Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Haido Tsantali"'
Autor:
Emmanuel Roilides, Evangelia Farmaki, Persephone Augoustides-Savvopoulou, Kalomoira Kefala-Agoropoulou, Eliza Karatza, John Tsiouris, Anna Lazaridou, Haido Tsantali
Publikováno v:
Hematology. 12:549-553
Background: Pearson syndrome is a rare mitochondrial disorder characterized by sideroblastic anemia, liver disease, renal tubulopathy and exocrine pancreas deficiency. Observations: We describe a female infant suffering from anemia since birth who gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5003c4b8cb4eb974b06dc9c8277512
https://doi.org/10.1080/10245330701400900
https://doi.org/10.1080/10245330701400900
Autor:
Miranda Athanassiou-Metaxa, Emmanouil Hatzipantelis, Athanasios Christoforidis, Eirini Kazantzidou, Ioanna Tsatra, George Katzos, George Koliakos, Haido Tsantali
Publikováno v:
HORMONES. 6:334-340
OBJECTIVE Osteopenia/osteoporosis of multi-factorial pathogenetic mechanism is reported to be a significant cause of morbidity in adult patients with beta-thalassaemia major. Even in young patients, decreased Bone Mineral Density (BMD) values are a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb909d59ad05d5a30d77a1f67d38394
https://doi.org/10.14310/horm.2002.1111030
https://doi.org/10.14310/horm.2002.1111030
Autor:
Alexandra Stamoulakatou, Amine Zorai, Piero C. Giordano, Kees Harteveld, Joanne Traeger-Synodinos, Miranda Athanasiou-Metaxa, Haido Tsantali, Ioannis Papassotiriou, Evangelos Premetis, Emmanuel Kanavakis, Christina Lazaropoulou
Publikováno v:
Blood Cells, Molecules, and Diseases. 32:118-123
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=doi_dedup___::6de0f19b8acad069b9c1a5fa2af4bb61
https://doi.org/10.1016/j.bcmd.2003.10.009
https://doi.org/10.1016/j.bcmd.2003.10.009
Autor:
Ioanna Tsatra, Athanasios Dimitriadis, Athanasios Christoforidis, Afroditi Haritandi, Miranda Athanassiou-Metaxa, Stavroula Karyda, Haido Tsantali, Ioannis Tsitouridis
Publikováno v:
Journal of pediatric hematology/oncology. 28(5)
Clinical complications resulting from unevenly iron accumulation in individual organs of patients with beta-thalassemia major can affect both expectancy and quality of life. Magnetic resonance imaging (MRI) offers a quantitative, noninvasive, accurat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd6bc862b8ae3fb0fef4314c42ec490
https://pubmed.ncbi.nlm.nih.gov/16772883
https://pubmed.ncbi.nlm.nih.gov/16772883