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D Castiglia

Showing results (41-50 of 43) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|December 4, 2020
Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub-classification of inherited epidermolysis bullosa: a single-centre retrospective comparative study of 87 cases with long-term follow-upS Rossi, D Castiglia, E Pisaneschi, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
The British Journal of Dermatology|June 1, 2011
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplexM García, J L Santiago, A Terrón, et al.
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Showing results (41-50 of 43) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 43 results.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 4, 2020
Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub-classification of inherited epidermolysis bullosa: a single-centre retrospective comparative study of 87 cases with long-term follow-upS Rossi, D Castiglia, E Pisaneschi, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
The British Journal of Dermatology|June 1, 2011
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplexM García, J L Santiago, A Terrón, et al.
Pageof 5