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

British journal of dermatology (1951), 2018-10, Vol.179 (4), p.933-939

2018

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Systematic review with meta‐analysis: the I148M variant of patatin‐like phospholipase domain‐containing 3 gene (PNPLA3) is significantly associated with alcoholic liver cirrhosis

Alimentary pharmacology & therapeutics, 2014-09, Vol.40 (6), p.571-581

2014

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Polymorphisms in autophagy genes are genetic susceptibility factors in glioblastoma development

BMC cancer, 2022-02, Vol.22 (1), p.146-146, Article 146

2022

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Comment on: Clinicopathological features and oncological outcomes of patients with young‐onset rectal cancer

British journal of surgery, 2020-07, Vol.107 (8), p.e277-e277

2020

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Molecular evidence of type 2 mosaicism in Gorlin syndrome

British journal of dermatology (1951), 2013-12, Vol.169 (6), p.1342-1345

2013

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Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin

Journal of the European Academy of Dermatology and Venereology, 2022-10, Vol.36 (10), p.e789-e790

2022

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Early‐onset acral basal cell carcinomas in Gorlin syndrome

British journal of dermatology (1951), 2014-11, Vol.171 (5), p.1227-1229

2014

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Epidermal growth factor receptor (EGFR) pathway polymorphisms as predictive markers of cetuximab toxicity in locally advanced head and neck squamous cell carcinoma (HNSCC) in a Spanish population

Oral oncology, 2016-12, Vol.63, p.38-43

2016

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Meta‐analysis: glutathione‐S‐transferase allelic variants are associated with alcoholic liver disease

Alimentary pharmacology & therapeutics, 2011-11, Vol.34 (10), p.1159-1172

2011

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Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome

Journal of the European Academy of Dermatology and Venereology, 2017-01, Vol.31 (1), p.e11-e13

2017

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Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature

British journal of dermatology (1951), 2012-04, Vol.166 (4), p.830-838

2012

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Recessive XLI: high prevalence of neurological disorders

British journal of dermatology (1951), 2018-10, Vol.179 (4), p.e180-e180

2018

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Acral peeling skin syndrome resulting from mutations in TGM5

Journal of the European Academy of Dermatology and Venereology, 2016-03, Vol.30 (3), p.477-480

2016

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Letter: PNPLA3 and alcoholic liver disease – an alert to methodological limitations. Authors’ reply

Alimentary pharmacology & therapeutics, 2015-03, Vol.41 (6), p.594-594

2015

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Gorlin Syndrome

Actas dermo-sifiliográficas (English ed.), 2018-04, Vol.109 (3), p.207-217

2018

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隐性 XLI: 神经系统疾病的高患病率

British journal of dermatology (1951), 2018-10, Vol.179 (4), p.e192-e192

2018

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X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient

Dermatology (Basel), 2010-01, Vol.221 (2), p.113-116

2010

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Gorlin Syndrome

Actas dermo-sifiliográficas (English ed.), 2018-04, Vol.109 (3), p.207-217

2018

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Síndrome de Gorlin

Actas dermo-sifiliográficas, 2018-04, Vol.109 (3), p.207-217

2018

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

British journal of dermatology (1951), 2017-12, Vol.177 (6), p.1654-1663

2017

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Análisis de la relación entre polimorfismos en regiones diana de micro-ARN y la enfermedad hepática alcohólica

Revista clínica espanõla, 2018-05, Vol.218 (4), p.170-176

2018

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X-linked ichthyosis: an update

British journal of dermatology (1951), 1999-10, Vol.141 (4), p.617-627

1999

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

British journal of dermatology (1951), 2018-01, Vol.178 (1), p.198-206

2018

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Relación de la presencia de polimorfismos de CFH , HTRA1 , ARMS2 , VEGF-A y VEGF-R con la aparición de los subtipos de degeneración macular asociada a la edad

Archivos de la Sociedad Española de Oftalmología, 2016-04, Vol.91 (4), p.177-183

2016

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Growth hormone expression in ontogenic development in gilthead sea bream

Cell and tissue research, 2003-07, Vol.313 (1), p.81-91

2003

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

Systematic review with meta‐analysis: the I148M variant of patatin‐like phospholipase domain‐containing 3 gene (PNPLA3) is significantly associated with alcoholic liver cirrhosis

Polymorphisms in autophagy genes are genetic susceptibility factors in glioblastoma development

Comment on: Clinicopathological features and oncological outcomes of patients with young‐onset rectal cancer

Molecular evidence of type 2 mosaicism in Gorlin syndrome

Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin

Early‐onset acral basal cell carcinomas in Gorlin syndrome

Epidermal growth factor receptor (EGFR) pathway polymorphisms as predictive markers of cetuximab toxicity in locally advanced head and neck squamous cell carcinoma (HNSCC) in a Spanish population

Meta‐analysis: glutathione‐S‐transferase allelic variants are associated with alcoholic liver disease

Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome

Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature

Recessive XLI: high prevalence of neurological disorders

Acral peeling skin syndrome resulting from mutations in TGM5

Letter: PNPLA3 and alcoholic liver disease – an alert to methodological limitations. Authors’ reply

Gorlin Syndrome

隐性 XLI: 神经系统疾病的高患病率

X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient

Gorlin Syndrome

Síndrome de Gorlin

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

Análisis de la relación entre polimorfismos en regiones diana de micro-ARN y la enfermedad hepática alcohólica

X-linked ichthyosis: an update

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

Relación de la presencia de polimorfismos de CFH , HTRA1 , ARMS2 , VEGF-A y VEGF-R con la aparición de los subtipos de degeneración macular asociada a la edad

Growth hormone expression in ontogenic development in gilthead sea bream

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