María Isabel Buedo

ORCID: 0000-0002-2967-1647
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About
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Research Areas
  • Osteomyelitis and Bone Disorders Research
  • Coronary Artery Anomalies
  • Orthopedic Infections and Treatments
  • Autoimmune Neurological Disorders and Treatments
  • Kawasaki Disease and Coronary Complications
  • Cardiac Structural Anomalies and Repair
  • Urticaria and Related Conditions
  • Infectious Diseases and Tuberculosis
  • Dupuytren's Contracture and Treatments
  • RNA regulation and disease
  • Polyomavirus and related diseases
  • Intramuscular injections and effects
  • Congenital limb and hand anomalies
  • Eosinophilic Disorders and Syndromes
  • Chromosomal and Genetic Variations
  • Head and Neck Surgical Oncology
  • CRISPR and Genetic Engineering
  • Cytomegalovirus and herpesvirus research
  • IgG4-Related and Inflammatory Diseases
  • Genital Health and Disease
  • Ophthalmology and Eye Disorders
  • Medicine and Dermatology Studies History
  • DNA Repair Mechanisms
  • Systemic Sclerosis and Related Diseases
  • Sympathectomy and Hyperhidrosis Treatments

Hospital General Universitario de Albacete
2024

Complejo Hospitalario Universitario de Albacete
2015-2022

Hospital Universitario La Paz
2011

Carlos Grasa Elisa Fernández-Cooke Sara Domínguez‐Rodríguez Javier Aracil-Santos Ana Barrios Tascón and 95 more Judith Sánchez-Manubens Beatriz Mercader Jordi Antón Esmeralda Núñez Cuadros Enrique Villalobos Matilde Bustillo Alonso Marisol Camacho Manuel Oltra Benavent Gemma Giralt Ana María Bello Naranjo Beatriz Rocandio Cristina Calvo Elisa Fernández-Cooke Cristina Calvo Ana Barrios Tascón Judith Sánchez-Manubens Jordi Antón Javier Aracil Santos Esmeralda Núñez Cuadros María Luisa Navarro Gómez David Moreno Pérez María Martín Cantero Pérez Esmeralda Nuñez Cuadros Pérez Begoña Carazo Gallego Pérez Fernando Sánchez García Marisol Camacho Lovillo Renata Marqués Olaf Neth Laura Fernández Silveira Miguel Forte Ángeles Ortega Montes Leticia Isabel Martínez Campos Beatriz Bravo Mancheño M. Camacho Antonio F Medina Claros Carlos Salido María Torres Rico Beatriz Ruiz Sáez Elena Fernadez de la Puebla Lechuga Ma José Lirola Cruz Kety Maya Carrasco Moisés Rodríguez‐González Enrique Blanca Jover José Uberos Fernández María Mercedes Ibáñez Alcalde Miguel Lafuente Hidalgo Lorenzo Jiménez Montañes Matilde Bustillo Alonso A. Ayerza Casas Bárbara Montes Zapico Carlos Pérez Mendez Javier Fernández Aracama Lucía Rodríguez María Aleida Ibáñez Fernández Silvia Escribá Bori María Concepción Mir Perelló Ma Ángeles de la Fuente Sánchez Patricia Aparicio García Carlos Briales Joaquín Castilla Crespí María Elena Colino Gil Nerea Delgado Cabrera Ana Bello Naranjo Jesús Poch Páez Moneyba García Yáñez Montse González García Maite Viadero Beatriz Jiménez Montero Olga Domínguez García Begoña Losada Pinedo Gema Íñigo Martín Lucía María Escribano Gómez Miguel Lillo María Isabel Buedo Laura Rey Elena Urbaneja Rodríguez Sara Rellán Rodríguez Teresa Cantero Beatriz Plata Izquierdo Luisa Álvarez Ignacio Oulego-Erróz Elena Pérez Santaolalla Carlos Alcalde Martín Fernándo Centeno Malfaz Elena Pérez Gutiérrez Ma Soledad Jiménez Casso Fredy Prada Rosa Bou E. Iglesias Joan Calzada Olga Calavia Garsaball Marc Tobeña Rue Gemma Giralt Zulema Lobato N. Rius Gordillo

10.1007/s10067-022-06319-4 article EN Clinical Rheumatology 2022-08-08

Abstract Fanconi anemia (FA) is a rare genetic disease characterized by high phenotypic and genotypic heterogeneity, extreme chromosome fragility. To better understand the natural history of FA, identify risk prognostic factors, develop novel therapeutic strategies, Spanish Registry Patients with FA collects data on clinical features, fragility, subtypes, DNA sequencing informed consent participating individuals. In this article, we describe evolution 227 patients followed up for to 30...

10.1002/ajh.27520 article EN cc-by-nc-nd American Journal of Hematology 2024-11-19
Ana Barrios-Tascón Masaru Miura Sara Domínguez‐Rodríguez Elisa Fernández-Cooke Geòrgia Sarquella-Brugada and 95 more Alfredo Tagarro Elisa Fernández-Cooke Cristina Calvo Judith Sánchez-Manubens Jordi Antón Javier Aracil Santos Esmeralda Núñez Cuadros María Luisa Navarro Gómez David Moreno Pérez María Martín Cantero Pérez Esmeralda Nuñez Cuadros Pérez Begoña Carazo Gallego Pérez Fernando Sánchez García Marisol Camacho Lovillo Renata Marqués Olaf Neth Laura Fernández Silveira Miguel Forte Ángeles Ortega Montes Leticia Isabel Martínez Campos Beatriz Bravo Mancheño M. Camacho Antonio F. Medina Claros Carlos Salido María Torres Rico Beatriz Ruiz Sáez Elena Fernadez de la Puebla Lechuga Ma José Lirola Cruz Kety Maya Carrasco Moisés Rodríguez‐González Enrique Blanca Jover José Uberos Fernández María Mercedes Ibáñez Alcalde Miguel Lafuente Hidalgo Lorenzo Jiménez Montañes Matilde Bustillo Alonso A. Ayerza Casas Bárbara Montes Zapico Carlos Pérez Mendez Javier Fernández Aracama Lucía Rodríguez María Aleida Ibáñez Fernández Sandra Navarro Campo Silvia Escribá Bori María Concepción Mir Perelló Ma Ángeles de la Fuente Sánchez Patricia Aparicio García Carlos Briales Joaquín Castilla Crespí María Elena Colino Gil Nerea Delgado Cabrera Ana Bello Naranjo Jesús Poch Páez Moneyba García Yáñez Montse González García Maite Viadero Beatriz Jiménez Montero Olga Domínguez García Begoña Losada Pinedo Gema Íñigo Martín Lucía María Escribano Gómez Antonio Cepillo Miguel Lillo María Isabel Buedo Laura Rey Elena Urbaneja Rodríguez Sara Rellán Rodríguez Teresa Cantero Beatriz Plata Izquierdo Luisa Álvarez Ignacio Oulego-Erróz Elena Pérez Santaolalla Carlos Alcalde Martín Fernándo Centeno Malfaz Elena Pérez Gutiérrez Ma Soledad Jiménez Casso Fredy Prada Rosa Bou E. Iglesias Joan Calzada Olga Calavia Garsaball Marc Tobeña Rue Gemma Giralt Zulema Lobato N. Rius Gordillo Montserrat Pascual Torres María Méndez Hernández Lourdes R. García Sergio Flores Villar Silvia Yevenes Ruiz Laura Minguell Domingo Anna Ballester Ana Miralles-Marco Berta Pujol Soler Anton Foguet Vidal

10.1016/j.jpeds.2021.05.023 article EN The Journal of Pediatrics 2021-05-15

Tolosa-Hunt syndrome, a diagnosis of exclusionLa oftalmoplejia dolorosa es una entidad infrecuente en Pediatría, caracterizada por dolor orbitario y parálisis oculomotora ipsilateral.Puede ser debido diferentes causas; de ellas el síndrome (STH), causado inflamación inespecífica seno cavernoso o fisura orbitaria superior.El STH un diagnóstico exclusión, lo que ante paciente con sospecha hay realizar los pertinentes exámenes complementarios, incluyen pruebas imagen cerebral, entre otras.El...

10.4321/s1139-76322015000100010 article ES cc-by-nc-nd Pediatría Atención Primaria 2015-03-01

Purpose A single center, prospective study was performed to assess the efficacy and safety of Griflow® Dual–-a gravity-fed device for intravenous delivery human immunoglobulin Flebogamma®. Methods total 2 infusions in visits per patient were assessed using G2 G3 Dual models that provide different flow rates adjusted patient's weight. To follow most common method administration, infusion through two-way commenced with low rate capillary (clamp closed) 30 minutes continued high rate, opening...

10.5301/jva.2011.8689 article EN The Journal of Vascular Access 2011-09-26
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