Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Petra Mátyás"'
Autor:
Petra Mátyás-Rausch
Publikováno v:
Historical Studies on Central Europe, Vol 4, Iss 1 (2024)
In the summer of 1604, the Transylvanian Council of Government, which had been formed shortly before, submitted a longer report to King Rudolf I of Hungary. They reported on the administration and financial situation of the newly pacified province of
Externí odkaz:
https://doaj.org/article/fa5aedd29f2e42b494ffddf2f840c4a6
Autor:
Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga, Petra Mátyás, Andrej Ficek, Miloslava Hučková, Martina Sůrová, Dana Šafka-Brožková, Saima Anwar, Judit Bene, Slavomír Straka, Ingrid Janicsek, Zubair M Ahmed, Pavel Seeman, Béla Melegh, Milan Profant, Iwar Klimeš, Saima Riazuddin, Ľudevít Kádasi, Daniela Gašperíková
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124232 (2015)
In the present study we aimed: 1) To establish the prevalence and clinical impact of DFNB49 mutations in deaf Roma from 2 Central European countries (Slovakia and Hungary), and 2) to analyze a possible common origin of the c.1331+2T>C mutation among
Externí odkaz:
https://doaj.org/article/2211c17f1c124b1f8927900caae4f350
Autor:
Petra Mátyás-Rausch
Publikováno v:
Erdélyi Múzeum. 84:61-71
Ez a cikk egy kincstári tisztviselő - Deli Farkas - motivációit kutatja, hogy saját jobbágya örökbefogadja. Ezt még a Lázár Mihályhoz hasonló jobbágyok esetében is számos ok indokolhatta, például ásványkincsbirtokai, az a törvén
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac43b089bb4139fcb9fbea2150ba81f8
https://doi.org/10.36373/em-2022-1-6
https://doi.org/10.36373/em-2022-1-6
Autor:
Petra Mátyás-Rausch
Publikováno v:
Erdélyi Múzeum. 83:41-53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24834ace336c4a30e073cf208d7c1b12
https://doi.org/10.36373/em-2021-1-4
https://doi.org/10.36373/em-2021-1-4
Autor:
Petra Mátyás-Rausch
Publikováno v:
Certamen. 3:271-282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a066c752c64877ce0a525c03612e66a4
https://doi.org/10.51384/cert-03.23
https://doi.org/10.51384/cert-03.23
Autor:
Anett, Fekete, Kinga, Hadzsiev, Judit, Bene, Antónia, Nászai, Petra, Mátyás, Ágnes, Till, Béla, Melegh
Publikováno v:
Orvosi hetilap. 158(12)
This article presents the case of a 62-year-old mother and her 41-year-old daughter, who have had severe neurological symptoms for a few decades. After a long investigation period the definite diagnosis of MERRF syndrome was confirmed. After DNA isol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcad059bc697c4b23a0b9fc88325490e
https://pubmed.ncbi.nlm.nih.gov/28328248
https://pubmed.ncbi.nlm.nih.gov/28328248
Autor:
Judit, Bene, Kinga, Hadzsiev, Katalin, Komlósi, Erzsébet, Kövesdi, Petra, Mátyás, Béla, Melegh
Publikováno v:
Orvosi hetilap. 156(49)
Severe myoclonic epilepsy in infancy (Dravet's syndrome) is a very rare form of epilepsy. Mutations of SCN1A gene encoding voltage-gated sodium channel alpha-1 subunit are major causes of the autosomal dominant disorder. Most cases are associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d148575c1b06b8b0f15ea045d61a3b28
https://pubmed.ncbi.nlm.nih.gov/26614543
https://pubmed.ncbi.nlm.nih.gov/26614543