Results 171 to 180 of about 4,884 (187)

De uitkomsten van de hulpverlening van MJD Groningen

2002
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Flikweert, M., Mak, J., Kromontono, E., Melief, W., van der Laan, G.   +4 more
openaire   +1 more source

Brain structural abnormalities in the preclinical stage of Machado–Joseph disease/spinocerebellar ataxia type 3 (MJD/SCA3): evaluation by MRI morphometry, diffusion tensor imaging and neurite orientation dispersion and density imaging

Journal of Neurology, 2021
Jianping Hu, Mengcheng Li
exaly  

Broad Influence of Mutant Ataxin-3 on the Proteome of the Adult Brain, Young Neurons, and Axons Reveals Central Molecular Processes and Biomarkers in SCA3/MJD Using Knock-In Mouse Model

Frontiers in Molecular Neuroscience, 2021
Emmanuel Brouillet, Lukasz Marczak, Kalina Wiatr   +2 more
exaly  

3.061 ANALYSIS OF SERUM MICRORNAS IN SCA3/MJD PATIENTS

Parkinsonism & Related Disorders, 2012
Y.T. Shi, B. Tang, H. Jiang
openaire   +1 more source

Case report: Short-term efficacy and changes in 18F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)

Frontiers in Neurology, 2023
Lou Xin
exaly  

Effectiveness of Levodopa/Carbidopa in Slowing the Progression of MJD/SCA3

Neurology Open Access
Mafalda Raposo, Zsuzsa Sárkány, Joana Damásio, Manuela Lima, Sandra Macedo-Ribeiro, Pedro Miguel Martins, Tetsuo Ashizawa, Andrew Billnitzer, Susan Perlman, Khalaf Bushara, Michael D. Geschwind, Cameron Dietiker, Christopher M. Gomez, Mahesh Padmanaban, Sheng-Han Kuo, Puneet Opal, Rizwan Akhtar, Henry Paulson, Sharan Srinivasan, Amy Ferng, Chiadi U. Onyike, Sarah Ying, Liana Rosenthal, Ashley Paul, Jeremy Schmahmann, Christopher Stephen, Anoopum Gupta, Chih-Chun Lin, S.H. Subramony, Matthew Burns, George Wilmot, Antoine Duquette, Theresa Zesiewicz, Marie Y. Davis, Ali G. Hamedani, Joaquin Vizcarra Pasapera, Vikram G. Shakkottai, Stefan Pulst, Lauren Moore   +38 more
openaire   +1 more source

MJD

2006
openaire   +1 more source

MJD

2011
openaire   +1 more source

Phenotype-genotype correlations in SCA1, SCA2, SCA3/MJD and SCA6

Neuromuscular Disorders, 1997
Alexandra Durr, Giovanni Stevanin, Geraldine Cancel, Olivier Didierjean, Alexis Brice   +4 more
openaire   +1 more source

Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6

Journal of the Neurological Sciences, 1999
Toru Kawanami
exaly