Felix Gonzalo-De La Fuente
Madrid, MD, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications
Development and validation of a multivariable prediction rule for detecting a severe acquired ADAMTS13 activity deficiency in patients with thrombotic microangiopathies.
Journal: Clinical chemistry and laboratory medicine
Published: May 17, 2017
Phenotype of mutations in the promoter region of the β-globin gene.
Journal: Journal of clinical pathology
Published: February 02, 2017
Hemoglobin Le Lamentin in the province of Albacete, Spain: Discovery of 32 cases.
Journal: Clinical biochemistry
Published: August 15, 2016
Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre.
Journal: Journal of clinical pathology
Published: May 18, 2016
Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.
Journal: Journal of clinical pathology
Published: December 06, 2015
HB Puerta del Sol [HBA1:c.148A>C], HB Valdecilla [HBA2:c.3G>T], HB Gran Vía [HBA2:c.98T>G], HB Macarena [HBA2:c.358C>T] and HB El Retiro [HBA2:c.364_366dupGTG]: description of five new hemoglobinopathies.
Journal: Clinical chemistry and laboratory medicine
Published: July 08, 2015
Different forms of Hb Le Lamentin. An unexpected finding in Hba1c quantification.
Journal: Clinical biochemistry
Published: July 08, 2015
Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies.
Journal: Clinical biochemistry
Published: December 04, 2014
Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype.
Journal: Journal of human genetics
Published: May 13, 2014
Last Updated: 09/26/2026