Nurasyikin Yusof
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Explore the profile of Nurasyikin Yusof including associated specialties, affiliations and a list of published articles.
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9
Citations
19
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Recent Articles
1.
Hamzah R, Yusof N, Tumian N, Abdul Aziz S, Mohammad Basri N, Leong T, et al.
J Blood Med
. 2022 Jun;
13:337-349.
PMID: 35761846
Background: Immune thrombocytopenia (ITP) is well characterized in Western, European and other Asia-Pacific countries. Nevertheless, the clinical epidemiology, treatment pattern and disease outcome of ITP in Malaysia are still limited...
2.
Syed Abas S, Abdul Karim N, Periyasamy P, Yusof N, Shah S, Leong T, et al.
Int J Environ Res Public Health
. 2022 Jan;
19(2).
PMID: 35055629
Dengue mortality remains high despite monitoring against warning signs (WS). The associations of WS at febrile phase (FP) and hemorrhage at defervescence with the levels and kinetics of ROTEM, platelet...
3.
Wan Mohd Zohdi W, Ismail A, Yusof N, Ithnin A, Shuib S, Masir N, et al.
Clin Pathol
. 2022 Jan;
15:2632010X211070774.
PMID: 35036912
Diffuse large B-cell lymphoma (DLBCL) is a type of non-Hodgkin Lymphoma commonly presenting as a solid tumor either by nodal or extra-nodal manifestations. Here we describe two atypical presentations of...
4.
Eldeen Bakheet O, Yusof N, Raja Zahratul A, Ithnin A, Abdul Aziz S, Alias H
Indian J Hematol Blood Transfus
. 2016 Jul;
32(Suppl 1):262-6.
PMID: 27408409
Secondary sea-blue histiocytosis occurs more frequently than the primary form and occurs consequent to a wide range of metabolic and haematologic disorders including thalassaemia. We report an 18-year-old Chinese boy...
5.
Yousuf R, Abdul Aziz S, Yusof N, Leong C
Indian J Hematol Blood Transfus
. 2014 Aug;
30(3):208-10.
PMID: 25114411
We report a 47-year-old Malay lady, para 4 + 1, with known medical history of hypertension whom presented at Emergency Department with severe anaemia, most likely secondary to menorrhagia caused...
6.
Yousuf R, Abdul Aziz S, Yusof N, Leong C
Indian J Hematol Blood Transfus
. 2014 Jan;
29(2):65-70.
PMID: 24426338
Red blood cell alloimmunization is a common complication among the transfusion recipients. In Malaysia, multiple ethnicity causes genetic heterogeneity among the population which in turn can cause a wide variation...
7.
Raja-Sabudin R, Hamid A, Yusof N, Alauddin H, Aziz S, Kulaveerasingam S, et al.
Saudi Med J
. 2012 Oct;
33(10):1131-3.
PMID: 23047221
No abstract available.
8.
Azma R, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, et al.
Malays J Pathol
. 2012 Aug;
34(1):57-62.
PMID: 22870600
Haemoglobin Constant Spring (Hb CS) mutation and single gene deletions are common underlying genetic abnormalities for alpha thalassaemias. Co-inheritance of deletional and non-deletional alpha (alpha) thalassaemias may result in various...
9.
Hemolytic disease of the fetus and newborn caused by anti-D and anti-S alloantibodies: a case report
Yousuf R, Abdul Aziz S, Yusof N, Leong C
J Med Case Rep
. 2012 Feb;
6:71.
PMID: 22348809
Introduction: Hemolytic disease of the fetus and newborn is most commonly caused by anti-D alloantibody. It is usually seen in Rhesus D (RhD)-negative mothers that have been previously sensitized. We...