Zobrazeno 1 - 10
of 116
pro vyhledávání: '"N. Gombakis"'
Publikováno v:
Case Reports in Pediatrics, Vol 2014 (2014)
Nephroblastomatosis (NB) has been considered as a precursor of Wilms tumor (WT). The natural history of NB seems to present significant variation as some lesions may regress spontaneously, while others may grow and expand or relapse and develop into
Externí odkaz:
https://doaj.org/article/358b9da5b78d4b8c8252d764a519a789
Publikováno v:
Balkan Journal of Medical Genetics, Vol 23, Iss 2, Pp 107-110 (2021)
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics : BJMG
Osteopetrosis refers to a group of rare hereditary disorders characterized by generalized skeletal densification due to limited bone resorption by osteoclasts. The infantile autosomal recessive form represents the most malignant one with onset early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f7ecd968d417a4c9498fbcb31639b4
https://doi.org/10.2478/bjmg-2020-0019
https://doi.org/10.2478/bjmg-2020-0019
Autor:
Maria Hatzistilianou, Athanasios Tragiannidis, Maria Palabougiouki, Ioannis Kyriakidis, N. Gombakis, Tatiani Moudiou, Eleni Vasileiou, Timoleon Vyzantiadis, Maria Stamou
Publikováno v:
Türk Pediatri Arşivi.
Both biliary atresia and hemoglobinopathies have been associated with a higher incidence of bloodstream infections. We hereby present the case of a female infant of Nigerian descent with extrahepatic biliary atresia and double heterozygocity for sick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b723a54b8999c4a5b2ea9e3809a68f8a
https://doi.org/10.14744/turkpediatriars.2019.67674
https://doi.org/10.14744/turkpediatriars.2019.67674
Autor:
A. Kargioti, Timoleon-Achilleas Vyzantiadis, Aikaterini Teli, Efthymia Vlachaki, Marina Economou, Vassilia Garypidou, Nikolaos Neokleous, Sofia Vakalopoulou, Fotios Papachristou, N. Gombakis, Stamatia Theodoridou
Publikováno v:
Acta Haematologica. 132:45-48
The aim of this study was to investigate platelet function in patients with thalassaemia and to detect any relation to chelation treatment (deferasirox or deferiprone/deferiprone plus desferioxamine). Thirty-three transfusion-dependent patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f10014dcaa2ff08e9cc11ebbd1982f8
https://doi.org/10.1159/000355817
https://doi.org/10.1159/000355817
Autor:
N. Gombakis, V Tzimouli, F. Kanakoudi, D. Kleta, D. J. Zafeiriou, A. Taparkou, M. Athanassiou, Zoe Dorothea Pana, V. Garipidou, Emmanuil S. Hatzipantelis
Publikováno v:
International Journal of Hematology. 98:158-163
Sickle cell disease pathogenesis is a complex interplay of multiple factors associated with vascular endothelial activation, intense oxidative stress, and increased sickle cell adhesion. The aim of this study was to determine and compare three panels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e21e12bc17abcfa93454eb383260fd
https://doi.org/10.1007/s12185-013-1392-y
https://doi.org/10.1007/s12185-013-1392-y
Autor:
Fani Athanassiadou-Piperopoulou, Athanasios Tragiannidis, Norma Vavatsi-Christaki, Miranda Athanassiou-Metaxa, Eliza Karatza, Andromachi Papagianni, Fekri Samarah, N. Gombakis, Marina Economou
Publikováno v:
Blood Coagulation & Fibrinolysis. 24:35-39
Primary immune thrombocytopenia (ITP) is the commonest acquired cause of bleeding in childhood. The aim of the present study was to evaluate the role of FcγRIIa and FcγRIIIa polymorphisms in the pathogenesis and therapeutic result of childhood ITP.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e83707f5a97936788a7c7d9d924b9118
https://doi.org/10.1097/mbc.0b013e328359bc3b
https://doi.org/10.1097/mbc.0b013e328359bc3b
Autor:
Emmanuel Hatzipantelis, Maria Papageorgiou, Theodotis Papageorgiou, Athanasios Tragiannidis, Maria Hatzistilianou, N. Gombakis
Publikováno v:
International journal of immunopathology and pharmacology. 29(4)
Treatment-related myelodysplastic syndrome (t-MDS)/acute myeloid leukemia (AML) is a devastating early or late complication of treatment for childhood cancer related with a significant morbidity and mortality. We retrospectively studied survivors of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0ca281ec4d092eeca0711275fc547e5
https://pubmed.ncbi.nlm.nih.gov/27647464
https://pubmed.ncbi.nlm.nih.gov/27647464
Autor:
Vasilia Garipidou, Vasiliki Sidi-Fragandrea, N. Gombakis, Vaso Tzimouli, Theothotis Papageorgiou, Miranda Athanassiou-Metaxa, Fani Athanasiadou-Piperopoulou, Emmanouel S. Hatzipantelis, Dimitrios Koliouskas, Drosia Kleta, Anna Taparkou
Publikováno v:
Acta Haematologica. 125:130-135
The severe endothelial dysfunction in children with acute lymphoblastic leukemia (ALL) can result from the disease itself, from treatment, or from other conditions (e.g. sepsis). The aim of this study was to determine the levels of markers of endothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c64e3ad83c24d57b4246dba50e19e2d
https://doi.org/10.1159/000322120
https://doi.org/10.1159/000322120
Autor:
D. Haas, Joél Smet, M. Tamiolaki, Adrian C. Sewell, Dimitrios I. Zafeiriou, R. van Coster, Christine Vianey-Saban, Persephone Augoustides-Savvopoulou, Euthymia Vargiami, Panagiota Triantafyllou, N. Gombakis, Niels Gregersen
Publikováno v:
Neuropediatrics. 38:78-82
Ethylmalonic encephalopathy (EE) is a rare, recently defined inborn error of metabolism which affects the brain, gastrointestinal system and peripheral blood vessels and is characterized by a unique constellation of clinical and biochemical features.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc6c52c446675b9a5d3e520d86e23a9
https://doi.org/10.1055/s-2007-984447
https://doi.org/10.1055/s-2007-984447
Autor:
Maria Kourti, Vasiliki Sidi, Dimitrios Koliouskas, Fani Athanassiadou, N. Gombakis, George Tzimagiorgis, Norma Vavatsi
Publikováno v:
Pediatric Hematology and Oncology. 23:489-494
Modern treatment protocols lead to complete remission in a high proportion of patients with childhood acute lymphoblastic leukemia (ALL). However, a large number of them show a relapse of the disease. Treatment failure in these patients is mainly att
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be8b7c48d1b7ed5f82486ac2cb2de39
https://doi.org/10.1080/08880010600719303
https://doi.org/10.1080/08880010600719303