Zobrazeno 1 - 7
of 7
pro vyhledávání: '"LIVIA, VIDA"'
Publikováno v:
Otolaryngology Case Reports, Vol 17, Iss , Pp 100243- (2020)
Tracheal agenesis – failure of trachea development - is an extremely rare and severe congenital disorder involving the respiratory system and in most cases it is associated with other abnormalities. Three anatomic types of tracheal agenesis were de
Externí odkaz:
https://doaj.org/article/ffc482bf480f41009ddd3bb8515c80ba
Publikováno v:
Magyar Onkologia; 2023, Vol. 67 Issue 4, p304-313, 10p
Autor:
Alexandra Csenkey, Emma Hargitai, Eszter Pakai, Bela Kajtar, Livia Vida, Aba Lorincz, Marin Gergics, Peter Vajda, Gergo Jozsa, Andras Garami
Publikováno v:
Injury. 53(12)
There are several options available for conservative treatment of partial-thickness burns, however, reliable, affordable, and easily obtainable animal testing models are hard to find for the comparison of the different treatment methods. We aimed at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d509f1aed3185069953923ad9f84274
https://pubmed.ncbi.nlm.nih.gov/36216616
https://pubmed.ncbi.nlm.nih.gov/36216616
Autor:
László Kereskai, Gábor Ottóffy, Livia Vida, Orsolya Tóth, Erzsébet Sziládi, Árpád Szomor, Béla Kajtár
Publikováno v:
Hematológia−Transzfuziológia. 51:151-158
Absztrakt: Bevezetes: A primer csontlimfomak rendkivul ritka entitasok, melyek patogeneziset illetően az alacsony esetszam miatt meg mindig keves informacio all rendelkezesunkre. A primer csontlimf...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1781340fef46596e5e80c7c43309a0a3
https://doi.org/10.1556/2068.2018.51.3.6
https://doi.org/10.1556/2068.2018.51.3.6
Autor:
Béla Kajtár, Barnabás Rózsai, Zoltán Nyul, Beáta Tóth, Gábor Ottóffy, József Stankovics, Livia Vida
Publikováno v:
Hematológia−Transzfuziológia. 51:86-91
Absztrakt: Az X kromoszomahoz kotott limfoproliferativ betegseg (XLP) ritka immundeficienciaval jaro szindroma, melyet az SH2D1A gen mutacioja okoz. A betegseget az Epstein–Barr-virusfertőzes aktiv...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abf06ab089a15b4799682dc3dd0cf6f4
https://doi.org/10.1556/2068.2018.51.2.6
https://doi.org/10.1556/2068.2018.51.2.6
Publikováno v:
Otolaryngology Case Reports, Vol 17, Iss, Pp 100243-(2020)
Tracheal agenesis – failure of trachea development - is an extremely rare and severe congenital disorder involving the respiratory system and in most cases it is associated with other abnormalities. Three anatomic types of tracheal agenesis were de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8803c65901dee5f0ad923330459ddd8b
https://doi.org/10.1016/j.xocr.2020.100243
https://doi.org/10.1016/j.xocr.2020.100243
Autor:
Csaba Bödör, Lilla Reiniger, Tamás Masszi, Judit Csomor, Tibor Krenács, András Matolcsy, Ambrus Gángó, Botond Timár, Judit Demeter, Hussain Alizadeh, Réka Mózes, Júlia Gaál-Weisinger, Adrienn Sulák, Béla Kajtár, Livia Vida
Publikováno v:
Pathology. 51(3)
Mutations of the multifunctional protein calreticulin (CALR) are recognised as one of the main driver alterations involved in the pathogenesis of Philadelphia negative myeloproliferative neoplasms (Ph- MPN) and also represent a major diagnostic crite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16028cb99b4794fac22b5dff1e1dd43f
https://pubmed.ncbi.nlm.nih.gov/30606612
https://pubmed.ncbi.nlm.nih.gov/30606612