Results 1 to 10 of about 1,383 (117)

Cardiovascular Effects of the Essential Oil of Croton argyrophylloides in Normotensive Rats: Role of the Autonomic Nervous System. [PDF]

open access: yesEvid Based Complement Alternat Med, 2016
Cardiovascular effects of the essential oil of Croton argyrophylloides Muell. Arg. (EOCA) were investigated in normotensive rats. In saline-pretreated anesthetized or conscious rats, intravenous (i.v.) injection of the EOCA induced dose-dependent ...
Alves-Santos TR   +3 more
europepmc   +5 more sources

Convolvulus arvensis: Antioxidant, Antibacterial, and Antifungal Properties of Chemically Profiled Essential Oils: An Approach against Nosocomial Infections [PDF]

open access: yesLife, 2022
Convolvulus arvensis is a medicinal plant in the family Convolvulaceae, which is used in traditional phytotherapy. The objective of this work was conducted to valorize essential oils of Convolvulus arvensis (EOCA) in terms of chemical composition ...
Ahmad Mohammad Salamatullah
doaj   +2 more sources

In Vitro Antiviral Potential, Antioxidant, and Chemical Composition of Clove (Syzygium aromaticum) Essential Oil [PDF]

open access: yesMolecules, 2023
Viral infections are spread all around the world. Although there are available therapies, their safety and effectiveness are constrained by their adverse effects and drug resistance. Therefore, new natural antivirals have been used such as essential oils,
Manal Jameel Kiki
doaj   +2 more sources

Prognostic Nomograms for Predicting Overall Survival and Cancer-Specific Survival of Patients With Early Onset Colon Adenocarcinoma [PDF]

open access: yesFrontiers in Oncology, 2020
BackgroundThe incidence of colon cancer in young patients is on the rise, of which adenocarcinoma is the most common pathological type. However, a reliable nomogram for early onset colon adenocarcinoma (EOCA) to predict prognosis is currently lacking ...
Huimin Jin   +3 more
doaj   +2 more sources

Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2013
Autosomal recessive cerebellar ataxias are a heterogeneous group of neurological disorders. In 1981, a neurological entity comprised by early onset progressive cerebellar ataxia, dysarthria, pyramidal weakness of the limbs and retained or increased upper
Jose Luiz Pedroso   +4 more
doaj   +5 more sources

Motor training-related brain reorganization in patients with cerebellar degeneration. [PDF]

open access: yesHum Brain Mapp, 2022
Voxel‐based morphometry analysis was used to obtain information on the neural correlates of visuomotor arm training in cerebellar degeneration. Whereas controls showed increased gray matter volumes in visual associative cortex, in cerebellar patients gray matter increased in premotor cortex.
Draganova R   +10 more
europepmc   +2 more sources

The genetic landscape and phenotypic spectrum of GAA-FGF14 ataxia in China: a large cohort studyResearch in context [PDF]

open access: yesEBioMedicine
Summary: Background: An intronic GAA repeat expansion in FGF14 was recently identified as a cause of GAA-FGF14 ataxia. We aimed to characterise the frequency and phenotypic profile of GAA-FGF14 ataxia in a large Chinese ataxia cohort.
Riwei Ouyang   +19 more
doaj   +2 more sources

Different altered stage correlative expression of high abundance acute-phase proteins in sera of patients with epithelial ovarian carcinoma [PDF]

open access: yesJournal of Hematology & Oncology, 2009
Background The general enhanced expression of α1-antichymotrypsin (ACT), clusterin (CLU), α1-antitrypsin (AAT), haptoglobin β-chain (HAP), and leucine rich glycoprotein (LRG) in the sera of patients with epithelial ovarian carcinoma (EOCa) was recently ...
Lim Boon-Kiong, Chen Yeng, Hashim Onn H
doaj   +2 more sources

Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix-Saguenay. [PDF]

open access: yesMol Genet Genomic Med
We present the first Bulgarian patients diagnosed by whole‐exome sequencing with ARSACS due to five different mutations in the SACS gene, three of which are novel. This expands the disorder's mutation and geographic spectrum and illustrates that brain MRI and optic coherence tomography are necessary supportive clinical tests.
Chamova T   +13 more
europepmc   +2 more sources

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