186 related articles for article (PubMed ID: 15097931)
1. Generalized mottled pigmentation with postnatal skin blistering in three generations.
Westerhof W; Dingemans KP
J Am Acad Dermatol; 2004 May; 50(5 Suppl):S65-9. PubMed ID: 15097931
[TBL] [Abstract][Full Text] [Related]
2. Epidermolysis bullosa simplex with mottled pigmentation - mutation analysis proved the diagnosis in a four-generation pedigree.
Glàsz-Bóna A; Medvecz M; Virágh Z; Hatvani Z; Blazsek A; Kárpáti S
Eur J Dermatol; 2010; 20(6):698-700. PubMed ID: 20923750
[TBL] [Abstract][Full Text] [Related]
3. Epidermolysis bullosa simplex with mottled pigmentation.
Coleman R; Harper JI; Lake BD
Br J Dermatol; 1993 Jun; 128(6):679-85. PubMed ID: 8338752
[TBL] [Abstract][Full Text] [Related]
4. Epidermolysis Bullosa Simplex with mottled pigmentation: mutation analysis in the first reported Hispanic pedigree with the largest single generation of affected individuals to date.
Shurman D; Losi-Sasaki J; Grimwood R; Kivirikko S; Tichy E; Uitto J; Richard G
Eur J Dermatol; 2006; 16(2):132-5. PubMed ID: 16581562
[TBL] [Abstract][Full Text] [Related]
5. [Piebaldism].
Küster W
Hautarzt; 1987 Aug; 38(8):481-3. PubMed ID: 3654219
[TBL] [Abstract][Full Text] [Related]
6. Epidermolysis bullosa herpetiformis with mottled pigmentation and an unusual punctate keratoderma.
Medenica-Mojsilović L; Fenske NA; Espinoza CG
Arch Dermatol; 1986 Aug; 122(8):900-8. PubMed ID: 2943231
[TBL] [Abstract][Full Text] [Related]
7. Retrospective diagnosis of Kindler syndrome in a 37-year-old man.
Thomson MA; Ashton GH; McGrath JA; Eady RA; Moss C
Clin Exp Dermatol; 2006 Jan; 31(1):45-7. PubMed ID: 16309479
[TBL] [Abstract][Full Text] [Related]
8. Epidermolysis bullosa simplex with mottled pigmentation due to de novo P25L mutation in keratin 5 in an Italian patient.
Pascucci M; Posteraro P; Pedicelli C; Provini A; Auricchio L; Paradisi M; Castiglia D
Eur J Dermatol; 2006; 16(6):620-2. PubMed ID: 17229601
[TBL] [Abstract][Full Text] [Related]
9. Epidermolysis bullosa simplex herpetiformis of Dowling-Meara with mottled pigmentation: the relationship between EBS herpetiformis and EBS with mottled pigmentation.
Tay YK; Weston WL
Pediatr Dermatol; 1996; 13(4):306-9. PubMed ID: 8844751
[TBL] [Abstract][Full Text] [Related]
10. Localized and generalized forms of blistering in junctional epidermolysis bullosa due to COL17A1 mutations in the Netherlands.
Pasmooij AM; Pas HH; Jansen GH; Lemmink HH; Jonkman MF
Br J Dermatol; 2007 May; 156(5):861-70. PubMed ID: 17263807
[TBL] [Abstract][Full Text] [Related]
11. [Simultaneous occurrence of metageria and Gottron's acrogeria in one family].
Kaufmann I; Thiele B; Mahrle G
Z Hautkr; 1985 Jun; 60(12):975-84. PubMed ID: 4024679
[TBL] [Abstract][Full Text] [Related]
12. Transient bullous dermolysis of the newborn in three generations.
Fassihi H; Diba VC; Wessagowit V; Dopping-Hepenstal PJ; Jones CA; Burrows NP; McGrath JA
Br J Dermatol; 2005 Nov; 153(5):1058-63. PubMed ID: 16225626
[TBL] [Abstract][Full Text] [Related]
13. Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family.
Ouragini H; Cherif F; Kassar S; Floriddia G; Pascucci M; Daoud W; Osman-Dhahri AB; Boubaker S; Castiglia D; Abdelhak S
J Dermatol Sci; 2009 May; 54(2):114-20. PubMed ID: 19261445
[TBL] [Abstract][Full Text] [Related]
14. Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features.
Fischer T; Gedde-Dahl T
Clin Genet; 1979 Mar; 15(3):228-38. PubMed ID: 421361
[TBL] [Abstract][Full Text] [Related]
15. Speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering: a clinical triad, with variable associations. A report of two families.
Boss JM; Matthews CN; Peachey RD; Summerly R
Br J Dermatol; 1981 Nov; 105(5):579-85. PubMed ID: 6457621
[No Abstract] [Full Text] [Related]
16. Acantholytic epidermolysis bullosa.
Hoffman MD; Fleming MG; Pearson RW
Arch Dermatol; 1995 May; 131(5):586-9. PubMed ID: 7741547
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant junctional epidermolysis bullosa.
Almaani N; Liu L; Dopping-Hepenstal PJ; Lovell PA; Lai-Cheong JE; Graham RM; Mellerio JE; McGrath JA
Br J Dermatol; 2009 May; 160(5):1094-7. PubMed ID: 19120338
[TBL] [Abstract][Full Text] [Related]
18. Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation.
Hamada T; Yasumoto S; Karashima T; Ishii N; Shimada H; Kawano Y; Imayama S; McGrath JA; Hashimoto T
Br J Dermatol; 2007 Sep; 157(3):605-8. PubMed ID: 17635506
[No Abstract] [Full Text] [Related]
19. Generalized Dowling-Degos disease.
Wu YH; Lin YC
J Am Acad Dermatol; 2007 Aug; 57(2):327-34. PubMed ID: 17637446
[TBL] [Abstract][Full Text] [Related]
20. Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations.
van den Akker PC; van Essen AJ; Kraak MM; Meijer R; Nijenhuis M; Meijer G; Hofstra RM; Pas HH; Scheffer H; Jonkman MF
J Dermatol Sci; 2009 Oct; 56(1):9-18. PubMed ID: 19665875
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
