Personas / Equipo Humano

Eulalia Baselga Torres

Buscador de publicaciones

Publicaciones

  • Hernandez-Martín A, Aranegui B, Escámez MJ, de Lucas R, Vicente-Villa MA, Rodríguez-Díaz E, Bernabeu-Wittel J, Gonzalez-Hermosa R, García-Patos V, Ginarte M, Mascaró JM, Corredera C, Baselga E, Santiago JL, Chaves A, Román C, Evole M, Martin-Santiago A, Torrelo A, Del Río M, Feito M, González-Enseñat MA, Romero G, Morcillo-Makow E, Abaitua I and García-Doval I.

    Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care.

    ACTAS DERMO-SIFILIOGRAFICAS . 104(10): 890-6. Nº de citas: 19

    [doi:10.1016/j.ad.2013.03.006]

  • Revencu N, Boon LM, Mendola A, Cordisco MR, Dubois J, Clapuyt P, Hammer F, Amor DJ, Irvine AD, Baselga E, Dompmartin A, Syed S, Santiago AM, Ades L, Collins F, Smith J, Sandaradura S, Barrio VR, Burrows PE, Blei F, Cozzolino M, Brunetti-Pierri N, Vicente-Villa MA, Abramowicz M, Désir J, Vilain C, Chung WK, Wilson A, Gardiner CA, Dwight Y, Lord DJ, Fishman L, Cytrynbaum C, Chamlin S, Ghali F, Gilaberte Y, Joss S, Boente MD, Léauté-Labrèze C, Delrue MA, Bayliss S, Martorell-Sampol L, Gonzalez MA, Mazereeuw-Hautier J, O'Donnell B, Bessis D, Pyeritz RE, Salhi A, Tan OT, Wargon O, Mulliken JB and Vikkula M.

    RASA1 Mutations and Associated Phenotypes in 68 Families with Capillary Malformation-Arteriovenous Malformation

    HUMAN MUTATION . 34(12): 1632-1641. Nº de citas: 206

    [doi:10.1002/humu.22431]

  • Novoa-Candia, MP, Baselga E, Aguilera, P and Tresserra, F.

    Atrophic Congenital Melanocytic Nevus Mimicking Rapidly Involuting Congenital Hemangioma

    PEDIATRIC DERMATOLOGY . 30(6): 164-165.

    [doi:10.1111/j.1525-1470.2012.01772.x]

  • Català-Temprano A, Roé E, Vikkula M and Baselga E.

    Capillary malformation-arteriovenous malformation syndrome: a report of 2 cases, diagnostic criteria, and management.

    ACTAS DERMO-SIFILIOGRAFICAS . 104(8): 710-713. Nº de citas: 8

    [doi:10.1016/j.adengl.2012.04.025]

  • Mendola A, Schlögel MJ, Ghalamkarpour A, Irrthum A, Nguyen HL, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken JB, Boon LM, Brouillard P and Vikkula M.

    Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

    Molecular syndromology . 4(6): 257-266. Nº de citas: 64

    [doi:10.1159/000354097]

  • Hernández-Martin A, de Lucas R, Vicente-Villa MA, Baselga E, Morcillo-Makow E, Arroyo Manzanal MI, Abaitua I and Torrelo A.

    Reference centers for epidermolysis bullosa and ichthyosis: an urgent need in Spain.

    ACTAS DERMO-SIFILIOGRAFICAS . 104(5): 363-366. Nº de citas: 4

    [doi:10.1016/j.adengl.2013.04.001]

  • Siegel, DH, Shieh, JTC, Kwon, EK, Baselga E, Blei, F, Cordisco, M, Dobyns, WB, Duffy, KJ, Garzon, MC, Gibbs, DL, Grimmer, JF, Hayflick, SJ, Krol, AL, Kwok, PY, Lorier, R, Matter, A, McWeeney, S, Metry, D, Mitchell, S, Pope, E, Santoro, JL, Stevenson, DA, Bayrak-Toydemir, P, Wilmot, B, Worthey, EA, Frieden, IJ, Drolet, BA and Broeckel, U.

    Copy Number Variation Analysis in 98 Individuals with PHACE Syndrome

    JOURNAL OF INVESTIGATIVE DERMATOLOGY . 133(3): 677-684. Nº de citas: 19

    [doi:10.1038/jid.2012.367]

  • Metry, D, Frieden, IJ, Hess, C, Siegel, D, Maheshwari, M, Baselga E, Chamlin, S, Garzon, M, Mancini, AJ, Powell, J and Drolet, BA.

    Propranolol Use in PHACE Syndrome with Cervical and Intracranial Arterial Anomalies: Collective Experience in 32 Infants

    PEDIATRIC DERMATOLOGY . 30(1): 71-89. Nº de citas: 58

    [doi:10.1111/j.1525-1470.2012.01879.x]

  • Drolet, BA, Frommelt, PC, Chamlin, SL, Haggstrom, A, Bauman, NM, Chiu, YE, Chun, RH, Garzon, MC, Holland, KE, Liberman, L, MacLellan-Tobert, S, Mancini, AJ, Metry, D, Puttgen, KB, Seefeldt, M, Sidbury, R, Ward, KM, Blei, F, Baselga E, Cassidy, L, Darrow, DH, Joachim, S, Kwon, EKM, Martin, K, Perkins, J, Siegel, DH, Boucek, RJ and Frieden, IJ.

    Initiation and Use of Propranolol for Infantile Hemangioma: Report of a Consensus Conference

    Pediatrics . 131(1): 128-140. Nº de citas: 397

    [doi:10.1542/peds.2012-1691]

  • Hernández-Martín A, Garcia-Doval I, Aranegui B, de Unamuno P, Rodríguez-Pazos L, González-Enseñat MA, Vicente-Villa MA, Martín-Santiago A, Garcia-Bravo B, Feito M, Baselga E, Círia S, de Lucas R, Ginarte M, González-Sarmiento R and Torrelo A.

    Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain

    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY . 67(2): 240-244. Nº de citas: 44

    [doi:10.1016/j.jaad.2011.07.033]