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Recenti Progressi in Medicina
|
June 5, 2001
[Genetic risk factors in ischemic cardiopathy]
D Girelli, N Martinelli
Recenti Progressi in Medicina
|
September 1, 1991
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension]
O Olivieri, D Girelli, R Corrocher
Minerva Medica
|
January 7, 1998
["Hyperferritinemia-cataract syndrome." Description of a new hereditary disease, from anamnesis to molecular diagnosis]
D Girelli, P Piccoli, R Corrocher
Haematologica
|
September 5, 2001
Extensive life-threatening thrombosis in a patient with heparin-induced thrombocytopenia and factor V Leiden mutation
F Pizzolo, D Girelli, O Olivieri
Internal Medicine Journal
|
January 19, 2007
Recurrent needle-tract metastases of hepatocellular carcinoma following fine-needle aspiration
C Pavan, A Parisi, D Girelli
Haematologica
|
September 1, 1990
Red blood cell molecular abnormalities in non haematological diseases
G De Sandre, D Girelli, O Olivieri
Blood
|
June 1, 1996
Molecular basis for the hereditary hyperferritinemia-cataract syndrome
D Girelli, O Olivieri, P Gasparini, et al.
Preventive Medicine
|
September 1, 1996
Relationships between serum uric acid and lipids in healthy subjects
C Russo, O Olivieri, D Girelli, et al.
The European Journal of Medicine
|
January 1, 1993
Delayed multiorgan non-neoplastic damage after exposure to radiotherapy in infancy
O Olivieri, D Girelli, C Russo, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 27, 2005
Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?
B Lunghi, D Scanavini, D Girelli, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 84) with videos related to
Sort By:
Page
of 9
Recenti Progressi in Medicina
|
June 5, 2001
[Genetic risk factors in ischemic cardiopathy]
D Girelli, N Martinelli
Recenti Progressi in Medicina
|
September 1, 1991
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension]
O Olivieri, D Girelli, R Corrocher
Minerva Medica
|
January 7, 1998
["Hyperferritinemia-cataract syndrome." Description of a new hereditary disease, from anamnesis to molecular diagnosis]
D Girelli, P Piccoli, R Corrocher
Haematologica
|
September 5, 2001
Extensive life-threatening thrombosis in a patient with heparin-induced thrombocytopenia and factor V Leiden mutation
F Pizzolo, D Girelli, O Olivieri
Internal Medicine Journal
|
January 19, 2007
Recurrent needle-tract metastases of hepatocellular carcinoma following fine-needle aspiration
C Pavan, A Parisi, D Girelli
Haematologica
|
September 1, 1990
Red blood cell molecular abnormalities in non haematological diseases
G De Sandre, D Girelli, O Olivieri
Blood
|
June 1, 1996
Molecular basis for the hereditary hyperferritinemia-cataract syndrome
D Girelli, O Olivieri, P Gasparini, et al.
Preventive Medicine
|
September 1, 1996
Relationships between serum uric acid and lipids in healthy subjects
C Russo, O Olivieri, D Girelli, et al.
The European Journal of Medicine
|
January 1, 1993
Delayed multiorgan non-neoplastic damage after exposure to radiotherapy in infancy
O Olivieri, D Girelli, C Russo, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 27, 2005
Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?
B Lunghi, D Scanavini, D Girelli, et al.
Page
of 9