Joaquin Mediavilla-Diaz

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 8 publications

Minimal residual disease evaluation by flow cytometry is a complementary tool to cytogenetics for treatment decisions in acute myeloid leukaemia.

Minimal residual disease evaluation by flow cytometry is a complementary tool to cytogenetics for treatment decisions in acute myeloid leukaemia.

Journal: Leukemia research
Published: July 08, 2015

Maternal and fetal outcomes in pregnant women with acute promyelocytic leukemia.

Maternal and fetal outcomes in pregnant women with acute promyelocytic leukemia.

Journal: Annals of hematology
Published: October 22, 2014

Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia.

Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia.

Journal: International journal of hematology
Published: April 25, 2014

Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: first case in Spain

Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: first case in Spain

Journal: Medicina clinica
Published: May 21, 2013

Association in cis of the mutations +20 (C>T) in the 5' untranslated region and IVS-II-745 (C>G) on the β-globin gene.

Association in cis of the mutations +20 (C>T) in the 5' untranslated region and IVS-II-745 (C>G) on the β-globin gene.

Journal: Hemoglobin
Published: February 22, 2013

Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.

Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.

Journal: Hemoglobin
Published: December 11, 2012

Study of three families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish population: three homozygous cases.

Study of three families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish population: three homozygous cases.

Journal: Hemoglobin
Published: October 26, 2012

Thrombosis and severe asthenia as priority manifestations in paroxysmal nocturnal haemoglobinuria.

Thrombosis and severe asthenia as priority manifestations in paroxysmal nocturnal haemoglobinuria.

Journal: Annals of hematology
Published: December 06, 2011
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Last Updated: 09/26/2026