinical features and MRI in families with SCA1, SCA2 and SCA3 Autor Katrin Bürk, Michael Abele, M. Fetter, J. Dichgans, Martin Skalej, Franco Laccone, Olivier Didierjean, Alexis Brice, Thomas Klockgether
Vydáno 1996Artigo -
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KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients Autor Karla P. Figueroa, Natali A. Minassian, Giovanni Stévanin, Michael D. Waters, Vartan Garibyan, Sylvie Forlani, Adam Strzelczyk, Katrin Bürk, Alexis Brice, Alexandra Dürr, Diane M. Papazian, Stefan M. Pulst
Vydáno 2009Artigo -
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The natural history of degenerative ataxia: a retrospective study in 466 patients Autor Thomas Klockgether, Rainer Lüdtke, B. Krämer, Michael Abele, Katrin Bürk, Lüdger Schöls, Olaf Rieß, Franco Laccone, Sylvia Boesch, Íscia Lopes‐Cendes, Alexis Brice, Rivka Inzelberg, Nelly Zilber, J. Dichgans
Vydáno 1998Artigo -
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Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico‐pathological insights Autor Udo Rüb, Katrin Bürk, Dagmar Timmann, Wilfred F.A. den Dunnen, Kay Seidel, Karima Farrag, E. R. Brunt, Helmut Heinsen, Rupert Egensperger, A. Bornemann, Stephan W. Schwarzacher, Horst‐Werner Korf, Lüdger Schöls, J. Böhl, Thomas Deller
Vydáno 2012Artigo -
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Onset features and time to diagnosis in Friedreich’s Ataxia Autor Elisabetta Indelicato, Wolfgang Nachbauer, Andreas Eigentler, Matthias Amprosi, Raffaella Matteucci Gothe, Paola Giunti, Caterina Mariotti, Javier Arpa, Alexandra Dürr, Thomas Klopstock, Lüdger Schöls, Ilaria Giordano, Katrin Bürk, Massimo Pandolfo, Claire Didszdun, Jörg B. Schulz, Sylvia Boesch
Vydáno 2020Artigo -
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Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families Autor Géraldine Cancel‐Tassin, Alexandra Dürr, Olivier Didierjean, G. Imbert, Katrin Bürk, Agnès Lézin, Samir Belal, Ali Benomar, M. Abada-Bendib, Christophe Vial, J. Guimarães, Hervé Chneiweiss, Giovanni Stévanin, Gaël Yvert, N. Abbas, Frédéric Saudou, Anne Sophie Lebre, M. Yahyaoui, Fayçal Hentati, J C Vernant, Thomas Klockgether, Jean‐Louis Mandel, Y. Agid, Alexis Brice
Vydáno 1997Artigo -
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Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study Autor Heike Jacobi, Sophie Tézenas du Montcel, Sandro Romanzetti, Florian Harmuth, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Grzegorz Makowicz, Alexandra Dürr, Marie-Lorraine Monin, Alessandro Filla, Alessandro Roca, Lüdger Schöls, Holger Hengel, Jon Infante, Jun-Suk Kang, Dagmar Timmann, Carlo Casali, Marcella Masciullo, László Balikó, Béla Melegh, Wolfgang Nachbauer, Katrin Bürk-Gergs, Jörg B. Schulz, Olaf Rieß, Kathrin Reetz, Thomas Klockgether
Vydáno 2020Artigo -
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The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group Autor Christoph Kamm, D G Healy, N Quinn, Ullrich Wüllner, J. Carsten Möller, Lüdger Schöls, Felix Geser, Katrin Bürk, Anders D. Børglum, Maria Teresa Pellecchia, Eduardo Tolosa, Francesca Del Sorbo, Christer Nilsson, Oliver Bandmann, Manu Sharma, Petra Mayer, Maria Gasteiger, A. Haworth, Tetsutaro Ozawa, Andrew J. Lees, Joan K. Short, Paola Giunti, Elke Holinski‐Feder, Thomas Illig, H.‐Erich Wichmann, Gregor K. Wenning, Nicholas Wood, Thomas Gasser
Vydáno 2005Artigo -
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Nonataxia symptoms in Friedreich Ataxia Autor Kathrin Reetz, Imis Dogan, Christian Hohenfeld, Claire Didszun, Paola Giunti, Caterina Mariotti, Alexandra Dürr, Sylvia Boesch, Thomas Klopstock, Francisco Javier Rodríguez de Rivera Garrido, Lüdger Schöls, Ilaria Giordano, Katrin Bürk, Massimo Pandolfo, Jörg B. Schulz, Wolfgang Nachbauer, Andreas Eigentler, Chantal Depondt, Sandra Benaich, Perrine Charles, Claire Ewenczyk, Marie‐Lorraine Monin, Kathrin Fedosov, Manuel Dafotakis, Thomas Klockgether, Dagmar Timmann, Ivan Karin, Christiane Neuhofer, Claudia Stendel, Jennifer Müller vom Hagen, Julia Wolf, Lidia Sarro, Lorenzo Nanetti, Anna Castaldo, Javier Arpa, Irene Sanz‐Gallego, Michael Parkinson, Mary G. Sweeney
Vydáno 2018Artigo -
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Progression characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study Autor Kathrin Reetz, Imis Dogan, R.-D Hilgers, Paola Giunti, Caterina Mariotti, Alexandra Dürr, Sylvia Boesch, Thomas Klopstock, Francisco Javier Rodríguez de Rivera Garrido, Lüdger Schöls, Thomas Klockgether, Katrin Bürk, Myriam Rai, Massimo Pandolfo, Jörg B. Schulz, Wolfgang Nachbauer, Andreas Eigentler, Chantal Depondt, Sandra Benaich, Perrine Charles, Claire Ewenczyk, Marie‐Lorraine Monin, Manuel Dafotakis, Kathrin Fedosov, Claire Didszun, Ummehan Ermis, Ilaria Giordano, Dagmar Timmann, Ivan Karin, Christiane Neuhofer, Claudia Stendel, Jennifer Müller vom Hagen, Julia Wolf, Marta Panzeri, Lorenzo Nanetti, Anna Castaldo, Javier Arpa, Irene Sanz‐Gallego, Michael Parkinson, Mary G. Sweeney
Vydáno 2016Artigo -
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A clinical diagnostic algorithm for early onset cerebellar ataxia Autor Rick Brandsma, Corien C. Verschuuren‐Bemelmans, Dina Amrom, Nina Barišić, Peter Baxter, Enrico Bertini, Lubov Blumkin, Vesna Branković-Srećković, Oebele F. Brouwer, Katrin Bürk, Coriene E. Catsman‐Berrevoets, Dana Craiu, I.F.M. de Coo, J. Gburek, C Kennedy, Tom J. de Koning, H.P.H. Kremer, Ram Kumar, Alfons Macaya, Alessia Micalizzi, Marisol Mirabelli-Badenier, Andrea H. Németh, Sara Nuovo, Bwee Tien Poll‐The, Tally Lerman‐Sagie, Maja Steinlin, Matthis Synofzik, Marina A.J. Tijssen, Gessica Vasco, Michèl A.A.P. Willemsen, Ginevra Zanni, Enza Maria Valente, Eugen Boltshauser, Deborah A. Sival
Vydáno 2019Revisão
Vyhledávací nástroje:
Související témata
Ataxia
Medicine
Internal medicine
Psychiatry
Pediatrics
Spinocerebellar ataxia
Neuroscience
Psychology
Biology
Disease
Pathology
Cerebellar ataxia
Gene
Genetics
Atrophy
Degenerative disease
Frataxin
Iron-binding proteins
Physical therapy
Age of onset
Audiology
Central nervous system disease
Clinical trial
Cohort
Cohort study
Etiology
Gastroenterology
Machado–Joseph disease
Natural history
Natural history study