Search results for "Sang"

Factor VII deficiency: evidence that in minor surgery one-day replacement therapy is sufficient

2011

Oral Communication

2012

Inherited factor VII (FVII) deficiency is the most common of the rare autosomal recessive bleeding disorders (RBD), with an estimated prevalence of 1 per 300,000 in European countries.1,2 It is likely that the prevalence is higher in those countries where consanguineous marriages are frequent.We here report STER study results on 112 evaluable enrolled cases

"Esse Malo Quam videri". Sangre y mérito en la orden de Malta a través de la literatura de ficción (Italia, siglos XVI-XVII)

2015

Textos de comunicaciones defendidas en la XIII Reunión Científica de la Fundación Española de Historia Moderna, previa evaluación ciega por pares.

Comparison of validation protocols for blood pressure measuring devices in children and adolescents

2022

Accuracy of blood pressure (BP) measurement is important for the evaluation of hypertension in children and adolescents, and it is critically dependent upon the accuracy of the BP measuring device. A device that could pass validated protocols with reliable accuracy would be desirable in clinical and research settings. Several scientific organizations have published recommendations on the validation of different BP measuring devices. Most of them focus on adults but separate recommendations and validation criteria for BP devices intended for use in children and adolescents are included in some validation protocols. In this review, we compare the validation criteria for BP measuring devices a…

Informe legal del sindico secular, y apostolico del Convento de la Sangre de Christo ... de Religiosos Menores Capuchinos, extra muros de la Ciudad d…

1743

Precedeix al tìt.: "Jesus, Maria, y Joseph, y el serafico Patriarca San Francisco P." Signatura ms. al final de "Fr Juan Btª Musoles"? Port. amb orla tip. i grav. xil. enmarcat de "S. Francisco de Asis." Caplletra ornada Sign.: [A]2, B-L2 Reclams

Thymus essential oil extraction, characterization and incorporation in phospholipid vesicles for the antioxidant/antibacterial treatment of oral cavi…

2018

The aim of the work was to extract, characterize, and formulate Thymus capitatus (Tymbra capitata) essential oil in phospholipid vesicles: liposomes, glycerosomes and Penetration Enhancer-containing Vesicles (PEVs). The steam-distilled essential oil was mainly composed of carvacrol. The oil was mixed with lecithin and water to produce liposomes, or different ratios of water/glycerol or water/propylene glycol (PG) to produce glycerosomes and PG-PEVs, respectively. Cryo-TEM showed the formation of unilamellar, spherical vesicles, and light scattering disclosed that their size increased in the presence of glycerol or PG, which improved long-term stability. The formulations were highly biocompa…

Renal tubular dysgenesis (RTD) - an important cause of the oligohydramnion-sequence

2000

Renal tubular dysgenesis (RTD) is a disorder characterized by neonatal renal failure and regular gross renal architecture, although the histological features of immature and shortened proximal tubules lead to neonatal death. The pathogenesis of this condition includes a congenital familial condition, a twin-twin transfusion syndrome, and an angiotensin-converting enzyme inhibitor intake by the mother. The clinical picture shows an association with oligohydramnia, pulmonary hypoplasia, and skull ossification defects. In the present paper, we report the occurrence of RTD in three infants of a consanguinous couple and compared our data with those of the literature. Our data confirm that late s…

The Expanding Spectrum of Mutations in Hereditary Angioedema.

2021

The evolution in the knowledge of rare genetic diseases such as hereditary angioedema (HAE) has increased at a parallel pace with the development of new molecular tools. The deficiency of C1 inhibitor (C1-INH) has been recognized as the main cause of HAE (HAE-C1-INH) since the 1960s, but the discovery of the wide spectrum of mutations affecting the C1-INH gene (SERPING1) was possible only from the late 1980s, when Sanger sequencing became available and more accessible worldwide. Nevertheless, the involvement of other genes in HAE was discovered only in 2006 with the description of mutations in the F12 gene in patients with HAE and normal C1-INH. In the last 3 years, advanced next-generation…

T Cell Large Granular Lymphocytic Leukemia in Association with Sjögren’s Syndrome

2009

T cell large granular lymphocytic (LGL) leukemia is a rare condition accounting for 2–3% of all mature lymphoid leukemias. Here, we present the case of a 73-year-old woman presenting with neutropenia and anemia (hemoglobin 9.9 g/dl). Hematological assessment revealed the presence of a T cell LGL leukemia. At the time of T cell LGL leukemia diagnosis, the patient developed xerophthalmia and xerostomia, and a diagnosis of Sjögren’s syndrome was made following salivary gland biopsy. The finding of large granular lymphocytes in the context of autoimmune disorders is well-known, though it often occurs with rheumatoid arthritis or in association with a positive autoantibody titer in the absence o…

STUDIO E VALIDAZIONE DI SISTEMI PER L’IDENTIFICAZIONE E IL MONITORAGGIO DI PARAMETRI BIOMEDICI ATTI ALLA PREVENZIONE DI EVENTI INDESIDERATI E ALL’ASS…

L’aumento delle patologie cronico-degenerative nella popolazione mondiale ha comportato un numero sempre maggiore di individui richiedenti assistenza sanitaria, generando, nell’ambito delle realtà ospedaliere, diverse problematiche relative al miglioramento della qualità di vita dei pazienti, ai costi e alla gestione di un numero sempre crescente di soggetti ammalati. Il trattamento sanitario e la ricerca di base si sono pertanto orientati verso la prevenzione delle condizioni che predispongono i soggetti ai peggioramenti clinici e ai ricoveri ospedalieri, puntando sia su nuovi sistemi indossabili di monitoraggio per individuare precocemente i segni di peggioramento, sia su sistemi che poss…