Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shamma A. Al-Shamisi"'
Autor:
Syed M Shah, Fatima Al Dhaheri, Ammar Albanna, Najla Al Jaberi, Shaikha Al Eissaee, Nouf Ahmed Alshehhi, Shamma A Al Shamisi, Maryam M Al Hamez, Said Y Abdelrazeq, Michal Grivna, Theresa S Betancourt
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227483 (2020)
BACKGROUND:Little is known about depressive symptoms among adolescents in the United Arab Emirates (UAE). This study aimed to identify the prevalence of depression and its association with self-esteem, individual, parental and family factors among ad
Externí odkaz:
https://doaj.org/article/d32d0aabb74e4a3db7228d2d2f04cb07
Self-esteem and other risk factors for depressive symptoms among adolescents in United Arab Emirates
Autor:
Fatima Al Dhaheri, Najla Al Jaberi, Michal Grivna, Ammar Albanna, Shaikha Al Eissaee, Shamma A. Al Shamisi, Syed M. Shah, Theresa S. Betancourt, Said Y. Abdelrazeq, Nouf Ahmed Alshehhi, Maryam M. Al Hamez
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 1, p e0227483 (2020)
PLoS ONE, Vol 15, Iss 1, p e0227483 (2020)
Background Little is known about depressive symptoms among adolescents in the United Arab Emirates (UAE). This study aimed to identify the prevalence of depression and its association with self-esteem, individual, parental and family factors among ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71b1436ea09693fd69ecaec8d705a4c4
http://europepmc.org/articles/PMC6959560
http://europepmc.org/articles/PMC6959560
Autor:
Bassam R Ali, Imen Ben-Rebeh, Anne John, Nadia A Akawi, Reham M Milhem, Nouf A Al-Shehhi, Mouza M Al-Ameri, Shamma A Al-Shamisi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://doaj.org/article/0c1361e492a343028561c1a1d16335c9
Autor:
Synan F. AbuQamar, Sofyan H Alyan, Arjun Sham, Rabah Iratni, Shamma A. Al-Shamisi, Khaled Moustafa
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172343 (2017)
PLoS ONE
PLoS ONE
The WRKY33 transcription factor was reported for resistance to the necrotrophic fungus Botrytis cinerea. Using microarray-based analysis, we compared Arabidopsis WRKY33 overexpressing lines and wrky33 mutant that showed altered susceptibility to B. c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8be9809f8bf770c981bb50e93cb2a178
http://europepmc.org/articles/PMC5313235?pdf=render
http://europepmc.org/articles/PMC5313235?pdf=render
Autor:
Nadia Akawi, Imen Ben-Rebeh, Shamma A. Al-Shamisi, Bassam R. Ali, Anne John, Reham M. Milhem, Mouza M. Al-Ameri, Nouf Ahmed Alshehhi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f47a53089e63c9fa74696c5967d36bf
https://doi.org/10.1371/journal.pone.0026206
https://doi.org/10.1371/journal.pone.0026206