Search research articles
Contact Us
Filters
Showing results (11-20 of 16) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 16 results.
Annals of Hematology
|
June 3, 2016
Hereditary xerocytosis, a misleading anemia
R Del Orbe Barreto, B Arrizabalaga, A B De la Hoz Rastrollo, et al.
International Journal of Laboratory Hematology
|
July 19, 2016
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing
R Del Orbe Barreto, B Arrizabalaga, A B De la Hoz, et al.
International Journal of Laboratory Hematology
|
December 24, 2015
Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation
R Del Orbe Barreto, B Arrizabalaga, A B de la Hoz, et al.
Haematologica
|
December 10, 1999
Erythropoietin plus granulocyte colony-stimulating factor in the treatment of myelodysplastic syndromes. Identification of a subgroup of responders. The Spanish Erythropathology Group
A F Remacha, B Arrizabalaga, A Villegas, et al.
Haematologica
|
May 15, 1998
Red blood cell phenotypes in alpha-thalassemias in the Spanish population
A Villegas, A Porres, J Sánchez, et al.
Leukemia
|
February 29, 2020
miR-146a rs2431697 identifies myeloproliferative neoplasm patients with higher secondary myelofibrosis progression risk
F Ferrer-Marín, A B Arroyo, B Bellosillo, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Annals of Hematology
|
June 3, 2016
Hereditary xerocytosis, a misleading anemia
R Del Orbe Barreto, B Arrizabalaga, A B De la Hoz Rastrollo, et al.
International Journal of Laboratory Hematology
|
July 19, 2016
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing
R Del Orbe Barreto, B Arrizabalaga, A B De la Hoz, et al.
International Journal of Laboratory Hematology
|
December 24, 2015
Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation
R Del Orbe Barreto, B Arrizabalaga, A B de la Hoz, et al.
Haematologica
|
December 10, 1999
Erythropoietin plus granulocyte colony-stimulating factor in the treatment of myelodysplastic syndromes. Identification of a subgroup of responders. The Spanish Erythropathology Group
A F Remacha, B Arrizabalaga, A Villegas, et al.
Haematologica
|
May 15, 1998
Red blood cell phenotypes in alpha-thalassemias in the Spanish population
A Villegas, A Porres, J Sánchez, et al.
Leukemia
|
February 29, 2020
miR-146a rs2431697 identifies myeloproliferative neoplasm patients with higher secondary myelofibrosis progression risk
F Ferrer-Marín, A B Arroyo, B Bellosillo, et al.
Page
of 2