Cutaneous manifestations in COVID‐19: familial cluster of urticarial rash von Cepeda‐Valdes, R., Carrion‐Alvarez, D., Trejo‐Castro, A., Hernandez‐Torre, M., Salas‐Alanis, J.

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Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines von 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.

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Haematidrosis and haemolacria in a young adult von Salas‐Alanis, J. C., Salas‐Garza, M., Goldust, M. Mohamad, Fajardo‐Ramirez, O. R.

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Heterogeneous addiction to transforming growth factor‐beta signalling in recessive dystrophic epidermolysis bullosa‐associated cutaneous squamous cell carcinoma von Dayal, J.H.S., Mason, S.M., Salas‐Alanis, J.C., McGrath, J.A., Taylor, R.G., Mellerio, J.E., Blyth, K., South, A.P., Inman, G.J.

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High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell m... von Pourreyron, C., Chen, M., McGrath, J.A., Salas-Alanis, J.C., South, A.P., Leigh, I.M.

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Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome von Chiu, F. P. -C., Salas‐Alanis, J. C., Amaya‐Guerra, M., Cepeda‐Valdes, R., McGrath, J. A., Hsu, C. ‐K.

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Seven novel COL7A1 mutations identified in patients with recessive dystrophic epidermolysis bullosa from Mexico von Saeidian, A. H., Youssefian, L., Moreno Trevino, M. G., Fortuna, G., Vahidnezhad, H., Atanasova, V. S., Uitto, J., Salas‐Alanis, J. C., South, A. P.

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First report of COL7A1 mutations in two patients with recessive dystrophic epidermolysis bullosa from Peru von Saeidian, A. H., Youssefian, L., Rosales‐Solis, G. M., Vahidnezhad, H., Atanasova, V. S., Uitto, J., South, A. P., Salas‐Alanis, J. C.

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Genotype–oropharyngeal phenotype correlation in Mexican patients with dystrophic epidermolysis bullosa von Fortuna, G, Pollio, A, Aria, M, Moreno-Trevino, M.G, Marasca, F, Salas-Alanís, J.C

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Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24 von Martinez-Mir, A, Zlotogorski, A, Londono, D, Gordon, D, Grunn, A, Uribe, E, Horev, L, Ruiz, I M, Davalos, N O, Alayan, O, Liu, J, Gilliam, T C, Salas-Alanis, J C, Christiano, A M

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Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait von Tadin-Strapps, M, Salas-Alanis, JC, Moreno, L, Warburton, D, Martinez-Mir, A, Christiano, AM

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Linear immunoglobulin A disease and vancomycin: two real ancestral enemies? von Fortuna, G., Aria, M., Marasca, F., Salas-Alanís, J.C.

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Sabinas syndrome in monozygotic twins von López-García, D. R., Salas-Alanis, J. C., Christiano, A. M., Ocampo-Candiani, J., Gómez-Flores, M.

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Moderation of Phenotypic Severity in Dystrophic and Junctional Forms of Epidermolysis Bullosa Through In-Frame Skipping of Exons Containing Non-Sense or Frameshift Mutations von McGrath, John A., Ashton, Gabrielle H.S., Mellerio, Jemima E., McMillan, James R., Eady, Robin A.J., Salas-Alanis, Julio Cesar, Swensson, Ole

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Allelic Heterogeneity of Dominant and Recessive COL7A1 Mutations Underlying Epidermolysis Bullosa Pruriginosa von Mellerio, Jemima E., Ashton, Gabrielle H.S., Mohammedi, Rafik, Eady, Robin A.J., McGrath, John A., Lyon, Calum C., Kirby, Brian, Harman, Karen E., Salas-Alanis, Julio C., Atherton, David J., Harrison, Phillip V., Griffiths, W. Andrew D., Black, Martin M.

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Oral plasmablastic lymphoma in an HIV-positive patient with an unusual survival rate von Fortuna, G., Pollio, A., Salas-Alanis, J. C., Mariani, U.

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A recurrent glycine substitution mutation, G2043R, in the type VII collagen gene (COL7A1) in dominant dystrophic epidermolysis bullosa von MELLERIO, J. E, SALAS-ALANIS, J. C, TALAMANTES, M. L, HORN, H, TIDMAN, M. J, ASHTON, G. H. S, EADY, R. A. J, MCGRATH, J. A

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Clinical features of gingival lesions in patients with dystrophic epidermolysis bullosa: a cross‐sectional study von Fortuna, G, Aria, M, Cepeda‐Valdes, R, Pollio, A, Moreno‐Trevino, MG, Salas‐Alanís, JC

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Fishing for new genes in skin biology: impact of cytogenetics on gene discovery von Tadin-Strapps, M, Warburton, D, Salas-Alanis, JC, Lopez-Cepeda, LD, Christiano, AM

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The molecular basis of dystrophic epidermolysis bullosa in Mexico von Salas-Alanis, Julio C., Amaya-Guerra, Mario, McGrath, John A.

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