Zobrazeno 1 - 10
of 5 768
pro vyhledávání: '"Cns anomalies"'
Autor:
Behnaz Moradi, Fatemeh Zare Bidoki, Javid Azadbakht, Mahboobeh Shirazi, Hassan Hashemi, Sedigheh Hantooshzadeh, Mohamad Ali Kazemi, Mohammad Shafiee, Mohammad Hossein Golezar
Publikováno v:
Neurology Letters, Vol 3, Iss 1, Pp 12-19 (2024)
Background: This study is aimed to compare the accuracy of prenatal standard brain ultrasound (US), neurosonography (NSG), and magnetic resonance imaging (MRI) for diagnosing central nervous system (CNS) anomalies.Methods: In this prospective study p
Externí odkaz:
https://doaj.org/article/022d711f6be1402e9267504d189522b0
Publikováno v:
Egyptian Journal of Medical Research, Vol 4, Iss 1, Pp 83-96 (2023)
Background: Great concerns have been obtained for CNS anomalies due to their maternal and fetal morbidities and mortality outcomes. The high prevalence of CNS anomalies has been linked to polyhydramnios in several studies. This study was conducted to
Externí odkaz:
https://doaj.org/article/59a29d39d46348149ff0b9d7661820ef
Akademický článek
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Akademický článek
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Autor:
C. Falamesca, S. Cappelletti, R. Vicario, P.G. Amante, C. Correale, F. Vigevano, L. Caforio, T. Grimaldi Capitello
Publikováno v:
European Psychiatry, Vol 65, Pp S616-S617 (2022)
Introduction Women receiving a prenatal diagnosis of fetal anomalies are a high-risk population for psychological distress leading to mood disorders. Even so, to date we have no evidence of studies who investigated the levels of maternal anxiety and
Externí odkaz:
https://doaj.org/article/e711b02f272648fe967520d0ad254c40
Autor:
Emanuela Ponzi, Mattia Gentile, Emanuele Agolini, Emilia Matera, Roberto Palumbi, Antonia Lucia Buonadonna, Antonia Peschechera, Alessandra Gabellone, Maria Fatima Antonucci, Lucia Margari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Chromosome 14q11‐q22 deletion syndrome (OMIM 613457) is a rare contiguous gene syndrome. Two regions of overlap (RO) of the 14q12q21.1 deletion have been identified: a proximal region (RO1), including FOXG1(*164874), NKX2‐1(*6
Externí odkaz:
https://doaj.org/article/c7a6e4f8e868449b82fdc9a74d62ed1f
Autor:
Ponzi, Emanuela1 (AUTHOR), Gentile, Mattia1 (AUTHOR) mattiagentile@libero.it, Agolini, Emanuele2 (AUTHOR), Matera, Emilia3 (AUTHOR), Palumbi, Roberto3 (AUTHOR), Buonadonna, Antonia Lucia1 (AUTHOR), Peschechera, Antonia3 (AUTHOR), Gabellone, Alessandra3 (AUTHOR), Antonucci, Maria Fatima1 (AUTHOR), Margari, Lucia3 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Jul2020, Vol. 8 Issue 7, p1-6. 6p.
Autor:
Miremberg, H.1,2 (AUTHOR), Leidner, N. Feldman1,2 (AUTHOR), Hartoov, J.1,2 (AUTHOR), Salemnick, Y.1,2 (AUTHOR), Birnbaum, R.1,2 (AUTHOR), Malinger, G.1,2 (AUTHOR), Haratz, K. Krajden1,2 (AUTHOR)
Publikováno v:
Ultrasound in Obstetrics & Gynecology. Sep2024 Supplement 1, Vol. 64, p90-91. 2p.
Publikováno v:
Egyptian Journal of Medical Research. 4:83-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80c421d2eac71031cbe57449937ff66d
https://doi.org/10.21608/ejmr.2023.284070
https://doi.org/10.21608/ejmr.2023.284070
Autor:
Zhuang, Jianlong1 (AUTHOR) 415913261@qq.com, Zhang, Na1 (AUTHOR) zn0402003@163.com, Chen, Yu'e2 (AUTHOR), Jiang, Yuying1 (AUTHOR), Chen, Xinying1 (AUTHOR), Chen, Wenli1 (AUTHOR), Chen, Chunnuan3 (AUTHOR) chenchunnuan1983@aliyun.com
Publikováno v:
Scientific Reports. 1/27/2024, Vol. 14 Issue 1, p1-8. 8p.