Results 21 to 30 of about 8,682 (200)

Mobility limitations and emotional dysfunction in old age: The moderating effects of physical activity and social ties

International Journal of Geriatric Psychiatry, Volume 38, Issue 7, July 2023., 2023
Abstract Background This study aims to examine the association between mobility limitations and emotional dysfunction among older Ghanaians and evaluate the buffering effect of physical activity (PA) and social ties in this association. Methods The analysis included 1201 adults aged ≥50 from the 2016‐17 Aging, Health, Psychological Well‐being, and ...
Razak M. Gyasi, Felix Asante, Mohammed Gazali Hambali, Julius Odei, Louis Jacob, Bernard Obeng, Prince Peprah, Edward Asamoah, Williams Agyemang‐Duah, Kabila Abass, Gershim Asiki, Anokye M. Adam   +11 more
wiley   +1 more source

The Implementation of E-Commerce Consumer Option Rights (Khiyar) in Realizing Transaction Justice: A Study of Maqasid Al-Shariah

Al-Manahij: Jurnal Kajian Hukum Islam, 2023
This article aims to reveal the optimization of option rights in realizing or stopping e-commerce transactions to achieve justice due to several problems in e-commerce transactions, including no meeting of two people who transact and no goods at that ...
Abdi Wijaya, Achmad Musyahid Idrus, Tahani Asri Maulidah, Mulham Jaki Asti, Nurjannah Nurjannah   +4 more
doaj   +1 more source

Nosology of genetic skeletal disorders: 2023 revision

American Journal of Medical Genetics Part A, Volume 191, Issue 5, Page 1164-1209, May 2023., 2023
Abstract The “Nosology of genetic skeletal disorders” has undergone its 11th revision and now contains 771 entries associated with 552 genes reflecting advances in molecular delineation of new disorders thanks to advances in DNA sequencing technology.
Sheila Unger, Carlos R. Ferreira, Geert R. Mortier, Houda Ali, Débora R. Bertola, Alistair Calder, Daniel H. Cohn, Valerie Cormier‐Daire, Katta M. Girisha, Christine Hall, Deborah Krakow, Outi Makitie, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Ravi Savarirayan, David Sillence, Marleen Simon, V. Reid Sutton, Matthew L. Warman, Andrea Superti‐Furga   +20 more
wiley   +1 more source

Mutation spectrum of non‐syndromic hearing loss in the UAE, a retrospective cohort study and literature review

Molecular Genetics &Genomic Medicine, Volume 10, Issue 11, November 2022., 2022
Abstract Background Hearing loss (HL) is a heterogeneous condition that causes partial or complete hearing impairment. Hundreds of variants in >60 genes have been reported to be associated with Hereditary HL (HHL), variants of the GJB2 gene are the most common cause of congenital SNHL, with >100 variants reported.
Omnia Elsayed, Aisha Al‐Shamsi
wiley   +1 more source

Refonder ou revivifier l’islam. Les stratégies d’écriture d’Abū Ḥāmid al-Ġazālī (m. 505/1111)

Cahiers d'Études du Religieux- Recherches Interdisciplinaires, 2023
At the end of the 11th century, Islam saw an upsurge of a takfīr bent toward exclusion, in reaction to a perceived infidelity to orthodoxy or orthopraxy.
Emmanuel Pisani
doaj   +1 more source

Qatar genome: Insights on genomics from the Middle East

Human Mutation, Volume 43, Issue 4, Page 499-510, April 2022., 2022
Abstract Despite recent biomedical breakthroughs and large genomic studies growing momentum, the Middle Eastern population, home to over 400 million people, is underrepresented in the human genome variation databases. Here we describe insights from Phase 1 of the Qatar Genome Program with whole genome sequenced 6047 individuals from Qatar.
Hamdi Mbarek, Geethanjali Devadoss Gandhi, Senthil Selvaraj, Wadha Al‐Muftah, Radja Badji, Yasser Al‐Sarraj, Chadi Saad, Dima Darwish, Muhammad Alvi, Tasnim Fadl, Heba Yasin, Fatima Alkuwari, Rozaimi Razali, Waleed Aamer, Fatemeh Abbaszadeh, Ikhlak Ahmed, Younes Mokrab, Karsten Suhre, Omar Albagha, Khalid Fakhro, Ramin Badii, Said I. Ismail, Asma Althani, Qatar Genome Program Research Consortium   +23 more
wiley   +1 more source

Genotype–phenotype correlates in Joubert syndrome: A review

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 190, Issue 1, Page 72-88, March 2022., 2022
Abstract Joubert syndrome (JS) is a genetically heterogeneous primary ciliopathy characterized by a pathognomonic cerebellar and brainstem malformation, the “molar tooth sign,” and variable organ involvement. Over 40 causative genes have been identified to date, explaining up to 94% of cases. To date, gene‐phenotype correlates have been delineated only
Simone Gana, Valentina Serpieri, Enza Maria Valente   +2 more
wiley   +1 more source

Maslahat Menurut Imam Malik Dan Imam Al-ghazali (Studi Perbandingan) [PDF]

, 2014
This article discusses Imam Malik's and Imam al-Gazali's theory of maslahat: First, both Malik and al-Gazali agreed that maslahat relevant to Islamic law.
Herawati, A. (Andi)
core   +3 more sources

A Moderated Mediation Model of Factors Influencing Intention to Adopt Cryptocurrency among University Students

Human Behavior and Emerging Technologies, Volume 2022, Issue 1, 2022., 2022
The goal of this study is to find out what people think about cryptocurrencies and how they feel about it. The study used a questionnaire to assess the factors that influence people’s willingness to accept cryptocurrency. The study used a pretest, posttest quantitative analysis to determine the level of awareness among users in the first phase.
Saher Zeast Hasan, Huma Ayub, Abida Ellahi, Mahnoor Saleem, Zheng Yan   +4 more
wiley   +1 more source

Demand for Imported versus Domestic Fish in Nigeria

Journal of Agricultural Economics, Volume 72, Issue 3, Page 782-804, September 2021., 2021
Abstract Fish is among the most important animal‐sourced foods in Africa and is crucial in combatting malnutrition. Fish demand in Africa has far outpaced supply as the import share rose from 16% in 1970 to 39% by 2017. Little is known about who is consuming the imports: rural versus urban, rich versus poor.
Lenis Saweda O. Liverpool‐Tasie, Awa Sanou, Thomas Reardon, Ben Belton   +3 more
wiley   +1 more source