Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Andreas Kaloterakis"'
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
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
Autor:
Andreas Kaloterakis, Constantin Papageorgiou, Alexandra Alexopoulou, Stephanos J. Hadziyannis, Spyros P. Dourakis
Publikováno v:
European Journal of Internal Medicine. 15:248-250
Sickle-cell trait has been characterized as a benign condition. However, life-threatening complications sometimes develop. Acute chest syndrome (ACS) is usually described in homozygous sickle cell disease, but it rarely develops in individuals with s
Autor:
Erwin Tschachler, Joannis Stratigos, Theresa Popow-Kraupp, Rudolf Berger, Dean L. Mann, Georg Stingl, Eva Zonzits, Angelos Hatzakis, Robert J. Biggar, Reinhard Gillitzer, Klemens Rappersberger, Andreas Kaloterakis, Klaus Wolff
Publikováno v:
Journal of Investigative Dermatology. 95:371-381
In 1984, Greek physicians reported on the clustering of cases of Kaposi's sarcoma (KS) on the Peloponnesus peninsula. To gain more insight into its pathogenesis, we studied the seroepidemiologic and clinicopathologic characteristics of 12 Greek KS pa
Autor:
Andreas, Kaloterakis, Ioannis, Rizos, Georgios, Goumas, Anna, Filiotou, John, Barbetseas, Sotiris, Papathanasiou, Pavlos, Toutouzas
Publikováno v:
The Journal of heart valve disease. 12(5)
A case is reported of isolated native tricuspid calve Candida parapsilosis endocarditis (INTVCE) in a male patient with no history of drug abuse or heart disease. The patient had received hyperalimentation and antibiotics for four months via a centra
Autor:
Spyros P., Dourakis, Alexandra, Alexopoulou, Constantin, Papageorgiou, Andreas, Kaloterakis, Stephanos J., Hadziyannis
Publikováno v:
European journal of internal medicine. 15(4)
Sickle-cell trait has been characterized as a benign condition. However, life-threatening complications sometimes develop. Acute chest syndrome (ACS) is usually described in homozygous sickle cell disease, but it rarely develops in individuals with s
Publikováno v:
Gastrointestinal endoscopy. 42(4)
The frequency and degree of gastrointestinal involvement in patients with Mediterranean Kaposi's sarcoma (non-AIDS), a newly recognized form of Kaposi's sarcoma, is unknown. Eighty-seven patients with Mediterranean Kaposi's sarcoma proven by skin and
Autor:
John Stratigos, C. Papasteriades, S. Hadjiyannis, Anna Filiotou, J. Economidou, Andreas Kaloterakis
Publikováno v:
Tissue antigens. 45(2)
Fifty-four (54) unrelated patients with Mediterranean Kaposi's sarcoma (MKS) and 8 patients members of 4 unrelated families with familial MKS were serotyped for HLA-A,B and DR antigens. The diagnosis was histologically confirmed and all patients were
Publikováno v:
European Journal of Haematology. 69:191-192
Autor:
Anna Filiotou, Andreas Kaloterakis
Publikováno v:
British Journal of Haematology. 106:836-836