BACKGROUND/PURPOSE Texture analysis (TA) is a branch of image processing, which attempts to convey "texture" information from digital images, such as magnetic resonance images (MRI). Machado-Joseph disease (MJD) affects mainly cerebellum and brainstem, but recent studies have shown that other cerebral structures may also be affected. OBJECTIVE To investigate subtle structural abnormalities in corpus callosum (CC), thalami, putamen, and caudate nuclei of patients with MJD using TA. METHODS Eighteen healthy volunteers and 18 patients with MJD were studied (mean age at disease onset = 34.7 years; disease duration = 9.6 years; mean expanded CAG in the MJD1 gene = 73). A TA approach based on the gray-level cooccurrence matrix was applied to T1-M...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Machado-Joseph disease, or spinocerebellar ataxia type 3(MJD/SCA3), is the most frequent late onset ...
BACKGROUND AND PURPOSE: TA is a branch of image processing that seeks to reduce image information by...
BACKGROUND AND PURPOSE: TA is a branch of image processing that seeks to reduce image information by...
Previous imaging studies in the Machado-Joseph disease (MJD/SCA3) have mostly concentrated on the ce...
We evaluated spectroscopy findings at the deep white matter in Machado-Joseph disease (MJD). We obta...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)BACKGROUND/PURPOSE Previous imaging stu...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)BACKGROUND AND PURPOSE Neuropathologica...
Juvenile myoclonic epilepsy (JME) is the most frequent subsyndrome of the idiopathic generalized epi...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Background/purpose: Juvenile myo...
Machado-Joseph disease (MJD) is one of the most frequently encountered spinocerebellar ataxias. Howe...
Background: Machado-Joseph disease (MJD) is one of the most frequently encountered spinocerebellar a...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)We evaluated spectroscopy findings at t...
AbstractBackground/purposeJuvenile myoclonic epilepsy (JME) is the most frequent subsyndrome of the ...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Machado-Joseph disease, or spinocerebellar ataxia type 3(MJD/SCA3), is the most frequent late onset ...
BACKGROUND AND PURPOSE: TA is a branch of image processing that seeks to reduce image information by...
BACKGROUND AND PURPOSE: TA is a branch of image processing that seeks to reduce image information by...
Previous imaging studies in the Machado-Joseph disease (MJD/SCA3) have mostly concentrated on the ce...
We evaluated spectroscopy findings at the deep white matter in Machado-Joseph disease (MJD). We obta...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)BACKGROUND/PURPOSE Previous imaging stu...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)BACKGROUND AND PURPOSE Neuropathologica...
Juvenile myoclonic epilepsy (JME) is the most frequent subsyndrome of the idiopathic generalized epi...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Background/purpose: Juvenile myo...
Machado-Joseph disease (MJD) is one of the most frequently encountered spinocerebellar ataxias. Howe...
Background: Machado-Joseph disease (MJD) is one of the most frequently encountered spinocerebellar a...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)We evaluated spectroscopy findings at t...
AbstractBackground/purposeJuvenile myoclonic epilepsy (JME) is the most frequent subsyndrome of the ...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Progressive myoclonic epilepsy type 1 (EPM1) is an autosomal recessively inherited neurodegenerative...
Machado-Joseph disease, or spinocerebellar ataxia type 3(MJD/SCA3), is the most frequent late onset ...