Zobrazeno 1 - 10
of 195
pro vyhledávání: '"Patimah Ismail"'
Autor:
Neda Ansari, Vasudevan Ramachandran, Nur Afiqah Mohamad, Elnaz Salim, Patimah Ismail, Mohamad Hazmi, Liyana Najwa Inchee Mat
Publikováno v:
Global Medical Genetics, Vol 10, Iss 01, Pp 012-018 (2023)
Background Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder, and the underlying causes remain unknown and have not been fully elucidated. Several candidate genes have been associated with T2DM in various populations with conflicting re
Externí odkaz:
https://doaj.org/article/b6c2cf513b054bc182a51b98df7c7ee6
Autor:
Salma Ahmadloo, King-Hwa Ling, Ahmad Fazli, Ghazaleh Larijani, Nooshin Ghodsian, Sanaz Mohammadi, Naser Amini, Vahid Hosseinpour Sarmadi, Patimah Ismail
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-15 (2022)
Abstract Background Coronary Heart Disease (CHD) is the leading cause of death in industrialized countries. There is currently no direct relation between CHD and type 2 diabetes mellitus (T2D), one of the major modifiable risk factors for CHD. This s
Externí odkaz:
https://doaj.org/article/0a8b1a2db7d343e18296bc51d2ad9fbe
Autor:
Elnaz Salim, Vasudevan Ramachandran, Neda Ansari, Patimah Ismail, Mohd Hazmi Mohamed, Nur Afiqah Mohamad, Liyana Najwa Inche Mat
Publikováno v:
Genetics Research, Vol 2022 (2022)
Objectives. Endothelin-1 (ET-1), the most potent endogenous vasoconstrictor, generated by enzymatic cleavage catalyzed by an endothelin-converting enzyme (ECE), plays a significant role in the regulation of hypertension. Methods. This study investiga
Externí odkaz:
https://doaj.org/article/b08530a4dfbd4d6d8be89c7ed567534f
Autor:
Norshakimah Md Bakri, Vasudevan Ramachandran, Fan Kee Hoo, Visvaraja Subrayan, Hazlita Isa, Nor Fariza Ngah, Nur Afiqah Mohamad, Siew Mooi Ching, Yoke Mun Chan, Patimah Ismail, Fazliana Ismail, Erma Suryana Sukiman, Wan Alia Wan Sulaiman
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 3, Pp 207-213 (2018)
Background: Several studies in various populations have been conducted to determine candidate genes that could contribute to age-related macular degeneration (AMD) pathogenesis. Objective: The present study was undertaken to determine the association
Externí odkaz:
https://doaj.org/article/2c75a6037f894482866cb80a576824ae
Autor:
Nur Afiqah Mohamad, Vasudevan Ramachandran, Patimah Ismail, Hazlita Mohd Isa, Yoke Mun Chan, Nor Fariza Ngah, Norshakimah Md Bakri, Siew Mooi Ching, Fan Kee Hoo, Wan Aliaa Wan Sulaiman
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 77-81 (2018)
Background: Genetic and environmental factors are known to be risk factors in development of neovascular age-related macular degeneration (nAMD). Genetic factors such as polymorphisms in the complement component pathway genes might play a role in pat
Externí odkaz:
https://doaj.org/article/46038742357a4c02a6e3ecfe88b2b3c0
Autor:
Nur Afiqah Mohamad, Vasudevan Ramachandran, Patimah Ismail, Hazlita Mohd Isa, Yoke Mun Chan, Nor Fariza Ngah, Norshakimah Md Bakri, Siew Mooi Ching, Fan Kee Hoo, Wan Aliaa Wan Sulaiman
Publikováno v:
International Journal of Ophthalmology, Vol 10, Iss 12, Pp 1889-1897 (2017)
AIM: To describe the prevalence and changes in treatment patterns of ranibizumab and photodynamic therapy (PDT) among retinal disease patients who attended the Ophthalmology Clinic in the tertiary care Hospital Selayang from 2010 to 2014. METHODS: S
Externí odkaz:
https://doaj.org/article/8c6deffbbe2a46a899e678101a99f26c
Autor:
Norshakimah Md Bakri, Vasudevan Ramachandran, Hoo Fan Kee, Visvaraja Subrayan, Hazlita Isa, Nor Fariza Ngah, Nur Afiqah Mohamad, Ching Siew Mooi, Chan Yoke Mun, Patimah Ismail, Fazliana Ismail, Erma Suryana Sukiman, Wan Alia Wan Sulaiman
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 33, Iss 12, Pp 602-608 (2017)
Age-related macular degeneration (AMD) is the most widely recognised cause of irreversible vision loss and previous studies have suggested that the advancement of wet AMD is influenced by both modifiable and non-modifiable elements. Single nucleotide
Externí odkaz:
https://doaj.org/article/f0961fe717664c3a917e15efd996f3d7
Autor:
null Hamidreza Saeidi, null Chandramathi Samudi Raju, null Patimah Ismail, null Sayyidi Hamzi Abdul Raub, null Noorjehan Omar, null Ikmal Hisyam Bakrin
Publikováno v:
Cellular and Molecular Biology. 68:22-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d8373d46cf201523cedd7d1b8256a10
https://doi.org/10.14715/cmb/2022.68.8.4
https://doi.org/10.14715/cmb/2022.68.8.4
Publikováno v:
In International Journal of Cardiology 15 July 2016 215:318-324
Autor:
Nur Afiqah Mohamad, Vasudevan Ramachandran, Patimah Ismail, Hazlita Mohd Isa, Yoke Mun Chan, Nor Fariza Ngah, Norshakimah Md Bakri, Siew Mooi Ching, Fan Kee Hoo, Wan Aliaa Wan Sulaiman, Liyana Najwa Inche Mat, Mohd Hazmi Mohamed
Publikováno v:
Biomolecules & Biomedicine, Vol 18, Iss 3 (2018)
Pharmacogenetic studies indicate that a variable response to anti-vascular endothelial growth factor (VEGF) therapy in patients with neovascular form of AMD (nAMD) may be due to polymorphisms in the complement factor H gene (CFH). This study is the f
Externí odkaz:
https://doaj.org/article/872e929952a44c169ec200b9c5dded3e