[PDF] Top 20 Arq. NeuroPsiquiatr. vol.65 número1

... Pela ousadia e pela oportunidade da iniciativa, as congratulações de Arquivos de Neuro-Psiquiatria à Academia Brasileira de Neurologia e seus membros. Antonio Spina França[r] ... See full document

... Histological and histochemical abnormalities in muscle biopsy: (A) selective atrophy of the type 2 fibers (case 29; ATPase pH 9.4); (B) type 1 fiber with lipid accumulation (case 23; Oil[r] ... See full document

... 1º CONGRESSO INTERNACIONAL DE PSIQUIATRIA DA INFÂNCIA E DA ADOLESCÊNCIA /e XIII ENCONTRO de AMIGOS pelo AUTISMO. De 21 a 24 março 2007 na cidade de São Paulo (Instituto de Psiquiatria, IPQ, do Hospital das Clínicas da ... See full document

... Os AA solicitam corrigir erro que inadvertidamente fi- zeram constar do título em inglês: onde se lê inibitor leia- se inhibitor e no lugar de over leia-se on, ficando:Neonatal treatment effect with selective inhibitor ... See full document

... Finally, mirror test probably is not sensitive to detect ToM deficits in subjects with unilateral fron- tal lesions, beeing necessary more extensive lesions affecting orbitofrontal areas[r] ... See full document

... patients with cerebellar pathology were selected without a control group, being the patient’s char- acteristic thirteen patients with stroke, three with postinfectious cerebellitis, thre[r] ... See full document

... Compression by a dolichoectasic basilar artery (DBA) has already been involved in ocular motor nerve paresis 6.. Al-.[r] ... See full document

... Typical features of Dandy-Walker variant on brain MRI: (A) large fourth ventricle in axial T1-weighted image; (B) small cerebellar vermis in axial T2-weighted image; (C) hydro- cephalus [r] ... See full document

... Congenital inclusion dermoid cyst located over the region of the anterior fontanel in adult Nigerians.. Cisto dermóide de inclusão localizado na região da fontanela anterior no adulto.[r] ... See full document

... In order to study metabolic changes within the brain, the authors performed a magnetic resonance spectroscopy (MRS) study in a 1- year-old girl with merosin-positive CMD (MP-CMD).. MRS o[r] ... See full document

... In our opinion, this study should be performed in all medically resistant epilepsy patient suspected to have apnea or unexplained daytime somnolence.. Better understanding the role of th[r] ... See full document

... phy of the basal ganglia and cerebellum (H-ABC) is a nosologic entity described in 2002, by van der Knaap and coworkers 2.. It is an extremely rare disease.[r] ... See full document

... We conclude that although a larger sample is needed in order to confirm our findings, the reduc- tion of one AED in selected children with refractory epilepsy can be associated with less[r] ... See full document

... For diagnostic purposes, she underwent evaluation by different scales, which provided ratings compatible with diagnosis of autism (Autism Rating Scale, with 40.5 points, and Evaluation o[r] ... See full document

... Therefore, in NCC was found several general pathologic processes (necrosis, interstitial deposits, fibrosis, gliosis, inflammation) amongst which are highlighted beta-fibrillose in 13 (7[r] ... See full document

... The investigation disclosed pilli torti and thrycorrexis nodosa in the hair, low serum levels of both copper and ceruloplasmin, brain magnetic resonance study showed atrophy and whit[r] ... See full document

... The present study aimed at investigating the spe- cific effects of bromazepam on the coupling of cor- tical areas and the strength of interhemispheric con- nectivity, as expressed in ter[r] ... See full document

... Juvenile onset bul- bospinal muscular atrophy with deafness: Vialetto-van Laere syndrome or Madras type motor neuron disease?. J Neurol 1987;234:440-442.[r] ... See full document

... ABSTRACT - Patients with Parkinson’s disease (PD) in whom symptoms start before the age of 45 years (EOPD) present different clinical characteristics from those with the late-onset form [r] ... See full document

... Association analysis of the catechol-o-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder. Cr[r] ... See full document