Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Marta, Feito Rodríguez"'
Autor:
Ana Elísabet López‐Sundh, Esperanza Escribano‐Palomino, Marta Feito‐Rodríguez, Jair Tenorio, María Emilia Brizzi, Khrystyna Krasnovska Zayets, Guillermo Servera‐Negra, Raúl de Lucas‐Laguna
Publikováno v:
American Journal of Medical Genetics Part A. 191:253-258
Autor:
Lucía Quintana-Castanedo, MD, Marta Feito-Rodríguez, MD, PhD, Iván Valero-López, MD, Clara Chiloeches-Fernández, MD, Elena Sendagorta-Cudós, MD, PhD, Pedro Herranz-Pinto, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 6, Iss 6, Pp 498-499 (2020)
Externí odkaz:
https://doaj.org/article/df3a175dc048493a977504e7aff315d3
Autor:
Maria, Gonzalez-Cao, Teresa, Puertolas, Clara, Martinez-Vila, Cristina, Carrera, Cayetana, Maldonado Seral, Pedro, Rodríguez-Jiménez, Silvia, Sequero, Pablo, Cerezuela-Fuentes, Rosa, Feltes Ochoa, Eva, Muñoz, Mónica, Antoñanzas Basa, Juan, Martín-Liberal, Ainara, Soria, Juan, Francisco Rodriguez Moreno, Ivan, Marquez-Rodas, Pilar, Lopez Criado, José, Luis Manzano, Rafael, Lopez-Castro, Pablo, Ayala de Miguel, Laura, Villalobos, Salvador, Martin Algarra, Ines, Gonzalez-Barrallo, Aram, Boada, Almudena, García Castaño, Susana, Puig, Guillermo, Crespo, Pablo, Luna Fra, Cristina, Aguayo Zamora, Marta, Feito Rodríguez, Lara, Valles, Ana, Drozdowskyj, Jesús, Gardeazabal, Luis, Antonio Fernandez-Morales, Alberto, Rodrigo, Raquel, Cruz, Oriol, Yelamos, Belen, Rubio, Karmele, Mujica, Mariano, Provencio, Alfonso, Berrocal
Background The Spanish Melanoma Group (GEM) developed a national registry of patients with melanoma infected by SARS-CoV-2 ( GRAVID ).Methods The main objective was to describe the COVID-19 fatality rate in patients with melanoma throughout the pande
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0f3f41e0e5a020dbbf18dbcc0d240b01
https://hdl.handle.net/10171/65982
https://hdl.handle.net/10171/65982
Autor:
A.I. Lorente-Lavirgen, C Salas-Márquez, L Quintana-Castanedo, Ana Martín-Santiago, S I Palencia-Pérez, E Baselga-Torres, José Bernabeu-Wittel, M T Montserrat-García, Ignacio García-Doval, A Azón-Masoliver, M Valdivieso-Ramos, A Giacaman, E Roé-Crespo, Javier Domínguez-Cruz, M de Vega-Martínez, J. del Boz-González, M Campos-Domínguez, Carlos Cuenca-Barrales, Asunción Vicente, Marta Feito-Rodríguez
Publikováno v:
Actas Dermo-Sifiliográficas, Vol 112, Iss 9, Pp 806-816 (2021)
Background: There are severaltherapeutic options for infantile haemangiomas (IH). Propranolol is used according to a pivotal trial. We aimed to describe the characteristics of IH in clinical practice, including the therapies used, and to compare the
Autor:
Diego Soto‐García, Jose Manuel Busto Leis, Ana Carmona‐Olveira, David Revilla‐Nebreda, Marta de Uribe Viloria, Marta Feito‐Rodríguez
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 37
Autor:
Kiril Magaletsky Kharachko, Marta Feito Rodríguez, Nelson M. Buitrago Sánchez, Juan Carlos López Gutiérrez
Publikováno v:
Pediatric dermatologyREFERENCES.
We report the case of a 12-month-old infant who presented with progressive lower limb enlargement associated with erythema mimicking an arteriovenous malformation. Computed tomography confirmed an arteriovenous fistula (AVF) between the deep femoral
Autor:
Marta Feito Rodríguez
Publikováno v:
Más Dermatología. :32-33
Autor:
Raúl de Lucas Laguna, Isabel Pérez-Conde, Clara Chiloeches-Fernández, Marta Feito-Rodríguez, Rocío Maseda-Pedrero, Lucía Quintana-Castanedo
Publikováno v:
Pediatric Dermatology. 37:1131-1134
Dyskeratosis congenita (DC) is an unusual inherited disease characterized by the triad of mucosal leukoplakia, nail dystrophy, and skin pigmentation. Hyperkeratosis of the palms and soles is another reported skin finding. This hyperkeratosis can lead
Autor:
Clara Chiloeches Fernández, Marta Feito Rodríguez, Nicholas Stewart, Marta Valdivielso‐Ramos, Ana Isabel Rodríguez Bandera
Publikováno v:
Australasian Journal of Dermatology. 61:349-352
High-frequency ultrasonography (HFUS) represents a useful adjunct for dermatologists in the diagnosis of capillary malformation-arteriovenous malformation (CM-AVM) syndrome. We present a paediatric case series of 6 patients with confirmed RASA1 gene
Autor:
Raúl de Lucas Laguna, Marta Feito Rodríguez, Clara Chiloeches Fernández, Rocío Maseda Pedrero, Lucía Quintana Castanedo, Daniel Nieto Rodríguez
Publikováno v:
Dermatologic Surgery. 47:61-64
Background Raynaud's phenomenon (RP) is a clinical syndrome characterized by recurrent episodes of digital vasospasm triggered by exposure to physical and chemical agents or emotional stress. Although many pharmacologic treatments have been tested, t