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	1.	Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review. [electronic resource] by Diociaiuti, A Castiglia, D Naim, M Condorelli, A G Zambruno, G El Hachem, M Producer: 20190826 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review. [electronic resource] by Diociaiuti, A Pisaneschi, E Rossi, S Condorelli, A G Carnevale, C Zambruno, G El Hachem, M Producer: 20210514 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short arm. [electronic resource] by Condorelli, A G Fortugno, P Cianfarani, F Proto, V Di Zenzo, G Didona, B Zambruno, G Castiglia, D Producer: 20191104 In: The British journal of dermatology vol. 178 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	MicroRNA-145-5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts. [electronic resource] by Condorelli, A G Logli, E Cianfarani, F Teson, M Diociaiuti, A El Hachem, M Zambruno, G Castiglia, D Odorisio, T Producer: 20210315 In: The British journal of dermatology vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)