» Authors » Mardhiah Mohammad

Mardhiah Mohammad

Explore the profile of Mardhiah Mohammad including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 6
Citations 54
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Jalal T, Khan A, Natto H, Abdull Rasad M, Kaderi M, Mohammad M, et al.
Nutr Cancer . 2019 Jan; 71(5):792-805. PMID: 30614285
Nine phenolic compounds were identified and quantified in Artocarpus altilia fruit. One of the main compounds was quercetin, which is the major class of flavonoids has been identified and quantified...
2.
Wang D, Mohammad M, Wang Y, Tan R, Murray L, Ricardo S, et al.
Kidney Int Rep . 2017 Nov; 2(4):739-748. PMID: 29142990
Introduction: X-linked Alport syndrome (OMIM 301050) is caused by missense variants in 40% of families. This study examined the effects of chemical chaperone treatment (sodium 4-phenylbutyrate) on fibroblast cell lines...
3.
Yusof A, Mohammad M, Abdullahi M, Mohamed Z, Zakaria R, Abdul Wahab R
Trop Life Sci Res . 2017 Feb; 28(1):23-32. PMID: 28228914
Intestinal parasitic infections are one of the most common causes of human diseases that result in serious health and economic issues in many developing and developed countries. Raw vegetables and...
4.
Hisamuddin N, Hashim N, Soffian S, Amin M, Abdul Wahab R, Mohammad M, et al.
Korean J Parasitol . 2016 May; 54(2):197-200. PMID: 27180579
Cryptosporidium, a protozoan parasite, can cause cryptosporidiosis which is a gastrointestinal disease that can infect humans and livestock. Cattle are the most common livestock that can be infected with this...
5.
Mohammad M, Nanra R, Colville D, Trevillian P, Wang Y, Storey H, et al.
Pediatr Nephrol . 2013 Dec; 29(3):481-5. PMID: 24337245
Background: Female subjects with X-linked Alport syndrome have a single COL4A5 mutation, germ cell mosaicism in affected tissues and typically develop renal failure later or less often than male subjects....
6.
Wang Y, Sivakumar V, Mohammad M, Colville D, Storey H, Flinter F, et al.
Pediatr Nephrol . 2013 Nov; 29(3):391-6. PMID: 24178893
Background: This study determined the family history and clinical features that suggested autosomal recessive rather than X-linked Alport syndrome. Methods: All patients had the diagnosis of Alport syndrome and the...