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Anna Elizabeth Martinez 医生

Consultant Dermatologist


Dr Anna Elizabeth Martinez is a Consultant Dermatologist who runs the skin fragility service. She is an international expert in epidermolysis bullosa (EB) and other genodermatosis. She runs the dermatology allergy service and her other areas of expertise include severe eczema, allergy, vascular malformations and birth marks. 

Dr Martinez publishes extensively. She has been awarded NIHR Principal Investigator award 2016/17. 


  • English
  • Spanish


  • Difficult eczema
  • Skin fragility disorders in particular epidermolysis bullosa
  • Birth marks and vascular malformations
  • Genetic skin diseases such as ichthyosis and Netherton syndrome
  • Clinical research and new treatments in paediatric dermatology 


  • MBBS having trained at St Bartholomew’s Hospital London
  • MRCH 
  • NIHR Principal Investigator award 2016-2017
  • Clinical excellence awards last awarded September 2017


  • British Society of Paediatric Dermatology (BSPD)
  • European Reference Network lead for EB and Ichthyosis 2017 onwards
  • Fellow of the Royal College of Paediatrics and Child Health (FRCPCH)
  • Associate member of the British Association of Dermatologists
  • European Society Paediatric Dermatology
  • Medical Advisor to the Ichthyosis Support Group
  • External Advisory Panel Cell therapy, Netherlands 2017
  • International Consensus Committee of the Classification EB from 2013
  • Expert working Group BSCI allergy eczema guidelines 2016

Dr Martinez is actively involved in clinical research having been awarded grants of over £1.5M in the last three years for research. She is the Principal Investigator/ Co-investigator for several clinical trials.


Mellerio, J.E., Robertson, S.J., Bernardis, C., Diem, A., Fine, J.D., George, R., Goldberg, D., Halmos, G.B., Harries, M., Jonkman, M.F., Lucky, A., Martinez, A.E., Maubec, E., Morris, S., Murrell, D.F., Palisson, F., Pillay, E.I., Robson, A., Salas-Alanis, J.C., McGrath, J.A., 2016. Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines. Br J Dermatol. 174 pp 56-67.

Rashidghamat, E., Ozoemena, L., Liu, L., McGrath, J.A., Martinez, A.E., Mellerio, J.E., 2015. Mutations in EXPH5 (exophilin-5) underlie a rare subtype of autosomal recessive epidermolysis bullosa simplex. Br J Dermatol.  

Petrof, G., Lwin, S.M., Martinez-Queipo, M., Abdul-Wahab, A., Tso, S., Mellerio, J.E., Slaper-Cortenbach, I., Boelens, J.J., Tolar, J., Veys, P., Ofuya, M., Peacock, J.L., Martinez, A.E., McGrath, J.A., 2015. Potential of Systemic Allogeneic Mesenchymal Stromal Cell Therapy for Children with Recessive Dystrophic Epidermolysis Bullosa. J Invest Dermatol.

Fuggle, N.R., Bragoli, W., Mahto, A., Glover, M., Martinez, A.E., Kinsler, V.A., The adverse effect profile of oral azathioprine in pediatric atopic dermatitis, and recommendations for monitoring. J Am Acad Dermatol. 72(1) pp. 108-14.

Goldschneider, K.R., Good, J., Harrop, E., Liossi, C., Lynch-Jordan, A., Martinez, A.E., Maxwell, L.G., Stanko-Lopp, D., 2014. Pain care for patients with epidermolysis bullosa: best care practice guidelines. BMC Med. 12(1) p. 178.

Waelchli, R., Aylett, S.E., Robinson, K., Chong, W.K., Martinez, A.E., Kinsler, V.A., 2014. New vascular classification of port-wine stains: improving prediction of Sturge-Weber risk. Br J Dermatol. 171(4) pp. 861-7.

Fine, J.D., Bruckner-Tuderman, L., Eady, R.A., Bauer, E.A., Bauer, J.W., Has, C., Heagerty, A., Hintner, H., Hovnanian, A., Jonkman, M.F., Leigh, I., Marinkovich, M.P., Martinez, A.E., McGrath, J.A., Mellerio, J.E., Moss, C., Murrell, D.F., Shimizu, H., Uitto, J., Woodley, D., Zambruno, G., 2014. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J Am Acad Dermatol. 70(6) pp. 1103-26.

Liu, L., Mellerio, J.E., Martinez, A.E., McMillan, J.R., Aristodemou, S., Parsons, M., McGrath, J.A., 2014. Mutations in EXPH5 result in autosomal recessive inherited skin fragility. Br J Dermatol. 170(1) pp. 196-9.

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