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M G Bisconte

Showing results (1-10 of 7) with videos related to

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Hemoglobin|January 1, 1989
Hb G-San Jose homozygosis in a Calabrian familyC Brancati, M Caracciolo, M Bria, et al.
Human Genetics|March 1, 1995
SP alpha I/65 hereditary elliptocytosis in Calabria (southern Italy)A Qualtieri, M G Bisconte, A Pasqua, et al.
British Journal of Haematology|May 1, 1997
Spectrin Cosenza: a novel beta chain variant associated with Sp alphaI/74 hereditary elliptocytosisA Qualtieri, A Pasqua, M G Bisconte, et al.
Italian Journal of Orthopaedics and Traumatology|June 1, 1991
Skeletal changes in thalassemia majorE Giuzio, M Bria, M G Bisconte, et al.
British Journal of Haematology|January 31, 1998
Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemiaA Qualtieri, V Pedace, M G Bisconte, et al.
La Chirurgia Degli Organi Di Movimento|October 1, 1991
Osteoporosis in patients affected with thalassemia. Our experienceE Giuzio, M Bria, M G Bisconte, et al.
Journal of Endocrinological Investigation|June 23, 2009
Autoimmune hemolityc anemia concomitant with sequential autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Hashimoto's thyroiditis: a new entity of autoimmune polyendocrine syndromeM Gentile, M Verta, E Vigna, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Hemoglobin|January 1, 1989
Hb G-San Jose homozygosis in a Calabrian familyC Brancati, M Caracciolo, M Bria, et al.
Human Genetics|March 1, 1995
SP alpha I/65 hereditary elliptocytosis in Calabria (southern Italy)A Qualtieri, M G Bisconte, A Pasqua, et al.
British Journal of Haematology|May 1, 1997
Spectrin Cosenza: a novel beta chain variant associated with Sp alphaI/74 hereditary elliptocytosisA Qualtieri, A Pasqua, M G Bisconte, et al.
Italian Journal of Orthopaedics and Traumatology|June 1, 1991
Skeletal changes in thalassemia majorE Giuzio, M Bria, M G Bisconte, et al.
British Journal of Haematology|January 31, 1998
Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemiaA Qualtieri, V Pedace, M G Bisconte, et al.
La Chirurgia Degli Organi Di Movimento|October 1, 1991
Osteoporosis in patients affected with thalassemia. Our experienceE Giuzio, M Bria, M G Bisconte, et al.
Journal of Endocrinological Investigation|June 23, 2009
Autoimmune hemolityc anemia concomitant with sequential autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Hashimoto's thyroiditis: a new entity of autoimmune polyendocrine syndromeM Gentile, M Verta, E Vigna, et al.
Pageof 1