Umbral Methods and Harmonic Numbers

The theory of harmonic based function is discussed here within the framework of umbral operational methods. We derive a number of results based on elementary notions relying on the properties of Gaussian integrals.Comment: 6 page

Deep Inelastic Scattering in Improved Lattice QCD. II. The second moment of structure functions

In this paper we present the 1-loop perturbative computation of the renormalization constants and mixing coefficients of the lattice quark operators of rank three whose hadronic elements enter in the determination of the second moment of Deep Inelastic Scattering (DIS) structure functions. We have employed in our calculations the nearest-neighbor improved ``clover-leaf'' lattice QCD action. The interest of using this action in Monte Carlo simulations lies in the fact that all terms which in the continuum limit are effectively of order $a$ ($a$ being the lattice spacing) have been demonstrated to be absent from on-shell hadronic lattice matrix elements. We have limited our computations to the quenched case, in which quark operators do not mix with gluon operators. We have studied the transformation properties under the hypercubic group of the operators up to the rank five (which are related to moments up to the fourth of DIS structure functions), and we discuss the choice of the operators considered in this paper together with the feasibility of lattice computations for operators of higher ranks. To perform the huge amount of calculations required for the evaluation of all the relevant Feynman diagrams, we have extensively used the symbolic manipulation languages Schoonschip and Form.Comment: 30 pages, latex + elsart + feynman (complete postscript file available upon request to [email protected]); submitted to Nuclear Physics

Prenatal screening and counseling for genetic disorders

Introduction: The carriers of the same autosomal recessive disorder are usually unaware of onset of the genetic diseases in the children even if screenings are available for many of these disorders. In this paper, we report the experience of the Prenatal Diagnosis Center of AOU Federico II and we discuss the role of the screening for beta-thalassemia (BT), cystic fibrosis (CF) and for other rare genetic disorders. Materials and Methods: We analyzed retrospectively the indication for Prenatal Diagnosis (PD) of all the couples referred to our center from January 1993 to May 2013. We divided our sample into three groups: couples at high risk for BT, for CF and for other rare genetic disorders. Results: From January 1993 to May 2013, we performed 1269 PD for genetic disorders. There are still couples who discovered to be carriers of BT by screening after the birth of the affected child (n=51 (11,3%)); the majority of the people were screened for CF carrier after the birth of an affected child (n=155 (80,7%)) or through the cascade screening (n=28 (14,6%)). Large-scale screenings for rare genetic conditions are not available and people were screened only if they have a positive familial history. Conclusion: Parental screening is available for many severe and rare diseases whose genetic origin is known. The proportion of patients referred for very high-risk indications increased over time with an higher demand for rare disease. An adequate counseling is fundamental to identify women at risk for having affected child. Screening, counseling and PD of genetic diseases is a complex matter and needs for a continuous update

Integrals of Special Functions and Umbral Methods

AbstractWe derive integrals of combination of Gauss and Bessel functions, by the use of umbral techniques. We show that the method allows the possibility of pursuing new and apparently fruitful avenues in the theory of special functions, displaying interesting links with the theory and the formalism of integral transforms

Archele, a web based acquisition, search and retrieval system

The problem of filing and storing paper and electronic documents is of great concern for public administration as well as private companies. We introduce a system that allows acquisition of images by means of one or more computer equipped with scanners, and associated with metadata for the subsequent search for and storage of data in a Document Repository protected by a system of access control lists (ACL).The system we describe here allows filing, search and retrieval of millions of documents by means of web interfaces. The architecture is fully compliant with web standards and with its design principles. The system we describe is called ArchEle (in Italian, Archiviazione Elettronica)

Novel agents for acute myeloid leukemia

Acute myeloid leukemia (AML) is a complex hematological disease characterized by genetic and clinical heterogeneity. Recent advances in the understanding of AML pathogenesis have paved the way for the development of new agents targeting specific molecules or mechanisms that contribute to finally move beyond the current standard of care, which is \u201c3 + 7\u201d regimen. In particular, new therapeutic options such as targeted therapies (midostaurin and enasidenib), monoclonal antibodies (gemtuzumab ozogamicin), and a novel liposomal formulation of cytarabine and daunorubicin (CPX-351) have been recently approved, and will be soon available for the treatment of adult patients with AML. In this review, we will present and describe these recently approved drugs as well as selected novel agents against AML that are currently under investigation, and show the most promising results as monotherapy or in combination with chemotherapy. The selection of these emerging treatments is based on the authors\u2019 opinion

Nuclear factor kB as a target for new drug development in myeloid malignancies.

The transcription nuclear factor k B (NF-kB) can intervene in oncogenesis through to its capacity to regulate the expression of a large number of genes that regulate apoptosis, cell proliferation and differentiation as well as inflammation, angiogenesis and tumor migration. Impaired NF-kB activity has been demonstrated not only in solid cancers but also in various types of hematologic malignancies including acute myeloid leukemia, chronic myelogenous leukemia and in a subset of myelodysplastic syndromes. The underlying mechanisms, illustrated in the text and although quite diverse in different diseases, provide the rationale for new therapeutic strategies combining different NF-kB or proteasome inhibitors. It has, therefore, been proposed that inhibition of NF-kB could be an adjuvant therapy for cancer and many phase I/II clinical studies are ongoing with different inhibitors. This review highlights the in vitro and in vivo results of NF-kB inhibition in myeloid malignancies

Risk of preeclampsia in of women who underwent chorionic villus sampling

OBJECTIVE: To assess the risk of preeclampsia in women who underwent chorionic villus sampling (CVS). STUDY DESIGN: This is a retrospective, single-center, cohort study. All consecutive singleton gestations who underwent chorionic villus sampling from January 2014 to January 2016 were included in the study. The primary outcome was the incidence of preeclampsia. Subgroup analysis in women with beta thalassemic trait was performed. Logistic regression, presented as adjusted odds ratio (aOR) with the 95% of confidence interval (CI), was performed. RESULTS: Five hundred forty-seven women who underwent CVS, and 1532 women who did not were analyzed. Women who underwent CVS had a significantly lower risk of preeclampsia (4.4 versus 8.0%; aOR 0.53, 95%CI 0.34-0.83), and late-onset preeclampsia (3.3 versus 6.1%; aOR 0.52, 95%CI 0.31-0.87). No statistically significant differences were found in preeclampsia with severe features, early-onset preeclampsia, and preterm birth (PTB). Women who underwent CVS due to thalassemic trait had a lower incidence of preeclampsia compare to those women who did not undergo CVS (3.3 versus 8.0%; aOR 0.39, 95%CI 0.14-0.87), while no differences were found comparing women who underwent CVS due to thalassemic trait with women who underwent CVS due to other reasons. CONCLUSIONS: Women who underwent first trimester CVS had a lower risk of preeclampsia compared to those who did not

Thrombotic microangiopathies during pregnancy : The obstetrical and neonatal perspective

Thrombotic Microangiopathies during pregnancy and puerperium are very rare and, if undiagnosed, can be lifethreating. Pregnancy and postpartum can represent a trigger in predisposed patients. Therefore, obstetricians are usually the first to observe clinical symptoms and laboratory abnormalities suggestive of Thrombotic Microangiopathies. The aim of this review is to briefly describe the obstetrical and perinatal outcome of these entities and highlight the clues for a correct diagnosis of pregnancy-related Thrombotic Microangiopathies. (C) 2019 Elsevier B.V. All rights reserved.Peer reviewe

Un client web EPP per la Regione Toscana

L\u27Istituto di Informatica e Telematica del CNR di Pisa (IIT-CNR) gestisce il Registro del country code Top Level Domain .it (Registro .it). Nel corso del 2009, il Registro .it ha attivato un nuovo sistema di registrazione, denominato "sistema sincrono", basato sul protocollo di comunicazione EPP (Extensible Provisioning Protocol). Al fine di supportare la Regione Toscana nell\u27evoluzione dei propri sistemi di gestione dei domini, conseguentemente al passaggio dal vecchio sistema asincrono al nuovo sistema sincrono, lo IIT-CNR, sulla base di una convenzione tra i due enti, ha fornito il supporto tecnico per la progettazione e realizzazione di un\u27interfaccia client web EPP che disponesse delle funzionalit? necessarie alla registrazione e al mantenimento dei nomi a dominio nel .it in modalit? sincrona. Il client web ? stato implementato con un\u27applicazione J2EE da deployare su un\u27opportuna istanza dell\u27application server JBoss