Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Sakir Erdem"'
Publikováno v:
Clinical Genetics. 6:46-50
A girl with the combination of hereditary spherocytosis and hereditary elliptocytosis is presented. She had a moderately severe haemolytic anaemia. This was the result either of a summation of the clinical effects of the involved genes or of the mutu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d3a8a7ac7b3ea501a00d0a06724cbd
https://doi.org/10.1111/j.1399-0004.1974.tb00629.x
https://doi.org/10.1111/j.1399-0004.1974.tb00629.x
Autor:
T. P. Molchanova, D. D. Pobedimskaya, Günçağ Dinçol, Koray Dinçol, Sakir Erdem, Z. Ye, Titus H.J. Huisman, J. B. Wilson, Brooke B. Webber
Publikováno v:
Hemoglobin. 18:57-60
A 28-year-old female from the city of Kars in Turkey was treated for a chronic iron deficiency anemia with oral iron. During the clinical evaluation a slowly moving hemoglobin (Hb) variant was detected which migrated about like Hb F in alkaline elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f57e2270afbc1ece712e5634b5152cb8
https://doi.org/10.3109/03630269409014146
https://doi.org/10.3109/03630269409014146
Publikováno v:
BIO Web of Conferences; 11/6/2024, Vol. 133, p1-10, 10p
Publikováno v:
Acta Haematologica. 71:116-120
7 cases of multiple myeloma with a history of exposure to benzene, radioactive iodine, chemotherapy for Hodgkin's disease and of repeated injections of autovaccine to Staphylococcus albus hemolyticus are described. The relationship between the develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45dd8153b6e8e5ec8adcb07588f56437
https://doi.org/10.1159/000206568
https://doi.org/10.1159/000206568
Publikováno v:
Human Heredity. 30:3-6
135 Turks living in the vicinity of Antalya, a Turkish city on the Mediterranean coast, were studied for haemoglobin variants, beta-thalassaemia G-6-PD deficiency and haptoglobin types. The incidence of Hb-S was 2.3%. 8 beta-thalassaemic individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e73b70637948385fbc41f601794221
https://doi.org/10.1159/000153079
https://doi.org/10.1159/000153079
Publikováno v:
Blut Zeitschrift für die Gesamte Blutforschung. 30:255-260
Two patients, one with myeloid metaplasia and the other one with PNH, both due to chronic exposure to benzene are presented. The patient with PNH exhibited also marked monocytosis as a rare hematologic finding of chronic benzene exposure. The etiolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c5c5d04b29ca86ec2e2744424e0e8e
https://doi.org/10.1007/bf01635357
https://doi.org/10.1007/bf01635357
Publikováno v:
Human Heredity. 29:272-278
Clinical and haematological findings of 164 Turkish beta-thalassaemic heterozygotes with increased Hb-A2 are presented. The series comprised of 19 children, 81 females and 64 males. The majority of these thalassaemic individuals were asymptomatic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::688d18f3dd0ecd91394d17912fc8ce2d
https://doi.org/10.1159/000153057
https://doi.org/10.1159/000153057
Publikováno v:
Human Heredity. 26:149-153
Two families in which two relatives with chronic exposure to benzene developed acute leukaemia are presented. The results of the cytogenetic studies are presented and the importance of the combination of genetic and environmental factors in the causa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcaf3ce273d40eb78fb59fb04be0b3cf
https://doi.org/10.1159/000152796
https://doi.org/10.1159/000152796
Publikováno v:
Blut Zeitschrift für die Gesamte Blutforschung. 28:293-298
Six cases ofHodgkin's disease with a history of chronic benzene exposure are presented. These patients were chronically exposed to benzene for a period ranging from 1 to 28 years with a mean of 11 years, before the onset ofHodgkin's disease. The poss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2df5f795230cfb7e52f9f43be0a2ce4
https://doi.org/10.1007/bf01631650
https://doi.org/10.1007/bf01631650
Publikováno v:
Acta Haematologica. 59:178-189
20 patients with β -thalassemia intermedia classified according to the results of genetic studies are presented. (1) 9 patients with β -thalassemia intermedia homoz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::161abdb891a7aa0032b710cf19d890cb
https://doi.org/10.1159/000207760
https://doi.org/10.1159/000207760