17 research outputs found
Miről mesélnek a kora újkori középiskolai adatsorok? : a kassai jezsuita gimnázium anyakönyvének elektronikus feldolgozása - egy kutatási projekt első eredményei = The electronical processing of the school register of the Jesuit Grammar School in Košice - the first results of a research project
In spite of the fact that the Society of Jesus had a quasi-monopoly position in Catholic ecclesiastical secondary education in the Kingdom of Hungary and Transylvania in the 17th and 18th centuries, until recently, registers of Jesuit grammar schools have not been utilised sufficiently. As referred to in the title, the study examines the possibilities of the electronical processing of the school register of the early modern Jesuit Grammar School in Kassa (Košice, present-day: Slovakia), introducing the first results. The project has started within the confines of the subproject of the “MTA–ELTE History of Universities Research Group” as a continuation of the project called “Catholic Schooling in Hungary in the Early Modern Period: the Students of the Győr, Nagyszombat and Pozsony Jesuit Colleges”. As results of the latter project, the school registers of the Jesuit grammar schools in Győr, Pozsony (Bratislava, present-day: Slovakia) and Nagyszombat (Trnava, present-day: Slovakia) had been already processed electronically and student databases had been created, which are currently available at the Hungaricana – Hungarian Cultural Heritage Portal. The importance of these student databases, including the Kassa one, lies primarily in the potential of complex queries. Statistical data series can be produced by using of them from an essentially pre-statistical period, which could provide a sharper insight into a well-defined broad segment of society of the early modern Kingdom of Hungary. Moreover, cohort analyses based on them could contribute to revealing school studies and educational paths, providing opportunities to make inductive reasonings. Nevertheless, especially combined with other databases, hopefully those will be also useful for researchers dealing with information history, because they aid to draw higher-order conclusions through the various logical queries
A 17. század közepi hatalmi és felekezeti küzdelmek Felső-Magyarországon egy rendhagyó ingatlanügylet tükrében : A kassai királyi ház jezsuitáknak adományozása és a felső- magyarországi főkapitányi székhely áthelyezése
A tanulmány a kassai királyi ház jezsuita rend számára törtĂ©nĹ‘ eladományozásának ĂĽgyĂ©t tárgyalja, bemutatva az alternatĂv elkĂ©pzelĂ©seket, az Ă©pĂĽlet kibĹ‘vĂtĂ©sĂ©ig Ă©s átadásáig vezetĹ‘ utat, valamint az azt övezĹ‘ politikai-felekezeti alapĂş konfliktusokat. Az Ă©pĂĽlet birtokba vĂ©tele mĂ©rföldkövet jelentett az 1650-es Ă©vek elejĂ©n mĂ©g rezidencia formában működĹ‘ jezsuiták számára a nagyobb intĂ©zmĂ©nyi önállĂłságot jelentĹ‘ kollĂ©giummá alakulás Ăştján. A királyi adomány egyĂşttal a felsĹ‘-magyarországi fĹ‘kapitányi szĂ©khelynek a szakirodalomban rendre feledĂ©sbe merĂĽlĹ‘ áthelyezĂ©sĂ©t Ă©s a Bornemissza-ház e cĂ©lbĂłl valĂł megvásárlását is jelentette. | he study discusses the donation of the Royal House of Kassa to the Jesuit Order,
presenting the alternative ideas preceding it, the road to the extension and hand-
over of the building, and the political-denominational conflicts surrounding the
transaction. Taking possession of the building marked a milestone on the road to
becoming a college with greater institutional autonomy for the Jesuits, who were
still operating in residence format in the early 1650s. The royal donation also meant
the relocation of the seat of the Royal Captain-general in Upper Hungary, which is often forgotten in the literature, as well as the purchase of the Bornemissza House
for this purpose
Screening for Mutations of 21-Hydroxylase Gene in Hungarian Patients with Congenital Adrenal Hyperplasia
Congenital adrenal hyperplasia (CAH) is a group of autosomal
recessive disorders, causing impaired secretion of cortisol and
aldosterone from the adrenal cortex, with subsequent
overproduction of adrenal androgens. The most common enzyme
defect causing CAH is steroid 21-hydroxylase deficiency. To
determine the mutational spectrum in the Hungarian CAH
population, the CYP21 active gene was analyzed using PCR. A
total of 297 Hungarian patients with 21-hydroxylase deficiency
are registered in the 2nd Department of Pediatrics, Budapest,
Hungary, and their clinical status was evaluated. Blood samples
for CYP21 genotype determination could be obtained from 167
patients (representing 306 unrelated chromosomes and 56.2% of
the total group of patients). Eight of the most common mutations
were screened [In2 (intron 2 splice mutation), I172N, Del (Del:
apparents large gene conversion), Q318X, R356W, 1761Tins,
ClusterE6, V281L] using allele-specific amplification. The most
frequent mutation in the Hungarian CAH population was found to
be In2. Our results have shown a good genotype/phenotype
correlation in case of most mutations; the In2 mutation is
associated mostly with the severe form of the disease, whereas
I172N was expressed in a wide spectrum of phenotypes. 1999
Minimum power multicasting in wireless networks under probabilistic node failures
Minimum power multicasting, Probabilistic mathematical models, Multihop networks,