Fundación Pública Galega de Medicina Xenómica
Centro de investigación
Publicacións nas que colabora con Jaime Toribio Pérez (12)
2014
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Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis
British Journal of Dermatology
2013
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Annular elastolytic giant cell granuloma associated to late-onset X-linked dominant protoporphyria
Dermatology, Vol. 227, Núm. 3, pp. 238-242
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Autosomal recessive congenital ichthyosis
Actas Dermo-Sifiliograficas
2012
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Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis
International Journal of Dermatology, Vol. 51, Núm. 4, pp. 427-430
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Clinical and molecular classification of ichthyosis
Piel
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Multiple local and recent founder effects of TGM1 in Spanish families.
PloS one, Vol. 7, Núm. 4
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Variable expression of naevoid basal cell carcinoma syndrome in a family with a novel mutation in the PTCH1 gene
Clinical and Experimental Dermatology
2011
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Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): Evidence of founder effects
British Journal of Dermatology, Vol. 165, Núm. 4, pp. 906-911
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Birt-Hogg-Dubé syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene
International Journal of Dermatology, Vol. 50, Núm. 8, pp. 968-971
2009
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Lamellar ichthyosis with a novel homozygous C-terminal mutation in the transglutaminase-1 gene
International Journal of Dermatology, Vol. 48, Núm. 11, pp. 1195-1197
2007
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Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)
International Journal of Dermatology, Vol. 46, Núm. 1, pp. 61-63
2001
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Identification of Mycobacterium marinum in sea-urchin granulomas
British Journal of Dermatology, Vol. 145, Núm. 1, pp. 114-116