Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Helen Tsapra"'
Autor:
Helen Tsapra, Andrew Fretzayas, Marianthi Galetseli, Maria Moustaki, Polyxeni Nicolaidou, P. Dimitriou
Publikováno v:
Scandinavian Journal of Urology and Nephrology. 42:462-465
Although urine production depends on numerous physiological variables there are no quantitative data regarding the effect of bladder decompression, by means of continuous catheter drainage, on urine production. The aim of this study was to investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f5eab2ec30ba13d5a1cf5b181016c5
https://doi.org/10.1080/00365590801933101
https://doi.org/10.1080/00365590801933101
Autor:
Andreas Fretzayas, Polyxeni Nicolaidou, Georges Tsiftis, Elizabeth Dimitriou, Aglaia Giannoulia-Karantana, Helen Georgouli, Talia Kakourou, Chryssa Bakoula, Helen Tsapra, Anna Papadopoulou, Georges Kavadias
Publikováno v:
Nutrition Research. 26:620-625
Vitamin D status in humans depends on the amount of sun exposure and vitamin D intake. Recent reports suggest that hypovitaminosis D (as defined by serum 25-hydroxyvitamin D [25(OH)D]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8c23cbff91d90705a7fdaf5e1b52037
https://doi.org/10.1016/j.nutres.2006.09.018
https://doi.org/10.1016/j.nutres.2006.09.018
Autor:
Yiannis G. Matsinos, Konstantinos Douros, Andreas Fretzayas, Aglaia Giannoulia-Karantana, Ioannis Papassotiriou, Polyxeni Nicolaidou, Helen Tsapra, Anna Papadopoulou, Helen Georgouli, Georges P Chrousos, Sophia Kitsiou
Publikováno v:
Hormone Research in Paediatrics. 65:83-88
Background/Aims: Hypocalcemic vitamin D-resistant rickets (HVDRR) is a rare monogenic autosomal recessive disorder associated with mutations in the gene of the vitamin D receptor (VDR), the mediator of 1,25(OH)2D3 action. Although many investigations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33b01626dafeb9916696861ea1fbefc
https://doi.org/10.1159/000091043
https://doi.org/10.1159/000091043
Autor:
Helen Georgouli, P. Nicolaidou, Yiannis G. Matsinos, Helen Tsapra, Fotini Psychou, Petros M. Zeis, Dimitris Gourgiotis, Vasiliki Getsi
Publikováno v:
Pediatric Nephrology. 18:1157-1160
Urinary excretion of endothelin-1 (ET-1) and plasma ET-1 were measured in 21 children with absorptive idiopathic hypercalciuria (AIH) and 22 controls. The absorptive type of idiopathic hypercalciuria was determined by a calcium loading test. Daily ur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6575654dce25e3a86f2395a5bbf68019
https://doi.org/10.1007/s00467-003-1263-5
https://doi.org/10.1007/s00467-003-1263-5
Autor:
Smaragdi Fessatou, George Maropoulos, Helen Michelakakis, Helen Tsapra, Anastasia Garoufi, Kleopatra H. Schulpis
Publikováno v:
Pediatric Pathology & Molecular Medicine. 22:153-157
Ornithine transcarbamylase deficiency, an X-linked disorder, is the most common inherited urea cycle defect. Previous reports have documented the existence of several different mutations that can, partly at least, explain the phenotypic variability o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36e14a2970da1e99ee2e53bed801d6dd
https://doi.org/10.1080/pdp.22.2.153.157
https://doi.org/10.1080/pdp.22.2.153.157