Publicaciones en las que colabora con Javier Cañueto Álvarez (12)

2023

  1. Cutaneous squamous cell carcinoma: From biology to therapy

    Advances in Surgical and Medical Specialties (Taylor and Francis), pp. 393-424

2020

  1. Cutaneous squamous cell carcinoma: From biology to therapy

    International Journal of Molecular Sciences, Vol. 21, Núm. 8

2018

  1. Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series

    British Journal of Dermatology, Vol. 179, Núm. 4, pp. 933-939

  2. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

    British Journal of Dermatology, Vol. 178, Núm. 1, pp. 198-206

2017

  1. Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome

    Journal of the European Academy of Dermatology and Venereology

2016

  1. Acral peeling skin syndrome resulting from mutations in TGM5

    Journal of the European Academy of Dermatology and Venereology

2015

  1. Emopamil binding protein mutation in Conradi-Hünermann-Happle syndrome representing plaque-type psoriasis

    Indian Journal of Dermatology, Vol. 60, Núm. 2, pp. 216

2014

  1. The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi-Hünermann-Happle syndrome

    Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, Vol. 1841, Núm. 3, pp. 336-344

2012

  1. Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: New insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature

    British Journal of Dermatology, Vol. 166, Núm. 4, pp. 830-838

2011

  1. Buschke-ollendorff syndrome with striking phenotypic variation resulting from a novel c.2203C>T nonsense mutation in LEMD3

    Pediatric Dermatology, Vol. 28, Núm. 4, pp. 447-450

  2. Una nueva mutación en el gen EDA en una familia española con displasia ectodérmica hipohidrótica ligada al cromosoma X

    Actas Dermo-Sifiliograficas, Vol. 102, Núm. 9, pp. 722-725

2010

  1. Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: A high frequency of partial deletions in a Spanish population

    Journal of the European Academy of Dermatology and Venereology, Vol. 24, Núm. 10, pp. 1226-1229