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D De Mattia

Showing results (41-50 of 90) with videos related to

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The Pediatric Infectious Disease Journal|June 1, 1990
Age-specific prevalence of hepatitis B virus infection among children in an endemic area in southern ItalyT Stroffolini, D De Mattia, A Compagnone, et al.
Acta Paediatrica Scandinavica|March 1, 1985
Post-natal development of protein C in full-term newbornsF Schettini, D De Mattia, M Altomare, et al.
Minerva Pediatrica|January 1, 1996
[Oromaxillofacial changes in thalassemia major]D De Mattia, P L Pettini, V Sabato, et al.
Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Acta Haematologica|January 13, 2001
Factors influencing effectiveness of deferiprone in a thalassaemia major clinical settingG C Del Vecchio, E Crollo, F Schettini, et al.
Angiology|September 1, 1993
Association of congenital afibrinogenemia and K-dependent protein C deficiency--a case reportD De Mattia, G Regina, P Giordano, et al.
Pediatric Hematology and Oncology|May 1, 1994
B-cell lymphoma in an HIV-1 positive childD De Mattia, D Pace, P Ferrante, et al.
Human Genetics|November 1, 1994
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemiaS Filosa, W Cai, R Galanello, et al.
Scandinavian Journal of Haematology|October 1, 1986
Cytochrome b and FAD content in polymorphonuclear leucocytes in a family with X-linked chronic granulomatous diseaseS Riccardi, D Giordano, F Schettini, et al.
La Ricerca in Clinica E in Laboratorio|October 1, 1988
Postnatal development of prekallikrein (Fletcher factor) in manF Schettini, D De Mattia, M M Manzionna, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
The Pediatric Infectious Disease Journal|June 1, 1990
Age-specific prevalence of hepatitis B virus infection among children in an endemic area in southern ItalyT Stroffolini, D De Mattia, A Compagnone, et al.
Acta Paediatrica Scandinavica|March 1, 1985
Post-natal development of protein C in full-term newbornsF Schettini, D De Mattia, M Altomare, et al.
Minerva Pediatrica|January 1, 1996
[Oromaxillofacial changes in thalassemia major]D De Mattia, P L Pettini, V Sabato, et al.
Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Acta Haematologica|January 13, 2001
Factors influencing effectiveness of deferiprone in a thalassaemia major clinical settingG C Del Vecchio, E Crollo, F Schettini, et al.
Angiology|September 1, 1993
Association of congenital afibrinogenemia and K-dependent protein C deficiency--a case reportD De Mattia, G Regina, P Giordano, et al.
Pediatric Hematology and Oncology|May 1, 1994
B-cell lymphoma in an HIV-1 positive childD De Mattia, D Pace, P Ferrante, et al.
Human Genetics|November 1, 1994
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemiaS Filosa, W Cai, R Galanello, et al.
Scandinavian Journal of Haematology|October 1, 1986
Cytochrome b and FAD content in polymorphonuclear leucocytes in a family with X-linked chronic granulomatous diseaseS Riccardi, D Giordano, F Schettini, et al.
La Ricerca in Clinica E in Laboratorio|October 1, 1988
Postnatal development of prekallikrein (Fletcher factor) in manF Schettini, D De Mattia, M M Manzionna, et al.
Pageof 9