A Hernandez-Martin

Summary

Affiliation: Hospital Universitario
Country: Spain

Publications

  1. doi request reprint Hyperpigmented macules on the face of young children: a series of 25 cases
    Angela Hernández-Martín
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    J Am Acad Dermatol 70:288-90. 2014
  2. doi request reprint First symposium of ichthyosis experts
    A Hernandez-Martin
    Servicio de Dermatologia, Hospital Infantil Niño Jesus, Madrid, España Electronic address
    Actas Dermosifiliogr 104:877-82. 2013
  3. doi request reprint First symposium of ichthyosis experts
    A Hernandez-Martin
    Servicio de Dermatologia, Hospital Infantil Niño Jesus, Madrid, Spain Electronic address
    Actas Dermosifiliogr 104:877-82. 2013
  4. doi request reprint Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care
    A Hernandez-Martin
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    Actas Dermosifiliogr 104:890-6. 2013
  5. doi request reprint A systematic review of clinical trials of treatments for the congenital ichthyoses, excluding ichthyosis vulgaris
    Angela Hernández-Martín
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    J Am Acad Dermatol 69:544-549.e8. 2013
  6. doi request reprint Eosinophilic pustular folliculitis of infancy: a series of 15 cases and review of the literature
    Angela Hernández-Martín
    Department of Dermatology, Hospital Nino Jesus, Madrid, Spain
    J Am Acad Dermatol 68:150-5. 2013
  7. doi request reprint Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain
    Angela Hernández-Martín
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain
    J Am Acad Dermatol 67:240-4. 2012
  8. doi request reprint Hereditary mucoepithelial dysplasia: report of two sporadic cases
    Angela Hernández-Martín
    Departments of Dermatology, Hospital Nino Jesus, Madrid, Spain
    Pediatr Dermatol 29:311-5. 2012
  9. doi request reprint X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient
    A Hernandez-Martin
    Department of Dermatology, Hospital Nino Jesus, Madrid, Spain
    Dermatology 221:113-6. 2010
  10. ncbi request reprint [Localized pityriasis lichenoides]
    A Hernandez-Martin
    Servicio de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
    Actas Dermosifiliogr 98:47-9. 2007

Collaborators

Detail Information

Publications24

  1. doi request reprint Hyperpigmented macules on the face of young children: a series of 25 cases
    Angela Hernández-Martín
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    J Am Acad Dermatol 70:288-90. 2014
    ..Acquired hyperpigmented lesions in early childhood can be the presenting sign of serious diseases or benign conditions and often cause significant parental anxiety...
  2. doi request reprint First symposium of ichthyosis experts
    A Hernandez-Martin
    Servicio de Dermatologia, Hospital Infantil Niño Jesus, Madrid, España Electronic address
    Actas Dermosifiliogr 104:877-82. 2013
    ..This article summarizes the presentations given at the symposium and is intended as a reference for anyone interested in the subject. ..
  3. doi request reprint First symposium of ichthyosis experts
    A Hernandez-Martin
    Servicio de Dermatologia, Hospital Infantil Niño Jesus, Madrid, Spain Electronic address
    Actas Dermosifiliogr 104:877-82. 2013
    ..This article summarizes the presentations given at the symposium and is intended as a reference for anyone interested in the subject. ..
  4. doi request reprint Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care
    A Hernandez-Martin
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    Actas Dermosifiliogr 104:890-6. 2013
    ..Dystrophic epidermolysis bullosa (DEB) is a rare disease that represents a heavy burden for both the patient and the health care system. There are currently no data on the prevalence of DEB in Spain...
  5. doi request reprint A systematic review of clinical trials of treatments for the congenital ichthyoses, excluding ichthyosis vulgaris
    Angela Hernández-Martín
    Department of Dermatology, Hospital Infantil del Niño Jesús, Madrid, Spain Electronic address
    J Am Acad Dermatol 69:544-549.e8. 2013
    ..The ichthyoses comprise a group of inherited disorders of keratinization. Because of the need for lifelong treatment, it is important that therapies are beneficial, safe, and well tolerated...
  6. doi request reprint Eosinophilic pustular folliculitis of infancy: a series of 15 cases and review of the literature
    Angela 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...
  7. doi request reprint Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain
    Angela 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...
  8. doi request reprint Hereditary mucoepithelial dysplasia: report of two sporadic cases
    Angela 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...
  9. doi request reprint X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient
    A 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...
  10. ncbi request reprint [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...
  11. ncbi request reprint Ulcerated sclerotic giant congenital melanocytic naevus: case report and review of the literature
    A 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...
  12. ncbi request reprint [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...
  13. ncbi request reprint [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...
  14. ncbi request reprint [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...
  15. doi request reprint [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...
  16. doi request reprint 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
    J 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...
  17. doi request reprint Ectodermal dysplasia-skin fragility syndrome: a novel mutation in the PKP1 gene
    A Hernandez-Martin
    Department of Dermatology, Hospital Nino Jesus, Madrid, Spain
    Clin Exp Dermatol 38:787-90. 2013
    ..It is caused by plakophilin-1 (PKP1) deficiency, which results in desmosomal abnormality and poor intercellular cohesion between the epidermal cells. We report a case with a novel PKP1 mutation in intron 6. ..
  18. ncbi request reprint [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
    ....
  19. doi request reprint Molecular evidence of type 2 mosaicism in Gorlin syndrome
    A Torrelo
    Department of Dermatology, Hospital del Nino Jesus, Menendez Pelayo 65, Madrid, 28034, Spain
    Br J Dermatol 169:1342-5. 2013
    ..In this way we provide for the first time molecular proof of a type 2 segmental involvement of this autosomal dominant trait. ..
  20. ncbi request reprint [Primary cutaneous aspergillosis in a leukemic child]
    A Torrelo
    Servicios de Dermatologia, Hospital del Nino Jesus, Madrid, Espana
    Actas Dermosifiliogr 98:276-8. 2007
    ....
  21. ncbi request reprint Congenital multiple clustered dermatofibroma
    P 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...
  22. doi request reprint Ectodermal dysplasias: a clinical and molecular review
    P Garcia-Martin
    Servicio de Dermatologia, Hospital Infantil del Niño Jesús, Madrid, Spain
    Actas Dermosifiliogr 104:451-70. 2013
    ..In recent decades, the genes responsible for at least 30 different types of ectodermal dysplasia have been identified, throwing light on the pathogenic mechanisms involved and their correlation with clinical findings. ..
  23. doi request reprint [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...
  24. doi request reprint Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population
    J 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...