Showing results (21-30 of 650) with videos related to

Sort By:
Pageof 65
Acta Haematologica|October 26, 1999
Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case reportP Giordano, D De Lucia, B Coppola, et al.
Bone Marrow Transplantation|April 3, 2001
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II)A Iolascon, V Sabato, D de Mattia, et al.
Fish & Shellfish Immunology|September 15, 2001
Heavy metals affect the circulating haemocyte number in the shrimp Palaemon elegansS Lorenz, M Francese, V J Smith, et al.
Annali Dell'Istituto Superiore Di Sanita|July 29, 1998
[Blood lead levels during pregnancy in th the newborn period. Study of the population of Bari]R Carbone, N Laforgia, E Crollo, et al.
Haematologica|May 21, 1998
Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infantE Miraglia del Giudice, S Perrotta, C Lombardi, et al.
Human Mutation|May 2, 2000
Characterization of the CYP21 gene 5' flanking region in patients affected by 21-OH deficiencyA Bobba, E Marra, P Lattanzio, et al.
Biology of the Neonate|June 9, 1998
Maternal and neonatal lead exposure in southern ItalyR Carbone, N Laforgia, E Crollo, et al.
European Journal of Haematology|August 31, 2000
Transfusion-dependent congenital dyserythropoietic anaemia with intraerythroblastic inclusions of a non-globin proteinA Iolascon, B Martire, M J Lee, et al.
Acta Haematologica|January 1, 1993
Atypical hereditary ovalocytosis associated with defective dyserythropoietic anemiaM Jankovic, G Sansone, V Conter, et al.
Haematologica|March 21, 1998
Resistance to activated protein C as a risk factor of stroke in a thalassemic patientP Giordano, V Sabato, F Schettini, et al.
Pageof 65