Zobrazeno 1 - 10
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pro vyhledávání: '"Premetis, E."'
Autor:
Papanikolaou, G., Chandrinou, H., Bouzas, E., Contopoulos-Ioannidis, D., Kalotychou, V., Prentzas, K., Lilakos, K., Asproudis, I., Palaiologou, D., Premetis, E., Papassotiriou, I., Sakellaropoulos, N.
Hereditary hyperferritinemia-cataract syndrome (HHCS) is a well-characterized autosomal dominant disease caused by mutations in the iron responsive element (IRE) of ferritin L-chain (FTL) mRNA. Mutations in the IRE result in reduced binding of the tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::30bb8afe4c148c640aa2529c01a0643a
http://olympias.lib.uoi.gr/jspui/handle/123456789/16051
http://olympias.lib.uoi.gr/jspui/handle/123456789/16051
Hereditary hyperferritinemia-cataract syndrome (HHCS) is a well-characterized autosomal dominant disease caused by mutations in the iron responsive element (IRE) of ferritin L-chain (FTL) mRNA. Mutations in the IRE result in reduced binding of the tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::ebaf945b89d62e2b83ed5325dd5a5e5d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3098095
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3098095
Iron deficiency anemia (IDA) and anemia of chronic disease (CDA) are often encountered in patients with inflammatory bowel disease (IBD). Inadequate intake or loss of iron is a clear cause of IDA, but mechanisms of CDA induction are multifactorial an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::81a7ed0496ea18b961a667c038c2b87c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3093342
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3093342
Abnormal globin chain biosynthesis may result in deficient quantity (thalassemia) or structural variation (abnormal hemoglobins) and traditionally, they represent two phenotypically distinct groups of disorders. However, the phenotypic expression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::75abeabc5186fa71896cdd85784b0ad5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084840
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084840
Autor:
Traeger-Synodinos, J Papassotiriou, I Karagiorga, M and Premetis, E Kanavakis, E Stamoulakatou, A
A single patient with a rare Haemoglobin H (HbH) disease genotype (–(Med)/alpha(TSaudi)alpha) was observed to have exceptionally high levels of HbH (> 60%) and paradoxically high total haemoglobin levels. Studies of haematological parameters, blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3fafb8a3704a20e351d2bbd970c4e53d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082373
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082373
Purpose: Measurement of liver T2 values seems to be an accurate and sensitive magnetic resonance imaging (MRI) method for the quantification of liver hemosiderosis in multiple transfused patients with thalassemia. Because many of these patients have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::ecf4cd5240c69c0ad168310c73437b6d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051568
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051568
Transfusional iron overload leading to cardiopathy and other severe complications continues to be a major problem in chronically transfused homozygous beta-thalassaemia patients. It is well known that young red cells (neocytes) survive longer after t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::65f2ebd1d0d52d0b79d88af394f26793
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047880
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047880
The interaction of rare Hb variants with beta degrees-thalassaemia results in a quasihomozygous state where the erythrocytes contain the variant as the only major adult Hb component, Such a situation is a unique model that enables functional studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::ad50d1cd68f2ac18be994a639d08e7d5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047614
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3047614
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