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Nur Afiqah Mohamad
Nur Afiqah Mohamad
Senior Lecturer, University College of MAIWP International
在 ucmi.edu.my 的电子邮件经过验证
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引用次数
引用次数
年份
Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects
NA Mohamad, V Ramachandran, H Mohd Isa, YM Chan, NF Ngah, ...
Human Genomics 13, 1-12, 2019
242019
Analysis of selected glutathione S-transferase gene polymorphisms in Malaysian type 2 diabetes mellitus patients with and without cardiovascular disease
A Etemad, R Vasudevan, AF Aziz, AK Yusof, S Khazaei, N Fawzi, ...
Genet Mol Res 15 (2), 1-9, 2016
182016
High-frequency repetitive transcranial magnetic stimulation at dorsolateral prefrontal cortex for migraine prevention: A systematic review and meta-analysis
NI Mohamad Safiai, NA Mohamad, H Basri, LN Inche Mat, FK Hoo, ...
Cephalalgia 42 (10), 1071-1085, 2022
142022
Analysis of the association between CFH Y402H polymorphism and response to intravitreal ranibizumab in patients with neovascular age-related macular degeneration (nAMD)
NA Mohamad, V Ramachandran, P Ismail, HM Isa, YM Chan, NF Ngah, ...
Bosnian Journal of Basic Medical Sciences 18 (3), 260, 2018
72018
Regional Emergency Stroke Quick-Response (RESQ) Network: A Proposed Paradigm of Malaysia Stroke Care Services
HB Peck Kee Chia, Nur Afiqah Mohamad, Liyana Najwa Inche Mat, Iskasymar Itam ...
Malaysian Journal of Medicine and Health Sciences 16 (4), 353-361, 2020
62020
Analysis of homocysteine metabolism enzyme gene polymorphisms in non-syndromic congenital heart disease patients among Malaysians
NA Mohamad, R Vasudevan, P Ismail, NI Jafar, A Etemad, AFA Aziz
Life Sci J 11 (8), 318-26, 2014
62014
Analysis of OCT1, OCT2 and OCT3 gene polymorphisms among Type 2 diabetes mellitus subjects in Indian ethnicity, Malaysia
SGA Al-Ashoor, V Ramachandran, LNI Mat, NA Mohamad, MH Mohamed, ...
Saudi Journal of Biological Sciences 29 (1), 453-459, 2022
52022
Transcranial direct current stimulation with multiple oral re-reading therapy for pure alexia without agraphia: a case report
NA Mohamad, SN Che Adinan, AHK Yusof Khan, NNH Nik Abdul Ghani, ...
Neurocase 27 (5), 391-395, 2021
52021
Analysis of angiotensin converting enzyme, endothelial nitric oxide synthase & serotonin gene polymorphisms among atrial septal defect subjects with and without pulmonary …
NI Jaafar, R Vasudevan, P Ismail, AF Abdul Aziz, NA Mohamad, ...
Journal of Cardiovascular Development and Disease 5 (3), 48, 2018
52018
Prevalence and treatment patterns of ranibizumab and photodynamic therapy in a tertiary care setting in Malaysia
NA Mohamad, V Ramachandran, P Ismail, HM Isa, YM Chan, NF Ngah, ...
International Journal of Ophthalmology 10 (12), 1889, 2017
52017
Genotyping of GATA4 gene variant (G296S) in Malaysian congenital heart disease subjects by real-time PCR high resolution melting analysis
N Fawzi, R Vasudevan, P Ismail, M Alwi, AAA Fazli, H Almeamar, ...
Journal of Medical Biochemistry 32 (2), 152, 2013
52013
A review of the neuroprotective effects of andrographolide in Alzheimer's disease
Z Abedi, H Basri, Z Hassan, LNI Mat, H Khaza’ai, NA Mohamad
Advances in Traditional Medicine 21, 253-266, 2021
42021
Inche Mat, LN; Mohamed, MH Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects
NA Mohamad, V Ramachandran, H Mohd Isa, YM Chan, NF Ngah, ...
Hum. Genom 13, 13, 2019
42019
Association of copy number variations in complement factor H-Related genes among age-related macular degenerative subjects
NM Bakri, V Ramachandran, HF Kee, V Subrayan, H Isa, NF Ngah, ...
The Kaohsiung Journal of Medical Sciences 33 (12), 602-608, 2017
42017
Analysis of human bradykinin receptor gene and endothelial nitric oxide synthase gene polymorphisms in end-stage renal disease among malaysians
R Vasudevan, P Ismail, NI Jaafar, NA Mohamad, E Etemad, WA WS, ...
Balkan Journal of Medical Genetics 17 (1), 37-40, 2014
42014
Association of GCK (rs1799884), GCKR (rs780094), and G6PC2 (rs560887) gene polymorphisms with type 2 diabetes among Malay ethnics
N Ansari, V Ramachandran, NA Mohamad, E Salim, P Ismail, M Hazmi, ...
Global Medical Genetics 10 (01), 012-018, 2023
32023
Inche Mat LN, Hoo FK, Abdul Rashid AM, et al.(2021) High-frequency repetitive transcranial magnetic stimulation at dorsolateral prefrontal cortex for migraine prevention: A …
NI Mohamad Safiai, NA Mohamad, H Basri
PLoS One 16 (6), e0251528, 2021
32021
VEGF Polymorphisms Among Neovascular Age-Related Macular Degenerative Subjects in a Multiethnic Population
NA Mohamad, V Ramachandran, P Ismail, H Mohd Isa, YM Chan, ...
Genetic testing and molecular biomarkers 21 (10), 600-607, 2017
32017
Association of Endothelin-Converting Enzyme and Endothelin-1 Gene Polymorphisms with Essential Hypertension in Malay Ethnics
E Salim, V Ramachandran, N Ansari, P Ismail, MH Mohamed, ...
Genetics Research 2022, e57, 2022
22022
R102G polymorphism of the complement component 3 gene in Malaysian subjects with neovascular age-related macular degeneration
NA Mohamad, V Ramachandran, P Ismail, HM Isa, YM Chan, NF Ngah, ...
Egyptian Journal of Medical Human Genetics 19 (2), 77-81, 2018
22018
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