Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Filiotou, A."'
Autor:
Kaloterakis, A., Filiotou, A., Konstantopoulos, K., Rombos, Y., Bossinakou, I., Hadziyannis, S.
Publikováno v:
Haematologia. 2001, Vol. 31 Issue 2, p153-159. 7p.
Publikováno v:
Human Heredity, 1983 Jan 01. 33(3), 188-191.
Externí odkaz:
https://www.jstor.org/stable/45102133
Publikováno v:
Annals of Gastroenterology : Quarterly Publication of the Hellenic Society of Gastroenterology
Scopus-Elsevier
Scopus-Elsevier
Patients with autoimmune disorders seem to have an elevated risk of lymphoma, especially non-Hodgkin’s lymphoma (NHL). The increased risk has been attributed to the disturbance of immune function found in these patients or to the immunosuppressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9f457b29ea31bb3ddd36b4f10d19f69a
http://europepmc.org/articles/PMC3959296
http://europepmc.org/articles/PMC3959296
Autor:
Christos Zovoilis, Alexandra Alexopoulou, Spyros P. Dourakis, Anna Filiotou, Athanasios J. Archimandritis, Aris Androulakis, Emmanouel Agapitos
Publikováno v:
International Journal of Hematology. 86:333-336
A 47-year-old woman presented with severe hemolytic uremic syndrome (HUS) followed by heart failure. An echocardiogram showed an ejection fraction of 20%, and a cardiac catheterization followed by a myocardial histologic evaluation demonstrated dilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8200b5194b525fb7f0b279a33515b24
https://doi.org/10.1532/ijh97.e0713
https://doi.org/10.1532/ijh97.e0713
Publikováno v:
Haematologia. 31:153-159
Multiple myeloma (MM) is rare among patients with sickle cell syndromes (SCS). We describe six Greek sickle cell patients aged 56 to 65 years: five haemoglobin Sbeta+thalassaemia (HbSbeta+ (thal), one sickle cell anaemia (HbSS), who developed MM (thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a93f191f8c6d6dba45d52e120295b90
https://doi.org/10.1163/15685590152492963
https://doi.org/10.1163/15685590152492963
Autor:
I. Raptis, C. Zouboulis, A. Filiotou, J. Koskinas, H. Michelakakis, Andreas Kaloterakis, S. Hadziyannis
Publikováno v:
Journal of Internal Medicine. 246:587-590
Chronic Gaucher disease [GD] in association with systemic AL amyloidosis is extremely rare. We describe a 46-year-old Greek male with chronic GD confirmed by low glucocerebroside activity in fibroblasts and N370S/L444P mutations at the cerebrosidase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd3a348d507a77c93a64270f5655032c
https://doi.org/10.1046/j.1365-2796.1999.00607.x
https://doi.org/10.1046/j.1365-2796.1999.00607.x
Autor:
Melanie Deutsch, Emmanuel Tsochatzis, Dimitrios Vassilopoulos, Anna Filiotou, Athanasios J. Archimandritis, Anna Tasidou
Publikováno v:
JCR: Journal of Clinical Rheumatology. 11:326-328
Angioimmunoblastic T-cell lymphoma (AITL) is a rare type of non-Hodgkin lymphoma with systemic manifestations, including fever, lymphadenopathy, rash, and rarely arthritis. We report the case of a patient who presented with symmetric inflammatory pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82795a28dad3c649ce9d3921f116817b
https://doi.org/10.1097/01.rhu.0000195105.20029.07
https://doi.org/10.1097/01.rhu.0000195105.20029.07
Publikováno v:
Lupus. 2002, Vol. 11 Issue 3, p190-192. 3p. 1 Chart.
Publikováno v:
Lupus. 11:190-192
The case of a Greek woman with acute intermittent porphyria (AIP) associated with systemic lupus erythematosus (SLE) is described and the literature on this association is reviewed. The coexistence of these two diseases may be determined by unknown m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91f66628ccfda57542ef258cdebca1e
https://doi.org/10.1191/0961203302lu159cr
https://doi.org/10.1191/0961203302lu159cr
Autor:
Maria-Vasiliki, Papageorgiou, Alexandra, Alexopoulou, Flora, Kontopidou, Anna, Filiotou, John, Koskinas, Dimitrios, Pectasides
Publikováno v:
Anticancer research. 31(4)
We describe here the rare coexistence, at the time of diagnosis, of a myeloproliferative neoplasm (MPN) and non-Hodgkin's lymphoma (NHL) in a 74-year-old patient who presented with thrombocytosis and signs of portal hypertension on physical examinati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::78c10377d80fd13e64b2540fd950d576
https://pubmed.ncbi.nlm.nih.gov/21508404
https://pubmed.ncbi.nlm.nih.gov/21508404