Search Results - "Nieto, Jorge Martínez"

Pincered red cells in hereditary spherocytosis by Escribano Serrat, Silvia, Del Campo Balguerías, Gonzalo, Martínez Nieto, Jorge, Medina Salazar, Fiorella, Benavente Cuesta, Celina, González Fernández, Fernando Ataúlfo

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Case Report: α-Spectrin Mutation Associated with αLELY Polymorphism Responsible for Hereditary Pyropoikilocytosis by Sánchez Villalobos, María, Salido Fiérrez, Eduardo, Martínez Nieto, Jorge, García Garay, Mª Carmen, Beltrán Videla, Asunción, Pérez Oliva, Ana Belen, Blanquer Blanquer, Miguel, Moraleda Jiménez, José María

“…Hereditary pyropoikilocytosis (HPP) is characterised by severe hemolytic anemia due to membrane instability. We report the case of a 13-day-old boy with…”
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P1609: CAPLACIZUMAB THERAPY IN OLDER PATIENTS (≥60 YEARS) WITH IMMUNE THROMBOTIC THROMBOCYTOPENIC PURPURA (ITTP). RESULTS OF THE SPANISH TTP REGISTRY by Rubia, Javier DE LA, Gómez‐Seguí, Inés, Cid, Joan, Valcárcel, David, Goterris, Rosa, Zarzoso, Miguel Fernández, Mingot‐Castellano, María Eva, Izquierdo, Cristina Pascual, Hernández, Ana Oliva, Nieto, Jorge Martínez, Idrovo, Laura F. Ávila, Coronel, María Liz Paciello, Hernández, Luis M.

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Reticulocyte parameters of delta beta thalassaemia trait, beta thalassaemia trait and iron deficiency anaemia by 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

“…To analyse the differences in reticulocyte indices between delta beta thalassaemia trait (δβ-TT), beta thalassaemia trait (β-TT) and iron deficiency anaemia…”
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P1605: IMMUNE THROMBOTIC THROMBOCYTOPENIC PURPURA IN OLDER PATIENTS: RESULTS FROM THE SPANISH TTP REGISTRY (REPTT) by Seguí, Inés Gómez, Aracil, Eva Frances, Eva, Mingot‐Castellano Maria, Pampliega, M Vara, Goterris, Rosa, Candel, F García, Izquierdo, Cristina Pascual, Garma, Julio del Rio, Dominguez, Luisa Guerra, Andrés, Isabel Vicuña, Peinado, Jose Garcia‐Arroba, Marcos, Saioa Zalba, Estevez, Julia Vidan, Gonzalez, Elena, Saavedra, Veronica Campuzano, Gala, Jose Maria Garcia, Sanchez, S Ortega, Nieto, Jorge Martínez, Gambarte, Laura Pardo, Rodríguez, Maria Sole, Docampo, Marta Fernandez, Idrovo, Laura F. Ávila, Hernández, Luis M., Cid, Joan, Rubia, Javier DE LA

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P1480: CLINICAL AND GENETIC STUDY OF HEREDITARY SPHEROCYTOSIS IN THE SPANISH POPULATION by Castilla, Lucia, Aspa, Jose, Nieto, Jorge Martínez, Cabrera, Ángel Zúñiga, Santiago, Marta, Feria, Ana Garcia, Marco Buades, Josefa Esperanza, Marina, María Argüello, Ayala Diaz, Rosa María, Sanchez, Ricardo, Orbe Barreto, Rafael Del, Lobo Olmedo, Ana, Dávila‐Valls, Julio, Martín‐Pérez, Sonia, Jativa Saez, Cristina, Rodriguez, Inés Hernández, Salido, Eduardo, Recasens, Valle, Fernández, Lucía Guerrero, Moreno Risco, Maria Belén, Fernández, Ataulfo González, Rubio, Montserrat Lopez

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δβ-Thalassemia trait: how can we discriminate it from β-thalassemia trait and iron deficiency anemia? by 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

“…To analyze the differences not only in classic hematologic parameters but also in RBC subpopulations among δβ-thalassemia trait (δβ-TT), β-thalassemia trait…”
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Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: First case in Spain by de la Fuente-Gonzalo, Félix, Ropero, Paloma, Martínez-Nieto, Jorge, Villegas, Ana, González, Fernando A., Díaz-Mediavilla, Joaquín

“…Thalassemias are the most frequent monogenic disorder around the world. α-Thalassemias are due to a deficiency of synthesis in the alpha-globin chain of the…”
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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 by Ropero, Paloma, González, Fernando A., Cela, Elena, Beléndez, Cristina, Cervera, Aurea, Martínez-Nieto, Jorge, Fuente-Gonzalo, Félix de la, Vinuesa, Lara, Villegas, Ana, Díaz-Mediavilla, Joaquín

“…In the 5′ untranslated region (5′UTR), which is transcribed but not translated and is involved in posttranscriptional regulation of the gene promoting and…”
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Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases by de la Fuente-Gonzalo, Felix, Baiget, Montserrat, Badell, Isabel, Ricard, Pilar, Vinuesa, Lara, Martínez-Nieto, Jorge, Ropero, Paloma, Villegas, Ana, González, Fernando A., Díaz-Mediavilla, Joaquin, The Erythropathology Spanish Group

“…Most α-thalassemia (α-thal) mechanisms are deletions of one or both α-globin genes and less than 5.0-10.0% are point mutations. Hb Agrinio [α29(B10)Leu→Pro,…”
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ADAMTS13 recovery in acute thrombotic thrombocytopenic purpura after caplacizumab therapy by Mingot-Castellano, María-Eva, García-Candel, Faustino, García-Arroba, José, de la Rubia-Comos, Javier, Gómez-Seguí, Inés, Paciello-Coronel, María-Liz, Valcárcel-Ferreiras, David, Jiménez, Moraima, Cid, Joan, García-Gala, José-María, Guerra-Domínguez, Luisa, Ávila-Idrobo, Laura-Francisca, Oliva-Hernandez, Ana, Zalba-Marcos, Saioa, Ortega-Sánchez, Sandra, Goterris-Viciedo, Rosa, Moreno-Jiménez, Gemma, Domínguez-Acosta, Lourdes, Hernández-Mateos, Luis, Flores-Ballesteros, Elena, Pascual-Izquierdo, Cristina, Albert, Albert, Alegre, Adrian, Alkorta Eizagirre, Aitziber, Alonso Madrigal, Cristina, Amunarriz, Cristina, Antelo Caamaño, María Luisa, Berberana Fernández de Murias, Margarita, Berrueco Moreno, Ruben, Bueno, Jose Luis, Calderón López, María Teresa, Chica Gullón, Esther, Cid Vidal, Joan, Contreras Barbeta, Enric, Cuéllar Pérez-Ávila, Clara, de la Rubia Comos, Javier, Del Río Garma, Julio, Díaz Valdés, José R., Diaz-Ricart, Maribel, Diez Gallarreta, Zuriñe, Dueñas Hernando, Virginia, Eguia, Blanca, Escoda, Lourdes, Fernández Muñoz, Hermogenes, Fernández Sánchez de Mora, Maria Carmen, Fernandez Zarzoso, Miguel, Fidalgo, Teresa, Fonte Feal, Cristina, García Candel, Faustino, Gimeno, JJ, Gómez, Delia, Gonzalez, Carlos, González Fernández, Fernando Ataulfo, Gonzalez Porras, Jose Ramon, Hernandez, Adoracion, Hernández Castellet, José Carlos, Hidalgo Soto, Marta, Kerguelen Fuentes, Ana Lilia, Lopes, Raquel, Martín Hernández, María Paz, Martinez Estefano, Elvira, Martinez Revuelta, Eva, Mingot Castellano, María Eva, Morales Sanz, María Dolores, Moreno, Gemma, Moreno Chulilla, Jose Antonio, Oliva Hernandez, Ana Yurena, Pecos, Patricia, Pereira Coelho, Daniela Sofia, Perez-Lopez, Olga, Ramiro, Laia, Richart López, Luis Alberto, Rodriguez Dominguez, Maria Jesus, Rodriguez Nuñez, Antonio, Saez Serrano, Isabel, Sanchez Anton, Piva, Sánchez Fernández, Mª Soledad, Sebastian, Elena, Solanich Moreno, Xabier, Soledad Casado, Soledad, Tallón, Jose David, Turcu, Violeta, Valledor Méndez, Manuel, Vidan Y Estevez, Julia, Bienert, Álvaro, Serrano, Alfons, Llorente, Laura, Campuzano, Verónica, Tallón, Inmaculada, Pons, Verónica, Linares, Mónica, Valles, Ana, Araujo, Enmanuel, Marco de Lucas, Fernando, Uribe Barrientos, Marisol, Calviño, Michael, Gómez Calafat, Montse, Marco Vera, Pascual, Zalba, Saioa, Escamilla, Virginia

“…•There is no delay in ADAMTS13 recovery after PEX start in caplacizumab–treated patients with iTTP from the Spanish registry.•Caplacizumab allows suspending…”
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Two new mutations in the GLRX5 gene cause sideroblastic anemia by Melo Arias, Andrés Felipe, Escribano Serrat, Silvia, Martínez Nieto, Jorge, Medina Salazar, Fiorella, Ropero Gradilla, Paloma, Benavente Cuesta, Celina, González Fernández, Fernando Ataúlfo

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Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: A New Molecular Analysis by Ropero, Paloma, Martín-Nuñez, Guillermo, González, F.A., Villegas, Ana, de la Fuente-Gonzalo, Félix, Martínez-Nieto, Jorge, Vinuesa, Lara, Díaz-Mediavilla, Joaquín

“…Unstable hemoglobin (Hb) variants account for 9.5% of structural hemoglobinopathies. The majority of these unstable variants are the result of gene point…”
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Largest comparison between onset and relapses of acquired thrombotic thrombocytopenic purpura reveals severe neurological involvement and worse analytic parameters at debut by Vegas Villalmanzo, Blanca, Cantera Estefanía, Rodrigo, Muñoz Madrid, Sara, Cerrato Salas, Mariana, Arnaiz Martín, Irene, Molina Pérez, Marta, Sagrista López, Beatriz, Ruiz Ramírez, Yolanda, Cucharero Martín, Javier, Estival Monteliú, Pablo, Ropero Gradilla, Paloma, Ferrer Benito, Sara, Martín Hernández, María Paz, González Fernández, Fernando Ataulfo, Gómez Álvarez, Miguel, Villegas Martínez, Ana, Benavente Cuesta, Celina, Martínez Nieto, Jorge

“…It has been proposed that the onset of Acquired Thrombotic Thrombocytopenic Purpura (iTTP) is more severe than subsequent relapses; however, existing studies…”
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Caplacizumab Treatment in Elderly Patients with iTTP: Updated Experience from the Spanish TTP Registry by Gómez Seguí, Inés, Sopeña Pell-Ilderton, Clara, Cid, Joan, Lozano, Miquel, Mingot Castellano, Maria Eva, Pascual Izquierdo, Maria Cristina, Gonzalez del Castillo, Luz Maria, Vidan Estevez, Julia Maria, Garcia-Candel, Faustino, Jiménez Balarezo, Moraima, Valcarcel, David, Cuellar Perez-Avila, Clara, Aguirre Arrizabalaga, Maria Aranzazu, Avila Idrovo, Laura Francisca, Moreno Jimenez, Maria Gemma, Oliva Hernandez, Ana Yurena, Garcia Gala, Jose Maria, Martínez Nieto, Jorge, Goterris, Rosa, Fernández Docampo, Marta, De La Rubia, Javier

“…Introduction Immune thrombotic thrombocytopenic purpura (iTPP) is a rare microangiopathic thrombotic disorder with severely reduced levels of ADAMTS13 due to…”
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Effect of Caplacizumab in the Recovery of ADAMTS13 Level in Patients with Autoimmune Thrombotic Thrombocytopenic Purpura. Analysis from the Spanish Registry (REPTT) by Mingot, Maria Eva, Pascual, Cristina Izquierdo, Garcia-Candel, Faustino, Martínez Nieto, Jorge, García-Arroba Peinado, José, De La Rubia, Javier, Gomez Segui, Ines, Pacielo Coronel, Maria Liz, Valcárcel, David, Jiménez Balarezo, Moraima, Cid, Joan, Lozano, Miquel, Garcia Gala, Jose Maria, Angos Vazquez, Sonia, Vara, Míriam, Guerra, Luisa, Avila Idrobo, Francisca, Oliva Hernandez, ANA Yurena, Zalba, Saoia, Tallon Ruiz, Inmaculada, Ortega Sánchez, Sandra, Goterris, Rosa, Moreno Jimenez, Maria, Dominguez Acosta, Lourdes, Arraiz Ramirez, Maria, Hernández, Luis, Flores Ballesteros, Elena, Del Rio Garma, Julio

“…INTRODUCTION Treatment of immune thrombotic thrombocytopenic purpura (iTTP) includes plasma exchanges (PEX) and immunosuppressive treatment with steroids with…”
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Caplacizumab As New Paradigm-Changing Therapy for Patients with Autoimmune Thrombotic Thrombocytopenic Purpura (aTTP): Real-World Data from TTP Spanish Registry by Garcia-Garcia, Irene, Jiménez, Moraima, Valcárcel, David, Mingot-Castellano, Maria Eva, Pascual Izquierdo, Maria Cristina, Viejo, Aurora, Lozano, Miquel, Goterris, Rosa, Martínez Nieto, Jorge, Oliva, Ana, Gómez-Seguí, Inés, Hernandez, Luis, Zalba, Saioa, Campuzano, Verónica, Martínez, Yolanda, González, Helena, Tallon, Inmaculada, Fernández Zarzoso, Miguel, Moreno Jiménez, Gemma, Lakhwani Lakhwani, Sunil, Ortega, Sandra, Solé, María, Atucha Fernández, Jon Ander, Del Rio-Garma, Julio, Cid, Joan

“…Introduction: Autoimmune thrombotic thrombocytopenic purpura (aTTP) is a severe disease caused by the production of autoantibodies against von Willebrand…”
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β-Intermediate Thalasemia: triplication of genes α / β thalassemia heterozygous in Spain by Ropero, Paloma, González Fernández, Fernando Ataulfo, Martínez Nieto, Jorge, Torres Jiménez, Williana Melissa, Benavente Cuesta, Celina

“…Objectives. Check with hematological data that the diagnosis and clinical grade of β-thalassemia intermedia can be established when a triplication of genes…”
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Consensus document for the diagnosis and treatment of pyruvate kinase deficiency by Morado, Marta, Villegas, Ana María, de la Iglesia, Silvia, Martínez-Nieto, Jorge, del Orbe Barreto, Rafael, Beneitez, David, Salido, Eduardo

“…Pyruvate Kinase deficiency (PKD) is the second most frequent enzymopathy and the most common cause of chronic hereditary non-spherocytic haemolytic anaemia…”
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Differential diagnosis of erythrocytosis. Hemoglobins with high oxygen affinitty by Villegas-Martínez, Ana, González-Fernández, Ataulfo, Ropero, Paloma, Martínez-Nieto, Jorge, Moreno, Nahir, Colás, Blanca, López, Alberto, Benavente, Celina

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