Leprosy. An update: definition, pathogenesis, classification, diagnosis, and treatment K Eichelmann, SEG González, JC Salas-Alanis, J Ocampo-Candiani Actas Dermo-Sifiliográficas (English Edition) 104 (7), 554-563, 2013 | 265 | 2013 |
Fibroblast-derived dermal matrix drives development of aggressive cutaneous squamous cell carcinoma in patients with recessive dystrophic epidermolysis bullosa YZ Ng, C Pourreyron, JC Salas-Alanis, JHS Dayal, R Cepeda-Valdes, ... Cancer research 72 (14), 3522-3534, 2012 | 138 | 2012 |
Innate sensing of microbial products promotes wound-induced skin cancer E Hoste, EN Arwert, R Lal, AP South, JC Salas-Alanis, DF Murrell, ... Nature communications 6 (1), 5932, 2015 | 136 | 2015 |
Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines JE Mellerio, SJ Robertson, C Bernardis, A Diem, JD Fine, R George, ... British Journal of Dermatology 174 (1), 56-67, 2016 | 135 | 2016 |
Allelic heterogeneity of dominant and recessive COL7A1 mutations underlying epidermolysis bullosa pruriginosa JE Mellerio, GHS Ashton, R Mohammedi, RAJ Eady, JA McGrath, ... Journal of investigative dermatology 112 (6), 984-987, 1999 | 127 | 1999 |
Coccidioidomycosis and the skin: a comprehensive review SC Garcia Garcia, JC Salas Alanis, MG Flores, SE Gonzalez Gonzalez, ... Anais brasileiros de dermatologia 90, 610-619, 2015 | 114 | 2015 |
CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells J Jacków, Z Guo, C Hansen, HE Abaci, YS Doucet, JU Shin, R Hayashi, ... Proceedings of the National Academy of Sciences 116 (52), 26846-26852, 2019 | 112 | 2019 |
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa RJ Cho, LB Alexandrov, NY Den Breems, VS Atanasova, M Farshchian, ... Science Translational Medicine 10 (455), eaas9668, 2018 | 107 | 2018 |
A critical reappraisal of the current data on drug-induced linear immunoglobulin A bullous dermatosis: a real and separate nosological entity? G Fortuna, JC Salas-Alanis, E Guidetti, MP Marinkovich Journal of the American Academy of Dermatology 66 (6), 988-994, 2012 | 105 | 2012 |
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy K Nakabayashi, D Amann, Y Ren, U Saarialho-Kere, N Avidan, S Gentles, ... The American Journal of Human Genetics 76 (3), 510-516, 2005 | 103 | 2005 |
Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations JA McGrath, GHS Ashton, JE Mellerio, JR McMillan, RAJ Eady, ... Journal of investigative dermatology 113 (3), 314-321, 1999 | 100 | 1999 |
Treatment of infantile hemangiomas with short-term application of imiquimod 5% cream O Welsh, Z Olazarán, M Gómez, J Salas, B Berman Journal of the American Academy of Dermatology 51 (4), 639-642, 2004 | 91 | 2004 |
Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression C Pourreyron, G Cox, X Mao, A Volz, N Baksh, T Wong, H Fassihi, K Arita, ... Journal of investigative dermatology 127 (10), 2438-2444, 2007 | 69 | 2007 |
A recurrent glycine substitution mutation, G2043R, in the type VII collagen gene (COL7A1) in dominant dystrophic epidermolysis bullosa JE Mellerio, JC Salas‐Alanis, ML Talamantes, H Horn, MJ Tidman, ... British Journal of Dermatology 139 (4), 730-737, 1998 | 69 | 1998 |
Lepra: puesta al día. Definición, patogénesis, clasificación, diagnóstico y tratamiento K Eichelmann, SEG González, JC Salas-Alanis, J Ocampo-Candiani Actas Dermo-Sifiliográficas 104 (7), 554-563, 2013 | 64 | 2013 |
Thrombospondin-1 is a major activator of TGF-β signaling in recessive dystrophic epidermolysis bullosa fibroblasts VS Atanasova, RJ Russell, TG Webster, Q Cao, P Agarwal, YZ Lim, ... Journal of Investigative Dermatology 139 (7), 1497-1505. e5, 2019 | 58 | 2019 |
Congenital epidermolysis bullosa: a review C Siañez-González, R Pezoa-Jares, JC Salas-Alanis Actas Dermo-Sifiliográficas (English Edition) 100 (10), 842-856, 2009 | 58 | 2009 |
Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24 A Martinez-Mir, A Zlotogorski, D Londono, D Gordon, A Grunn, E Uribe, ... Journal of medical genetics 40 (12), 872-878, 2003 | 57 | 2003 |
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis GM DeStefano, KA Fantauzzo, L Petukhova, M Kurban, M Tadin-Strapps, ... Proceedings of the National Academy of Sciences 110 (19), 7790-7795, 2013 | 54 | 2013 |
Epithelial HMGB1 delays skin wound healing and drives tumor initiation by priming neutrophils for NET formation E Hoste, C Maueröder, L Van Hove, L Catrysse, HK Vikkula, M Sze, ... Cell Reports 29 (9), 2689-2701. e4, 2019 | 52 | 2019 |