Similar articles for PMID: 7550320

Year	Number of Results
1986	2
1987	1
1988	1
1990	1
1991	3
1992	2
1993	4
1994	10
1995	15
1996	15
1997	25
1998	26
1999	11
2000	10
2001	16
2002	7
2003	7
2004	5
2005	6
2006	6
2007	6
2008	5
2009	2
2010	9
2011	9
2012	9
2013	7
2014	8
2015	8
2016	7
2017	8
2018	9
2019	6
2020	9
2021	9
2022	15
2023	1
2024	0

1

Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa.

McGrath JA, Gatalica B, Christiano AM, Li K, Owaribe K, McMillan JR, Eady RA, Uitto J. McGrath JA, et al. Nat Genet. 1995 Sep;11(1):83-6. doi: 10.1038/ng0995-83. Nat Genet. 1995. PMID: 7550320

2

Generalized atrophic benign epidermolysis bullosa.

Darling TN, Bauer JW, Hintner H, Yancey KB. Darling TN, et al. Adv Dermatol. 1997;13:87-119; discussion 120. Adv Dermatol. 1997. PMID: 9551142 Review.

3

Autosomal dominant junctional epidermolysis bullosa.

Almaani N, Liu L, Dopping-Hepenstal PJ, Lovell PA, Lai-Cheong JE, Graham RM, Mellerio JE, McGrath JA. Almaani N, et al. Br J Dermatol. 2009 May;160(5):1094-7. doi: 10.1111/j.1365-2133.2008.08977.x. Epub 2009 Dec 16. Br J Dermatol. 2009. PMID: 19120338

4

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

McGrath JA, Gatalica B, Li K, Dunnill MG, McMillan JR, Christiano AM, Eady RA, Uitto J. McGrath JA, et al. Am J Pathol. 1996 Jun;148(6):1787-96. Am J Pathol. 1996. PMID: 8669466 Free PMC article.

5

Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa.

Kiritsi D, Kern JS, Schumann H, Kohlhase J, Has C, Bruckner-Tuderman L. Kiritsi D, et al. J Med Genet. 2011 Jul;48(7):450-7. doi: 10.1136/jmg.2010.086751. Epub 2011 Feb 28. J Med Genet. 2011. PMID: 21357940 Free article.

6

A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia.

Ruzzi L, Gagnoux-Palacios L, Pinola M, Belli S, Meneguzzi G, D'Alessio M, Zambruno G. Ruzzi L, et al. J Clin Invest. 1997 Jun 15;99(12):2826-31. doi: 10.1172/JCI119474. J Clin Invest. 1997. PMID: 9185503 Free PMC article.

7

Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa.

Pulkkinen L, Marinkovich MP, Tran HT, Lin L, Herron GS, Uitto J. Pulkkinen L, et al. J Invest Dermatol. 1999 Dec;113(6):1114-8. doi: 10.1046/j.1523-1747.1999.00793.x. J Invest Dermatol. 1999. PMID: 10636730 Free article.

8

Generalized atrophic benign epidermolysis bullosa in 2 siblings complicated by multiple squamous cell carcinomas.

Swensson O, Christophers E. Swensson O, et al. Arch Dermatol. 1998 Feb;134(2):199-203. doi: 10.1001/archderm.134.2.199. Arch Dermatol. 1998. PMID: 9487212

9

Ultrastructural findings in epidermolysis bullosa.

Smith LT. Smith LT. Arch Dermatol. 1993 Dec;129(12):1578-84. Arch Dermatol. 1993. PMID: 7504435

10

Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa.

Darling TN, McGrath JA, Yee C, Gatalica B, Hametner R, Bauer JW, Pohla-Gubo G, Christiano AM, Uitto J, Hintner H, Yancey KB. Darling TN, et al. J Invest Dermatol. 1997 Apr;108(4):463-8. doi: 10.1111/1523-1747.ep12289718. J Invest Dermatol. 1997. PMID: 9077475 Free article.

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