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1.
Rev Med Liege ; 76(9): 656-660, 2021 Sep.
Article in French | MEDLINE | ID: mdl-34477335

ABSTRACT

In order to limit the spread of the COVID-19 infection, the Belgian authorities established a lockdown from the 18th of March to the 3rd of May 2020. To our knowledge, an analysis of the effect of the lockdown on the Emergency Department attendance by patients with non-urgent pathologies has not been realized yet. We reviewed the files of patients who presented to the Emergency Department of the Brugmann Hospital in Bruxelles during the lockdown period with affections that were evaluated at 4-5 according to the Manchester Triage System (MTS). We then calculated the proportion of these passages with respect to the total passages to the Emergency Department, and subsequently compared the results with the data referring to the same period in the previous year (from 18/03/2019 to 03/05/2019). The results show a clear decrease in the Emergency Department attendance by patients with non-urgent affections during the 2020 lockdown period.


Afin de limiter la dissémination de la COVID-19, un confinement a été instauré par les autorités Belges du 18 mars au 3 mai 2020. Les conséquences du confinement sur le nombre d'admissions aux Urgences, en général, et sur les différents types d'urgences, en particulier, n'ont pas, à notre connaissance, été étudiées. Nous avons revu les dossiers des patients qui se sont présentés au Service des Urgences de l'Hôpital Brugmann à Bruxelles pendant cette période, et qui ont été triés 4 ou 5 selon le «Manchester Triage System¼ (MTS). On a ensuite comparé la proportion de ces passages au nombre total d'inscriptions. Ces données ont ensuite été confrontées à la même période, mais sur l'année 2019 (du 18/03/2019 au 03/05/2019). Durant le confinement, nous avons observé une nette diminution des passages de patients avec des pathologies moins urgentes.


Subject(s)
COVID-19 , Communicable Disease Control , Emergency Service, Hospital , Hospitals , Humans , SARS-CoV-2
2.
J Prev Med Hyg ; 59(1): E1-E7, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29938233

ABSTRACT

The influenza viruses have the ability to agglutinate erythrocytes by binding to sialic acid receptors on the host cell. Human influenza viruses preferentially bind to sialic acid linked to galactose by α 2.6 linkage, while avian influenza viruses preferentially bind to sialic acid linked to Gal by α 2.3 linkage. There is a close correlation between the ability of influenza A viruses to agglutinate erythrocytes from different animal species and their receptor specificity. The haemagglutination and haemagglutination inhibition assays are influenced by the species of erythrocytes. To provide an overview of the expression of sialic acid receptors on different erythrocytes, avian (turkey, chicken, pigeon) and mammalian (sheep, horse, human) species have been analysed by flow cytometry. Chicken, turkey and human erythrocytes display both types of linkages. Horse and sheep erythrocytes show almost exclusively α 2.3 Gal linkages, while pigeon erythrocytes express almost exclusively α 2.6 Gal linkages. The erythrocytes from the same avian and mammalian species have been evaluated by haemagglutination and haemagglutination inhibition assays with seasonal and avian strains. Chicken and turkey erythrocytes seem to be the most appropriate for both assays with seasonal influenza strains, in addition to pigeon erythrocytes, particularly for the B strains. In the case of the avian strain, chicken erythrocytes are suitable for haemagglutination assay and horse erythrocytes for haemagglutination inhibition assay. The choice of erythrocytes has a significant impact on the titres measured by both assays.


Subject(s)
Erythrocytes/virology , Influenza A virus/metabolism , Receptors, Cell Surface/metabolism , Animals , Birds , Hemagglutination Inhibition Tests/methods , Horses , Humans , Influenza in Birds , Influenza, Human , Sheep
3.
Neuromuscul Disord ; 28(2): 122-128, 2018 02.
Article in English | MEDLINE | ID: mdl-29305139

ABSTRACT

The aim of our prospective observational study was to assess profiles of cognitive function and a possible impairment of executive functions in a cohort of boys with Duchenne muscular dystrophy without intellectual and behavior disability. Forty Duchenne boys (range of age: 6 years to 11 years and 6 months) were assessed by Wechsler Intelligence scale and battery of tests including tasks assessing working memory and executive functions (inhibition and switching, problem solving and planning). In our cohort some aspects of cognitive function were often impaired. These included multitasking, problem solving, inhibition and working memory necessary to plan and direct goal oriented behavior. Our results support the suggestion that aspects of cognitive function could be impaired even in boys without intellectual disability and support the hypothesis that executive functions may play an important role in specific aspects of cognitive impairment in Duchenne muscular dystrophy.


Subject(s)
Cognition , Executive Function , Muscular Dystrophy, Duchenne/psychology , Child , Humans , Intelligence , Male , Memory, Short-Term , Neuropsychological Tests , Prospective Studies
4.
Genes Brain Behav ; 16(6): 627-634, 2017 07.
Article in English | MEDLINE | ID: mdl-28378436

ABSTRACT

Ventral and dorsal streams are visual pathways deputed to transmit information from the photoreceptors of the retina to the lateral geniculate nucleus and then to the primary visual cortex (V1). Several studies investigated whether one pathway is more vulnerable than the other during development, and whether these streams develop at different rates. The results are still discordant. The aim of the present study was to understand the functionality of the dorsal and the ventral streams in two populations affected by different genetic disorders, Noonan syndrome (NS) and 22q11.2 deletion syndrome (22q11.2DS), and explore the possible genotype-phenotype relationships. 'Form coherence' abilities for the ventral stream and 'motion coherence' abilities for the dorsal stream were evaluated in 19 participants with NS and 20 participants with 22q11.2DS. Collected data were compared with 55 age-matched controls. Participants with NS and 22q11.2DS did not differ in the form coherence task, and their performance was significantly lower than that of controls. However, in the motion coherence task, the group with NS and controls did not differ, and both obtained significantly higher scores than the group with 22q11.2DS. Our findings indicate that deficits in the dorsal stream are related to the specific genotype, and that in our syndromic groups the ventral stream is more vulnerable than the dorsal stream.


Subject(s)
22q11 Deletion Syndrome/physiopathology , Noonan Syndrome/physiopathology , Visual Perception , Brain/physiopathology , Child , Female , Humans , Male
5.
Clin Genet ; 91(1): 86-91, 2017 01.
Article in English | MEDLINE | ID: mdl-27062503

ABSTRACT

Congenital ataxias are nonprogressive neurological disorders characterized by neonatal hypotonia, developmental delay and ataxia, variably associated with intellectual disability and other neurological or extraneurological features. We performed trio-based whole-exome sequencing of 12 families with congenital cerebellar and/or vermis atrophy in parallel with targeted next-generation sequencing of known ataxia genes (CACNA1A, ITPR1, KCNC3, ATP2B3 and GRM1) in 12 additional patients with a similar phenotype. Novel pathological mutations of ITPR1 (inositol 1,4,5-trisphosphate receptor, type 1) were found in seven patients from four families (4/24, ∼16.8%) all localized in the IRBIT (inositol triphosphate receptor binding protein) domain which plays an essential role in the regulation of neuronal plasticity and development. Our study expands the mutational spectrum of ITPR1-related congenital ataxia and indicates that ITPR1 gene screening should be implemented in this subgroup of ataxias.


Subject(s)
Genetic Predisposition to Disease/genetics , Inositol 1,4,5-Trisphosphate Receptors/genetics , Mutation , Spinocerebellar Ataxias/genetics , Adult , Amino Acid Sequence , Binding Sites/genetics , Child , Exome/genetics , Family Health , Female , Humans , Lectins, C-Type/metabolism , Male , Membrane Proteins/metabolism , Middle Aged , Pedigree , Sequence Analysis, DNA/methods , Sequence Homology, Amino Acid , Young Adult
6.
J Prev Med Hyg ; 56(2): E51-6, 2015 Aug 05.
Article in English | MEDLINE | ID: mdl-26789988

ABSTRACT

INTRODUCTION: Vaccines and antiviral drugs are the most widely used methods of preventing or treating Influenza virus infection. The role of sea buckthorn (SBT) bud dry extract as a natural antiviral drug against Influenza was investigated. METHODS: Influenza virus was cultured in the MDCK cell line, with or without SBT bud extract, and virus growth was assessed by HA and TCID50 virus titration in terms of cytopathic effect on cells. Several concentrations of extract were tested, the virus titer being measured on day 4 after infection. RESULTS: After infection, the virus titer in the control sample was calculated to be 2.5 TCID50/ml; treatment with SBT bud extract reduced the virus titer to 2.0 TCID50/ml at 50 µg/ml, while the HA titer was reduced from 1431 (control) to 178. Concentrations lower than 50µg/ml displayed an inhibitory effect in the HA assay, but not in the TCID50 virus titration; however, observation of the viral cultures confirmed a slowdown of viral growth at all concentrations. DISCUSSION: Natural dietary supplements and phytotherapy are a growing market and offer new opportunities for the treatment of several diseases and disorders. These preliminary experiments are the first to show that SBT bud extract is able to reduce the growth of the Influenza A H1N1 virus in vitro at a concentration of 50 µg/ml. This discovery opens up the possibility of using SBT bud extract as a valid weapon against Influenza and, in addition, as the starting-point for the discovery of new drugs.

7.
G Ital Med Lav Ergon ; 29(3 Suppl): 313-5, 2007.
Article in Italian | MEDLINE | ID: mdl-18409702

ABSTRACT

The percentage of bladder cancer as occupational disease in West-Europe is of 5/10%, but only a few amount of them are recognized as occupational disease from INAIL. The above mentioned research project is realized in order to decrease the gap between expected and claimed cases of occupational disease and it is conducted with the collaboration of ASL of Pisa, ASL of Empoli, Azienda Ospedaliera Universitaria Pisana and INAIL. 677 patients with bladder cancer were interviewed by phone, among them 64 subjects had a working experience compatible with neoplastic risks because had a previous occupational exposure to aromatic amines and metal working fluids. These cases were discussed into a Medical Staff and 40 cases were considered "probable" for occupational disease, 18 "possible", 3 cases are suspended for more research, 3 cases are considered "no professional disease". The research allows finding out a great number of bladder cancer, increasing the total amount of workers with occupational disease. The integrated approach with the collaboration among different institutions is surely the best way to allow and guarantee a suitable and right protection of workers with occupational disease.


Subject(s)
Occupational Diseases/epidemiology , Urinary Bladder Neoplasms/epidemiology , Female , Humans , Italy/epidemiology , Male , Middle Aged , Population Surveillance
8.
Minerva Urol Nefrol ; 53(2): 57-9, 2001 Jun.
Article in Italian | MEDLINE | ID: mdl-11455311

ABSTRACT

BACKGROUND: Elevated serum levels of homocysteine have increasingly been associated as a risk factor of cardiovascular disease. Recent reports demonstrated that supplements of folates, vitamin B12 (B12) and vitamin B6 (B6) are effective in correcting serum Hcy levels in hemodialysed patients. AIM: to assess the effectiveness of oral supplements of folates, B12 and B6, in order to reduce serum Hcy levels in our cohort of hemodialysed patients. METHODS: Sixty-one hemodialysed patients have been enrolled in the study (age 68+/-13 years; hemodialysis 62+/-42 months). Oral supplements of calcium folinate (30 mg 3 times a week), B12 (500 mg 3 times a week) and B6 (200 mg 3 times a week) were administered at the end of each hemodialysis session. Serum levels of Hcy, folic acid and B12 were tested at the beginning of the study and at 2 month intervals. RESULTS: After 5 months of follow-up, serum levels of Hcy were normalised in 19% of our patients and in total 70% of them showed a reduction >8% when compared with the basal Hcy levels. No side effects related to folates, B12 or B6 supplementation were observed. CONCLUSIONS: Oral supplements of folates, B12 and B6 are a safe and effective treatment of hyperhomocysteinemia in hemodialysed patients.


Subject(s)
Dietary Supplements , Folic Acid/administration & dosage , Renal Dialysis , Vitamin B 12/administration & dosage , Vitamin B 6/administration & dosage , Administration, Oral , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Humans , Male , Middle Aged , Time Factors
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