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ArticlesPeer ReviewedFull Text
Clinical and Pathological Features of Persistent Decorative Tattoo Reactions
Author / Creator:Suárez-Peñaranda, José ; Fachal, Carmen ; Blanco-Bellas, Maria ; Ginarte, Manuel ; Monteagudo, Benigno ; León, Alvaro ; González-Carril, Fernando
Publisher:Kolkata: Medknow
Journal title:Indian Journal of Dermatology, 2022-03, Vol.67 (2), p.152-156
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ArticlesPeer ReviewedFull Text
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation
Author / Creator:Esperón-Moldes, Uxia ; Ginarte-Val, Manuel ; Rodríguez-Pazos, Laura ; Fachal, Laura ; Martín-Santiago, Ana ; Vicente, Asunción ; Jiménez-Gallo, David ; Guillén-Navarro, Encarna ; Sampol, Loreto Martorell ; González-Enseñat, María Antonia ; Vega, Ana
Publisher:United States: Public Library of Science
Journal title:PloS one, 2020-02, Vol.15 (2), p.e0229025-e0229025
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ArticlesPeer ReviewedFull Text
Multiple Local and Recent Founder Effects of TGM1 in Spanish Families
Author / Creator:Fachal, Laura ; Rodríguez-Pazos, Laura ; Ginarte, Manuel ; Toribio, Jaime ; Salas, Antonio ; Vega, Ana
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-04, Vol.7 (4), p.e33580
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ArticlesPeer ReviewedFull Text
A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations
Author / Creator:Montalván‐Suárez, Martha ; Esperón‐Moldes, Uxia Saraiva ; Rodríguez‐Pazos, Laura ; Ordóñez‐Ugalde, Andrés ; Moscoso, Fernanda ; Ugalde‐Noritz, Nora ; Santomé, Luis ; Fachal, Laura ; Tettamanti‐Miranda, Daniel ; Ruiz, Juan Carlos ; Ginarte, Manuel ; Vega, Ana
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2019-05, Vol.7 (5), p.e608-n/a
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ArticlesPeer ReviewedFull Text
Bier’s Spots in Association with Hypoplasia of the Aorta
Author / Creator:Cabanillas, Miguel ; Suárez-Amor, Oscar ; Loureiro, Manuel ; Ginarte, Manuel ; Toribio, Jaime
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Dermatology (Basel), 2007-01, Vol.215 (2), p.166-167
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ArticlesPeer ReviewedFull Text
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis . Study of the CYP4F22 c.1303CT founder mutation
Author / Creator:Esperón-Moldes, Uxia ; Ginarte-Val, Manuel ; Rodríguez-Pazos, Laura ; Fachal, Laura ; Martín-Santiago, Ana ; Vicente, Asunción ; Jiménez-Gallo, David ; Guillén-Navarro, Encarna ; Sampol, Loreto Martorell ; González-Enseñat, María Antonia ; Vega, Ana
Publisher:Public Library of Science
Journal title:PloS one, 2020-02, Vol.15 (2), p.e0229025
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ArticlesPeer ReviewedFull Text
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis
Author / Creator:Esperón-Moldes, Uxia ; Ginarte-Val, Manuel ; Rodríguez-Pazos, Laura ; Fachal, Laura ; Martín-Santiago, Ana ; Vicente, Asunción ; Jiménez-Gallo, David ; Guillén-Navarro, Encarna ; Sampol, Loreto Martorell ; González-Enseñat, María Antonia ; Vega, Ana
Publisher:Public Library of Science
Journal title:PloS one, 2020-02, Vol.15 (2), p.e0229025
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ArticlesPeer ReviewedFull Text
Adherence to drug treatments and adjuvant barrier repair therapies are key factors for clinical improvement in mild to moderate acne: the ACTUO observational prospective multicenter cohort trial in 64...
Author / Creator:de Lucas, Raúl ; Moreno-Arias, Gerardo ; Perez-López, Montserrat ; Vera-Casaño, Ángel ; Aladren, Sonia ; Milani, Massimo
Publisher:England: BioMed Central Ltd
Journal title:BMC dermatology, 2015-09, Vol.15 (1), p.17-17, Article 17
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ArticlesFull Text
Treatment of α1-antitrypsin-deficiency panniculitis with minocycline
Author / Creator:GINARTE, Manuel ; ROSON, Elena ; PETEIRO, Carmen ; TORIBIO, Jaime
Publisher:Chatham, NJ: Quadrant HealthCom
Journal title:Cutis (New York, N.Y.), 2001, Vol.68 (2), p.86-88
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ArticlesFull Text
Treatment of (alpha(1))-antitrypsin-deficiency panniculitis with minocycline
Author / Creator:Ginarte, Manuel ; Roson, Elena ; Peteiro, Carmen ; Toribio, Jaime
Publisher:Chatham: Quadrant HealthCom Inc
Journal title:Cutis (New York, N.Y.), 2001-08, Vol.68 (2), p.86
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ReportsFull Text
Bier's spots in association with hypoplasia of the aorta
Author / Creator:Cabanillas, Miguel ; Suárez-Amor, Oscar ; Loureiro, Manuel ; Ginarte, Manuel ; Toribio, Jaime
Journal title:Dermatology (Basel, Switzerland), 2007, Vol.215 (2), p.166-167
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Clinical and Pathological Features of Persistent Decorative Tattoo Reactions

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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

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Multiple Local and Recent Founder Effects of TGM1 in Spanish Families

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A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations

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Bier’s Spots in Association with Hypoplasia of the Aorta

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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis . Study of the CYP4F22 c.1303CT founder mutation

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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis

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Adherence to drug treatments and adjuvant barrier repair therapies are key factors for clinical improvement in mild to moderate acne: the ACTUO observational prospective multicenter cohort trial in 64...

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Treatment of α1-antitrypsin-deficiency panniculitis with minocycline

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Treatment of (alpha(1))-antitrypsin-deficiency panniculitis with minocycline

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Bier's spots in association with hypoplasia of the aorta

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