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

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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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Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy von Nakabayashi, Kazuhiko, Amann, Daniela, Ren, Yan, Saarialho-Kere, Ulpu, Avidan, Nili, Gentles, Simone, MacDonald, Jeffrey R., Puffenberger, Erik G., Christiano, Angela M., Martinez-Mir, Amalia, Salas-Alanis, Julio C., Rizzo, Renata, Vamos, Esther, Raams, Anja, Les, Clifford, Seboun, Eric, Jaspers, Nicolaas G.J., Beckmann, Jacques S., Jackson, Charles E., Scherer, Stephen W.

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Leprosy. An Update: Definition, Pathogenesis, Classification, Diagnosis, and Treatment von Eichelmann, K, González González, S.E, Salas-Alanis, J.C, Ocampo-Candiani, J

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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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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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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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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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Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1 von Wessagowit, V., Ashton, G. H. S., Mohammedi, R., Salas-Alanis, J. C., Denyer, J. E., Mellerio, J. E., Eady, R. A. J., McGrath, J. A.

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Frameshift mutations in the type VII collagen gene (COL7A1) in five Mexican cousins with recessive dystrophic epidermolysis bullosa von SALAS-ALANIS, J. C, MELLERIO, J. E, AMAYA-GUERRA, M, ASHTON, G. H. S, EADY, R. A. J, MCGRATH, J. A

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Frequency of the CCR5 gene 32-basepair deletion in Hispanic Mexicans von Salas-Alanis, J C, Mellerio, J E, Ashton, G H, McGrath, J A

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A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosa von Mellerio, J. E., Salas-Alanis, J. C., Amaya-Guera, M., Tamez, E., Ashton, G. H. S., Mohammedi, R., Eady, R. A. J., McGrath, J. A.

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Fishing for new genes in skin biology: impact of cytogenetics on gene discovery: Section Editors: 
Roderick R McInnes, e‐mail: mcinnes@sickkids.on.ca
Jacques Michaud, e‐mail: jmich... von Tadin‐Strapps, M, Warburton, D, Salas‐Alanis, JC, Lopez‐Cepeda, LD, Christiano, AM

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Overexpression of Desmoglein 2 in a mouse model of Gorlin syndrome enhances spontaneous basal cell carcinoma formation through STAT3-mediated Gli1 expression von Brennan-Crispi, DM, Overmiller, AM, Tamayo-Orrego, L, Marous, MR, Sahu, J, McGuinn, KP, Cooper, F, Georgiou, IC, Frankfurter, M, Salas-Alanis, JC, Charron, F, Millar, SE, Mahoney, MG, Riobo-Del Galdo, NA

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Lepra: puesta al día. Definición, patogénesis, clasificación, diagnóstico y tratamiento von Eichelmann, K, González González, S.E, Salas-Alanis, J.C, Ocampo-Candiani, J

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