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Haematologica
|
January 4, 1998
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis
P Sivera, A Roetto, U Mazza, et al.
International Journal of Laboratory Hematology
|
May 11, 2016
The mutual control of iron and erythropoiesis
C Camaschella, A Pagani, A Nai, et al.
Leukemia & Lymphoma
|
July 27, 2016
Granulocyte Macrophage Colony-Stimulating Factor (GM-CSF) Reduces Pancytopenia After Rescue Therapy in a Patient with Hodgkin's Lymphoma
W Piacibello, C Camaschella, A C Stern, et al.
British Journal of Haematology
|
September 1, 1991
A spontaneous mutation causing unstable Hb Hammersmith: detection of the beta 42 TTT----TCT change by CCM and direct sequencing
I Dianzani, S Ramus, R G Cotton, et al.
Trends in Genetics : TIG
|
December 1, 1993
Dilemmas and progress in mutation detection
I Dianzani, C Camaschella, A Ponzone, et al.
Minerva Chirurgica
|
October 31, 1977
[Diagnostic laparotomy in Hodgkin's disease]
F Rolfo, G Ardizzone, C Camaschella, et al.
PCR Methods and Applications
|
April 1, 1995
An efficient method for PCR analysis of mitochondrial DNA from paraffin-embedded archival heart tissue
A Bobba, R Lippolis, S Giannattasio, et al.
Thrombosis and Haemostasis
|
August 28, 2001
A new mutation trans to I278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease
S Bosio, G Cavallero, E Brusa, et al.
British Journal of Haematology
|
February 1, 1994
Clinical and haematological improvement induced by etidronate in a patient with idiopathic myelofibrosis and osteosclerosis
P Sivera, L Cesano, A Guerrasio, et al.
British Journal of Obstetrics and Gynaecology
|
May 1, 1990
Thrombotic thrombocytopenic purpura in pregnancy with maternal and fetal survival. Case report
A Maina, V Donvito, O Giachino, et al.
Page
of 15
Search research articles
Search
Showing results (11-20 of 141) with videos related to
Sort By:
Page
of 15
Haematologica
|
January 4, 1998
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis
P Sivera, A Roetto, U Mazza, et al.
International Journal of Laboratory Hematology
|
May 11, 2016
The mutual control of iron and erythropoiesis
C Camaschella, A Pagani, A Nai, et al.
Leukemia & Lymphoma
|
July 27, 2016
Granulocyte Macrophage Colony-Stimulating Factor (GM-CSF) Reduces Pancytopenia After Rescue Therapy in a Patient with Hodgkin's Lymphoma
W Piacibello, C Camaschella, A C Stern, et al.
British Journal of Haematology
|
September 1, 1991
A spontaneous mutation causing unstable Hb Hammersmith: detection of the beta 42 TTT----TCT change by CCM and direct sequencing
I Dianzani, S Ramus, R G Cotton, et al.
Trends in Genetics : TIG
|
December 1, 1993
Dilemmas and progress in mutation detection
I Dianzani, C Camaschella, A Ponzone, et al.
Minerva Chirurgica
|
October 31, 1977
[Diagnostic laparotomy in Hodgkin's disease]
F Rolfo, G Ardizzone, C Camaschella, et al.
PCR Methods and Applications
|
April 1, 1995
An efficient method for PCR analysis of mitochondrial DNA from paraffin-embedded archival heart tissue
A Bobba, R Lippolis, S Giannattasio, et al.
Thrombosis and Haemostasis
|
August 28, 2001
A new mutation trans to I278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease
S Bosio, G Cavallero, E Brusa, et al.
British Journal of Haematology
|
February 1, 1994
Clinical and haematological improvement induced by etidronate in a patient with idiopathic myelofibrosis and osteosclerosis
P Sivera, L Cesano, A Guerrasio, et al.
British Journal of Obstetrics and Gynaecology
|
May 1, 1990
Thrombotic thrombocytopenic purpura in pregnancy with maternal and fetal survival. Case report
A Maina, V Donvito, O Giachino, et al.
Page
of 15