Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ali N. Al Odaib"'
Autor:
Maha H. Daghestani, Arjumand Warsy, Mazin H. Daghestani, Ali N. Al-odaib, Abdelmoneim Eldali, Nadia A. Al-Eisa, Sawsan A. Omer, Zeinab K. Hassan
Publikováno v:
International Journal of Endocrinology, Vol 2012 (2012)
Background. Several studies have shown an association between codon 16 polymorphism of the β2AR gene and obesity. Methods. We studied the association between Arg16Gly polymorphism and obesity and its influence on anthropometric parameters, lipids, i
Externí odkaz:
https://doaj.org/article/6d17115364844494a6625f823ac81495
Publikováno v:
Saudi medical journal. 28(8)
To studied the relationship that exists between leptin, ghrelin, insulin, neuropeptide Y (NPY), anthropometric, and metabolic variables in Saudi females.The study was conducted at the Department of Genetics, King Faisal Specialist HospitalResearch Ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb31af529e11ab29cd37dc867b183834
https://pubmed.ncbi.nlm.nih.gov/17676200
https://pubmed.ncbi.nlm.nih.gov/17676200
Publikováno v:
Community genetics. 8(1)
In this paper, we address the preventive health aspects of genetic problems in the Middle East and provide guidelines to prioritize preventive strategies. Applications of various novel genetic techniques such as comprehensive neonatal screening, high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::578af806d53677e5ac17216d6ec3d3ff
https://pubmed.ncbi.nlm.nih.gov/15767755
https://pubmed.ncbi.nlm.nih.gov/15767755
Publikováno v:
Saudi medical journal. 24(11)
In the Arabian Peninsula, high percentages of consanguineous marriages and the tribal nature of marriages have resulted in high incidence of genetically based disorders. The successful management of these disorders incurs a high financial cost, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f1e40d67bd09c366f10f5b08333ec18
https://pubmed.ncbi.nlm.nih.gov/14647548
https://pubmed.ncbi.nlm.nih.gov/14647548
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 335(1-2)
Background : Type 3 glycogen storage disease is an inborn error of metabolism in young infants that often requires extensive workup. However, this disease manifests with few symptoms other than hepatosplenomegaly. At adolescence, this disease may cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::213093d70b1ac74bb699303a5aaddfaf
https://pubmed.ncbi.nlm.nih.gov/12927680
https://pubmed.ncbi.nlm.nih.gov/12927680