Results 131 to 140 of about 26,249 (178)

Exploring functional and structural connectivity disruptions in spinocerebellar ataxia type 3: Insights from gradient analysis. [PDF]

CNS Neurosci Ther
Wang X, Chen H, Wen R, Ou P, Huang Y, Deng L, Shi L, Chen W, Chen H, Wang J, He C, Liu C.   +11 more
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The volume of the subthalamic nucleus in spinocerebellar ataxia type 3: potential relevance for the clinical phenotype and treatment of parkinsonian symptoms with deep brain stimulation. [PDF]

J Neurol
Minnerop M, Pieperhoff P, Elben S, Hartmann CJ, Müttel T, Kahlen U, Wüllner U, Klockgether T, Wojtecki L, Caspers S, Amunts K, Vesper J, Schnitzler A, Groiss SJ.   +13 more
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Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic Review of Their Potential Uses in Disease Staging and Treatment Assessment. [PDF]

Int J Mol Sci
Soto-Piña AE, Pulido-Alvarado CC, Dulski J, Wszolek ZK, Magaña JJ.   +4 more
europepmc   +1 more source

Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort

Berger M, Garcia-Moreno H, Ferreira M, Hubener-Schmid J, Schaprian T, Wegner P, Elter T, Teichmann K, Santana MM, Grobe-Einsler M, Onder D, Koyak B, Bernsen S, Pereira de Almeida L, Silva P, Ribeiro JA, Cunha I, Gonzalez-Robles C, Khan S, Heslegrave A, Zetterberg H, Lima M, Raposo M, Ferreira AF, Vasconcelos J, van de Warrenburg BP, van Gaalen J, van Prooije TH, de Vries J, Schols L, Riess O, Synofzik M, Timmann D, Thieme A, Erdlenbruch F, Infante J, Pelayo AL, Manrique L, Reetz K, Dogan I, Oz G, Joers JM, Bushara K, Onyike C, Povazan M, Jacobi H, Schmahmann JD, Ratai E, Schmid M, Giunti P, Klockgether T, Faber J.   +51 more
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Phonoarticulation in spinocerebellar ataxia type 3

European Archives of Oto-Rhino-Laryngology, 2016
Phonoarticulation is characterized by changes in resonance, diadochokinesis, prosody, sound frequency, vocal quality, and intraoral pressure. The main aim of this study was to characterize the phonoarticulation in spinocerebellar ataxia type 3 (SCA3) and correlate it with clinical and genetic factors. Thirty-one patients with SCA3 who were subjected to
A E, Wolf, L, Mourão, M C, França, A J, Machado Júnior, A N, Crespo   +4 more
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“Pinball” intrusions in spinocerebellar ataxia type 3

Neurology, 2018
Saccadic intrusions are involuntary saccades that interrupt fixation and are usually conjugate between eyes.1 Although saccadic intrusions may be seen in healthy individuals, they also accompany certain neurologic disorders (usually manifesting higher frequency or amplitude) including cerebellar disease.2 We present a patient with spinocerebellar ...
João, Lemos, Ana, Novo, Cristina, Duque, João, Castelhano, Eric, Eggenberger, Cristina, Januário   +5 more
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Tremor-spectrum in spinocerebellar ataxia type 3

Journal of Neurology, 2012
Spinocerebellar ataxia type 3 (SCA3) can be present with a combination of cerebellar, neuropathic, pyramidal, or extrapyramidal symptoms. Tremor is a classical but not frequent manifestation of SCA3 and there is a lack of detailed knowledge regarding its origin.
Cecilia, Bonnet, Emmanuelle, Apartis, Mathieu, Anheim, Andre P, Legrand, Jose F, Baizabal-Carvallo, Anne M, Bonnet, Alexandra, Durr, Marie, Vidailhet   +7 more
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Spinocerebellar Ataxia-Type 3

2012
Spinocerebellar ataxia-type 3 (SCA3) or Machado-Joseph disease (MJD) is a clinically heterogeneous, neurodegenerative disorder characterized by varying degrees of ataxia, ophthalmoplegia, peripheral neuropathy, pyramidal dysfunction, and movement disorder.
Roongroj Bhidayasiri, Daniel Tarsy
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Homozygosity Enhances Severity in Spinocerebellar Ataxia Type 3

Pediatric Neurology, 2008
Spinocerebellar ataxia type 3, or Machado-Joseph disease, is an autosomal dominant neurodegenerative disease characterized by a wide spectrum of clinical findings that include progressive cerebellar ataxia. All affected individuals have an expanded CAG repeat mutation in one allele of the ATXN3 gene.
Daniel R, Carvalho, Alessandra, La Rocque-Ferreira, Isabela M, Rizzo, Erica U, Imamura, Carlos E, Speck-Martins   +4 more
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Transcranial sonography in spinocerebellar ataxia type 3

2004
Transcranial sonography (TCS) identifies hyperechogenic basal ganglia in extrapyramidal disorders such as Parkinson's disease or dystonia and reveals brain atrophy reflecting the stage of degeneration in Huntington's disease. Aim of the present study was to evaluate the diagnostic potential of TCS in spinocerebellar ataxia type 3 (SCA3), a ...
Th, Postert, J, Eyding, D, Berg, H, Przuntek, G, Becker, M, Finger, L, Schöls   +6 more
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