Search research articles
Contact Us
Filters
Showing results (71-80 of 138) with videos related to
Page
of 14
Sort By:
Clinical Genetics
|
November 1, 1989
The prevention of thalassemia in Sardinia
A Cao, C Rosatelli, R Galanello, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
March 1, 1996
Blood glucose normalization-induced haemolysis in three adolescents with type 1 diabetes mellitus at onset and unknown G-6-PD deficiency
M Vanelli, L Lucentini, P Picco, et al.
British Journal of Haematology
|
February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian families
M Furbetta, R Galanello, A Ximenes, et al.
Human Genetics
|
September 1, 1994
Y418C: a novel mutation in exon 9 of the glucocerebrosidase gene of a patient with Gaucher disease creates a new Bgl I site
R Tuteja, N Tuteja, F Lilliu, 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 anaemia
S Filosa, W Cai, R Galanello, et al.
Minerva Medica
|
March 17, 1981
[Our experience in screening and genetic counseling for beta-thalassemia]
A Cao, R Galanello, M A Melis, et al.
Journal of Medical Genetics
|
October 1, 1980
alpha-Thalassaemia in Sardinian infants
R Galanello, G Diana, M Furbetta, et al.
Blood
|
April 1, 1993
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphism
R Galanello, A Meloni, D Gasperini, et al.
Blood
|
January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy
A Podda, R Galanello, L Maccioni, et al.
Haematologica
|
July 1, 1990
Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia
R Galanello, M P Turco, S Barella, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 138) with videos related to
Sort By:
Page
of 14
Clinical Genetics
|
November 1, 1989
The prevention of thalassemia in Sardinia
A Cao, C Rosatelli, R Galanello, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
March 1, 1996
Blood glucose normalization-induced haemolysis in three adolescents with type 1 diabetes mellitus at onset and unknown G-6-PD deficiency
M Vanelli, L Lucentini, P Picco, et al.
British Journal of Haematology
|
February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian families
M Furbetta, R Galanello, A Ximenes, et al.
Human Genetics
|
September 1, 1994
Y418C: a novel mutation in exon 9 of the glucocerebrosidase gene of a patient with Gaucher disease creates a new Bgl I site
R Tuteja, N Tuteja, F Lilliu, 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 anaemia
S Filosa, W Cai, R Galanello, et al.
Minerva Medica
|
March 17, 1981
[Our experience in screening and genetic counseling for beta-thalassemia]
A Cao, R Galanello, M A Melis, et al.
Journal of Medical Genetics
|
October 1, 1980
alpha-Thalassaemia in Sardinian infants
R Galanello, G Diana, M Furbetta, et al.
Blood
|
April 1, 1993
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphism
R Galanello, A Meloni, D Gasperini, et al.
Blood
|
January 15, 1991
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy
A Podda, R Galanello, L Maccioni, et al.
Haematologica
|
July 1, 1990
Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia
R Galanello, M P Turco, S Barella, et al.
Page
of 14