Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Abdulla A. Alharthi"'
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Akademický článek
Screening of gene sequence variants in Saudi Arabian children with idiopathic short stature
Autor: Abdulla A. Alharthi, Ehab I. El-Hallous, Iman M. Talaat, Hamed A. Alghamdi, Matar I. Almalki, Ahmed Gaber
Publikováno v: Korean Journal of Pediatrics, Vol 60, Iss 10, Pp 327-332 (2017)
PurposeShort stature affects approximately 2%–3% of children, representing one of the most frequent disorders for which clinical attention is sought during childhood. Despite assumed genetic heterogeneity, mutations or deletions in the short statur
Externí odkaz: https://doaj.org/article/1bef468b74cf4a16b040516f86fd1a17
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2
Molecular Screening of PAX2 Gene Polymorphism in Primary Vesicoureteral Reflux Patients in Taif Governorate, KSA
Autor: Abdulla A. Alharthi, Ehab I. El-Hallous, Ahmed Gaber, Mohamed M. Hassan
Publikováno v: Pakistan Journal of Biological Sciences. 24:492-499
lbgBackground and Objective:l/bg Primary Nonsyndromic Vesicoureteral Reflux (PVUR) is a widespread genetic malformation and considered a prevalent Congenital Abnormality of the Kidney and Urinary Tract (CAKUT). Mutations in the ligPAX2 l/iggene have
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ac08e97ee75e94e85ae54cea4aac09c4
https://doi.org/10.3923/pjbs.2021.492.499
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4
Molecular Screening of
Autor: Ehab, I El-Hallous, Abdulla A, Alharthi, Ahmed, Gaber, Mohamed, M Hassan
Publikováno v: Pakistan journal of biological sciences : PJBS. 24(4)
lt;bgt;Background and Objective:lt;/bgt; Primary Nonsyndromic Vesicoureteral Reflux (PVUR) is a widespread genetic malformation and considered a prevalent Congenital Abnormality of the Kidney and Urinary Tract (CAKUT). Mutations in thelt;igt;PAX2lt;/
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1444a6b9fd8287f49df2ced4b2619be7
https://pubmed.ncbi.nlm.nih.gov/34486308
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8
Screening of gene sequence variants in Saudi Arabian children with idiopathic short stature
Autor: Matar I. Almalki, Ahmed Gaber, Abdulla A. Alharthi, Ehab I. El-Hallous, Iman M. Talaat, Hamed A. Alghamdi
Publikováno v: Korean Journal of Pediatrics, Vol 60, Iss 10, Pp 327-332 (2017)
Purpose Short stature affects approximately 2%-3% of children, representing one of the most frequent disorders for which clinical attention is sought during childhood. Despite assumed genetic heterogeneity, mutations or deletions in the short stature
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b544391dc0be900af69cd70c3fa09920
http://kjp.or.kr/upload/pdf/kjped-60-327.pdf
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10
Patterns of Childhood Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome in Saudi Children
Autor: Abdulla A. Alharthi
Publikováno v: Clinical Pediatrics. 56:177-183
Nephrotic syndrome (NS) is one of the most common causes of chronic kidney disease in children. Mostly, NS is controlled by steroids. In spite of this, 10% to 20% of the patients have steroid resistant NS (SRNS), and the rest have steroid sensitive N
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1083f62f83ea728ff6849743e3246cb1
https://doi.org/10.1177/0009922816645521
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