Mohamed-Syarif Mohamed-Yassin

15PUBLICATIONS
41CO-AUTHORS
Infant and child healthCardiology (incl. cardiovascular diseases)Applications in healthMedical biotechnology diagnostics (incl. biosensors)Cultural responsiveness and working with Pacific Peoples communities education
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Publications (15)

|Aug 20, 2026
Autosomal Dominant Polycystic Kidney Disease Presenting as a Painless Epigastric Mass: A Case Report.

|Feb 27, 2026
Variable phenotype associated with compound LDLR gene mutations in familial hypercholesterolemia patients: Case series and clinical implications.

Noor Alicezah Mohd Kasim, Yung-An Chua, Siti Hamimah Sheikh Abdul Kadir

|Apr 04, 2024
Factors associated with usability of the EMPOWER-SUSTAIN Self-management mobile app© among individuals with cardiovascular risk factors in primary care.

Siti M Abu Hussain, Hayatul N Miptah, Nur A Shibraumalisi

|Mar 01, 2024
A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care.

Mohamad Abu Zar Abdul-Halim, Hasidah Abdul-Hamid, Noorhida Baharudin

|Jun 14, 2023
Design, development, utility and usability testing of the EMPOWER-SUSTAIN Self-Management Mobile App© among primary care physicians and patients with metabolic syndrome.

Maryam Hannah Daud, Fakhrul Hazman Yusoff, Suraya Abdul-Razak

|May 03, 2023
Reducing Premature Coronary Artery Disease in Malaysia by Early Identification of Familial Hypercholesterolemia Using the Familial Hypercholesterolemia Case Ascertainment Tool (FAMCAT): Protocol for a Mixed Methods Evaluation Study.

Anis Safura Ramli, Nadeem Qureshi, Hasidah Abdul-Hamid

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Frequent Collaborators

8 joint publications

Anis Safura Ramli

6 joint publications

Noorhida Baharudin

3 joint publications

Nadeem Qureshi

2 joint publications

Noor Alicezah Mohd Kasim