Zobrazeno 1 - 10
of 46
pro vyhledávání: '"K, Sofroniadou"'
Autor:
K. Panayotopoulou, L. Kavalierou, E. Papoulia, T. Mandalaki, L. Fountoulaki, P. Tsiroyani, K. Loizou, K. Hatzidimitriou, C. Politi, N. Renieri, K. Sofroniadou, I. Spiliotopoulou, I. Kontopoulou, Argyri Gialeraki
Publikováno v:
Vox Sanguinis. 61:215-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f26869407535d0f4ec348308b5918b8f
https://doi.org/10.1111/j.1423-0410.1991.tb00948.x
https://doi.org/10.1111/j.1423-0410.1991.tb00948.x
Publikováno v:
Blood. 49:981-986
The frequency of thalassemia was determined in a group of 541 healthy adult black males. Individuals with decreased mean corpuscular hemoglobin (MCH) values were evaluated further with hemoglobin analysis, iron studies, and globin chain synthesis. Of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8736cd0e79f1acc8949f7ca89a150b5
https://doi.org/10.1182/blood.v49.6.981.bloodjournal496981
https://doi.org/10.1182/blood.v49.6.981.bloodjournal496981
Publikováno v:
Clinical Endocrinology. 20:435-443
Thyroid and pituitary function tests using hypothalamic releasing factors were performed in seven patients with thalassaemia and secondary haemosiderosis and in a control group of seven healthy subjects. The TSH level in the thalassaemic patients (18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8b03ad7d0b024c53dcfbb175a99bb1
https://doi.org/10.1111/j.1365-2265.1984.tb03439.x
https://doi.org/10.1111/j.1365-2265.1984.tb03439.x
Publikováno v:
BMJ. 2:38-42
Frequencies of the thalassaemias in Cyprus were examined by a survey of hospital inpatients and haematological investigations of adult and newborn population samples. The data indicate that 15% of the Greek and Turkish Cypriots are carriers of beta-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa42ff9272c95840e168e5ac001edab
https://doi.org/10.1136/bmj.2.5857.38
https://doi.org/10.1136/bmj.2.5857.38
Autor:
John B. Clegg, William G. Wood, A. Metaxatou-Mavromati, Christos Kattamis, David J. Weatherall, K. Sofroniadou
Publikováno v:
British journal of haematology. 43(4)
Haemoglobin F has been isolated from the red cells of individuals with the Greek form of hereditary persistence of fetal haemoglobin (HPFH), and the glycine/alanine composition of the gamma CB3 peptides determined. In contrast to previous reports we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::139f1ea697eaaba5ebe6002a7b836503
https://pubmed.ncbi.nlm.nih.gov/93488
https://pubmed.ncbi.nlm.nih.gov/93488
Autor:
R. Stathopoulou, K. Sofroniadou, V. Merianou, G. Papaevangelou, M. Karagiorga, V. Malliarakis, Constantina Politis, N. Zoumbos, A. Roumeliotou
Publikováno v:
Vox sanguinis. 56(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb627fb3457630658830222d26e11a4c
https://pubmed.ncbi.nlm.nih.gov/2658318
https://pubmed.ncbi.nlm.nih.gov/2658318
Publikováno v:
Blood. 49(6)
The frequency of thalassemia was determined in a group of 541 healthy adult black males. Individuals with decreased mean corpuscular hemoglobin (MCH) values were evaluated further with hemoglobin analysis, iron studies, and globin chain synthesis. Of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc4826126e52c031e8136a20c04af12a
https://pubmed.ncbi.nlm.nih.gov/861379
https://pubmed.ncbi.nlm.nih.gov/861379
Autor:
E. Temler, K Sofroniadou, D P Livadas, E Economou, J P Felber, G. Van Melle, H Fotiadou-Pappa
Publikováno v:
Clinical endocrinology. 27(4)
An increased incidence of diabetes mellitus and glucose intolerance has been reported in thalassaemia major treated with a high transfusion programme (HTP). To investigate beta-cell function, serum immunoreactive insulin (IRI), C-peptide (CP) and glu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c4afee5687c41e09316d38fb5b11b6
https://pubmed.ncbi.nlm.nih.gov/3325197
https://pubmed.ncbi.nlm.nih.gov/3325197
Publikováno v:
Acta endocrinologica. Supplementum. 265
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3d3e069c1abc99c8e9d81e9aae8a803
https://pubmed.ncbi.nlm.nih.gov/6593986
https://pubmed.ncbi.nlm.nih.gov/6593986
Autor:
P G, Waber, M A, Bender, R E, Gelinas, C, Kattamis, A, Karaklis, K, Sofroniadou, G, Stamatoyannopoulos, F S, Collins, B G, Forget, H H, Kazazian
Publikováno v:
Blood. 67(2)
In the Greek A gamma beta + type of hereditary persistence of fetal hemoglobin (HPFH), adult heterozygotes produce about 20% fetal hemoglobin (HbF), which is predominantly of the A gamma chain variety. The affected beta-globin gene cluster produces n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8fd0f7fce5060024c7679d5704be3563
https://pubmed.ncbi.nlm.nih.gov/2417646
https://pubmed.ncbi.nlm.nih.gov/2417646