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1.
Rev Neurol (Paris) ; 179(1-2): 114-117, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36473746

RESUMO

We describe four male patients with wasted-leg syndrome, with predominant asymmetric thigh atrophy and weakness that stabilized after a period of slow progression (follow-up 7-18 years). Two patients had an Indian ethnic background and two were Portuguese, without known Indian ancestry. Other mimicking disorders were excluded, but one Indian patient was later diagnosed with CADASIL. Electromyography (EMG) revealed severe chronic neurogenic changes in proximal leg muscles, and mild changes in distal leg muscles, but EMG of the upper limbs was normal. Upper motor neuron signs were absent clinically and on transcranial magnetic stimulation. This seems to represent a variant of the common wasted-leg syndrome presentation.


Assuntos
Esclerose Lateral Amiotrófica , Doença dos Neurônios Motores , Humanos , Masculino , Perna (Membro) , Doença dos Neurônios Motores/complicações , Doença dos Neurônios Motores/diagnóstico , Músculo Esquelético , Eletromiografia , Estimulação Magnética Transcraniana , Esclerose Lateral Amiotrófica/diagnóstico
2.
Front Neurosci ; 14: 428, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32528241

RESUMO

It may seem useless to propose preventive measures for a disease without established pathogenesis and successful therapy, such as amyotrophic lateral sclerosis (ALS). However, we will show that ALS shares essential molecular mechanisms with aging and that established anti-aging strategies, such as healthy diet or individually adjusted exercise, may be successfully applied to ameliorate the condition of ALS patients. These strategies might be applied for prevention if persons at ALS risk could be identified early enough. Recent research advances indicate that this may happen soon.

4.
Acta Neurol Scand ; 137(2): 233-237, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28967121

RESUMO

OBJECTIVES: The club cell protein (CC-16) is a biomarker associated with respiratory distress and pulmonary inflammation. We evaluated CC-16 as a candidate biomarker for respiratory failure in amyotrophic lateral sclerosis (ALS). MATERIALS AND METHODS: We studied 81 ALS patients and 30 matched controls. We used an ALS-related measure of functional capacity, and tested forced vital capacity (FVC) and the amplitude of the diaphragmatic response by phrenic nerve stimulation (PhrenAmpl). Plasma CC-16 levels were measured in venous blood. Kaplan-Meier survival curves were plotted to evaluate risk to non-invasive ventilation and death in patients with abnormal CC-16 levels. RESULTS: CC-16 levels were significantly raised in ALS patients (10.56 ng/mL ± 6.84 vs 8.34 ng/mL ± 3.10, P = .02), and in 17% of them, CC-16 level was above the upper cutoff value (mean + 2.5SD). CC-16 levels did not correlate with age, onset region, disease duration, functional status, FVC, and PhrenAmpl. In patients with increased CC-16 level, the risk of non-invasive was greater in the following 6 months (P = .01) and tended to have higher mortality in the following 30 months (P = .07). CONCLUSIONS: We propose that increased CC-16 levels is a marker of lung inflammatory response that associated with ventilatory insufficiency are related to impending respiratory failure, not fully predicted by conventional respiratory tests. The latter are limited by the moment of testing.


Assuntos
Esclerose Lateral Amiotrófica/sangue , Esclerose Lateral Amiotrófica/complicações , Insuficiência Respiratória/sangue , Insuficiência Respiratória/etiologia , Uteroglobina/sangue , Adulto , Idoso , Idoso de 80 Anos ou mais , Esclerose Lateral Amiotrófica/mortalidade , Biomarcadores/sangue , Feminino , Humanos , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Ventilação não Invasiva , Testes de Função Respiratória , Insuficiência Respiratória/mortalidade , Adulto Jovem
5.
Cytogenet Genome Res ; 109(4): 507-11, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15905646

RESUMO

Despite the growing outcome of results that put doubt upon the reliability of silver (Ag) staining and chromomycin A3 (CMA3) fluorescent banding in the detection of major ribosomal gene sites (NORs), these methods have been widely used, especially in fishes. In order to clarify the previous patterns obtained with those techniques, we performed fluorescence in situ hybridisation (FISH) with 28S rDNA probe followed by sequential CMA3 and Ag staining in diploid non-hybrid males of the Squalius alburnoides complex and in Squalius pyrenaicus. The results from all the studied specimens revealed a lack of correlation between classical and molecular techniques. Not just some other regions besides NORs were stained with CMA3 and Ag, but also the majority of the 28S rDNA sites were not detected. Care should then be taken in considering CMA3- and Ag-stained sites as NORs since their accuracy for that purpose may not always correspond to the expectations.


Assuntos
Cyprinidae/genética , Marcadores Genéticos/genética , Proteínas Ribossômicas/genética , Coloração pela Prata , Animais , Cromomicina A3 , Bandeamento Cromossômico , Sondas de DNA/genética , DNA Ribossômico/genética , Diploide , Proteínas de Peixes/genética , Hibridização in Situ Fluorescente/métodos , Masculino , Região Organizadora do Nucléolo
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