Epidermolisi bollosa distrofica (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Epidermolisi bollosa distrofica" in Italian language version.

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Fine JD, Epidemiology of Inherited Epidermolysis Bullosa Based on Incidence and Prevalence Estimates From the National Epidermolysis Bullosa Registry, in JAMA Dermatol, vol. 152, n. 11, novembre 2016, pp. 1231–1238, DOI:10.1001/jamadermatol.2016.2473, PMID 27463098.
Fortuna G, Di Lorenzo M, Cepeda-Valdes R, Garcia-Garcia C, Salas-Alanis JC, The largest family of the Americas with dominant dystrophic epidermolysis bullosa pruriginosa: a 18-year longitudinal genotype-phenotype study, in J. Dermatol. Sci., vol. 71, n. 3, settembre 2013, pp. 217–21, DOI:10.1016/j.jdermsci.2013.04.025, PMID 23688405.
Fine JD, Bruckner-Tuderman L, Eady RA, Bauer EA, Bauer JW, Has C, Heagerty A, Hintner H, Hovnanian A, Jonkman MF, Leigh I, Marinkovich MP, Martinez AE, McGrath JA, Mellerio JE, Moss C, Murrell DF, Shimizu H, Uitto J, Woodley D, Zambruno G, Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification, in J. Am. Acad. Dermatol., vol. 70, n. 6, giugno 2014, pp. 1103–26, DOI:10.1016/j.jaad.2014.01.903, PMID 24690439.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 367–84; quiz 385–6, DOI:10.1016/j.jaad.2009.03.052, PMID 19700010.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part II. Other organs, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 387–402; quiz 403–4, DOI:10.1016/j.jaad.2009.03.053, PMID 19700011.
Bruckner-Tuderman L, Dystrophic epidermolysis bullosa: pathogenesis and clinical features, in Dermatol Clin, vol. 28, n. 1, gennaio 2010, pp. 107–14, DOI:10.1016/j.det.2009.10.020, PMID 19945622.
von Bartenwerffer W, Has C, Arin MJ, Tantcheva-Poór I, Kreuter A, Kremer K, Arshah T, Hoffmann M, Eming SA, Kohlhase J, Krieg T, Bruckner-Tuderman L, Hartmann K, Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations, in Eur J Dermatol, vol. 21, n. 2, 2011, pp. 170–2, DOI:10.1684/ejd.2010.1247, PMID 21382783.

nih.gov

ncbi.nlm.nih.gov

Fine JD, Epidemiology of Inherited Epidermolysis Bullosa Based on Incidence and Prevalence Estimates From the National Epidermolysis Bullosa Registry, in JAMA Dermatol, vol. 152, n. 11, novembre 2016, pp. 1231–1238, DOI:10.1001/jamadermatol.2016.2473, PMID 27463098.
Fortuna G, Di Lorenzo M, Cepeda-Valdes R, Garcia-Garcia C, Salas-Alanis JC, The largest family of the Americas with dominant dystrophic epidermolysis bullosa pruriginosa: a 18-year longitudinal genotype-phenotype study, in J. Dermatol. Sci., vol. 71, n. 3, settembre 2013, pp. 217–21, DOI:10.1016/j.jdermsci.2013.04.025, PMID 23688405.
Fine JD, Bruckner-Tuderman L, Eady RA, Bauer EA, Bauer JW, Has C, Heagerty A, Hintner H, Hovnanian A, Jonkman MF, Leigh I, Marinkovich MP, Martinez AE, McGrath JA, Mellerio JE, Moss C, Murrell DF, Shimizu H, Uitto J, Woodley D, Zambruno G, Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification, in J. Am. Acad. Dermatol., vol. 70, n. 6, giugno 2014, pp. 1103–26, DOI:10.1016/j.jaad.2014.01.903, PMID 24690439.
Lee JY, Chen HC, Lin SJ, Pretibial epidermolysis bullosa: a clinicopathologic study, in J. Am. Acad. Dermatol., vol. 29, n. 6, dicembre 1993, pp. 974–81, PMID 8245264.
McGrath JA, Schofield OM, Eady RA, Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features, in Br. J. Dermatol., vol. 130, n. 5, maggio 1994, pp. 617–25, PMID 8204470.
Dharma B, Moss C, McGrath JA, Mellerio JE, Ilchyshyn A, Dominant dystrophic epidermolysis bullosa presenting as familial nail dystrophy, in Clin. Exp. Dermatol., vol. 26, n. 1, gennaio 2001, pp. 93–6, PMID 11260188.
Hashimoto K, Matsumoto M, Iacobelli D, Transient bullous dermolysis of the newborn, in Arch Dermatol, vol. 121, n. 11, novembre 1985, pp. 1429–38, PMID 3901931.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 367–84; quiz 385–6, DOI:10.1016/j.jaad.2009.03.052, PMID 19700010.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part II. Other organs, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 387–402; quiz 403–4, DOI:10.1016/j.jaad.2009.03.053, PMID 19700011.
Bruckner-Tuderman L, Dystrophic epidermolysis bullosa: pathogenesis and clinical features, in Dermatol Clin, vol. 28, n. 1, gennaio 2010, pp. 107–14, DOI:10.1016/j.det.2009.10.020, PMID 19945622.
Horn HM, Tidman MJ, The clinical spectrum of dystrophic epidermolysis bullosa, in Br. J. Dermatol., vol. 146, n. 2, febbraio 2002, pp. 267–74, PMID 11903238.
von Bartenwerffer W, Has C, Arin MJ, Tantcheva-Poór I, Kreuter A, Kremer K, Arshah T, Hoffmann M, Eming SA, Kohlhase J, Krieg T, Bruckner-Tuderman L, Hartmann K, Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations, in Eur J Dermatol, vol. 21, n. 2, 2011, pp. 170–2, DOI:10.1684/ejd.2010.1247, PMID 21382783.
Pearson RW, Paller AS, Dermolytic (dystrophic) epidermolysis bullosa inversa, in Arch Dermatol, vol. 124, n. 4, aprile 1988, pp. 544–7, PMID 3355197.
Fine JD, Osment LS, Gay S, Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarring, in Arch Dermatol, vol. 121, n. 8, agosto 1985, pp. 1014–7, PMID 4026337.

oadoi.org

Fine JD, Epidemiology of Inherited Epidermolysis Bullosa Based on Incidence and Prevalence Estimates From the National Epidermolysis Bullosa Registry, in JAMA Dermatol, vol. 152, n. 11, novembre 2016, pp. 1231–1238, DOI:10.1001/jamadermatol.2016.2473, PMID 27463098.
Fortuna G, Di Lorenzo M, Cepeda-Valdes R, Garcia-Garcia C, Salas-Alanis JC, The largest family of the Americas with dominant dystrophic epidermolysis bullosa pruriginosa: a 18-year longitudinal genotype-phenotype study, in J. Dermatol. Sci., vol. 71, n. 3, settembre 2013, pp. 217–21, DOI:10.1016/j.jdermsci.2013.04.025, PMID 23688405.
Fine JD, Bruckner-Tuderman L, Eady RA, Bauer EA, Bauer JW, Has C, Heagerty A, Hintner H, Hovnanian A, Jonkman MF, Leigh I, Marinkovich MP, Martinez AE, McGrath JA, Mellerio JE, Moss C, Murrell DF, Shimizu H, Uitto J, Woodley D, Zambruno G, Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification, in J. Am. Acad. Dermatol., vol. 70, n. 6, giugno 2014, pp. 1103–26, DOI:10.1016/j.jaad.2014.01.903, PMID 24690439.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 367–84; quiz 385–6, DOI:10.1016/j.jaad.2009.03.052, PMID 19700010.
Fine JD, Mellerio JE, Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part II. Other organs, in J. Am. Acad. Dermatol., vol. 61, n. 3, settembre 2009, pp. 387–402; quiz 403–4, DOI:10.1016/j.jaad.2009.03.053, PMID 19700011.
Bruckner-Tuderman L, Dystrophic epidermolysis bullosa: pathogenesis and clinical features, in Dermatol Clin, vol. 28, n. 1, gennaio 2010, pp. 107–14, DOI:10.1016/j.det.2009.10.020, PMID 19945622.
von Bartenwerffer W, Has C, Arin MJ, Tantcheva-Poór I, Kreuter A, Kremer K, Arshah T, Hoffmann M, Eming SA, Kohlhase J, Krieg T, Bruckner-Tuderman L, Hartmann K, Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations, in Eur J Dermatol, vol. 21, n. 2, 2011, pp. 170–2, DOI:10.1684/ejd.2010.1247, PMID 21382783.