Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nor Azimah Abdul Aziz"'
Autor:
Rohana Abdul Jalil, Nur Atiqah Shaari, Nor Azimah Abdul Aziz, Wan-Hitam Wh, Liza-Sharmini At, Ahmad Nurfahmi Akhtar Ali, Azhany Y
Introduction: Anchovy sauce is a known appetizer in many Asian’s cuisines. Based on the bio-physical content of anchovysauce, there is a possibility of the frequent consumption can affect severity and progression of glaucoma. The aim of thisstudy w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5037320e7395975c7522d6e2b2d294f1
Autor:
Nor Azimah Abdul Aziz
Publikováno v:
Journal of Financial Crime. 20:25-38
Purpose – The objective of this paper is to encourage compliance amongst the corporate community and to examine how statutory provisions will assist companies to implement internal control mechanisms and in managing risks, so as to achieve business
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cecddef3ae7964e103332edbacfa31c
https://doi.org/10.1108/13590791311287328
https://doi.org/10.1108/13590791311287328
Autor:
Huey Yin Leong, Nor Azimah Abdul Azize, Hui Bein Chew, Wee Teik Keng, Meow Keong Thong, Mohd Khairul Nizam Mohd Khalid, Liang Choo Hung, Norzila Mohamed Zainudin, Azura Ramlee, Muzhirah Aisha Md Haniffa, Yusnita Yakob, Lock Hock Ngu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive lysosomal storage disease due to N-acetylgalactosamine-6-sulfatase (GALNS) deficiency. It results in accumulation of the glycosaminoglycans, keratan sulfate and chondro
Externí odkaz:
https://doaj.org/article/3ceceb60b033493d83a1a1fe11a77f3f
Autor:
M. Mardhiah, Nor Azimah Abdul Azize, Yusnita Yakob, O. Affandi, Ngu Lock Hock, M.R. Rowani, Anasufiza Habib
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 22, Iss , Pp - (2020)
Introduction: Biotinidase deficiency (BD) is an autosomal recessively inherited disorder characterized by developmental delay, seizures, hypotonia, ataxia, skin rash/eczema, alopecia, conjunctivitis/visual problem/optic atrophy and metabolic acidosis
Externí odkaz:
https://doaj.org/article/e9ed4e87957142ccac1218cc00e2089a
Autor:
Lip Hen Moey, Nor Azimah Abdul Azize, Yusnita Yakob, Huey Yin Leong, Wee Teik Keng, Bee Chin Chen, Lock Hock Ngu
Publikováno v:
Pediatrics and Neonatology, Vol 59, Iss 4, Pp 397-403 (2018)
Background: Fructose-1,6-bisphosphatase (FBPase) deficiency is a rare autosomal recessive inborn error of gluconeogenesis. We reported the clinical findings and molecular genetic data in seven Malaysian patients with FBPase deficiency. Methods: All p
Externí odkaz:
https://doaj.org/article/282a9eb66cab47bb9e181f0db23b8c83