Zobrazeno 1 - 10
of 3 652
pro vyhledávání: '"Woodbury-Smith"'
Autor:
Koczkodaj, W. W., Mazurek, M., Pedrycz, W., Rogalska, E., Roth, R., Strzalka, D., Szymanska, A., Wolny-Dominiak, A., Woodbury-Smith, M., Xue, O. S., Zbyrowski, R.
Harmful Internet use (HIU) is a term coined for the unintended use of the Internet. In this study, we propose a more accurate HIU measuring method based on the peer assessment and differential evolution approach. The sample data comprises a juvenile
Externí odkaz:
http://arxiv.org/abs/2301.10232
Autor:
Akter, Hosneara 1, 2, Rahaman, Md. Atikur 1, Eshaque, Tamannyat Binte 1, Mohamed, Nesrin 3, Islam, Amirul 1, 4, Morshed, Mehzabin 1, Shahin, Zaha 5, Muhaimin, Al 1, Foyzullah, Arif Md. 1, Mim, Rabeya Akter 1, Omar, Farjana Binta 1, Hasan, Md. Nahid 1, 4, Satsangi, Dharana 6, Ahmed, Nahid 1, Al Saba, Abdullah 2, Jahan, Nargis 7, Hossen, Md. Arif 7, Mondol, Md. Ashadujjaman 7, Sakib, Ahammad Sharif 7, Kabir, Rezwana 7, Jahan Chowdhury, Mohammod Shah 7, Shams, Nusrat 7, Afroz, Shireen 8, Kanta, Shayla Imam 8, Bhuiyan, Sarwar Jahan 9, Biswas, Rabi 8, Hanif, Shehzad 3, Tambi, Richa 3, Nassir, Nasna 3, 6, Rahman, Muhammad Mizanur 10, Duan, Jinjie 11, 12, 13, D. Børglum, Anders 11, 12, 13, Amin, Robed 14, Basiruzzaman, Mohammed 7, Kamruzzaman, Md. 8, Sarker, Shaoli 7, 8, Woodbury-Smith, Marc 15, Uddin, K.M. Furkan 1, 16, Nabi, A.H.M. Nurun 2, Uddin, Mohammed 3, 4, 6, ∗
Publikováno v:
In Genetics in Medicine January 2025 27(1)
Autor:
Shaoli Sarker, Tamannyat Binte Eshaque, Anjana Soorajkumar, Nasna Nassir, Binte Zehra, Shayla Imam Kanta, Md Atikur Rahaman, Amirul Islam, Shimu Akter, Mohammad Kawsar Ali, Rabeya Akter Mim, K. M. Furkan Uddin, Mohammod Shah Jahan Chowdhury, Nusrat Shams, Md. Abdul Baqui, Elaine T. Lim, Hosneara Akter, Marc Woodbury-Smith, Mohammed Uddin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Duchenne muscular dystrophy (DMD) is a severe rare neuromuscular disorder caused by mutations in the X-linked dystrophin gene. Several mutations have been identified, yet the full mutational spectrum, and their phenotypic consequences, will
Externí odkaz:
https://doaj.org/article/b12c0b69d34d43fc96da4a42d0764a7d
Akademický článek
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Autor:
Stephen Tyrer
Publikováno v:
British Journal of Psychiatry. 209:87-88
Clinical Topics in Disorders of Intellectual Development Edited by Marc Woodbury-Smith RCPsych Publications. 2015. £30.00 (pb). 328 pp. ISBN 9781909726390 Between 1996 and 2012 a number of articles about disorders of intellectual development (now th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbd87cbe7b33c6a5bd078b881dff8a1c
https://doi.org/10.1192/bjp.bp.115.178723
https://doi.org/10.1192/bjp.bp.115.178723
Autor:
Woodbury-Smith, Marc, D’Abate, Lia, Stavropoulos, Dimitri J., Howe, Jennifer, Drmic, Irene, Ny Hoang, Zarrei, Mehdi, Trost, Brett, Iaboni, Alana, Anagnostou, Evdokia, Scherer, Stephen W.
Publikováno v:
Journal of Medical Genetics; Dec2023, Vol. 60 Issue 12, p1153-1160, 37p
Autor:
Nasna Nassir, Asma Bankapur, Bisan Samara, Abdulrahman Ali, Awab Ahmed, Ibrahim M. Inuwa, Mehdi Zarrei, Seyed Ali Safizadeh Shabestari, Ammar AlBanna, Jennifer L. Howe, Bakhrom K. Berdiev, Stephen W. Scherer, Marc Woodbury-Smith, Mohammed Uddin
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-16 (2021)
Abstract Background In recent years, several hundred autism spectrum disorder (ASD) implicated genes have been discovered impacting a wide range of molecular pathways. However, the molecular underpinning of ASD, particularly from the point of view of
Externí odkaz:
https://doaj.org/article/00dc4650ae5a4c8da8d8c168cea1f017
Autor:
Nassir, Nasna, Tambi, Richa, Bankapur, Asma, Al Heialy, Saba, Karuvantevida, Noushad, Khansaheb, Hamda Hassan, Zehra, Binte, Begum, Ghausia, Hameid, Reem Abdel, Ahmed, Awab, Deesi, Zulfa, Alkhajeh, Abdulmajeed, Uddin, K.M. Furkan, Akter, Hosneara, Safizadeh Shabestari, Seyed Ali, Almidani, Omar, Islam, Amirul, Gaudet, Mellissa, Kandasamy, Richard Kumaran, Loney, Tom, Tayoun, Ahmad Abou, Nowotny, Norbert, Woodbury-Smith, Marc, Rahman, Proton, Kuebler, Wolfgang M., Yaseen Hachim, Mahmood, Casanova, Jean-Laurent, Berdiev, Bakhrom K., Alsheikh-Ali, Alawi, Uddin, Mohammed
Publikováno v:
In iScience 24 September 2021 24(9)
Autor:
Hosneara Akter, Mohammad Shahnoor Hossain, Nushrat Jahan Dity, Md. Atikur Rahaman, K. M. Furkan Uddin, Nasna Nassir, Ghausia Begum, Reem Abdel Hameid, Muhammad Sougatul Islam, Tahrima Arman Tusty, Mohammad Basiruzzaman, Shaoli Sarkar, Mazharul Islam, Sharmin Jahan, Elaine T. Lim, Marc Woodbury-Smith, Dimitri James Stavropoulos, Darren D. O’Rielly, Bakhrom K. Berdeiv, A. H. M. Nurun Nabi, Mohammed Nazmul Ahsan, Stephen W. Scherer, Mohammed Uddin
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
Abstract Collectively, rare genetic diseases affect a significant number of individuals worldwide. In this study, we have conducted whole-exome sequencing (WES) and identified underlying pathogenic or likely pathogenic variants in five children with
Externí odkaz:
https://doaj.org/article/be7577baefe0449d9e32b34e4247a672
Publikováno v:
Journal of autism and developmental disorders [J Autism Dev Disord] 2006 Nov; Vol. 36 (8), pp. 1141-2. Date of Electronic Publication: 2006 Nov 01.