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Early‐onset acral basal cell carcinomas in Gorlin syndrome

Torrelo, A.; Vicente, A.; Navarro, L.; Planaguma, M.; González Sarmiento, Rogelio; Hernández‐Martín, A.; Noguera‐Morel, L.; Requena, L.; Colmenero, I.; Parareda, A.; González‐Enseñat, M.A.; Happle, R.; Bueno Martínez, Elena (2014)
Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6

Citterio, Cintia E.; Morales, Cecilia M.; Bouhours-Nouet, Natacha; Machiavelli, Gloria A.; Gatelais, Frédérique; Coutant, Regis; González Sarmiento, Rogelio; Rivolta, Carina M.; Targovnik, Héctor M.; Bueno Martínez, Elena (2015)
Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series

Rodrigo-Nicolás, B.; Martín-Santiago, A.; Cañueto, J.; Vicente, A.; Torrelo, A.; Noguera-Morel, L.; Duat-Rodríguez, A.; Jorge Finnigan, Conrado ; Palacios-Álvarez, I.; García-Hernández, J.L.; Sebaratnam, Deshan; González Sarmiento, Rogelio; Hernández Martín, Ángela; Bueno Martínez, Elena (2018)
Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

Alonso, N.; Cañueto, J.; Ciria, S.; Palacios‐Alvarez, I.; Alegre, M.; Badenas, C.; Barreiro, A.; Pena, L.; Maldonado, C.; Nespeira‐Jato, M.V.; Peña‐Penabad, C.; Azon, A.; Gavrilova, M.; Ferrer, I.; Sanmartin, O.; Robles, L.; Hernandez‐Martin, A.; Urioste, M.; Puig, S.; Puig, L.; Gonzalez‐Sarmiento, R.; Bueno Martínez, Elena (2017)
Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas

Bella Navarro, R.; García García, Ana Bárbara; González Sarmiento, Rogelio; Navarro, L.; Sánchez Sendra, B.; Revert, A.; Jordá, E.; Monteagudo, C.; Bueno Martínez, Elena (2017)

DEP06 - Artículos de revista: Recent submissions

Early‐onset acral basal cell carcinomas in Gorlin syndrome ﻿

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6 ﻿

Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series ﻿

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome ﻿

Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas ﻿

Early‐onset acral basal cell carcinomas in Gorlin syndrome

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6

Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas