Detalhe da pesquisa
1.
A randomized, controlled trial of oral propranolol in infantile hemangioma.
N Engl J Med
; 372(8): 735-46, 2015 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25693013
2.
Diacerein orphan drug development for epidermolysis bullosa simplex: A phase 2/3 randomized, placebo-controlled, double-blind clinical trial.
J Am Acad Dermatol
; 78(5): 892-901.e7, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29410318
3.
Types of congenital nonsyndromic ichthyoses.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
; 164(4): 357-365, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087941
4.
Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases.
Orphanet J Rare Dis
; 15(1): 142, 2020 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32505191
5.
Inherited ichthyoses: molecular causes of the disease in Czech patients.
Orphanet J Rare Dis
; 14(1): 92, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31046801
6.
Epidermolysis bullosa simplex with muscular dystrophy. Review of the literature and a case report.
J Dermatol Case Rep
; 10(3): 39-48, 2016 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28400893
7.
AEC syndrome caused by heterozygous mutation in the SAM domain of p63 gene.
Eur J Dermatol
; 20(3): 411-3, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20156774
8.
Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases.
Pediatrics
; 129(2): e523-8, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22271700
9.
Analysis of the COL7A1 gene in Czech patients with dystrophic epidermolysis bullosa reveals novel and recurrent mutations.
J Dermatol Sci
; 59(2): 136-40, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20598510