Search results for "Inheritance"
showing 10 items of 160 documents
ICOOLPS 2010 and MASPEGHI 2010.
2012
International audience; At ECOOP 2010 in Maribor, Slovenia, the two workshops MASPEGHI (MechAnisms for SPEcialization, Generalization and inHerItance) and ICOOOLPS (Implementation, Compilation, Optimization of Object-Oriented Languages, Programs and Systems) were combined because both were rather small and shared common concerns, their topic areas being strongly related. Six papers had been accepted to MASPEGHI, but only five were presented because the authors of one paper could not attend the conference and workshop. Three papers had been accepted to ICOOOLPS, and all were also presented. The workshop authors were later asked to submit extended versions of their papers for possible publica…
Le limitazioni al regime di circolazione e valorizzazione delle azioni e quote, profili civilistici
2022
Il presente contributo propone l'analisi di alcuni strumenti giuridici offerti dall’autonomia privata in ambito societario, in modo da permettere all’imprenditore – in tutte le ipotesi in cui quest’ultimo intenda determinare, prima della sua morte, la successione dell’azienda di famiglia – di pianificare in modo efficace il passaggio generazionale, avvantaggiando o sfavorendo, a seconda dei casi, il trasferimento delle partecipazioni societarie, con il proposito di disinnescare i rischi di disgregazione dell’unità dell’impresa e di conflitti tra i membri della famiglia. This contribution proposes the analysis of some legal instruments offered by private autonomy in the corporate sphere, in …
Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease
2001
BACKGROUNDHirschsprung disease (HSCR) is a frequent congenital disorder with an incidence of 1 in 5000 live births, characterised by the absence of parasympathetic intramural ganglion cells in the hindgut resulting in intestinal obstruction in neonates and severe constipation in infants and adults. Intestinal neuronal dysplasia (IND) shares clinical features with HSCR but the submucosal parasympathetic plexus is affected. IND has been proposed as one of the most frequent causes of chronic constipation and is often associated with HSCR.METHODSWe examined 29 patients diagnosed with sporadic HSCR, 20 patients with IND, and 12 patients with mixed HSCR/IND for mutations in the coding regions of …
Differential Gene Expression of Medullary Thyroid Carcinoma Reveals Specific Markers Associated with Genetic Conditions
2013
Maliszewska, Agnieszka et al.
Febrile seizure and related syndromes
2018
Abstract Febrile seizures (FS) are the result of particular sensitivity to fever in the developing brain, have a major genetic predisposition, and nearly always have a benign outcome. Febrile seizures are the most common for of seizures in childhood. They have been observed in 2–6% of children before the age of 5 years, but in some populations this figure increase to 15%. Febrile seizures could be the first manifestations of epilepsy. About 13% of epileptic patients have a history of febrile seizures, and 30% have had recurrent febrile seizures Their phenotypic characteristics allow, in the majority of cases, a classification of the seizure, an elaboration of a prognosis and to assume a spe…
Plants mentioned in the Islamic Scriptures (Holy Qur'ân and Ahadith): Traditional uses and medicinal importance in contemporary times.
2019
Abstract Ethnopharmacological relevance Over the past thousand years, Islamic physicians have collected cultural, philosophical, sociological and historical backgrounds for understanding diseases and medications. The Prophet Mohammed (Peace Be Upon Him (PBUH) said: “There is no disease that Allah has created, except that Allah also has created its cure.” Therefore, Islamic scholars are encouraged to explore and use both traditional and modern forms of medicine. Aim of the study (1) To identify some of the medicinal plants mentioned in the Holy Qur'ân and Ahadith textbooks of the period 700–1500 AD; (2) to compare them with presently used traditional medicines; (3) to evaluate their value ba…
Violence and the Peasant Elite in Lower Satakunta (1550–1680)
2016
“The lengthy quarrels over inheritance hint that these people had fiery tempers”, wrote Mauno Jokipii in his pioneering article on the history of the Lavila family—one of the prominent families of freeholders in Lower Satakunta.1 In our study on the women from that same family, Virpi Nissila and I have encountered about 100 court cases from the 1620 to the 1650s, in which six women from two generations have been present. The most prominent of them is Anna Martensdotter who appeared in court 28 times in the four years for which we have the court minutes still intact. These records tell of her offensive behaviour: neighbours complaining about her physical violence, insults, appropriations, an…
Quantized Dissensus in switching networks with nodes death and duplication* *Research supported by MURST-PRIN “Robust Techniques for uncertain system…
2009
Abstract In this paper we discuss agents exchanging quantized flows to diverge one from the others according to a dissensus protocol. A Quantized Gossip algorithm is considered. Evolutions of the states during switching intervals and at switching instants and their property are described and analyzed. The modeling of switching systems describing networks where death and duplication processes occur is described. Some properties of the topology reached by the network when different rules of duplication and inheritance are implemented.
On the genetics of psoriasis
1973
To elucidate the mode of inheritance in psoriasis, Falconer's model for estimating heritability which is under the assumption of multifactorial inheritance, was applied to the data of Hellgren (1967) from Sweden. The heritability estimates were based on both manifest and potential psoriasis since a clear separation of these two categories was impossible. These estimates were 64% for parents, 60% for siblings and 52% for all first degree relatives which included the children of psoriatic cases. For second degree relatives it was 48%. None of these differences are statistically significant. The results are discussed.
Retinoblastoma: History of His Identification, Characterization and Treatment
2015
The first description of a tumor resembling retinoblastoma (RB) was provided on 1597 by Pieter Pauw, who described a malignancy invading the orbit, the temporal region, and the cranium, filled with a "substance similar to brain tissue mixed with thick blood and like crushed stone". Since then, a number of retinal tumors were described and named until the 1922 when Verhoeff called these tumors RB, a term that the American Ophthalmological Society adopted in 1926. In 1971 Knudson focused on RB, and proposed his ‘two-hit’ theory of the molecular etiology of RB. In 1986, the RB1 gene was identified and the ‘two-hit’ theory of Knudson was validated. Successively, new studies in developing retina…