An fMRI study of visuo-vestibular interactions following vestibular neuritis

Autor: R.E. Roberts, H. Ahmad, M. Patel, Danai Dima, R. Ibitoye, M. Sharif, R. Leech, Q. Arshad, A.M. Bronstein

Publikováno v: NeuroImage: Clinical, Vol 20, Iss , Pp 1010-1017 (2018)

Vestibular neuritis (VN) is characterised by acute vertigo due to a sudden loss of unilateral vestibular function. A considerable proportion of VN patients proceed to develop chronic symptoms of dizziness, including visually induced dizziness, specif

Externí odkaz: https://doaj.org/article/5fea5a8a98e44ff1aef1a4f237f10731

Sexual autonomy and violence against women in Nigeria: Assessing the impact of Covid-19 pandemic

Autor: Folakemi Ajagunna, Tolulope R Ibitoye

Publikováno v: De Jure Law Journal, Volume: 54, Issue: 1, Pages: 141-159, Published: 2021

Sexual and reproductive rights are centred on an individual's autonomy. However, these rights are jeopardised when women and girls are faced with sexual violence. Recently, there was reported increase in violence against women and girls, constituting

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a78284174f4751fbd37396752eb4914
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S2225-71602021000100009&lng=en&tlng=en

De novo variants in CNOT3 cause a variable neurodevelopmental disorder

Autor: A. van Haeringen, Laurence Faivre, S Tomkins, Amélie Piton, Shelagh Joss, Emmelien Aten, C I de Bie, Ruth Newbury-Ecob, Emma Kivuva, R Ibitoye, Els A. J. Peeters, Miranda Splitt, Bronwyn Kerr, F Tranmauthem, Nicola Foulds, Andrew Collins, J Kennedy, David Geneviève, Marije Koopmans, Richard Martin, Sarah F. Smithson, Nolwenn Jean-Marçais, Jacques C. Giltay

Publikováno v: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2019, 27 (11), pp.1677-1682. ⟨10.1038/s41431-019-0413-6⟩
Eur J Hum Genet
European Journal of Human Genetics, 27(11), 1677-1682. NATURE PUBLISHING GROUP

International audience; As a result of exome-based sequencing work performed by the DDD study, de novo variants in CNOT3 have emerged as a newly recognised cause of a developmental disorder. This paper describes molecular and clinical details of 16 p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38c5ce5af3218a196ec119798557339e
https://hdl.handle.net/1887/122775

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