Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Christakis, J."'
Publikováno v:
Psychotherapy and Psychosomatics, 1988 Jan 01. 49(3/4), 171-178.
Externí odkaz:
https://www.jstor.org/stable/45115752
Juvenile hemochromatosis is an early-onset autosomal recessive disorder of iron overload resulting in cardiomyopathy, diabetes and hypogonadism that presents in the teens and early 20s (refs. 1,2). Juvenile hemochromatosis has previously been linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6028d877b43f6083d437395d5e7828fc
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085075
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085075
Animal models indicate that the antimicrobial peptide hepcidin (HAMP; OMIM 606464) is probably a key regulator of iron absorption in mammals. Here we report the identification of two mutations (93delG and 166C–>T) in HAMP on 19q13 in two families w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::140f8ddd7ee5a318615e944ecbf9b612
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082995
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082995
Purpose : Waldenstrom’s macroglobulinemia (WM) is a low-grade lymphoplasmacytic lymphoma in which CD20 is usually expressed on tumor cells. There is evidence that patients with WM may benefit from treatment with the anti-CD20 monoclonal antibody ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::0518c385b602184f7263d06ce16f1a92
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081807
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081807
Waldenstrom’s macroglobulinernia is a low-grade lymphoplasmacytoid lymphoma characterized by CD20 expression on malignant cells. Several studies have indicated that the anti-CD20 monoclonal antibody rituximab has activity against this disease. Thus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6dfb7015a29811aef36df35f5ba801f8
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082655
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3082655
THE ORIGIN OF THE SICKLE MUTATION IN GREECE - EVIDENCE FROM BETA-S GLOBIN GENE-CLUSTER POLYMORPHISMS
Study of the Hpa I polymorphism 3’ to the beta-globin gene in the Greek population revealed absence of the site in 238 beta-S chromosomes, in contrast to a much larger sample of chromosomes carrying the beta-A gene, where this site was consistently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c00f5085cf3266399a31d9bfa3b7f67d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044163
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044163
Haematological and clinical characteristics have been examined in 30 patients with homozygous sickle cell (SS) disease, 28 with sickle cell-beta-degrees thalassaemia, and 21 with sickle cell-beta+ thalassaemia. The latter could be divided into three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::91b67f94bb24d8b04b92bce8c9e627f4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044307
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044307
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