Zobrazeno 1 - 10
of 166
pro vyhledávání: '"homozygous beta thalassemia"'
Autor:
Guluzar Ozbolat, Abdullah Tuli
Publikováno v:
The Ukrainian Biochemical Journal, Vol 90, Iss 4, Pp 115-120 (2018)
β-Tthalassemia is common genetic disorders in Turkey that characterized by the reduced synthesis (β+) or absence (βo) of the β-globin chains in the HbA molecule. In this study, we aimed to determine the effect of the mutation type of the β-globi
Externí odkaz:
https://doaj.org/article/f9cbadcf2d0e446982c0163f77dfac4e
Free testosterone level in patients with homozygous beta thalassemia on regular transfusions regimen
Publikováno v:
Paediatrica Indonesiana, Vol 44, Iss 2, Pp 73-9 (2016)
Background Patients with homozygous beta thalassemia require regular transfusions which will lead to iron deposition in tissues including testicles. Objective This study aimed to evaluate testicular function in syn- thesizing testosterone by measurin
Externí odkaz:
https://doaj.org/article/a1a03f6f748b447bad8459d199c7d3f9
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 35(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd62ae69be296a1ec057e70e86ad242
https://pubmed.ncbi.nlm.nih.gov/30828179
https://pubmed.ncbi.nlm.nih.gov/30828179
Akademický článek
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Free testosterone level in patients with homozygous beta thalassemia on regular transfusions regimen
Publikováno v:
Paediatrica Indonesiana, Vol 44, Iss 2, Pp 73-9 (2016)
Background Patients with homozygous beta thalassemia require regular transfusions which will lead to iron deposition in tissues including testicles. Objective This study aimed to evaluate testicular function in synthesizing testosterone by measuring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b3401164e2f5a201e3155c1420f40f7
https://doi.org/10.14238/pi44.2.2004.73-9
https://doi.org/10.14238/pi44.2.2004.73-9
Autor:
Z. Margellis, Maria Tsironi, Ch. Kattamis, Athanasios Aessopos, Vassilis Ladis, Spyros Deftereos
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 120(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4069678918ea140667df2d7b0f62205d
https://pubmed.ncbi.nlm.nih.gov/15866098
https://pubmed.ncbi.nlm.nih.gov/15866098
Autor:
Efthymia Alexopoulou, Nikolaos Kelekis, Elias Brountzos, Angeliki Boussiotou, Vasilis Ladis, Dimitrios A. Kelekis
Publikováno v:
Journal of magnetic resonance imaging : JMRI. 18(5)
Giant adrenal myelolipoma is an uncommon entity. We present the atypical MR imaging findings of a giant adrenal myelolipoma in a patient with homozygous beta-thalassemia with histopathology correlation. The tumor showed a drop in signal on the oppose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e21cd66e79028f64118dd1d11ff8c052
https://pubmed.ncbi.nlm.nih.gov/14579404
https://pubmed.ncbi.nlm.nih.gov/14579404
Autor:
Graham D. Sher, Anne F. Collins, Douglas M. Templeton, Peter P. Liu, Jagdish Butany, William H. Francombe, Paul D. Greig, Nancy F. Olivieri, Paul A. Daly, Patricia J. McCusker
Publikováno v:
New England Journal of Medicine. 330:1125-1127
Most patients with homozygous β-thalassemia require red-cell transfusions to survive beyond the first decade of life. Although this intervention clearly prolongs survival,1 it also results in the accumulation of iron in tissue, which is itself fatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e12d148b3d30b03dc21a449583c2f5fa
https://doi.org/10.1056/nejm199404213301605
https://doi.org/10.1056/nejm199404213301605
Publikováno v:
Pediatric Blood & Cancer. 54:627-628
Clinically apparent jaundice is unusual in patients with beta-thalassemia major. Co-inheritance of Gilbert syndrome has been reported to cause hyperbilirubinemia in these subjects. Crigler-Najjar syndrome is another rare disorder of bilirubin metabol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a010a7573578e19c3e0395a5123086ac
https://doi.org/10.1002/pbc.22313
https://doi.org/10.1002/pbc.22313
Publikováno v:
Clinical Biochemistry. 23:529-531
G γ: A γ chain ratios were determined in homozygous beta thalassemia and cord blood samples using triton—urea polyacrylamide gel electrophoresis. The mean G γ/ G γ + A γ proportion in the two groups were 0.62 ± 0.10 and 0.72 ± 0.03, respecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7babbf380204f572901f51359b9b093a
https://doi.org/10.1016/0009-9120(90)80044-j
https://doi.org/10.1016/0009-9120(90)80044-j