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Annals of Hematology
|
December 1, 1993
Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques
D Caprino, M Acquila, P G Mori
British Journal of Haematology
|
July 1, 1992
GAA(Glu)272----AAA(Lys) and CGA(Arg)1941----CAA(Gln) in the factor VIII gene in two haemophilia A patients of Czech origin
A Krepelová, Z Vorlová, M Acquila, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 9, 2011
Molecular analysis of severe factor XI deficiency in three Italian patients
M P Bicocchi, F Marotta, L Banov, et al.
Nucleic Acids Research
|
August 25, 1990
DGGE detection of HhaI polymorphism in the F9 gene
D Caprino, M Acquila, M Pecorara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 20, 2008
An uncommon case of a female carrier of two distinct X-linked disorders
C Fabiano, M Acquila, M P Bicocchi, et al.
European Journal of Haematology
|
July 29, 2000
More on the relationship between cystic fibrosis and venous thrombosis
P G Mori, M Acquila, M P Bicocchi, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52
C Panarello, M Acquila, D Caprino, et al.
Blood
|
January 15, 1995
A skewed lyonization phenomenon as cause of hemophilia A in a female patient
M Acquila, D Caprino, P Bicocchi, et al.
European Journal of Pediatrics
|
February 9, 2000
Recurrent antiphospholipid-related deep vein thrombosis as presenting manifestation of systemic lupus erythematosus
M Gattorno, A C Molinari, A Buoncompagni, et al.
British Journal of Haematology
|
September 1, 1991
A pediatric case of pure red cell aplasia: successful treatment with anti-lymphocyte globulin and correlation with in vitro T cell-mediated inhibition of erythropoiesis
A Corcione, M Pasino, A C Molinari, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
Annals of Hematology
|
December 1, 1993
Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques
D Caprino, M Acquila, P G Mori
British Journal of Haematology
|
July 1, 1992
GAA(Glu)272----AAA(Lys) and CGA(Arg)1941----CAA(Gln) in the factor VIII gene in two haemophilia A patients of Czech origin
A Krepelová, Z Vorlová, M Acquila, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 9, 2011
Molecular analysis of severe factor XI deficiency in three Italian patients
M P Bicocchi, F Marotta, L Banov, et al.
Nucleic Acids Research
|
August 25, 1990
DGGE detection of HhaI polymorphism in the F9 gene
D Caprino, M Acquila, M Pecorara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 20, 2008
An uncommon case of a female carrier of two distinct X-linked disorders
C Fabiano, M Acquila, M P Bicocchi, et al.
European Journal of Haematology
|
July 29, 2000
More on the relationship between cystic fibrosis and venous thrombosis
P G Mori, M Acquila, M P Bicocchi, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52
C Panarello, M Acquila, D Caprino, et al.
Blood
|
January 15, 1995
A skewed lyonization phenomenon as cause of hemophilia A in a female patient
M Acquila, D Caprino, P Bicocchi, et al.
European Journal of Pediatrics
|
February 9, 2000
Recurrent antiphospholipid-related deep vein thrombosis as presenting manifestation of systemic lupus erythematosus
M Gattorno, A C Molinari, A Buoncompagni, et al.
British Journal of Haematology
|
September 1, 1991
A pediatric case of pure red cell aplasia: successful treatment with anti-lymphocyte globulin and correlation with in vitro T cell-mediated inhibition of erythropoiesis
A Corcione, M Pasino, A C Molinari, et al.
Page
of 3