Research Topics
Species | A Hernandez-MartinSummaryAffiliation: Hospital Universitario Country: Spain Publications
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Detail Information
Publications
Eosinophilic pustular folliculitis of infancy: a series of 15 cases and review of the literatureAngela Hernández-Martín
Department of Dermatology, Hospital Nino Jesus, Madrid, Spain
J Am Acad Dermatol 68:150-5. 2013..Eosinophilic pustular folliculitis (EPF) of infancy is characterized by the presence of pustular lesions containing eosinophils. It is the least well-characterized of the EPF diseases...- Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in SpainAngela Hernández-Martín
Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain
J Am Acad Dermatol 67:240-4. 2012..Previous reports on the prevalence of autosomal recessive congenital ichthyosis (ARCI) were based on single source data, such as lists of members in a patient association. These sources are likely to be incomplete... - Hereditary mucoepithelial dysplasia: report of two sporadic casesAngela Hernández-Martín
Departments of Dermatology, Hospital Nino Jesus, Madrid, Spain
Pediatr Dermatol 29:311-5. 2012..We report on two unrelated patients who presented with typical clinical and histologic features of HMD along with other unreported clinical findings... 
[Inherited epidermolysis bullosa: from diagnosis to reality]A Hernandez-Martin
Servicio de Dermatologia, Hospital Infantil del Niño Jesús, Madrid, Espana
Actas Dermosifiliogr 101:495-505. 2010..As dermatologists, we must be aware of the potential complications of EB because our intervention is essential for the correct referral of patients and coordination of all the specialists involved in their care...- X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patientA Hernandez-Martin
Department of Dermatology, Hospital Nino Jesus, Madrid, Spain
Dermatology 221:113-6. 2010..We report the first case of a patient with both XLI and DEB in whom a partial deletion of the STS gene and a recessive point mutation in COL7A1 were demonstrated... - [Analysis of surgical treatment for nonmelanoma skin cancer performed by dermatologists in a public hospital: clinical-pathological correlation, use of hospital resources, and waiting list time from diagnosis]A Hernandez-Martin
Unidad de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
Actas Dermosifiliogr 98:694-701. 2007..No studies have been published addressing differences in the management of surgical treatment for nonmelanoma skin cancer according to the specialties involved... - Ulcerated sclerotic giant congenital melanocytic naevus: case report and review of the literatureA Hernandez-Martin
Dermatology Unit, Hospital del Nino Jesus, Madrid, Spain
Clin Exp Dermatol 32:529-32. 2007..We review the published cases and propose the term 'sclerotic hypopigmented GCMN as a common descriptor of this type of congenital melanocytic naevus... - [Localized pityriasis lichenoides]A Hernandez-Martin
Servicio de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
Actas Dermosifiliogr 98:47-9. 2007..We report a 9-year-old patient with recurrent crops of pitiryasis lichenoides lesions exclusively involving the lower abdomen... - [Solitary giant cell collagenoma]A Hernandez-Martin
Servicio de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
Actas Dermosifiliogr 97:406-8. 2006..Histology studies show an increase of collagen fibers in the dermis and a variable decrease in elastic fibers. We discuss the case of a child with a solitary giant cerebriform collagenoma on the lumbar region of her back... - [Rasopathies: developmental disorders that predispose to cancer and skin manifestations]A Hernandez-Martin
Servicio de Dermatologia, Hospital Infantil del Niño Jesús, Madrid, Spain ahernandez
Actas Dermosifiliogr 102:402-16. 2011..Recognizing the skin manifestations of rasopathies can facilitate diagnosis of these syndromes... - [Lymphomatoid papulosis in children: report of 9 cases and review of the literature]A Martorell-Calatayud
Hospital Infantil Niño Jesus, Madrid, Espana
Actas Dermosifiliogr 101:693-701. 2010.... - 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 literatureJ Canueto
Department of Dermatology, University Hospital of Salamanca, Salamanca, Spain
Br J Dermatol 166:830-8. 2012..CDPX2 results from mutations in EBP (emopamil binding protein), and presents with increased levels of sterol precursors 8(9)-cholesterol and 8-dehydrocholesterol... - [Primary cutaneous aspergillosis in a leukemic child]A Torrelo
Servicios de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
Actas Dermosifiliogr 98:276-8. 2007.... - Congenital multiple clustered dermatofibromaP de Unamuno
Department of Dermatology, University Hospital of Salamanca, Paseo de San Vicente s n, 37007 Salamanca, Spain
Br J Dermatol 142:1040-3. 2000..We report a man in whom the MCD was congenital, although during the first few years of his second decade it extended to involve a broad zone on the left hip, gluteal region and upper thigh... - [Rasopathies: developmental disorders that predispose to cancer and skin manifestations]A Hernandez-Martin
Servicio de Dermatologia, Hospital Infantil del Niño Jesús, Madrid, Spain ahernandez
Actas Dermosifiliogr 102:402-16. 2011..Recognizing the skin manifestations of rasopathies can facilitate diagnosis of these syndromes... - Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish populationJ Canueto
Department of Dermatology, University Hospital of Salamanca, Salamanca, Spain
J Eur Acad Dermatol Venereol 24:1226-9. 2010..RXLI is caused by a deficiency in steroid sulphatase (STS), whose gene has been located on the X chromosome (locus Xp22.3). Up to 90% of the mutations described in this gene are complete deletions...