Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancy
García‐Martínez, Francisco Javier, Azorín, Daniel, Duat‐Rodríguez, Anna, Hernández‐Martín, Ángela
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.01.2021)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.01.2021)
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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias
Martínez-Rubio, Dolores, Hinarejos, Isabel, Sancho, Paula, Gorría-Redondo, Nerea, Bernadó-Fonz, Raquel, Tello, Cristina, Marco-Marín, Clara, Martí-Carrera, Itxaso, Martínez-González, María Jesús, García-Ribes, Ainhoa, Baviera-Muñoz, Raquel, Sastre-Bataller, Isabel, Martínez-Torres, Irene, Duat-Rodríguez, Anna, Janeiro, Patrícia, Moreno, Esther, Pías-Peleteiro, Leticia, Gordo, Mar O’Callaghan, Ruiz-Gómez, Ángeles, Muñoz, Esteban, Martí, Maria Josep, Sánchez-Monteagudo, Ana, Fuster, Candela, Andrés-Bordería, Amparo, Pons, Roser Maria, Jesús-Maestre, Silvia, Mir, Pablo, Lupo, Vincenzo, Pérez-Dueñas, Belén, Darling, Alejandra, Aguilera-Albesa, Sergio, Espinós, Carmen
Published in International journal of molecular sciences (01.10.2022)
Published in International journal of molecular sciences (01.10.2022)
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Clinical and Sonographic Classification of Neurofibromas in Children with Neurofibromatosis Type 1 - A Cluster Analysis
García-Martínez, Francisco Javier, Alfageme, Fernando, Duat-Rodríguez, Anna, Andrés Esteban, Eva María, Hernández-Martín, Angela
Published in Ultraschall in der Medizin (01.04.2023)
Published in Ultraschall in der Medizin (01.04.2023)
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Tocilizumab in pediatric refractory status epilepticus and acute epilepsy: Experience in two patients
Cantarín-Extremera, Verónica, Jiménez-Legido, María, Duat-Rodríguez, Anna, García-Fernández, Marta, Ortiz-Cabrera, Nelmar Valentina, Ruiz-Falcó-Rojas, María Luz, González-Gutiérrez-Solana, Luis
Published in Journal of neuroimmunology (15.03.2020)
Published in Journal of neuroimmunology (15.03.2020)
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Enterovirus A71 Infection and Neurologic Disease, Madrid, Spain, 2016
Taravilla, Carmen Niño, Pérez-Sebastián, Isabel, Salido, Alberto García, Serrano, Claudia Varela, Extremera, Verónica Cantarín, Rodríguez, Anna Duat, Marín, Laura López, Sanz, Mercedes Alonso, Traba, Olga María Suárez, González, Ana Serrano
Published in Emerging infectious diseases (01.01.2019)
Published in Emerging infectious diseases (01.01.2019)
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Angeborene kutane Neurofibrome bei Neurofibromatose Typ 1: Klinisch‐pathologische Merkmale in der frühen Kindheit
García‐Martínez, Francisco Javier, Azorín, Daniel, Duat‐Rodríguez, Anna, Hernández‐Martín, Ángela
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.01.2021)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.01.2021)
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ATP1A3-related disorders in the differential diagnosis of acute brainstem and cerebellar dysfunction
Duat-Rodríguez, Anna, Prochazkova, Michaela, Sebastian, Isabel Perez, Extremera, Veronica Cantarin, Legido, Maria Jimenez, Palero, Serafin Rodriguez, Ortiz Cabrera, Nelmar Valentina
Published in European journal of paediatric neurology (01.09.2021)
Published in European journal of paediatric neurology (01.09.2021)
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Neuropsychiatric comorbidities and cognition in epilepsy with eyelid myoclonia: A retrospective pediatric case series
Ballarà Petitbò, Maria, González Alguacil, Elena, Gutiérrez Delicado, Eva, Ortiz Cabrera, Nelmar Valentina, Duat Rodríguez, Anna, García Peñas, Juan José, Soto Insuga, Victor
Published in Epileptic disorders (01.10.2023)
Published in Epileptic disorders (01.10.2023)
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Early diagnosis of CAPOS syndrome before acute-onset ataxia - review of the literature and a new family
Rodriguez, Anna Duat, Prochazkova, Michaela, Santos, Saturnino Santos, Cabezas, Oscar Rubio, Extremera, Veronica Cantarin, Gonzalez-Gutierrez-Solana, Luis
Published in Pediatric neurology (01.06.2017)
Published in Pediatric neurology (01.06.2017)
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Hemicerebellitis: Report of three paediatric cases and review of the literature
Carceller Lechón, Fernando, Duat Rodríguez, Anna, Sirvent Cerdá, Sara I, Khabra, Komel, de Prada, Inmaculada, García-Peñas, Juan Jose, Madero López, Luis
Published in European journal of paediatric neurology (01.05.2014)
Published in European journal of paediatric neurology (01.05.2014)
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Clinical Case of Anti- N -methyl- d -aspartate Receptor Encephalitis in an 8-Month-Old Patient With Hyperkinetic Movement Disorder
Cantarín-Extremera, Verónica, MD, Duat-Rodríguez, Anna, MD, González-Gutiérrez-Solana, Luis, MD, López-Marín, Laura, MD, Armangue, Thaís, MD
Published in Pediatric neurology (01.05.2013)
Published in Pediatric neurology (01.05.2013)
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MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature
López-Marín, Laura, Martín-Belinchón, Mónica, Gutiérrez-Solana, Luis G, Morte-Molina, Beatriz, Duat-Rodríguez, Anna, Bernal, Juan
Published in Revista de neurologiá (16.06.2013)
Published in Revista de neurologiá (16.06.2013)
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Complejo esclerosis tuberosa: análisis de los ámbitos de afectación, progreso en el tratamiento y traslación a la práctica clínica habitual en una cohorte de pacientes pediátricos
Cantarín Extremera, Verónica, Bernardino Cuesta, Beatriz, Martín Villaescusa, Celia, Melero Llorente, Javier, Hernández Martín, Ángela, Aparicio López, Cristina, de Lucas Collantes, Carmen, Tamariz-Martel Moreno, Amalia, Duat Rodríguez, Anna, Ruiz-Falcó Rojas, María Luz
Published in Revista de neurologiá (09.01.2021)
Published in Revista de neurologiá (09.01.2021)
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Inducción de crisis de ausencia atípica durante el tratamiento con perampanel
Duat Rodríguez, Anna, Cantarín Extremera, Verónica, García Fernández, Marta, García Peñas, Juan José, Ruiz-Falcó Rojas, María Luz
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.11.2019)
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.11.2019)
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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation
Rojnueangnit, Kitiwan, Xie, Jing, Gomes, Alicia, Sharp, Angela, Callens, Tom, Chen, Yunjia, Liu, Ying, Cochran, Meagan, Abbott, Mary-Alice, Atkin, Joan, Babovic-Vuksanovic, Dusica, Barnett, Christopher P., Crenshaw, Melissa, Bartholomew, Dennis W., Basel, Lina, Bellus, Gary, Ben-Shachar, Shay, Bialer, Martin G., Bick, David, Blumberg, Bruce, Cortes, Fanny, David, Karen L., Destree, Anne, Duat-Rodriguez, Anna, Earl, Dawn, Escobar, Luis, Eswara, Marthanda, Ezquieta, Begona, Frayling, Ian M., Frydman, Moshe, Gardner, Kathy, Gripp, Karen W., Hernández-Chico, Concepcion, Heyrman, Kurt, Ibrahim, Jennifer, Janssens, Sandra, Keena, Beth A, Llano-Rivas, Isabel, Leppig, Kathy, McDonald, Marie, Misra, Vinod K., Mulbury, Jennifer, Narayanan, Vinodh, Orenstein, Naama, Galvin-Parton, Patricia, Pedro, Helio, Pivnick, Eniko K., Powell, Cynthia M., Randolph, Linda, Raskin, Salmo, Rosell, Jordi, Rubin, Karol, Seashore, Margretta, Schaaf, Christian P., Scheuerle, Angela, Schultz, Meredith, Schorry, Elizabeth, Schnur, Rhonda, Siqveland, Elizabeth, Tkachuk, Amanda, Tonsgard, James, Upadhyaya, Meena, Verma, Ishwar C., Wallace, Stephanie, Williams, Charles, Zackai, Elaine, Zonana, Jonathan, Lazaro, Conxi, Claes, Kathleen, Korf, Bruce, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine
Published in Human mutation (01.11.2015)
Published in Human mutation (01.11.2015)
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