763 research outputs found

    The Economic Valuation of Ecosystem Services of Biodiversity Components in Protected Areas: A Review for a Framework of Analysis for the Gargano National Park

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    Protected areas play an important role in the conservation and protection of biodiversity of particular territories, especially of ecosystems that provide resources for living organisms, including human beings. Different studies highlight the importance of biodiversity and its associated benefits in terms of ecosystem services of protected areas. The economic assessment of ecosystem services and biodiversity becomes a viable solution to help the policy maker to make decisions on the environmental preservation of these areas according to the Agenda 2030 for Sustainable Development. Nonetheless, very few studies provide an economic evaluation of the benefits of protected areas. To advance the current debate on the economic evaluation of the benefits provided by protected areas, the present paper purposes an integrated approach. It presents an overview of main ecosystem services’ mapping techniques currently available to researchers and policy makers and offers a systematic review carried out for the period 2015–2020 at an international level. The main findings are particularly attractive for the Gargano National Park (GNP) in the south of Italy, which is recognised as being a biodiversity hot spot at global level. The current study provides useful guidance for the assessment of trade-offs, the support to policy makers, and the provision of efficient allocation of public resources for protected area

    the choice of the iodinated radiographic contrast media to prevent contrast induced nephropathy

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    In patients with preexisting renal impairment, particularly those who are diabetic, the iodinated radiographic contrast media may cause contrast-induced nephropathy (CIN) or contrast-induced acute kidney injury (CI-AKI), that is, an acute renal failure (ARF), usually nonoliguric and asymptomatic, occurring 24 to 72 hours after their intravascular injection in the absence of an alternative aetiology. Radiographic contrast media have different osmolalities and viscosities. They have also a different nephrotoxicity. In order to prevent CIN, the least nephrotoxic contrast media should be chosen, at the lowest dosage possible. Other prevention measures should include discontinuation of potentially nephrotoxic drugs, adequate hydration with i.v. infusion of either normal saline or bicarbonate solution, and eventually use of antioxidants, such as N-acetylcysteine, and statins

    Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease.

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    BACKGROUND: We present the case of a white 35-year-old male with a diagnosis of Fabry disease and negative family history. CASE PRESENTATION: At the age of 31, he underwent a renal biopsy with a diagnosis of hypertension-induced nephroangiosclerosis. At the age of 35, he was referred to our hospital and started dialysis: the unusual finding of left ventricular hypertrophy with a normal ejection fraction and of myocardial fibrosis at the cardiac magnetic resonance suggested a diagnosis of Fabry disease, although there was no apparent family history—so extensive tests were subsequently undertaken. The patient had low plasma levels of α-galactosidase A and the genetic analysis showed a single nucleotide point mutation in hemizygosis at nucleotide c.901 C>T in exon 6 of the GLA gene, confirming the diagnosis of Fabry disease. We extended the genetic analysis to all family members of the patient (mother, sister and brothers) and none of them had any alteration in the GLA gene, suggesting a de novo mutation in the patient. CONCLUSIONS: In a family, it is rare to find only one Fabry disease affected subject with a de novo mutation. These findings emphasize the importance of early diagnosis, genetic counseling and studying the genealogical tree of suspicious patients, even in absence of a typical family history

    A rational approach to elucidate human monoamine oxidase molecular selectivity

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    Designing highly selective human monoamine oxidase (hMAO) inhibitors is a challenging goal on the road to a more effective treatment of depression and anxiety (inhibition of hMAO-A isoform) as well as neurodegenerative diseases (inhibition of hMAO-B isoform). To uncover the molecular rationale of hMAOs selectivity, two recently prepared 2H-chromene-2-ones, namely compounds 1 and 2, were herein chosen as molecular probes being highly selective toward hMAO-A and hMAO-B, respectively. We performed molecular dynamics (MD) studies on four different complexes, cross-simulating one at a time the two hMAO-isoforms (dimer embedded in a lipid bilayer) with the two considered probes. Our comparative analysis on the obtained 100 ns trajectories discloses a stable H-bond interaction between 1 and Gln215 as crucial for ligand selectivity toward hMAO-A whereas a water-mediated interaction might explain the observed hMAO-B selectivity of compound 2. Such hypotheses are further supported by binding free energy calculations carried out applying the molecular mechanics generalized Born surface area (MM-GBSA) method and allowing us to evaluate the contribution of each residue to the observed isoform selectivity. Taken as whole, this study represents the first attempt to explain at molecular level hMAO isoform selectivity and a valuable yardstick for better addressing the design of new and highly selective MAO inhibitors

    Mathematical aspects relative to the fluid statics of a self-gravitating perfect-gas isothermal sphere

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    In the present paper we analyze and discuss some mathematical aspects of the fluid-static configurations of a self-gravitating perfect gas enclosed in a spherical solid shell. The mathematical model we consider is based on the well-known Lane-Emden equation, albeit under boundary conditions that differ from those usually assumed in the astrophysical literature. The existence of multiple solutions requires particular attention in devising appropriate numerical schemes apt to deal with and catch the solution multiplicity as efficiently and accurately as possible. In sequence, we describe some analytical properties of the model, the two algorithms used to obtain numerical solutions, and the numerical results for two selected cases.Comment: Revision accepted for publication in "Communications in Computational Physics"; 23 pages, 9 figure

    Embryological considerations on a case of coexistence of persistent left superior vena cava and partially left inferior vena cava

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    The persistent left superior vena cava (PLSVC) is the most common venous thoracic congenital anomaly. The PLSCV generally drains into the right atrium, which it reaches through a dilated coronary sinus. Its presence is usually unrecognized, until a venous approach is performed. Abnormalities of the inferior vena cava (IVC) are rare (0.2-0.3% of healthy subjects and 0.6-2% of patients with cardiovascular defects). A single left IVC (LIVC) is very rare (11.9% of all the abnormalities) [1]. To the best of our knowledge, the coexistence of PLSCV and LICV has not been previously described. We present a case of a 32-year-old woman on hemodialysis for more than 12 years. An angiography demonstrated both a normal right SVC and a PLSCV and a single IVC with a lower left course, an intermediate circumaortic ring and an upper normal right course. The double SVC can be consequent to the failed development of the anastomosis between the anterior cardinal veins and the patency of the caudal part of the left anterior cardinal vein forming the PLSCV. As to the partially LIVC, its iliac and subrenal parts can be the results of the persistence of the left supracardinal vein. The circumaortic venous ring might indicate that a persistent intersupracardinal anastomosis receiving the left and the right renal veins was maintained around the abdominal aorta [2], while the superior part represents the normal right subcardinal and hepatic derivatives. The existence of anomalies should be considered, as they can have important implications in invasive procedures such as venous catheter placement, and may represent a speculative bridge between clinicians and embryologists

    The Role of Quantic Molecular Resonance (QMR) in the Treatment of Inferior Turbinate Hypertrophy (ITH): Our Experience With Long-Term Follow-Up in Allergic and Nonallergic Rhinitis Refractory to Medical Therapy. Preliminary Results.

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    Objective: The aim of this study was to assess the long-term effectiveness of quantic molecular resonance (QMR) in the treatment of inferior turbinate hypertrophy (ITH) in allergic and nonallergic rhinitis refractory to medical therapy. Methods: This study enrolled 281 patients, 160 males (56.9%) and 121 females (43.1%), mean age 37.8 ± 4.1 years, range 18 to 71. Fifty-four patients have been lost to follow up and have been therefore excluded from the final analysis. Based on skin prick test results, 69 patients were considered allergic (group A) and 158 nonallergic (group B). All subjects underwent before surgery (T0) and 3 (T1), 12 (T2), 24 (T3), and 36 months (T4) after QMR treatment to: 4-phase rhinomanometric examination, nasal endoscopy evaluation, and visual analogue scale to quantify the subjective feelings about nasal obstruction. Results: Subjective and objective parameters showed statistically significant improvement in both groups. Group B parameters not changed during follow-up, while group A showed significant worsening between T1 and subsequent assessments. T4 outcome indicates a better result in nonallergic patients. Conclusions: In accordance with the literature, our preliminary data validate QMR treatment as a successful therapeutic option for nasal obstruction due to ITH. Nonallergic patients had a very good T4 outcome. Allergic patients showed a worsening trend after 1 year probably due to other causes
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