Search results for "Sang"

Moderate-Vigorous Physical Activity across Body Mass Index in Females : Moderating Effect of Endocannabinoids and Temperament

2014

Altres ajuts: This manuscript was supported by grants from Instituto Salud Carlos III (FIS PI11/210 and CIBERobn). Sarah Sauchelli is recipient of a pre-doctoral Grant (2013-17) by IDIBELL. Jose C. Fernández-García is recipient of a 'Rio Hortega' contract from 'Instituto de Salud Carlos III', Madrid, Spain (CM12/00059). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. Endocannabinoids and temperament traits have been linked to both physical activity and body mass index (BMI) however no study has explored how these factors interact in females. The aims of this cross-sectional study were to 1) examine differences…

Un contrato inédito de Juan de Juanes. El retablo de la Cofradía de la Sangre de Cristo de Valencia (1539)

2012

This article is based on an unpublished contract signed in 1539 by Vicente and Juan Macip for an altarpiece for the Valencian Brotherhood of the Blood of Christ. The agreement stipulates that Juan, later known as Juan de Juanes, had to paint the scenes. Thus the document reinforces the hypothesis that Juan Macip was the most important painter in the Macip workshop during the 1530’s. It also fills a documental void in between the completion of the Silversmith’s Guild altarpiece (1534-1539) and the contract for the Fuente la Higuera altarpiece (1548). This study also verifies the popularity of the iconography of the seven sheddings of the Blood of Christ and processions of disciplinants.<b…

Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindred.

2008

Thirty-four members of a single Sardinian kindred with lecithin-cholesterol-acyltransferase deficiency have been studied. The kindred spans four generations and the parents of the two affected siblings are blood relatives. Segregation of the acyltransferase deficiency gene in the family clearly demonstrated an autosomal recessive mode of inheritance. Thirteen family members, including all obligate heterozygotes, had roughly half-normal acyltransferase activities (mean +/- S.D. = 0.39 +/- 0.06 mU/ml) when compared to 17 intrafamilial controls and spouses (mean +/- S.D. = 0.72 +/- 0.09 mU/ml) and 40 blood donors from Marburg/Lahn (mean +/- S.D. =0.76 +/- 0.1 mU/ml). Characterization of the he…

Segunda parte, En que prosigue la verdadera relacion del lastimoso estrago acaecido en la Ciudad de Sanguesa, del Reyno de Navarra, la noche del vein…

Grav. xil. enmarcat de la Mare de Déu Banda tip. al final de la primera part Sign.: [ ]4 Text a dues col Reclams

Blood absorption capacity of different xenograft bone substitutes. An in-vitro study

2019

Background Commercially available xenograft blocks, claim to have adequate characteristics to interact with biological media and thus permitting biological fluid absorption. The objective of this in vitro study was to compare the blood absorption capacity of four different xenograft block materials of different composition of collagen and porosity. Material and Methods Four brands of xenograft block materials were used (NuOss®, Bio-Oss®, Osteobiol® and Smartbone®). Five samples of each brand were analyzed, making a total of 20 tests. Human blood was used as the absorption liquid for the present experiment. The time period, in which the block remains in contact with the blood, was registered…

IL FATTORE IDROSTATICO

2007

La pressione idrostatica di un fluido è l’aumento della pressione in profondità rispetto a quella di superficie. Nelle arterie e vene cerebrali la pressione idrostatica del sangue se soggetta a continue oscillazioni può danneggiare il sistema capillare interposto e incidere negativamente sugli scambi di ossigeno e altre sostanze con il tessuto nervoso circostante. Il controllo vasomotorio del sistema nervoso autonomo è inefficace determinando una contrazione lenta e duratura nel tempo a livello delle arteriole di medio e piccolo calibro. Esiste perciò un importante fattore di bilanciamento della pressione sanguigna a livello cranico in grado di contenere la pressione idrostatica eccessiva: …

A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity.

2013

Inherited retinal dystrophies are a major cause of childhood blindness. Here, we describe the identification of a homozygous frameshift mutation (c.1194_1195delAG, p.Arg398Serfs*9) in TUB in a child from a consanguineous UK Caucasian family investigated using autozygosity mapping and whole-exome sequencing. The proband presented with obesity, night blindness, decreased visual acuity, and electrophysiological features of a rod cone dystrophy. The mutation was also found in two of the proband's siblings with retinal dystrophy and resulted in mislocalization of the truncated protein. In contrast to known forms of retinal dystrophy, including those caused by mutations in the tubby-like protein …

Protein Identification and Haplotype Description of Homozygote Mutation Causing Congenital Plasminogen Deficiency

2021

Severe type I Plasminogen (PLG) deficiency was clinically diagnosed after hyaline-positive periodic acid Schiff material was detected in the histologic study of superior tarsal conjunctiva and vulvar pseudomembrane of the patient. Direct immunofluorescence also confirmed multiple deposits of fibrinogen in the dermis. Plasma plasminogen activity was calculated in a <5% value (reference values, 75% to 150%) and sequencing of the PLG gene evidenced the homozygous mutation in c.2377T/A (p.Tyr793Asn), confirming the molecular diagnosis of congenital deficiency of plasminogen type 1. Genotype-Phenotype correlation among family members evidenced the recessive hereditary pattern of clinical manifes…

Altered cerebral blood flow velocity features in fibromyalgia patients in resting-state conditions

2017

[EN] The aim of this study is to characterize in resting-state conditions the cerebral blood flow velocity (CBFV) signals of fibromyalgia patients. The anterior and middle cerebral arteries of both hemispheres from 15 women with fibromyalgia and 15 healthy women were monitored using Transcranial Doppler (TCD) during a 5-minute eyes-closed resting period. Several signal processing methods based on time, information theory, frequency and time-frequency analyses were used in order to extract different features to characterize the CBFV signals in the different vessels. Main results indicated that, in comparison with control subjects, fibromyalgia patients showed a higher complexity of the envel…

Demographic and clinical data in acquired hemophilia A

2012

Summary.  Background:  Acquired hemophilia A (AHA) is a rare autoimmune disease caused by autoantibodies against coagulation factor VIII and characterized by spontaneous hemorrhage in patients with no previous family or personal history of bleeding. Although data on several AHA cohorts have been collected, limited information is available on the optimal management of AHA. Objectives:  The European Acquired Hemophilia Registry (EACH2) was established to generate a prospective, large-scale, pan-European database on demographics, diagnosis, underlying disorders, bleeding characteristics, treatment and outcome of AHA patients. Results:  Five hundred and one (266 male, 235 female) patients from …