Showing results (301-310 of 431) with videos related to

Sort By:
Pageof 44
Bollettino Della Societa Italiana Di Biologia Sperimentale|August 31, 1984
Human leukemic K562 cells: differential effects of 5-azacytidine on DNA methylation of epsilon-, gamma-globin and 7SL RNA genesL del Senno, F Conconi, R Barbieri, et al.
Pediatric Pulmonology|November 1, 1986
Modification of nonspecific bronchial reactivity in hypothyroid children under different regimens of substitutive opotherapyM P Villa, G Cerimoniale, F Bernardi, et al.
Pituitary|February 15, 2013
Thrombin generation in Cushing's Syndrome: do the conventional clotting indices tell the whole truth?S Koutroumpi, L Spiezia, N Albiger, et al.
Thrombosis and Haemostasis|March 1, 1996
The risk of abortion and stillbirth in antithrombin-, protein C-, and protein S-deficient womenB J Sanson, P W Friederich, P Simioni, et al.
Archives of Internal Medicine|January 13, 1997
Upper-extremity deep vein thrombosis. Risk factors, diagnosis, and complicationsP Prandoni, P Polistena, E Bernardi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery diseaseP Ferraresi, G Marchetti, C Legnani, et al.
The Aging Male : the Official Journal of the International Society for the Study of the Aging Male|January 28, 2005
Long-term low-dose dehydroepiandrosterone replacement therapy in aging males with partial androgen deficiencyA R Genazzani, S Inglese, I Lombardi, et al.
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
British Journal of Haematology|March 1, 1990
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogeneF Bernardi, G Marchetti, A Casonato, et al.
Human Genetics|July 1, 1992
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)G Marchetti, P Patracchini, D Gemmati, et al.
Pageof 44