Can we use peripheral tissue biopsies to diagnose Parkinson's disease? A review of the literature
Schneider, S. A., Boettner, M., Alexoudi, A., Zorenkov, D., Deuschl, G., Wedel, T.
Published in European journal of neurology (01.02.2016)
Published in European journal of neurology (01.02.2016)
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Journal Article
Neuroimaging Features of Neurodegeneration with Brain Iron Accumulation
KRUER, M. C, BODDAERT, N, SCHNEIDER, S. A, HOULDEN, H, BHATIA, K. P, GREGORY, A, ANDERSON, J. C, ROONEY, W. D, HOGARTH, P, HAYFLICK, S. J
Published in American journal of neuroradiology : AJNR (01.03.2012)
Published in American journal of neuroradiology : AJNR (01.03.2012)
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Journal Article
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine
Gardiner, Alice R, Bhatia, Kailash P, Stamelou, Maria, Dale, Russell C, Kurian, Manju A, Schneider, Susanne A, Wali, G M, Counihan, Tim, Schapira, Anthony H, Spacey, Sian D, Valente, Enza-Maria, Silveira-Moriyama, Laura, Teive, Hélio A G, Raskin, Salmo, Sander, Josemir W, Lees, Andrew, Warner, Tom, Kullmann, Dimitri M, Wood, Nicholas W, Hanna, Michael, Houlden, Henry
Published in Neurology (20.11.2012)
Published in Neurology (20.11.2012)
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Journal Article
THAP1 mutations (DYT6) are an additional cause of early-onset dystonia
Houlden, H, Schneider, S A, Paudel, R, Melchers, A, Schwingenschuh, P, Edwards, M, Hardy, J, Bhatia, K P
Published in Neurology (09.03.2010)
Published in Neurology (09.03.2010)
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Journal Article
Abnormal Motor Cortex Excitability in Preclinical and Very Early Huntington's Disease
Schippling, Sven, Schneider, Susanne A, Bhatia, Khailash P, Münchau, Alexander, Rothwell, John C, Tabrizi, Sarah J, Orth, Michael
Published in Biological psychiatry (1969) (01.06.2009)
Published in Biological psychiatry (1969) (01.06.2009)
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Journal Article
Severe tongue protrusion dystonia: clinical syndromes and possible treatment
Schneider, S A, Aggarwal, A, Bhatt, M, Dupont, E, Tisch, S, Limousin, P, Lee, P, Quinn, N, Bhatia, K P
Published in Neurology (26.09.2006)
Published in Neurology (26.09.2006)
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Journal Article
Genotype–phenotype interactions in primary dystonias revealed by differential changes in brain structure
Draganski, B., Schneider, S.A., Fiorio, M., Klöppel, S., Gambarin, M., Tinazzi, M., Ashburner, J., Bhatia, K.P., Frackowiak, R.S.J.
Published in NeuroImage (Orlando, Fla.) (01.10.2009)
Published in NeuroImage (Orlando, Fla.) (01.10.2009)
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Journal Article
Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study
Martino, D., Gajos, A., Gallo, V., Cif, L., Coubes, P., Tinazzi, M., Schneider, S. A., Fiorio, M., Zorzi, G., Nardocci, N., Ben-Shlomo, Y., Edwards, M. J., Bhatia, K. P.
Published in Journal of neurology (01.04.2013)
Published in Journal of neurology (01.04.2013)
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Journal Article
Modulatory effects of 5Hz rTMS over the primary somatosensory cortex in focal dystonia-An fMRI-TMS study
Schneider, Susanne A., Pleger, Burkhard, Draganski, Bogdan, Cordivari, Carla, Rothwell, John C., Bhatia, Kailash P., Dolan, Ray J.
Published in Movement disorders (15.01.2010)
Published in Movement disorders (15.01.2010)
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Journal Article
Idiopathic NBIA - clinical spectrum and transcranial sonography findings
Brüggemann, N., Wuerfel, J., Petersen, D., Klein, C., Hagenah, J., Schneider, S. A.
Published in European journal of neurology (01.06.2011)
Published in European journal of neurology (01.06.2011)
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Journal Article
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
Alazami, AM, Schneider, SA, Bonneau, D, Pasquier, L, Carecchio, M, Kojovic, M, Steindl, K, De Kerdanet, M, Nezarati, MM, Bhatia, KP, Degos, B, Goh, E, Alkuraya, FS
Published in Clinical genetics (01.12.2010)
Published in Clinical genetics (01.12.2010)
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Journal Article
A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
Steindl, K, Alazami, AM, Bhatia, KP, Wuerfel, JT, Petersen, D, Cartolari, R, Neri, G, Klein, C, Mongiardo, B, Alkuraya, FS, Schneider, SA
Published in Clinical genetics (01.12.2010)
Published in Clinical genetics (01.12.2010)
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Journal Article
Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family
Schneider, S A, van de Warrenburg, B P C, Hughes, T D, Davis, M, Sweeney, M, Wood, N, Quinn, N P, Bhatia, K P
Published in Neurology (14.11.2006)
Published in Neurology (14.11.2006)
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Journal Article
Genotypeaphenotype interactions in primary dystonias revealed by differential changes in brain structure
Draganski, B, Schneider, SA, Fiorio, M, Kloppel, S, Gambarin, M, Tinazzi, M, Ashburner, J, Bhatia, K P, Frackowiak, RSJ
Published in NeuroImage (Orlando, Fla.) (01.10.2009)
Published in NeuroImage (Orlando, Fla.) (01.10.2009)
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Journal Article
Familial dopa-responsive cervical dystonia
Schneider, S A, Mohire, M D, Trender-Gerhard, I, Asmus, F, Sweeney, M, Davis, M, Gasser, T, Wood, N W, Bhatia, K P
Published in Neurology (28.02.2006)
Published in Neurology (28.02.2006)
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Journal Article
Time dependent reduction of striatal hypertrophy in Parkin mutation carriers. A longitudinal VBM study
Reetz, K, Hagenah, J, Gaser, C, Schneider, SA, Pramstaller, PP, Siebner, HR, Klein, C, Binkofski, F
Published in NeuroImage (Orlando, Fla.) (01.07.2009)
Published in NeuroImage (Orlando, Fla.) (01.07.2009)
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Journal Article