Showing 1 - 11 results of 11 for search 'Wan Aliaa Wan Sulaiman', query time: 0.04s
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Repetitive transcranial magnetic stimulation of the primary motor cortex in stroke survivors-more than motor rehabilitation: A mini-review by Abdulhameed Tomeh, Abdul Hanif Khan Yusof Khan, Abdul Hanif Khan Yusof Khan, Wan Aliaa Wan Sulaiman, Wan Aliaa Wan Sulaiman
Published 2022-09-01
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R102G polymorphism of the complement component 3 gene in Malaysian subjects with neovascular age-related macular degeneration by 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
Published 2018-04-01
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Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects by 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
Published 2019-02-01
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Bilateral facial nerve palsy: a rare post-dengue fever complication by Ng Kim Khim, Wei Chao Loh, Anna Misya’il Abdul Rashid, Abdul Hanif Yusof KhanKhan, Janudin Baharin, Azliza Ibrahim, Liyana Najwa Inche Mat, Wan Aliaa Wan Sulaiman, Fan Kee Hoo, Hamidon Basri
Published 2022-11-01
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Analysis of the association between CFH Y402H polymorphism and response to intravitreal ranibizumab in patients with neovascular age-related macular degeneration (nAMD) by 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
Published 2018-08-01
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Establishing a hyperacute stroke service during the COVID-19 pandemic: our institution’s one year experience by 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
Published 2023-02-01
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Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family by Nurul Huda Musa, Nurul Huda Musa, Karuppiah Thilakavathy, Karuppiah Thilakavathy, Nur Afiqah Mohamad, Nur Afiqah Mohamad, Marina L. Kennerson, 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
Published 2023-01-01
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