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Recenti Progressi in Medicina|October 1, 1989
Hypothalamic pituitary adrenal function in patients with thalassemia majorD Bisbocci, C Camaschella, D Sperone, et al.Minerva Pediatrica|February 12, 1999
[Oxatomide in the treatment of atopic dermatitis]M Duse, R Merlini, R Gardenghi, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1995
Characterization of mitochondrial DNA in primary cardiomyopathiesA Bobba, S Giannattasio, A Pucci, et al.Haematologica|August 16, 2000
Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietinM De Gobbi, P Pasquero, F Brunello, et al.Blood|August 9, 2001
Natural history of congenital dyserythropoietic anemia type IIA Iolascon, J Delaunay, S N Wickramasinghe, et al.Human Mutation|November 26, 1999
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, ItalyI Dianzani, U Landegren, C Camaschella, et al.British Journal of Haematology|April 1, 1992
Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFHE Gottardi, M Losekoot, R Fodde, et al.British Journal of Haematology|May 1, 1976
Clinical and haematological data in 254 cases of beta-thalassaemia trait in ItalyU Mazza, G Saglio, F C Cappio, et al.American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.Pageof 11