Detalhe da pesquisa
1.
Real-time mobile teledermoscopy for skin cancer screening targeting an agricultural population: an experiment on 289 patients in France.
J Eur Acad Dermatol Venereol
; 30(1): 20-4, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26568080
2.
[Ainhum and "African acral keratoderma": three cases]. / Aïnhum et « kératodermies acrales africaines ¼ : trois cas.
Ann Dermatol Venereol
; 142(3): 170-5, 2015 Mar.
Artigo
em Francês
| MEDLINE | ID: mdl-25624138
3.
A homozygous insertion-deletion in the type VII collagen gene (COL7A1) in Hallopeau-Siemens dystrophic epidermolysis bullosa.
Nat Genet
; 5(3): 287-93, 1993 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-8275094
4.
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer.
Nat Genet
; 6(1): 106-10, 1994 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-7511021
5.
Association of glycerol and paraffin in the treatment of ichthyosis in children: an international, multicentric, randomized, controlled, double-blind study.
J Eur Acad Dermatol Venereol
; 26(8): 1014-9, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22118417
6.
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis.
Br J Dermatol
; 165(5): 1087-94, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21729027
7.
[Surgical treatment of keratosis palmaris in Mal de Meleda]. / Peut-on traiter chirurgicalement le Mal de Meleda (kératodermie palmoplantaire diffuse de Siemens) ?
Ann Chir Plast Esthet
; 54(2): 152-5, 2009 Apr.
Artigo
em Francês
| MEDLINE | ID: mdl-19042068
8.
Mutations in GJB6 cause hidrotic ectodermal dysplasia.
Nat Genet
; 26(2): 142-4, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11017065
9.
Herlitz junctional epidermolysis bullosa keratinocytes display heterogeneous defects of nicein/kalinin gene expression.
J Clin Invest
; 93(2): 862-9, 1994 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-8113417
10.
Exclusion of linkage between the collagenase gene and generalized recessive dystrophic epidermolysis bullosa phenotype.
J Clin Invest
; 88(5): 1716-21, 1991 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-1658051
11.
Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.
J Clin Invest
; 90(3): 1032-6, 1992 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1355776
12.
Using Urgotul dressing for the management of epidermolysis bullosa skin lesions.
J Wound Care
; 14(10): 490-1, 494-6, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16304926
13.
Clinical observations, virologic studies, and treatment trials in patients with epidermodysplasia verruciformis, a disease induced by specific human papillomaviruses.
J Invest Dermatol
; 83(1 Suppl): 18s-25s, 1984 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-6330217
14.
DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrence.
J Invest Dermatol
; 104(4): 456-61, 1995 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-7706758
15.
Predominance of the recurrent mutation R635X in the LAMB3 gene in European patients with Herlitz junctional epidermolysis bullosa has implications for mutation detection strategy.
J Invest Dermatol
; 109(2): 232-7, 1997 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-9242513
16.
Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome.
J Invest Dermatol
; 117(6): 1657-61, 2001 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11886537
17.
Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region.
Eur J Hum Genet
; 5(3): 156-60, 1997.
Artigo
em Inglês
| MEDLINE | ID: mdl-9272739
18.
Lamellar ichthyosis: further narrowing, physical and expression mapping of the chromosome 2 candidate locus.
Eur J Hum Genet
; 7(1): 77-87, 1999 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-10094194
19.
Bullous amyloidosis. Report of 3 cases and review of the literature.
Medicine (Baltimore)
; 72(1): 38-44, 1993 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8426536
20.
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome.
Am J Med Genet
; 75(3): 265-72, 1998 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-9475595