Zobrazeno 1 - 10
of 26
pro vyhledávání: '"S. Petmezaki"'
Autor:
M. Moya, G. Greisen, S. Reiter-Theil, E. Saliba, N. Nelson, N. Leroux, D. Bratlid, P. Morrogh, L. Hellstrom-westas, N. Modi, S.A. Mason, C.A. Ryan, V. Fellman, C. Megone, G. Russell, A. B. Gill, P.J. Allmark, A.M. Weindling, G. Latini, A. Phillips, P. Dalla-Vorgia, S. Petmezaki
Publikováno v:
European Neonatal Research ISBN: 9781003073444
European Neonatal Research ISBN: 9781315203157
European Neonatal Research ISBN: 9781315203157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2508fe17030c706e36729b3a9584c1
https://doi.org/10.4324/9781003073444-21
https://doi.org/10.4324/9781003073444-21
Autor:
N Roy-Chowdhury, B Deocharan, HR Bejjanki, J Roy-Chowdhury, C Koliopoulos, S Petmezaki, T Valaes
Publikováno v:
Acta Paediatrica. 91:100-102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::171ab4e7e37c3b7b60a614aedec8362f
https://doi.org/10.1111/j.1651-2227.2002.tb01650.x
https://doi.org/10.1111/j.1651-2227.2002.tb01650.x
Autor:
N, Roy-Chowdhury, B, Deocharan, H R, Bejjanki, J, Roy-Chowdhury, C, Koliopoulos, S, Petmezaki, T, Valaes
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 91(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5965c5e7559c84ccac5a075b4703e2ac
https://pubmed.ncbi.nlm.nih.gov/11883809
https://pubmed.ncbi.nlm.nih.gov/11883809
Publikováno v:
American journal of medical genetics. 4(2)
The proband and his elder brother had intrauterine growth retardation, hypospadias, cryptorchism, a high palate, distally placed axial triradii, and a functional and maturational CNS defect that improved with age and included the inability to suck, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::446c76aa8a422f11fe65a621cba36ea9
https://pubmed.ncbi.nlm.nih.gov/293130
https://pubmed.ncbi.nlm.nih.gov/293130
Publikováno v:
Pediatrics. 81(4)
In two separate studies, in which two different treatment regimens of Sn-protoporphyrin were used, a total of 69 control and 53 treated infants were studied to determine whether this potent inhibitor of the enzyme, heme oxygenase, could ameliorate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d83f8c8450d7aa4d1cf46fc458d8c5a4
https://pubmed.ncbi.nlm.nih.gov/3281127
https://pubmed.ncbi.nlm.nih.gov/3281127
Publikováno v:
Annales de genetique. 21(4)
A case of oligohydramnios syndrome was found to have an XYY karyotype and an inherited 9qh inversion. It is suggested that normal and extra Y chromosomes are a predisposing factor in the aetiology of severe congenital renal anomalies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c772596b67dba46f2bed563f7c432a46
https://pubmed.ncbi.nlm.nih.gov/314260
https://pubmed.ncbi.nlm.nih.gov/314260
Publikováno v:
Birth defects original article series. 6(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cfa5b71bc96324050c49fb9af3a9f2e7
https://pubmed.ncbi.nlm.nih.gov/4941650
https://pubmed.ncbi.nlm.nih.gov/4941650
Publikováno v:
Pediatric Research. 13:74-74
Serum 25-OHD, serum calcium (Ca)and serum phosphorus (P) were measured in 40 full-term infants, 25 prematures and 39 mothers during 2 periods of the year. Mean values of serum 25-OHD in full-term and premature infants as well as in the mothers were f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cbb9e846ca737a183af709cf4d0ed38
https://doi.org/10.1203/00006450-197901000-00031
https://doi.org/10.1203/00006450-197901000-00031
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