Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Erzsébet, Kövesdi"'
Autor:
Zsolt Bánfai, Erzsébet Kövesdi, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Valerián Ádám, Ferenc Pálos, Attila Miseta, Miklós Kásler, Béla Melegh
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background German-derived ethnicities are one of the largest ethnic groups in Hungary, dating back to the formation of the Kingdom of Hungary, which took place at the beginning of the 11th century. Germans arrived in Hungary in many waves. T
Externí odkaz:
https://doaj.org/article/800fd80deb8c4610a9d248e581b683f2
Autor:
Erzsébet Kövesdi, Ildikó Udvarácz, Angéla Kecskés, Szilárd Szőcs, Szidónia Farkas, Péter Faludi, Tibor Z. Jánosi, István M. Ábrahám, Gergely Kovács
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
The striatum is an essential component of the basal ganglia that is involved in motor control, action selection and motor learning. The pathophysiological changes of the striatum are present in several neurological and psychiatric disorder including
Externí odkaz:
https://doaj.org/article/9810b2a5da12446a88a02f325b8fccc2
Autor:
Klaudia Barabás, Gergely Kovács, Viola Vértes, Erzsébet Kövesdi, Péter Faludi, Ildikó Udvarácz, Dániel Pham, Dóra Reglődi, Istvan M. Abraham, Zsuzsanna Nagy
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
The hypothalamic gonadotropin-releasing hormone (GnRH)–kisspeptin neuronal network regulates fertility in all mammals. Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide isolated from the hypothalamus that is involved in t
Externí odkaz:
https://doaj.org/article/3a91c1dfb90a4b4aa4bc09e1029b9440
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 1, p 11 (2020)
Patients surviving traumatic brain injury (TBI) face numerous neurological and neuropsychological problems significantly affecting their quality of life. Extensive studies over the past decades have investigated pharmacological treatment options in d
Externí odkaz:
https://doaj.org/article/393a7c0dd4544475b186f1b178670bbb
Autor:
Zsolt Bánfai, Erzsébet Kövesdi, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Valerián Ádám, Ferenc Pálos, Attila Miseta, Miklós Kásler, Béla Melegh
Background German-derived ethnicities are one of the largest ethnic groups in Hungary, dating back to the formation of the Kingdom of Hungary, which took place at the beginning of the 11th century. Germans arrived in Hungary in many waves. The most s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf474dd1f0f2ef8ba6caf72d943d62f4
https://doi.org/10.21203/rs.3.rs-1407483/v2
https://doi.org/10.21203/rs.3.rs-1407483/v2
Autor:
Erzsébet Kövesdi, Péter Bukovics, Valérie Besson, József Nyirádi, János Lückl, József Pál, Balázs Sümegi, Tamás Dóczi, István Hernádi, András Büki
Publikováno v:
International Journal of Molecular Sciences, Vol 11, Iss 4, Pp 1253-1268 (2010)
We examined the neuro/axono-protective potential of a novel poly (ADP-ribose) polymerase (PARP) inhibitor L-2286 in a rat impact acceleration brain injury model. Male Wistar rats (n = 70) weighing 300-350 grams were used to determine the most effecti
Externí odkaz:
https://doaj.org/article/7c072eb7b4714e649f939c6347f84417
Autor:
János Sándor, Tamás Dóczi, Orsolya Farkas, József Pál, Erzsébet Kövesdi, Péter Bukovics, Endre Czeiter, András Büki
Publikováno v:
Molecules, Vol 14, Iss 12, Pp 5115-5123 (2009)
Calcium-induced, calpain-mediated proteolysis (CMSP) has recently been implicated to the pathogenesis of diffuse (traumatic) axonal injury (TAI). Some studies suggested that subaxolemmal CMSP may contribute to axolemmal permeability (AP) alterations
Externí odkaz:
https://doaj.org/article/2d9bfa5825c54a57b9948cd73c116b87
Autor:
Ágnes, Till, Renáta, Szalai, Márta, Hegyi, Erzsébet, Kövesdi, Gergely, Büki, Kinga, Hadzsiev, Béla, Melegh
Publikováno v:
Orvosi hetilap. 160(21)
The advances in molecular genetic methods has lead to the discovery of the genetic alterations that underlie the etiology of most diseases previously held to be idiopathic. Targeted genetic examination of a pediatric male patient showing a normal int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aee86bd22af7d951285cefbf1c149eeb
https://pubmed.ncbi.nlm.nih.gov/31104500
https://pubmed.ncbi.nlm.nih.gov/31104500
Autor:
Erzsébet, Kövesdi, Judit, Bene, Nikoletta, Nagy, Ágnes, Horváth, Béla, Melegh, Kinga, Hadzsiev
Publikováno v:
Orvosi hetilap. 158(30)
Tuberous sclerosis complex is a rare disease with high phenotypic heterogeneity, characterized by the appearance of multiplex hamartomas in the different organs. The disease is inherited by autosomal dominant manner, due to the mutations of two genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b7dce17613aeb7bf83149e8f7c748f0
https://pubmed.ncbi.nlm.nih.gov/28737457
https://pubmed.ncbi.nlm.nih.gov/28737457
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