Ngā hua rapu - Eulàlia Baselga

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  1. 1
    PIK3CA mutations in vascular malformations

    PIK3CA mutations in vascular malformations mā Sandra D. Castillo, Eulàlia Baselga, Mariona Graupera

    I whakaputaina 2019
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    Revisão
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  2. 2
    Sturge-Weber Syndrome: A Review

    Sturge-Weber Syndrome: A Review mā E. Higueros, Esther Roé, Esther Granell, Eulàlia Baselga

    I whakaputaina 2017
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    Revisão
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  3. 3
    Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache

    Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache mā Luis Fernando Sánchez‐Espino, Marta Ivars, Javier Antoñanzas, Eulàlia Baselga

    I whakaputaina 2023
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    Revisão
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  4. 4
    Erythema Multiforme-like Secondary to Paraphenylenediamine Due to Henna Tattoo Plus Residual Hypopigmentation

    Erythema Multiforme-like Secondary to Paraphenylenediamine Due to Henna Tattoo Plus Residual Hypopigmentation mā Levancini, Cristian Fischer, Sancho, Maribel Iglesias, Serrano, Vicente Exposito, Torres, Eulalia Baselga

    I whakaputaina 2015
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  5. 5
    Microcystic Lymphatic Malformation Successfully Treated With Topical Rapamycin

    Microcystic Lymphatic Malformation Successfully Treated With Topical Rapamycin mā P. García‐Montero, J. del Boz, Miguel Ángel Sánchez-Martínez, Isabel María Escudero Santos, Eulàlia Baselga

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Interventions for infantile haemangiomas of the skin

    Interventions for infantile haemangiomas of the skin mā Mónica Novoa, Eulàlia Baselga, Sandra Beltrán, Lucía Giraldo, Ali Shahbaz, Héctor Pardo‐Hernández, Ingrid Arévalo-Rodríguez

    I whakaputaina 2018
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  7. 7
    Infantile Hemangiomas With Unusually Prolonged Growth Phase

    Infantile Hemangiomas With Unusually Prolonged Growth Phase mā Heather A. Brandling‐Bennett, Denise W. Metry, Eulàlia Baselga, Anne W. Lucky, Denise M. Adams, Maria Cordisco, Ilona J. Frieden

    I whakaputaina 2008
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    Artigo
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  8. 8
    Lesiones pernióticas y acrales en España durante el confinamiento por COVID: análisis retrospectivo de 12 casos

    Lesiones pernióticas y acrales en España durante el confinamiento por COVID: análisis retrospectivo de 12 casos mā J. Romaní, Eulàlia Baselga, Natàlia Casamitjana, Nuria Martí, P. Garbayo, Asunción Vicente, M. Casals, Victòria Fumadó, Clàudia Fortuny, Sònia Calzado

    I whakaputaina 2020
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    Artigo
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  9. 9
    Chilblain and Acral Purpuric Lesions in Spain during Covid Confinement: Retrospective Analysis of 12 Cases

    Chilblain and Acral Purpuric Lesions in Spain during Covid Confinement: Retrospective Analysis of 12 Cases mā J. Romaní, Eulàlia Baselga, Natàlia Casamitjana, Nuria Martí, P. Garbayo, Asunción Vicente, M. Casals, Victòria Fumadó, Clàudia Fortuny, Sònia Calzado

    I whakaputaina 2020
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    Artigo
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  10. 10
    Efficacy and Safety of Topical Timolol for the Treatment of Infantile Hemangioma in the Early Proliferative Stage

    Efficacy and Safety of Topical Timolol for the Treatment of Infantile Hemangioma in the Early Proliferative Stage mā Fania Zamantta Muñoz‐Garza, Mónica Ríos, E. Roé-Crespo, José Bernabeu‐Wittel, M.T. Montserrat-García, L. Puig, Ignasi Gich, Eulàlia Baselga

    I whakaputaina 2021
    Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation

    Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation mā Milena Petkova, Marle Kraft, Simon Stritt, Inés Martínez‐Corral, Henrik Ortsäter, Michael Vanlandewijck, Bojana Jakic, Eulàlia Baselga, Sandra D. Castillo, Mariona Graupera, Christer Betsholtz, Taija Mäkinen

    I whakaputaina 2023
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    Artigo
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  12. 12
    Somatic <i>PIK3CA</i> mutations as a driver of sporadic venous malformations

    Somatic <i>PIK3CA</i> mutations as a driver of sporadic venous malformations mā Pau Castel, F. Javier Carmona, Joaquím Grego‐Bessa, Michael F. Berger, Agnès Viale, Kathryn V. Anderson, Sílvia Bagué, Maurizio Scaltriti, Cristina R. Antonescu, Eulàlia Baselga, José Baselga

    I whakaputaina 2016
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    Artigo
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  13. 13
    Propranolol Use in <scp>PHACE</scp> Syndrome with Cervical and Intracranial Arterial Anomalies: Collective Experience in 32 Infants

    Propranolol Use in <scp>PHACE</scp> Syndrome with Cervical and Intracranial Arterial Anomalies: Collective Experience in 32 Infants mā Denise W. Metry, Ilona J. Frieden, Christopher P. Hess, Dawn H. Siegel, Mohit Maheshwari, Eulàlia Baselga, Sarah L. Chamlin, Maria C. Garzón, Anthony J. Mancini, Julie Powell, Beth A. Drolet

    I whakaputaina 2012
    Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    Disease characteristics, comorbidities, treatment patterns and quality of life impact in children &lt;12 years old with atopic dermatitis: Interim results from the PEDISTAD Real-World Registry

    Disease characteristics, comorbidities, treatment patterns and quality of life impact in children &lt;12 years old with atopic dermatitis: Interim results from the PEDISTAD Real-Wo... mā Amy S. Paller, Emma Guttman‐Yassky, Marie L. A. Schuttelaar, Alan D. Irvine, Eulàlia Baselga, Yoko Kataoka, Martti Antila, Marjolein de Bruin‐Weller, Danielle Marcoux, Alvina Abramova, E. Rizova, Chunyuan Liu, Annie Zhang

    I whakaputaina 2022
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    Artigo
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  15. 15
    Severe adverse events during sirolimus “off‐label” therapy for vascular anomalies

    Severe adverse events during sirolimus “off‐label” therapy for vascular anomalies mā Jochen Rößler, Eulàlia Baselga, Victoria Lucía Dávila Osorio, Verónica Celis, Andrea Diociaiuti, Maya El Hachem, Sandrine Mestre, Dario Haeberli, Aram Prokop, Christof Hanke, Wolfgang Loichinger, I. Quéré, Iris Baumgärtner, Charlotte M. Niemeyer, Friedrich Kapp

    I whakaputaina 2021
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    Artigo
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  16. 16
    Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

    Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema mā Antonella Mendola, Matthieu J. Schlögel, Arash Ghalamkarpour, Alexandre Irrthum, Ha‐Long Nguyen, Elodie Fastré, Anette Bygum, Cees van der Vleuten, Christina Fagerberg, Eulàlia Baselga, I. Quéré, John B. Mulliken, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula

    I whakaputaina 2013
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    Artigo
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  17. 17
    Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies

    Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies mā Michel Wassef, Francine Blei, Denise M. Adams, Ahmad I. Alomari, Eulàlia Baselga, Alejandro Berenstein, Patricia E. Burrows, Ilona J. Frieden, Maria C. Garzón, Juan Carlos López‐Gutiérrez, David Lord, Sally Mitchel, Julie Powell, Julie Prendiville, Miikka Vikkula

    I whakaputaina 2015
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    Revisão
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  18. 18
    Oncogenic <i>PIK3CA</i> mutations occur in epidermal nevi and seborrheic keratoses with a characteristic mutation pattern

    Oncogenic <i>PIK3CA</i> mutations occur in epidermal nevi and seborrheic keratoses with a characteristic mutation pattern mā Christian Hafner, Elena López‐Knowles, Nuno Miguel Luis, Agustí Toll, Eulàlia Baselga, Alex Fernández-Casado, Sílvia Hernández, Adriana Ribé, Thomas Mentzel, Robert Stoehr, Ferdinand Hofstaedter, Michael Landthaler, Thomas Vogt, Ramón M. Pujol, Arndt Hartmann, Francisco X. Real

    I whakaputaina 2007
    Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    Real-world treatment outcomes of systemic treatments for moderate-to-severe atopic dermatitis in children aged less than 12 years: 2-year results from PEDISTAD

    Real-world treatment outcomes of systemic treatments for moderate-to-severe atopic dermatitis in children aged less than 12 years: 2-year results from PEDISTAD mā Amy S. Paller, Marjolein de Bruin‐Weller, Danielle Marcoux, Eulàlia Baselga, Vânia Oliveira Carvalho, Ledit Ardusso, Suzanne G.M.A. Pasmans, Mirna Toledo‐Bahena, Cory Rubin, Joel C. Joyce, Lara Wine Lee, Bryan Adams, Rajan Gupta, Marius Ardeleanu, Annie Zhang

    I whakaputaina 2024
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    Artigo
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  20. 20
    Keratinocytic epidermal nevi are associated with mosaic<i>RAS</i>mutations

    Keratinocytic epidermal nevi are associated with mosaic<i>RAS</i>mutations mā Christian Hafner, Agustí Toll, Susanne Gantner, Andreas Mauerer, Irene Lurkin, Francesco Acquadro, Alejandro Fernández-Casado, Ellen C. Zwarthoff, Wolfgang Dietmaier, Eulàlia Baselga, Elisabet Parera, Asunción Vicente, Ariel Casanova, Juan C. Cigudosa, Thomas Mentzel, Ramón M. Pujol, Michael Landthaler, Francisco X. Real

    I whakaputaina 2012
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    Artigo
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