Items where Author is "Zainal Abidin, Mohd Azri"
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Number of items: 11.
Article
Jamaluddin, Jalilah and Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri and Mohamad, Siti Mardhiana and Mahayidin, Hasni
(2026)
Preliminary reference range for B cell subpopulations in peripheral blood of healthy Malaysian children aged 2–15 years.
Scientific Reports, 16 (1).
art. no. 11765.
pp. 1-8.
ISSN 2045-2322
Mohamed Nashrudin, Khairoon Nisa and Zainal Abidin, Mohd Azri and Ng, Shi Eng and Razali, Hadibiah and Jawin, Vida and Zakaria, Atiqah Farah and Mohd Ali, Razana and Othman, Ida Shahnaz and Mohamed Unni, Mohamed Najib and Hung, Christina Yuh-Ron and Ismail, Intan Hakimah
(2025)
Rasgrp1 deficiency associated with diffuse mesangial sclerosis infantile nephrotic syndrome and Epstein-Barr virus-induced Hodgkin’s lymphoma.
Pediatric Allergy, Immunology, and Pulmonology, 38 (1).
pp. 11-20.
ISSN 2151-321X; eISSN: 2151-3228
Chang, Wai Leng and Mohd Noh, Lokman and Abdul Latiff, Amir Hamzah and Woo, Kent Chee Keen and Ismail, Intan Hakimah and Abd Hamid, Intan Juliana and Siniah, Sangeetha and Zainal Abidin, Mohd Azri and Sham, Marina and Mat Ripen, Adiratna and Baharin, Mohd Farid and Abdul Wahab, Asrul and Zainudeen, Zarina Thasneem and Hashim, Ilie Fadzilah and Wong, Yee Ming and Ahmad Shawaludin, Mohamad Qazreen and Ali, Adli
(2024)
Newborn screening for severe combined immunodeficiency in Malaysia: current status, challenges and progress.
Frontiers in Immunology, 15.
art. no. 1456769.
ISSN 1664-3224; eISSN: 1664-3224
Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri and Mohd Radzi, Farah Syuhada and Ramlan, Saidatul Saadah and Adam, Julia and Mat Ripen, Adiratna
(2021)
Ecthyma gangrenosum as the presenting clinical feature of X-linked agammaglobulinaemia: report of three cases and a review of literature.
Current Allergy and Clinical Immunology, 34 (4).
238 - 245.
ISSN 1609-3607
Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri
(2020)
Congenital nasal pyriform aperture stenosis with holoprosencephaly and Dandy–Walker malformation.
Journal of Clinical Neonatology, 9 (4).
292 - 294.
ISSN 2249-4847; ESSN: 1658-6093
Darussalam, Siti Eliza and Tompell, Afryan and Juni, Muhamad Hanafiah and Zainal Abidin, Mohd Azri
(2017)
A cross sectional study to assess knowledge and practice regarding antibiotic used among parents of children attending paediatric clinic.
International Journal of Public Health and Clinical Sciences (IJPHC), 4 (5).
172 - 181.
ISSN ESSN: 2289-7577
Atmawidjaja, Raymond Warouw and Zainal Abidin, Mohd Azri and Ismail, Intan Hakimah
(2016)
Cardiac tamponade: a rare but preventable complication of central venous catheter in neonates.
Medical Journal of Malaysia, 71 (3).
pp. 147-148.
ISSN 0300-5283
Conference or Workshop Item
Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri and Mohamed Nashrudin, Khairoon Nisa
(2024)
Aspergilloma in a young patient with autosomal-dominant hyper-IgE syndrome.
In: Asia Pacific Association of Allergy, Asthma, and Clinical Immunology (APAAACI) Congress 2024, 13-15 Dec. 2024, Kuala Lumpur, Malaysia. .
Mohamed Nashrudin, Khairoon Nisa and Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri and Zakaria, Noorzeehan and Safwan, Muhammad Shafiq and Abdul Jabar, Siti Wardah and Ramli, Farizza Hazlin and Thong, Pui Ling and Ng, Ruey Terng and Ong, Sik Yong
(2024)
Phenotypic diversity and immunodeficiency in Trichohepatoenteric Syndrome: a case series analysis.
In: Asia Pacific Association of Allergy, Asthma, and Clinical Immunology (APAAACI) Congress 2024, 13-15 Dec. 2024, Kuala Lumpur, Malaysia. .
Abdul Jabar, Siti Wardah and Safwan, Muhammad Shafiq and Ramli, Farizza Hazlin and Zakaria, Noorzeehan and Mohamed Nashrudin, Khairoon Nisa and Zainal Abidin, Mohd Azri and Ismail, Intan Hakimah
(2024)
Subcutaneous immunoglobulin: the game-changer in immunodeficiency treatment.
In: Asia Pacific Association of Allergy, Asthma, and Clinical Immunology (APAAACI) Congress 2024, 13-15 Dec. 2024, Kuala Lumpur, Malaysia. .
Ismail, Intan Hakimah and Zainal Abidin, Mohd Azri and Mohamed Nashrudin, Khairoon Nisa
(2024)
An interesting case of CYBB mutation in a Malay boy with normal maternal dihydroxidation test and matched mother-child haplotype.
In: 5th Asia-Pacific Society for Immunodeficiency (APSID), Congrss, 22-24 Mar. 2024, Tokyo, Japan. .
