طبيب آنا اليزابيت مارتينز

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.