Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype von Nieto, Jorge M, Villegas, Ana, De La Fuente-Gonzalo, Felix, González, Fernando A, Ropero, Paloma

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Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia von de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Vinuesa, Lara, Sevilla, Julián, Díaz-Mediavilla, Joaquín, Villegas, Ana, González, Fernando A., Ropero, Paloma

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Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014 von de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Villegas, Ana, González, Fernando A., Martínez, Rafael, Ropero, Paloma

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Phenotype of mutations in the promoter region of the β-globin gene von Ropero, Paloma, Erquiaga, Sara, Arrizabalaga, Beatriz, Pérez, Germán, de la Iglesia, Silvia, Torrejón, María José, Gil, Celia, Elena, Cela, Tenorio, María, Nieto, Jorge M, de la Fuente-Gonzalo, Félix, Villegas, Ana, González Fernández, Fernando-Ataúlfo, Martínez, Rafael

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Reticulocyte parameters of delta beta thalassaemia trait, beta thalassaemia trait and iron deficiency anaemia von Velasco-Rodríguez, Diego, Alonso-Domínguez, Juan-Manuel, González-Fernández, Fernando-Ataúlfo, Villarrubia, Jesús, Sopeña, María, Abalo, Lorena, Ropero, Paloma, Martínez-Nieto, Jorge, de la Fuente Gonzalo, Félix, Cava, Fernando

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Development and validation of a multivariable prediction rule for detecting a severe acquired ADAMTS13 activity deficiency in patients with thrombotic microangiopathies von Nieto, Jorge M., De La Fuente-Gonzalo, Félix, González, Fernando A., Villegas, Ana, Martínez, Rafael, Fuentes, Manuel E., Ropero, Paloma

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Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies von de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Ricard, Pilar, Anguita, Javier, Martínez, Rosalina, Cervera, Aurea, Villegas, Ana, González, Fernando A., Ropero, Paloma

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Hemoglobin Le Lamentin in the province of Albacete, Spain: Discovery of 32 cases von Martínez-López, Rosalina, Ropero, Paloma, Ballesteros Gallar, Cristina, Romero Román, Carlos, de la Fuente-Gonzalo, Félix, M. Nieto, Jorge, Navarro Casado, Laura, González, Fernando A.

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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... von de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Velasco, Diego, Cela, Elena, Pérez, Germán, Fernández-Teijeiro, Ana, Escudero, Antonio, Villegas, Ana, González-Fernández, Fernando A., Ropero, Paloma

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Different forms of Hb Le Lamentin. An unexpected finding in Hba1c quantification von Martínez-López, Rosalina, de la Fuente-Gonzalo, Félix, Nieto, Jorge M., Gallar, Cristina Ballesteros, Román, Carlos Romero, Villegas, Ana, González, Fernando A., Martínez, Rafael, Casado, Laura Navarro, Ropero, Paloma

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Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype von Nieto, Jorge M, Villegas, Ana, De La Fuente-Gonzalo, Felix, González, Fernando A, Ropero, Paloma

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Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: First case in Spain von de la Fuente-Gonzalo, Félix, Ropero, Paloma, Martínez-Nieto, Jorge, Villegas, Ana, González, Fernando A., Díaz-Mediavilla, Joaquín

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Design and Development of an All-Terrain Wheelchair for Rural Areas in Mexico: The First Stage of the Project von Rossa-Sierra, Alberto, Diaz-Pinal, Ana Paula, Cortes-Chavez, Fabiola, de la Fuente, Felix Maldonado, Carrillo-Alvarado, Gilberto

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δβ-Thalassemia trait: how can we discriminate it from β-thalassemia trait and iron deficiency anemia? von Velasco-Rodríguez, Diego, Alonso-Domínguez, Juan-Manuel, González-Fernández, Fernando-Ataúlfo, Villarrubia, Jesús, Ropero, Paloma, Martínez-Nieto, Jorge, de la Fuente, Félix, Guillén, Raquel, Acedo, Natalia, Serí, Cristina, Cava, Fernando

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Value Of Magnetic Resonance Imaging In The Study and Follow-Up Of Paroxysmal Nocturnal Hemoglobinuria von Villegas, Ana, Gonzalez, Ataulfo, Matute, Fatima, Nieto, Jorge Martinez, de la Fuente, Felix

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Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait von Velasco-Rodríguez, Diego, Alonso-Domínguez, Juan-Manuel, González-Fernández, Fernando-Ataúlfo, Muriel, Alfonso, Abalo, Lorena, Sopeña, María, Villarrubia, Jesús, Ropero, Paloma, Plaza, María Paz, Tenorio, María, Jiménez-Martín, Ana, Moreno, Gemma, Martínez-Nieto, Jorge, de la Fuente-Gonzalo, Félix, Fernández-Escribano, Marina, López-Jiménez, Francisco Javier, Cava, Fernando

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Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre von Villegas, Ana, González, Fernando Ataúlfo, Nieto, Jorge M, de la Fuente-Gonzalo, Félix, Martínez, Rafael, Torrejón, María Josefa, Ropero, Paloma

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Haemoglobinopathies that occur with decreased HbA 2 levels: a gene mutation set involving the δ gene at a Spanish centre von Villegas, Ana, González, Fernando Ataúlfo, Nieto, Jorge M, de la Fuente-Gonzalo, Félix, Martínez, Rafael, Torrejón, María Josefa, Ropero, Paloma

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Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the [delta] gene at a Spanish centre von Villegas, Ana, Gonzalez, Fernando Ataúlfo, Nieto, Jorge M, de la Fuente-Gonzalo, Félix, Martinez, Rafael, Torrejón, Maria Josefa, Ropero, Paloma

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FP137PREDICTION OF SEVERE ADAMTS13 DEFICIENCY IN PATIENTS WITH THROMBOTIC MICROANGIOPATHIES von Martinez Nieto, Jorge, De La Fuente-Gonzalo, Félix, González Fernández, Fernando Ataúlfo, Ropero, Paloma, Villegas, Ana

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