Zobrazeno 1 - 10
of 673
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, Rahaman, Md. Atikur, Eshaque, Tamannyat Binte, Mohamed, Nesrin, Islam, Amirul, Morshed, Mehzabin, Shahin, Zaha, Muhaimin, Al, Foyzullah, Arif Md., Mim, Rabeya Akter, Omar, Farjana Binta, Hasan, Md. Nahid, Satsangi, Dharana, Ahmed, Nahid, Al Saba, Abdullah, Jahan, Nargis, Hossen, Md. Arif, Mondol, Md.Ashadujjaman, Sakib, Ahammad Sharif, Kabir, Rezwana, Jahan Chowdhury, Mohammod Shah, Shams, Nusrat, Afroz, Shireen, Kanta, Shayla Imam, Bhuiyan, Sarwar Jahan, Biswas, Rabi, Hanif, Shehzad, Tambi, Richa, Nassir, Nasna, Rahman, Muhammad Mizanur, Duan, Jinjie, D. Børglum, Anders, Amin, Robed, Basiruzzaman, Mohammed, Kamruzzaman, Md., Sarker, Shaoli, Woodbury-Smith, Marc, Uddin, K.M. Furkan, Nabi, A.H.M. Nurun, Uddin, Mohammed
Publikováno v:
In Genetics in Medicine January 2025 27(1)
Autor:
Woodbury-Smith, Kara
This thesis argues for a novel understanding of the relationship between law and coercion. One of the relationships H.L.A. Hart sought to clarify is between law and coercion. In his work, Hart denies that coercion is a conceptually necessary feature
Externí odkaz:
http://hdl.handle.net/11375/25536
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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Publikováno v:
Behavioral and Brain Functions, Vol 4, Iss 1, p 11 (2008)
Abstract Background Autism Spectrum Conditions (ASCs) are characterized by a high degree of clinical heterogeneity, but the extent to which this variation represents a severity gradient versus discrete phenotypes is unclear. This issue has complicate
Externí odkaz:
https://doaj.org/article/2487a1dd0ec84a73b69705147748702f
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