[PDF] Top 20 Conjugal amyotrophic lateral sclerosis in Brazil

... normalities in her limbs or bladder ...weakness in the upper limbs alongside muscle at- rophy and ...neurons in the four limbs and tongue characterized by spontaneous activity (positive waves, ... See full document

... born in Pernambuco and coming from ...weakness in the left lower limb that progressed with atrophy of the left hand, being diagnosed six months later with ...decrease in voluntary ...resulting ... See full document

... with Amyotrophic Lateral Sclerosis through ...articles in the database, using controlled ...bulbar Amyotrophic Lateral Sclerosis, communication and feeding were more ... See full document

... resulted in only 32 significant events and did not reveal any functional pathways enriched by these events (Table S2 in File ...S1). In contrast, knock-down of FUS expression resulted in 579 ... See full document

... Amyotrophic lateral sclerosis (ALS) is characterized by progressive degeneration of both cortical and alpha mo- tor neurons of the inal common ...and in long survivors afects many sub- ... See full document

... Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects motor neurons in the cerebral cortex, brainstem, and spinal cord, brain regions in which ... See full document

... reported in the central nervous system, hepatocytes and peripheral blood lymphocytes from patients with sporadic amyotrophic lateral sclerosis ...reported, in spite of the fact that ... See full document

... – Amyotrophic Lateral Sclerosis (ALS) is a multifactorial disease, with pathophysiological mechanisms that show a complex interaction between genetic and molecular pathways, most of them related with ... See full document

... ALS patients with approximately one average year of illness duration provided the sera for the pool of IgGs for experimental applications. Healthy donors of comparable age (around 50 years old) served as control. IgGs ... See full document

... implicated in the pathogen- esis of ALS, the causes leading to most cases remain ...resulting in aberrant gene ...changes in global 5mC or 5 HmC associated with neurodegen- eration ...methylation ... See full document

... of amyotrophic lateral ...ventilation. In the first year after admission, the patient showed anxious and depres- sive symptoms, associated with a permanent refusal of his condition, with great hopes ... See full document

... HLA-DR antibody (Dakopatts, Santa Barbara, CA), directed against the common framework of MHC class II antigens; a rabbit antiserum to the 200 KD subunit of human neurofilament protein ([r] ... See full document

... Amyotrophic lateral sclerosis (ALS) is a neurodegenerative condition characterized by degeneration of upper motor neurons (UMN) arising from the motor cortex in the brain and lower motor ... See full document

... The study design consisted of a pragmatic, case-control, retrospective clinical study. The sample analyzed consisted of 223 ALS patients and 474 controls (two controls per case), matched for age and sex, who were ... See full document

... Amyotrophic lateral sclerosis (ALS) is a multiple-system neurodegenerative disease, and its extra-motor disorders have received increasing concern in recent ...present in ALS ... See full document

... Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative dis- ease of nervous central system, that cause progressive atrophy of breathing muscles and members, moreover bulbar symtoms like ... See full document

... aloud in patients with amyotrophic lateral scle- rosis (ALS) and those with frontotemporal dementia (FTD), in order to determine whether dif- ferences in patterns of speaking and ... See full document

... either cerebral peduncle, at the axial level showing the superior cerebellar peduncle decussation – identified on color maps by its transverse orientation – and all streamlines passing through this first ROI were ... See full document

... contra lateral acquisitions but the group of subjects, presents higher values of PLF and coherence for all frequencies, es- pecially for beta ...chrony in any frequency, specially for beta ...present ... See full document

... progression in ALS. The H63D mutation in the HFE gene was shown to be a risk factor for ALS in four independent studies, although no increased iron body storage is associated with this particular ... See full document