Publicacions
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Maruri-Aransolo, A, Caballero, JD, Michelena, M, Medina-Pascual, MJ, Carrasco, G, Asensio, O, Cols M and Cantón, R.
Evaluation of CHROMagar™ B. cepacia agar for the detection of Burkholderia cepacia complex species from sputum samples of patients with cystic fibrosis
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES . 43(7): 1349-1353. Nº de cites: 1
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Sierra-Núñez D, Bosch-Alcaraz A, Falcó A, Segura-Matute S, García-Godoy C, Otero-Arús C, Corral C and Zuriguel-Pérez E.
Multicenter study. Nursing professionals' perception of training needs in pain assessment in pediatric patients with cognitive dysfunction.
enfermeria intensiva . 35(3): 161-170.
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Caux, F, Patsatsi, A, Karakioulaki, M, Antiga, E, Baselga E, Borradori, L, Caproni, M, Cardones, AR, Chandran, NS, Dräger, S, Drenovska, K, Goebeler, M, Günther, C, Hofmann, SC, Ioannides, D, Joly, P, Marinovic, B, Mariotti, EB, Marzano, AV, Morel, KD, Murrell, DF, Prost, C, Sárdy, M, Setterfield, J, Skiljevic, D, Uzun, S, Vassileva, S, Zambruno, G and Schmidt, E.
S2k guidelines on diagnosis and treatment of linear IgA dermatosis initiated by the European Academy of Dermatology and Venereology
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY . 38(6): 1006-1023. Nº de cites: 12
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De Bortoli M, Ivars M, Revencu N, Nassogne MC, Lavarino C, Paco-Mercader S, Lammens M, Renders A, Dumitriu D, Helaers R, Boon LM, Baselga E and Vikkula M.
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants
AMERICAN JOURNAL OF MEDICAL GENETICS PART A . 194(6): . Nº de cites: 3
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Revencu N, Eijkelenboom A, Bracquemart C, Alhopuro P, Armstrong-Moron J, Baselga E, Cesario C, Dentici ML, Eyries M, Frisk S, Karstensen HG, Gene-Olaciregui N, Kivirikko S, Lavarino C, Mero IL, Michiels R, Pisaneschi E, Schönewolf-Greulich B, Wieland I, Zenker M and Vikkula M.
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA
ORPHANET JOURNAL OF RARE DISEASES . 19(1): 213-213. Nº de cites: 5
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Mora J, Climent A, Roldan-Molina M, Flores MC, Varo A, Pérez-Jaume S, Jou-Munoz C, Celma MS, Lazaro JJ, Cheung I, Castañeda-Heredia A, Gorostegui M, Rodriguez E, Chamorro S, Muñoz JP and Cheung NK.
Desensitizing the autonomic nervous system to mitigate anti-GD2 monoclonal antibody side effects
Frontiers in oncology . 14: 1380917-1380917.
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Downey C, Metry D, Garzon MC, Morales LK and Baselga E.
Reply to: "Letter to the Editor regarding Cutis marmorata telangiectatica congenita: Incidence of extracutaneous manifestations and a proposed clinical definition"
PEDIATRIC DERMATOLOGY . 41(3): 567-568.
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Alos L, Carrasco A, Teixidó C, Szumera-Cieckiewicz A, Vicente-Villa MA, Massi D and Carrera C.
Melanoma on congenital melanocytic nevi
PATHOLOGY RESEARCH AND PRACTICE . 256: 155262-155262.
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Ribeiro J, Tristan-Noguero A, Martinez-Calvo FF, Ibanez-Mico S, Peña-Segura JL, Ramos-Fernandez JM, Carlos Valera Dávila, O'Callaghan-Gordo M, Campistol-Plana J, Serrano M, Xenia Alonso, Illescas KS, Ramírez-Camacho A, Sans-Capdevila O, Garcia-Cazorla A, Bayés A and Alonso-Colmenero I.
Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy
Frontiers in Cell and Developmental Biology . 12: 1321282-1321282. Nº de cites: 3
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Baz-Redón N, Sánchez-Bellver L, Fernández-Cancio M, Rovira-Amigo S, Burgoyne T, Ranjit R, Aquino V, Toro-Barrios N, Carmona R, Polverino E, Cols M, Moreno-Galdó A, Camats-Tarruella N and Marfany G.
Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene
Cells . 13(6): .