Software-Defined-Networking-Based One-versus-Rest Strategy for Detecting and Mitigating Distributed Denial-of-Service Attacks in Smart Home Internet of Things Devices.

The number of connected devices or Internet of Things (IoT) devices has rapidly increased. According to the latest available statistics, in 2023, there were approximately 17.2 billion connected IoT devices; this is expected to reach 25.

Radiolysis performance of ibuprofen using ionizing processes: kinetics and energy consumption.

Ionizing technologies are used for disinfection and treatment of different industrial wastewaters. For this purpose, the radiolytic degradation of ibuprofen (IBP), selected within the main detected pharmaceuticals in different water locations with different concentrations, was investigated. Irradiation was performed with a gamma irradiator (Co) and with electron beam accelerator.

Current vaccine technology with an emphasis on recombinant measles virus as a new perspective for vaccination against SARS-CoV-2.

The novel coronavirus disease 2019 (COVID-19) that emerged in China has spread to more than 212 countries to date. COVID-19 can cause serious acute respiratory syndrome (SARS). Therefore, research advances on the associated SARS-coronavirus-2 (CoV-2) may enable the scientific community to establish effective vaccines to prevent SARS-CoV-2 infections by increasing understanding of viral pathogenesis.

Unexpected infant death secondary to a pulmonary infiltration due to acute myelocytic leukaemia.

Acute myeloid leukaemia (AML) often presents with non-specific symptoms such as fatigue, anaemia or infection. Pulmonary involvement is uncommon in AML during the course of the disease and is usually caused by infection, haemorrhage, leukaemic pulmonary infiltrates and leukostasis. Lung localization of AML is very uncommon and potentially life threatening if not diagnosed and treated rapidly.

Efficient heterologous expression, functional characterization and molecular modeling of annular seabream digestive phospholipase A.

Here we report the cDNA cloning of a phospholipase A (PLA) from five Sparidae species. The deduced amino acid sequences show high similarity with pancreatic PLA. In addition, a phylogenetic tree derived from alignment of various available sequences revealed that Sparidae PLA are closer to avian PLA group IB than to mammals' ones.

Fast multiple sclerosis progression in North Africans: Both genetics and environment matter.

Objective: To compare multiple sclerosis (MS) disability progression among North Africans (NAs) living in France (NAF) and in Tunisia (NAT) and Caucasian patients born and living in France (CF).

Methods: Patients with MS admitted to the day hospital in the Neurology Department at Pitié-Salpêtrière Hospital (France) and Razi Hospital (Tunisia) were questioned on their place of birth and the place of birth of their parents. To compare delay to outcomes, log-rank tests were used.

Two cases of sudden death due to pulmonary tumor thrombotic microangiopathy caused by occult gastric carcinoma.

We present two cases of occult gastric carcinoma associated to a large pulmonary tumors thrombosis microangiopathy (PTTM). The first case is a 28 years-old man. He was dead due to a respiratory failure.

Evaluation of an Arabic version of the non-motor symptoms scale in Parkinson's disease.

Non-motor symptoms (NMS) of Parkinson Disease (PD) are common and can cause severe disability. They are often under-recognized and remain untreated. Tools to evaluate these symptoms in Arabic-speaking patients are still lacking.

Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.

The aim of this study is to investigate the genetic basis of autosomal recessive congenital cataract and intellectual disability phenotype in a consanguineous Tunisian family. The whole genome scan of the studied family was performed with single nucleotide polymorphisms (SNPs). The resulted runs of homozygosity (ROH) were analyzed through the integrated Systems Tool for Eye gene discovery (iSyTE) in order to prioritize candidate genes associated with congenital cataract.

Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.

Background: To identify the genetic defect associated with autosomal recessive congenital cataract (ARCC), mental retardation (MR) and ARCC, MR and microcephaly present in most patients in four Tunisian consanguineous families.

Methods: We screened four genes implicated in congenital cataract by direct sequencing in two groups of patients; those affected by ARCC associated to MR and those who presented also microcephaly. Among its three genes PAX6, PITX3 and HSF4 are expressed in human brain and one gene LIM2 encodes for the protein MP20 that interact with the protein galectin-3 expressed in human brain and plays a crucial role in its development.