Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Nur Afiqah Mohamad"'
Autor:
Anna Misya’il Abdul Rashid, Mohamad Syafeeq Faeez Md Noh, Abdul Hanif Khan Yusof Khan, Wei Chao Loh, Janudin Baharin, Azliza Ibrahim, Fadhilah Hani Ishak, Aminuddin Sardi, Ahmad Firdaus Hanapai, Nur Afiqah Mohamad, Liyana Najwa Inche Mat, Fan Kee Hoo, Wan Aliaa Wan Sulaiman, Hamidon Basri
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background and aims The corononavirus 2019 (COVID-19) pandemic resulted in modifications in the workflow and redistribution of human resources, causing challenges in setting up of an acute stroke service. We would like to share our prelimina
Externí odkaz:
https://doaj.org/article/d71acbf39de7417bbdbd5f9d778fc961
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:
Nurul Huda Musa, Karuppiah Thilakavathy, Nur Afiqah Mohamad, Marina L. Kennerson, Liyana Najwa Inche Mat, Wei Chao Loh, Anna Misyail Abdul Rashid, Janudin Baharin, Azliza Ibrahim, Wan Aliaa Wan Sulaiman, Fan Kee Hoo, Hamidon Basri, Abdul Hanif Khan Yusof Khan
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Myotonia congenita (MC) is a rare neuromuscular disease caused by mutations within the CLCN1 gene encoding skeletal muscle chloride channels. MC is characterized by delayed muscle relaxation during contraction, resulting in muscle stiffness. There is
Externí odkaz:
https://doaj.org/article/dddab79db5184ef7b8dbefbf6ccc0f28
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:
Nur Afiqah Mohamad, Vasudevan Ramachandran, Hazlita Mohd Isa, Yoke Mun Chan, Nor Fariza Ngah, Siew Mooi Ching, Fan Kee Hoo, Wan Aliaa Wan Sulaiman, Liyana Najwa Inche Mat, Mohd Hazmi Mohamed
Publikováno v:
Human Genomics, Vol 13, Iss 1, Pp 1-12 (2019)
Abstract Background The association of HTRA1 rs11200638 and ARMS2 rs10490924 gene polymorphisms with response to intravitreal ranibizumab therapy among neovascular AMD (nAMD) subjects in Malaysia was determined in this study, followed by the expressi
Externí odkaz:
https://doaj.org/article/7526802e10414643b2b0fb706a97dae7
Autor:
Nabil Izzaatie Mohamad Safiai, Nur Afiqah Mohamad, Hamidon Basri, Liyana Najwa Inche Mat, Fan Kee Hoo, Anna Misyail Abdul Rashid, Abdul Hanif Khan Yusof Khan, Wei Chao Loh, Janudin Baharin, Aaron Fernandez, Intan Nureslyna Samsudin, Mohd Hazmi Mohamed, Mooi Ching Siew, Kai Wei Lee, Vasudevan Ramachandran, Patricia Pozo-Rosich, Wan Aliaa Wan Sulaiman
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0251528 (2021)
BackgroundMigraine may lead to a negative impact on the patients' quality of life with a subsequent substantial burden to society. Therapy options for treatment and prevention of migraine have progressed over the years and repetitive transcranial mag
Externí odkaz:
https://doaj.org/article/782c56199b0546ec9588d755fcfe03d8
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