Search Results - "Oliveira, A.S.B"
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Effect of L-carnitine on exercise performance in patients with mitochondrial myopathy
Published in Brazilian journal of medical and biological research (01-04-2015)“…Exercise intolerance due to impaired oxidative metabolism is a prominent symptom in patients with mitochondrial myopathy (MM), but it is still uncertain…”
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New findings in facial-onset sensory and motor neuronopathy (FOSMN) syndrome
Published in Revue neurologique (01-04-2019)“…Facial-onset sensory and motor neuronopathy (FOSMN) syndrome represents a rare, slowly progressive, lower motor neuron disease with sensory compromise,…”
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Physicochemical and sensory characterization of refined and deodorized tuna (Thunnus albacares) by-product oil obtained by enzymatic hydrolysis
Published in Food chemistry (15-09-2016)“…•Deodorized fish oil rich in PUFA from tuna heads by enzymatic hydrolysis was produced.•Physicochemical characterization and fatty acid profile were…”
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C.P.11 Centronuclear and myotubular myopathies: Clinical, histological and molecular findings in a large series of Brazilian patients
Published in Neuromuscular disorders : NMD (01-10-2012)“…Abstract Myotubular and centronuclear myopathies (MTM/CNM) are congenital muscle diseases with a wide clinical spectrum and typical histopathological findings…”
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Enzymatic extraction of oil from yellowfin tuna (Thunnus albacares) by‐products: a comparison with other extraction methods
Published in International journal of food science & technology (01-03-2017)“…Summary This study evaluated the quality of oil extracted from yellowfin tuna (Thunnus albacares) by enzymatic hydrolysis (EHO) compared with oil extracted by…”
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249P Clinical characteristics of the spinal muscular atrophy patients identified in the Brazilian public health system
Published in Neuromuscular disorders : NMD (01-10-2024)“…Spinal muscular atrophy (SMA) is a rare disease characterized by progressive loss of motor neurons. The most common form of SMA (5q-SMA), classified into…”
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Expanding the spectrum of TBK1-related disorders: Adult-onset non-5q spinal muscular atrophy
Published in Revue neurologique (01-11-2022)“…•Non-5q SMA represents an expanding group of neurogenetic diseases.•TBK1 is associated with Frontotemporal dementia and Amyotrophic Lateral Sclerosis.•We…”
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Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology
Published in Revue neurologique (01-04-2019)“…Motor neuron disease (MND) represents a wide and heterogeneous expanding group of disorders involving the upper or lower motor neurons, mainly represented by…”
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SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype
Published in Revue neurologique (01-10-2019)Get full text
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Motor neuron disease with leukodystrophy due to CSF1R mutation
Published in Revue neurologique (01-03-2020)Get full text
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Rapidly progressive bulbar-onset ALS due to SS18L1 mutation
Published in Revue neurologique (01-03-2020)Get full text
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Dengue. Muscle biopsy findings in 15 patients
Published in Arquivos de neuro-psiquiatria (01-06-1993)“…Dengue is known to produce a syndrome involving muscles, tendons and joints. The hallmark of this syndrome is severe myalgia but includes fever, cutaneous…”
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O'Sullivan–McLeod syndrome: Unmasking a rare atypical motor neuron disease
Published in Revue neurologique (01-01-2019)“…Atypical motor neuron disease represents a rare heterogeneous group of neurodegenerative disorders with clinical, genetic and neuroimaging features distinct…”
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Expression of HLA-DR in pheripheral nerve of amyotrophic lateral sclerosis
Published in Arquivos de neuro-psiquiatria (01-12-1994)“…To investigate the possibility of local antigen presentation within the peripheral nerve in amyotrophic lateral sclerosis (ALS), cryostat sections of 83…”
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Effect of L-carnitine on exercise performance in patients with mitochondrial myopathy
Published in Brazilian journal of medical and biological research (01-02-2015)“…Exercise intolerance due to impaired oxidative metabolism is a prominent symptom in patients with mitochondrial myopathy (MM), but it is still uncertain…”
Get full text
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Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia
Published in Journal of the neurological sciences (25-11-1997)“…We report herein on eleven Brazilian patients with mitochondrial DNA (mtDNA) deletions, found among thirteen patients with chronic progressive external…”
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Polineuropatia nutricional entre índios Xavantes
Published in Revista da Associação Médica Brasileira (1992) (01-03-1997)Get full text
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