Zobrazeno 1 - 10
of 151
pro vyhledávání: '"Eberlinc, A."'
Autor:
Jakob Sajovic, Gorazd Drevenšek, Alja Plut, Andreja Eberlinc, Manca Kosmač Vrabec, Anina Setnikar Lesjak, Polona Selič Zupančič, Martina Drevenšek
Publikováno v:
iScience, Vol 27, Iss 9, Pp 110738- (2024)
Summary: Orofacial clefts are the most common congenital anomaly of the face, and they significantly affect appearance. The combined effects of demographics, psychology, neurophysiology, and cleft characteristics to explain satisfaction with appearan
Externí odkaz:
https://doaj.org/article/6b395f21a2554e4d890d52f028bef98b
Autor:
Sajovic, Jakob, Drevenšek, Gorazd, Plut, Alja, Eberlinc, Andreja, Kosmač Vrabec, Manca, Setnikar Lesjak, Anina, Selič Zupančič, Polona, Drevenšek, Martina
Publikováno v:
In iScience 20 September 2024 27(9)
Autor:
Sajovic, Jakob, Setnikar Lesjak, Anina, Plut, Alja, Eberlinc, Andreja, Primožič, Jasmina, Drevenšek, Eva, Drevenšek, Martina
Publikováno v:
In Journal of Stomatology oral and Maxillofacial Surgery February 2023 124(1) Supplement
Publikováno v:
Zdravniški Vestnik, Vol 91, Iss 3-4, Pp 141-149 (2022)
Pierre Robinova sekvenca je triada, ki jo sestavljajo mikro- in/ali retrognatija, glosoptoza in zapora zgornjih dihal, ki se ji v 90 % pridruži palatoshiza. Pri otrocih s Pierre Robinovo sekvenco sta glavni funkcionalni težavi obstrukcija zgornjih
Externí odkaz:
https://doaj.org/article/d53b1a578b7244028b4679060c16ccf6
Publikováno v:
Slovenska pediatrija, Vol 28, Iss 2, Pp 67-77 (2021)
Izhodišče. Kraniosinostoze so redke prirojene bolezni lobanje, ki nastanejo ob prezgodnji zakostenitvi enega ali več lobanjskih šivov. Ker možgani ne morejo več prosto rasti, pride do deformacij lobanje, ki lahko dolgoročno povzročijo znotraj
Externí odkaz:
https://doaj.org/article/f8fb82f0f5aa49948dbbe3ba94cc40d4
Publikováno v:
Slovenska pediatrija, Vol 28, Iss 2, Pp 67-77 (2021)
Background. Craniosynostosis is a group of rare congeni-tal diseases of the skull. They arise from premature ossification of one or more cranial sutures. This represents an obstruction to normal brain growth and leads to specific deformations of th
Externí odkaz:
https://doaj.org/article/bd92e872ecdd49a2921149ca18b54c81
Autor:
Lara Slavec, Ksenija Geršak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4262 (2023)
Although the aetiology of non-syndromic orofacial clefts (nsOFCs) is usually multifactorial, syndromic OFCs (syOFCs) are often caused by single mutations in known genes. Some syndromes, e.g., Van der Woude syndrome (VWS1; VWS2) and X-linked cleft pal
Externí odkaz:
https://doaj.org/article/4f5fa5c43eda45a392d321c0dfcabc18
Publikováno v:
Zdravniški Vestnik, Vol 88, Iss 9-10, Pp 405-14 (2019)
Izhodišče: Orofacialni razcep je najpogostejša prirojena obrazna nepravilnost. Otroci z razcepi v orofacialnem področju imajo poleg težav z govorom tudi težave na področju hranjenja in požiranja. Raziskave kažejo, da so simptomi težav s hra
Externí odkaz:
https://doaj.org/article/5b3276d81f124e05b021f58b25f96923
Publikováno v:
Journal of Integrative Neuroscience, Vol 21, Iss 4, p 106 (2022)
Background: Craniosynostosis is a rare congenital disease of the skull. They arise when one or more cranial sutures ossify prematurely. This causes an obstruction to normal brain growth and leads to specific deformations of the skull, which may resul
Externí odkaz:
https://doaj.org/article/3d7295efcec043a9bd62bc661ffb64e6
Publikováno v:
In International Journal of Oral & Maxillofacial Surgery November 2018 47(11):1381-1388