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European Journal of Haematology
|
April 21, 1998
An unusual case of familial aplastic anaemia: in vitro and in vivo evidence for a multipotent progenitor responsive to G-CSF
C Dufour, J Maher, N Murray, et al.
Haematologica
|
February 1, 1979
The PNH abnormality in myeloproliferative disorders: association of PNH and acute erythremic myelosis in two children
L Luzzatto, J B Familusi, C K Williams, et al.
Annals of Tropical Medicine and Parasitology
|
February 1, 1988
Decreased malaria morbidity in the Tharu people compared to sympatric populations in Nepal
L Terrenato, S Shrestha, K A Dixit, et al.
Nucleic Acids Research
|
June 24, 1988
Polymerase chain reaction automated at low cost
N S Foulkes, P P Pandolfi de Rinaldis, J Macdonnell, et al.
BMJ (Clinical Research Ed.)
|
January 27, 1990
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-)
S Galiano, G F Gaetani, A Barabino, et al.
Haematologica
|
November 1, 1996
Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis
K Nafa, M Bessler, P Mason, et al.
Blood
|
June 14, 2000
Mild spherocytic hereditary elliptocytosis and altered levels of alpha- and gamma-adducins in beta-adducin-deficient mice
A F Muro, M L Marro, S Gajović, et al.
Nature
|
July 14, 2000
Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin
C May, S Rivella, J Callegari, et al.
Acta Haematologica
|
January 1, 1984
Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza)
A Ventura, F Panizon, M R Soranzo, et al.
European Journal of Biochemistry
|
December 1, 1988
The production of normal and variant human glucose-6-phosphate dehydrogenase in cos cells
P J Mason, T J Vulliamy, N S Foulkes, et al.
Page
of 26
Search research articles
Search
Showing results (181-190 of 259) with videos related to
Sort By:
Page
of 26
European Journal of Haematology
|
April 21, 1998
An unusual case of familial aplastic anaemia: in vitro and in vivo evidence for a multipotent progenitor responsive to G-CSF
C Dufour, J Maher, N Murray, et al.
Haematologica
|
February 1, 1979
The PNH abnormality in myeloproliferative disorders: association of PNH and acute erythremic myelosis in two children
L Luzzatto, J B Familusi, C K Williams, et al.
Annals of Tropical Medicine and Parasitology
|
February 1, 1988
Decreased malaria morbidity in the Tharu people compared to sympatric populations in Nepal
L Terrenato, S Shrestha, K A Dixit, et al.
Nucleic Acids Research
|
June 24, 1988
Polymerase chain reaction automated at low cost
N S Foulkes, P P Pandolfi de Rinaldis, J Macdonnell, et al.
BMJ (Clinical Research Ed.)
|
January 27, 1990
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-)
S Galiano, G F Gaetani, A Barabino, et al.
Haematologica
|
November 1, 1996
Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis
K Nafa, M Bessler, P Mason, et al.
Blood
|
June 14, 2000
Mild spherocytic hereditary elliptocytosis and altered levels of alpha- and gamma-adducins in beta-adducin-deficient mice
A F Muro, M L Marro, S Gajović, et al.
Nature
|
July 14, 2000
Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin
C May, S Rivella, J Callegari, et al.
Acta Haematologica
|
January 1, 1984
Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza)
A Ventura, F Panizon, M R Soranzo, et al.
European Journal of Biochemistry
|
December 1, 1988
The production of normal and variant human glucose-6-phosphate dehydrogenase in cos cells
P J Mason, T J Vulliamy, N S Foulkes, et al.
Page
of 26