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R Corrocher

Showing results (91-100 of 212) with videos related to

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Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
Clinical and Experimental Rheumatology|May 1, 1989
Thrombocytopenia in a case of Wegener's granulomatosisG B Gabrielli, G Pavarana, M Casaril, et al.
Human Genetics|August 14, 2001
A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous diseaseL Borgato, A Bonizzato, C Lunardi, et al.
Blood|July 1, 1994
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemiasO Olivieri, L De Franceschi, M D Capellini, et al.
Minerva Cardioangiologica|September 1, 1979
[Arterial hypertension and multiple renal arteries]F Bonfanti, R Corrocher, L M Bambara, et al.
Tumori|December 31, 1986
Reduction of liver glutathione peroxidase activity and deficiency of serum selenium in patients with hepatocellular carcinomaR Corrocher, M Casaril, G Bellisola, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
Serum laminin P1 in chronic viral hepatitis: correlations with liver histological activity and diagnostic valueG B Gabrielli, F Capra, M Casaril, et al.
Minerva Medica|November 17, 1984
[Persistent generalized lymphadenopathy: pre-AIDS. First description of a case observed in Italy]G B Gabrielli, R Nortilli, P Mezzelani, et al.
Thrombosis and Haemostasis|December 14, 1999
Differential effects of dietary supplementation with fish oil or soy lecithin on human platelet adhesionG Andrioli, A Carletto, P Guarini, et al.
The Journal of Clinical Investigation|January 15, 1997
Deficiency of Src family kinases Fgr and Hck results in activation of erythrocyte K/Cl cotransportL De Franceschi, L Fumagalli, O Olivieri, et al.
Pageof 22

Showing results (91-100 of 212) with videos related to

Sort By:
Pageof 22
Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
Clinical and Experimental Rheumatology|May 1, 1989
Thrombocytopenia in a case of Wegener's granulomatosisG B Gabrielli, G Pavarana, M Casaril, et al.
Human Genetics|August 14, 2001
A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous diseaseL Borgato, A Bonizzato, C Lunardi, et al.
Blood|July 1, 1994
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemiasO Olivieri, L De Franceschi, M D Capellini, et al.
Minerva Cardioangiologica|September 1, 1979
[Arterial hypertension and multiple renal arteries]F Bonfanti, R Corrocher, L M Bambara, et al.
Tumori|December 31, 1986
Reduction of liver glutathione peroxidase activity and deficiency of serum selenium in patients with hepatocellular carcinomaR Corrocher, M Casaril, G Bellisola, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
Serum laminin P1 in chronic viral hepatitis: correlations with liver histological activity and diagnostic valueG B Gabrielli, F Capra, M Casaril, et al.
Minerva Medica|November 17, 1984
[Persistent generalized lymphadenopathy: pre-AIDS. First description of a case observed in Italy]G B Gabrielli, R Nortilli, P Mezzelani, et al.
Thrombosis and Haemostasis|December 14, 1999
Differential effects of dietary supplementation with fish oil or soy lecithin on human platelet adhesionG Andrioli, A Carletto, P Guarini, et al.
The Journal of Clinical Investigation|January 15, 1997
Deficiency of Src family kinases Fgr and Hck results in activation of erythrocyte K/Cl cotransportL De Franceschi, L Fumagalli, O Olivieri, et al.
Pageof 22