1,706 research outputs found
"La materia quando inizia a soffrire": Denial Figures in Guido Morselli's Work
No full textopenIl presente lavoro si propone di indagare la questione della crisi del soggetto così come discussa dall'autore italiano Guido Morselli, nelle diverse sedi dei romanzi, della produzione saggistica e del diario personale. Da qui si analizzeranno temi quali il solipsismo e gli interrogativi esistenziali, fin dai loro primi riverberi nella filosofia centro-europea di fine Ottocento, inizio Novecento.The present work aims yo investigate the issue of the crisis of the subject, as it is discussed by the Italian author Guido Morselli, on his novels, essays and personal diary. We will also analyze topics such as solipsism and existential questions from their first reverberations on the late eighteen century and early nineteen century middle European philosophy
Adverse pregnancy outcomes in women exposed to gabapentin and pregabalin: data from a population-based study
No full textEruption delay in a 47 XXY male: a case report.
No full textThe 47,XXY syndrome, or Klinefelter syndrome, though it is a rare occurrence, it is the most common sex choromosome disorder affecting male subjects. This syndrome is underdiagnosed and seldomly before puberty. In this case, diagnosis was made before birth, through chorion villus sampling.
CASE REPORT:
A 16 month-old Italian male with 47 XXY syndrome showed the absence of primary teeth, with a delay of about 8-10 months, whereas during the first 15 months of life the auxological development has been normal both in weight and height (about 50th percentile). We assumed that this delay may be linked with Klinefelter syndrome, as sexual chromosomes play an important role in the dental development
Applicazione dell'analisi reologica allo studio della stabilità fisica di sospensioni di antibiotici
No full textIl sistema di qualificazione degli operatori economici negli appalti pubblici di lavori: possibili scenari futuri
No full textLa qualificazione negli appalti pubblici di lavori. L'organizzazione e il funzionamento del sistema SOA. Possibili scenari futuri del sistema di qualificazione
Disseminate Recurrent Folliculitis and Hidradenitis Suppurativa Are Associated Conditions: Results From a Retrospective Study of 131 Patients With Down Syndrome and a Cohort of 12,351 Pediatric Controls
No full textHidradenitis suppurativa (HS) is a chronic, inflammatory, recurrent skin disease of the pilosebaceous unit characterized by protean manifestations. Several studies have found an increased incidence and earlier presentation of this disease in patients carrying trisomy 21. Patients with Down syndrome (DS) have a higher risk of developing a wide range of cutaneous manifestations, including HS and chronic folliculitis. Recently, disseminate recurrent folliculitis (DRF) has been reported as an atypical monosymptomatic feature of HS at its onset
IMMUNOLOGICAL PATTERNS IN CHILDREN WITH DOWN SYNDROME: IS THERE A TEMPORAL TREND?
No full textDown syndrome is associated with an increased susceptibility to infections due to a deficiency of specific and nonspecific immunity.
Aim: The aim of the study was to analyze the temporal trends, if any, of some variables related tothe immunological status of children affected by Down syndrome.
Result: in the first 5 years of life, we observed a progressive decrease in the medium values of lymphocytes, CD4+ and plasma zinc levels, and an increase in CD8+, immunoglobulin A, immunoglobulin A, immunoglobulin G, immunoglobulin M and Natural killer, but generally without exceeding the interval of normality.
Conclusions: in Down syndrome children, the immune cellular status is similar to the normal population as far as white blood cell, lymphocyte, CD4+, CD8+, natural killer and immunoglobulins are concerned. Plasma level of zinc is normal from birth until 5 years but with a temporal trend of progressive reduction. This observation supports the hypothesis that a pharmacological supplementation may be necessary in Down syndrome children only after 5 years of age
Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173 109 consecutive births
No full textEpidemiological and genetic variables in limb reduction defects (LRD) were analysed during the years 1978 to 1987 in a case control study in Emilia Romagna, northern Italy. During the observation period, 83 neonates out of 173 109 consecutive
births had LRD (4-8 per 10 000). Cases were divided into five subgroups: transverse, intercalary, longitudinal, split, and multiple types of LRD. Of all cases, 64% were upper limb, 21% lower limb, and 15% both. Coexisting non-limb malformations
were found in 10 cases (12%), five with recognised syndromes and five with other associated defects.
About 7-2% of first degree relatives had defects involving the skeletal system. In two cases the mother had the same type of LRD (a split). No recurrence among sibs was observed. Risk factors correlated with LRD were found to be low birth
weight (2500 g or less), vaginal bleeding, and threatened abortion
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