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Author/Creator Mencía, Ángeles

1. Identical COL71A1 heterozygous mutations resulting in different dystrophic epidermolysis bullosa phenotypes. Issue 2 (22nd December 2017)

Authors:
Knöpfel, Nicole; Noguera‐Morel, Lucero; Hernández‐Martin, Angela; García‐Martin, Adela; García, Marta; Mencía, Ángeles; Pedrero, Rocío Maseda; de Lucas, Raúl; Escámez, Maria José; Torrelo, Antonio
Journal:
Pediatric dermatology
Issue:
Volume 35:Issue 2(2018)
Page Start:
e94
Record Type:
Journal Article
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2. Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia. Issue 4 (13th February 2016)

Authors:
Mencía, Ángeles; García, Marta; García, Eva; Llames, Sara; Charlesworth, Alexandra; de Lucas, Raúl; Vicente, Asunción; Trujillo‐Tiebas, María José; Coto, Pablo; Costa, Marta; Vera, Ángel; López‐Pestaña, Arantxa; Murillas, Rodolfo; Meneguzzi, Guerrino; Jorcano, José Luis; Conti, Claudio J; Escámez...
Journal:
Experimental dermatology
Issue:
Volume 25:Issue 4(2016)
Page Start:
269
Record Type:
Journal Article
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3. Keratinocyte cell lines derived from severe generalized recessive Epidermolysis Bullosa patients carrying a highly recurrent COL7A1 homozygous mutation: models to assess cell and gene therapies in vitro and in vivo. Issue 9 (16th August 2013)

Authors:
Chamorro, Cristina; Almarza, David; Duarte, Blanca; Llames, Sara G.; Murillas, Rodolfo; García, Marta; Cigudosa, Juan C.; Espinosa‐Hevia, Luis; Escámez, Maria José; Mencía, Ángeles; Meana, Álvaro; García‐Escudero, Ramón; Moro, Rosa; Conti, Claudio J.; Del Río, Marcela; Larcher, Fernando
Journal:
Experimental dermatology
Issue:
Volume 22:Issue 9(2013:Sep.)
Page Start:
601
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗