Nur Aizati Athirah Daud (Aizati N A Daud)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 5

Top Topics

Genome Wide Analysis

Platelet Rich Plasma

Nursing Students

Top Venues

Journal of personalized medicine

International journal of clinical pharmacy

Journal of cardiovascular development and disease

European journal of medical research

This page only lists publications with an associated author ORCID identifier.

Publications

Mohammed G Maslub, Mahasen A Radwan, Nur Aizati Athirah Daud, Abubakar Sha'aban
Association between CYP3A4/CYP3A5 genetic polymorphisms and treatment outcomes of atorvastatin worldwide: is there enough research on the Egyptian population? European journal of medical research 28 (1) (2023)
Mohammed Ahmed Akkaif, Ahmad Naoras Bitar, Laith A I K Al-Kaif, Nur Aizati Athirah Daud, Abubakar Sha'aban, Dzul Azri Mohamed Noor, Fatimatuzzahra' Abd Aziz, Arturo Cesaro, Muhamad Ali Sk Abdul Kader, Mohamed Jahangir Abdul Wahab, Chee Sin Khaw, Baharudin Ibrahim
The Management of Myocardial Injury Related to SARS-CoV-2 Pneumonia. Journal of cardiovascular development and disease 9 (9) (2022)
Balamurugan Tangiisuran, Vijitha Rajendran, Abubakar Sha'aban, Nur Aizati Athirah Daud, Siti Nurbaya Mohd Nawi
Physicians' perceived barriers and enablers for deprescribing among older patients at public primary care clinics: a qualitative study. International journal of clinical pharmacy (2021)
Ali Fadhel Ahmed, Chonlaphat Sukasem, Majeed Arsheed Sabbah, Nur Fadhlina Musa, Dzul Azri Mohamed Noor, Nur Aizati Athirah Daud
Genetic Determinants in HLA and Cytochrome P450 Genes in the Risk of Aromatic Antiepileptic-Induced Severe Cutaneous Adverse Reactions. Journal of personalized medicine 11 (5) (2021)
Nur Aizati Athirah Daud, Jorieke E H Bergman, Monika P Oktora, Wilhelmina S Kerstjens-Frederikse, Henk Groen, Jens H Bos, Eelko Hak, Bob Wilffert
Maternal use of drug substrates of placental transporters and the effect of transporter-mediated drug interactions on the risk of congenital anomalies. PloS one 12 (3) (2017)