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1.
Eur J Neurol ; 27(3): 454-460, 2020 03.
Artigo em Inglês | MEDLINE | ID: mdl-31696586

RESUMO

BACKGROUND AND PURPOSE: Existing research studies have demonstrated a relationship between magnetic resonance imaging (MRI) neuroimaging measures and walking speed in people with multiple sclerosis (PwMS). However, to date there are no data as to the brain structures involved in gait coordination and control in PwMS. Therefore, the aim of our study was to investigate the association between walk ratio, an indicator of gait coordination, and related brain structures in PwMS. METHODS: A brain MRI was performed by a 3.0-T MR scanner in conjunction with a volumetric analysis based on three-dimensional T1-weighted images. Regions of interest were volumes of the hippocampus, amygdala, putamen, caudate, pallidum, thalamus, cerebellum and the corpus callosum regions. Walking speed and walk ratio, defined as step length divided by step rate, was measured whilst walking on an electronic walkway. RESULTS: In all, 343 PwMS (41.1 ± 13.4 years, 69.1% female, median Expanded Disability Status Scale 2.5) were included in the study. A significant association was found between the left cerebellum volume and walk ratio after controlling for age, gender, total cranial volume and disability; R2  = 0.379, P = 0.002. A similar association was found between the right cerebellum volume and walk ratio, R2  = 0.364, P = 0.002. No correlations were observed between walk ratio and the thalamus, basal ganglia, hippocampus, amygdala and the corpus callosum volumes. No association was found between walking speed and all brain measures. CONCLUSIONS: The walk ratio should be considered when evaluating and assessing PwMS presenting with ataxia. Furthermore, it is also hypothesized that a low walk ratio indicates a lower cerebellum volume in the MS population.


Assuntos
Cerebelo/diagnóstico por imagem , Marcha/fisiologia , Esclerose Múltipla/diagnóstico por imagem , Caminhada/fisiologia , Adulto , Encéfalo/diagnóstico por imagem , Cerebelo/fisiopatologia , Avaliação da Deficiência , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Esclerose Múltipla/fisiopatologia
2.
Seizure ; 22(3): 189-93, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23298604

RESUMO

PURPOSE: To study the usefulness of EEG in the diagnosis of lissencephaly, a rare cortical developmental disorder associated with abnormal cellular proliferation. Currently, the clinical emphasis is placed on the radiological and genetic aspects for the diagnosis of lissencephaly. METHODS: This is a retrospective review of consecutive EEG recordings and imaging data from 14 children, with the diagnosis of lissencephaly, who were admitted from January 1998 to January 2010. All EEG recordings were performed with the 10-20 system of electrode placement, in both awake and sleep states. All EEG recordings were reviewed using anterior-posterior bipolar and transverse montages and then they were interpreted blindly, with respect to the imaging and genetic investigations for each patient. RESULTS: All children showed one of the three characteristic EEG patterns reported in the literature of lissencephaly. The EEG pattern I, showed an anterior posterior gradient that corresponded to the severity of the imaging study abnormality. All patients were on two or more AEDs and reported to continue having active epilepsy. CONCLUSION: In a child with clinical characteristics of lissencephaly, one of these three reported EEG patterns can prove useful in making the diagnosis very probable, preceding imaging and genetic testing.


Assuntos
Encéfalo/fisiopatologia , Epilepsia/diagnóstico , Lisencefalia/fisiopatologia , Pré-Escolar , Eletroencefalografia , Epilepsia/etiologia , Epilepsia/fisiopatologia , Feminino , Humanos , Lactente , Lisencefalia/complicações , Masculino , Estudos Retrospectivos
3.
Mediterr J Hematol Infect Dis ; 3(1): e2011029, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21869915

RESUMO

Cerebral Venous Sinus (sinovenous) Thrombosis (CSVT) is a serious and rare disorder, increasingly recognized and diagnosed in pediatric patients. The etiology and pathophisiology has not yet been completely clarified, and unlike adults with CSVT, management in children and neonates remains controversial. However, morbidity and mortality are significant, highlighting the continued need for high-quality studies within this field. The following review will highlight aspects of CSVT in the mediteranian area in children.

4.
Harefuah ; 140(2): 89-91, 192, 2001 Feb.
Artigo em Hebraico | MEDLINE | ID: mdl-11242934

RESUMO

Intraventricular hemorrhage in full-term neonates is rare; it may develop without any clinical signs. Its cause is not fully understood although some risk factors have been identified. A higher index of suspicion would ensure earlier diagnosis and treatment, which might reduce the rate of severe complications. We describe 2 cases in full-term neonates.


Assuntos
Hemorragia Cerebral/diagnóstico , Ventrículos Cerebrais , Hemorragia Cerebral/terapia , Humanos , Hidrocefalia/complicações , Lactente , Recém-Nascido , Masculino
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