Search results for "NHE"
showing 10 items of 1058 documents
La violència física i econòmica contra les dones a la Mallorca del segle XVII : una aproximació
2020
Resum: En aquesta primera aproximació a la Mallorca del segle XVII, es pot veure com les dones patien diferents tipus de violència. Per una banda, la física, que era exercida tant per part de desconeguts com per part dels marits dins de l’entorn conjugal. La fugida de la maltractada era la solució més habitual i, en moltes ocasions, la disputa acaba amb divorci. per altra banda, s’ha documentat l’existència d’una violència que es pot denominar econòmica i que es basa en l’exclusió de la dona de les seves pròpies possessions, cosa que conduïa a llargs litigis per a la restitució dotal o per a reclamar una herència. Generalment, aquesta violència es donava quan les dones quedaven soles i en s…
Monozygotic twins in history: enlightenment by mythology and ethnography
2020
Abstract Birth in mankind is planned in single. The birth of twins is a rare event, occurring in about 1% of pregnancies. This chapter presents different aspects of mythology, history and ethnography for the better understanding of the meaning of twins throughout times. Twins are and will always be a source of artistic inspiration, cultural inheritance and social (re)interpretation.
Girl With Partial Turner Syndrome and Absence Epilepsy
2007
This report describes a 16-year-old girl with short stature (-5 standard deviations), normal puberty, panic attacks, absence epilepsy, some stigmata of Turner syndrome, and a Madelung deformity. Routine chromosomal analysis revealed a female karyotype with one abnormal chromosome X, with the suspicion of additional material on the short arm. With fluorescent in situ hybridization and array-multiplex amplifiable probe hybridization methodology, a complex aberration was detected, with a deletion of the distal part of Xp22.33 (including the short-stature homeobox gene) and a duplication of Xp22.32-p22.12 proximal to the deleted segment. The deletion in our patient involves the Xp22.33 region. …
Jälleenrakentamisen ajan lapsesta tulevaisuuden lapseen : suomalaisten lastenkirjojen lapsikäsitykset ja sosiologinen lapsitutkimus
1998
Espungere e interpretare: a proposito dell’esodo di Ifigenia in Aulide
2014
L’articolo mostra che l’espunzione dell’esodo di Ifigenia in Aulide, su cui concordano quasi tutti gli editori, può comportare conseguenze decisive sul piano dell’interpretazione della tragedia. Infatti, in alcuni studi recenti, basati sull’edizione Kovacs (Loeb Classical Library, London 2002), che espunge la parte finale relativa al racconto del messaggero con la sostituzione animale, la morte di Ifigenia viene considerata la vera conclusione della tragedia. Da qui è derivata un’interpretazione in chiave politica del sacrificio, secondo la quale, conclusasi negativamente la guerra con Sparta e in assenza di una valida classe dirigente, la morte di un’innocente sarebbe necessaria alla reali…
Dissensus, death and division
2009
The modeling of switching systems describing networks where death and duplication processes occur is described. A dissensus protocol, complementary to consensus protocol, is introduced and the convergence or divergence of the agents' state evolution is studied. We discuss some properties of the topology reached by the network when different rules of duplication and inheritance are implemented.
An SPM-Enriched Marine Oil Supplement Shifted Microglia Polarization toward M2, Ameliorating Retinal Degeneration in rd10 Mice
2022
Retinitis pigmentosa (RP) is the most common inherited retinal dystrophy causing progressive vision loss. It is accompanied by chronic and sustained inflammation, including M1 microglia activation. This study evaluated the effect of an essential fatty acid (EFA) supplement containing specialized pro-resolving mediators (SPMs), on retinal degeneration and microglia activation in rd10 mice, a model of RP, as well as on LPS-stimulated BV2 cells. The EFA supplement was orally administered to mice from postnatal day (P)9 to P18. At P18, the electrical activity of the retina was examined by electroretinography (ERG) and innate behavior in response to light were measured. Retinal degeneration was …
Genetic Pattern and Haemorheological Determinants in Type 1 Diabetics
2016
Factor VII deficiency: evidence that in minor surgery one-day replacement therapy is sufficient
2011
Oral Communication
2012
Inherited factor VII (FVII) deficiency is the most common of the rare autosomal recessive bleeding disorders (RBD), with an estimated prevalence of 1 per 300,000 in European countries.1,2 It is likely that the prevalence is higher in those countries where consanguineous marriages are frequent.We here report STER study results on 112 evaluable enrolled cases