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of 83
pro vyhledávání: '"Ahmadzadeh,Ali"'
Publikováno v:
Benchmarking: An International Journal, 2020, Vol. 28, Issue 4, pp. 1164-1185.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/BIJ-08-2020-0411
Autor:
Jamshidiantehrani, Mohammadreza1, Ahmadzadeh, Ali2, Rahimisadr, Mahtab3, Abdolmohammadi, Milad4 abdolmohammadi@agrikavosh.ir
Publikováno v:
Systematic Reviews in Pharmacy. 2020, Vol. 11 Issue 7, p371-381. 11p.
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 20, Iss 3, Pp 454-457 (2009)
A 4-year old boy was referred for evaluation of renal failure, posterior urethral valve (PUV) and urinary tract infection. His parents added complaints of polyuria, polydipsia, enuresis, shortness of stature, and inappropriate obesity. Serum blood ur
Externí odkaz:
https://doaj.org/article/16d2602d2810461bb0fed47eb332d0f6
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 20, Iss 2, Pp 246-250 (2009)
Hydronephrosis is the most common abnormal finding in the urinary tract on prenatal screening with ultrasonography (U/S). Hydronephrosis may be obstructive or non-obstructive; obstructive lesions are more harmful to the developing kidneys. The aim of
Externí odkaz:
https://doaj.org/article/0f5357686db042f68560dd94061348e8
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 19, Iss 5, Pp 756-760 (2008)
To assess clinical characteristics, pathological findings, and therapeutic response in children with lupus nephritis (LN), we retrospectively studied 25 children under 16 years of age with LN at the Abozar children′s hospital from 1995 to 2006. The
Externí odkaz:
https://doaj.org/article/4d9b18f682a64829aa6b62b4a75123b3
Akademický článek
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Publikováno v:
International Journal of Procurement Management; 2021, Vol. 14 Issue: 1 p126-145, 20p
Publikováno v:
Nefrología (Madrid) v.33 n.3 2013
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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Objective: Nephropatic Cystinosis (NC) is a rare metabolic disorder due to mutation in the CTNS gene in which more than 90 different mutations have already been reported so far. This study was performed to investigate mutations of the CTNS gene and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::2c3e1b47bf6ed0b7685727c2cf54a327
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952013000400004
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952013000400004