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British Journal of Haematology
|
March 1, 1995
Clinical and laboratory effects of long-term administration of hydroxyurea to patients with sickle-cell/beta-thalassaemia
E Voskaridou, V Kalotychou, D Loukopoulos
Minerva Pediatrica
|
May 31, 2008
Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report
V Kalotychou, A Kanta, Y Rombos, et al.
Blood Cells, Molecules & Diseases
|
December 9, 2000
Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece
D Loukopoulos, E Voskaridou, V Kalotychou, et al.
Panminerva Medica
|
July 13, 2001
Clinical significance of the molecular detection of melanoma cells circulating in the peripheral blood in melanoma patients
K Konstantopoulos, M Psatha, V Kalotychou, et al.
American Journal of Hematology
|
January 12, 2000
Neutrophil elastase in patients with homozygous beta-thalassemia and pseudoxanthoma elasticum-like syndrome
M Samarkos, A Aessopos, C Fragodimitri, et al.
Postgraduate Medical Journal
|
November 8, 2005
Systolic and diastolic function in middle aged patients with sickle beta thalassaemia. An echocardiographic study
I Moyssakis, R Tzanetea, P Tsaftaridis, et al.
The West Indian Medical Journal
|
July 20, 2012
Mediterranean fever gene mutations in Greek patients with Behcet's disease
K Konstantopoulos, E Kanta, V Papadopoulos, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Hydroxyurea therapy in thalassemia
D Loukopoulos, E Voskaridou, A Stamoulakatou, et al.
Haematologica
|
February 22, 2000
Chelation therapy in patients with thalassemia using the orally active iron chelator deferiprone (L1)
Y Rombos, R Tzanetea, K Konstantopoulos, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
British Journal of Haematology
|
March 1, 1995
Clinical and laboratory effects of long-term administration of hydroxyurea to patients with sickle-cell/beta-thalassaemia
E Voskaridou, V Kalotychou, D Loukopoulos
Minerva Pediatrica
|
May 31, 2008
Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report
V Kalotychou, A Kanta, Y Rombos, et al.
Blood Cells, Molecules & Diseases
|
December 9, 2000
Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece
D Loukopoulos, E Voskaridou, V Kalotychou, et al.
Panminerva Medica
|
July 13, 2001
Clinical significance of the molecular detection of melanoma cells circulating in the peripheral blood in melanoma patients
K Konstantopoulos, M Psatha, V Kalotychou, et al.
American Journal of Hematology
|
January 12, 2000
Neutrophil elastase in patients with homozygous beta-thalassemia and pseudoxanthoma elasticum-like syndrome
M Samarkos, A Aessopos, C Fragodimitri, et al.
Postgraduate Medical Journal
|
November 8, 2005
Systolic and diastolic function in middle aged patients with sickle beta thalassaemia. An echocardiographic study
I Moyssakis, R Tzanetea, P Tsaftaridis, et al.
The West Indian Medical Journal
|
July 20, 2012
Mediterranean fever gene mutations in Greek patients with Behcet's disease
K Konstantopoulos, E Kanta, V Papadopoulos, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Hydroxyurea therapy in thalassemia
D Loukopoulos, E Voskaridou, A Stamoulakatou, et al.
Haematologica
|
February 22, 2000
Chelation therapy in patients with thalassemia using the orally active iron chelator deferiprone (L1)
Y Rombos, R Tzanetea, K Konstantopoulos, et al.
Page
of 1