Detalhe da pesquisa
1.
T-cell activation and bacterial infection in skin wounds of recessive dystrophic epidermolysis bullosa patients.
Exp Dermatol
; 31(9): 1431-1442, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35620886
2.
CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells.
Proc Natl Acad Sci U S A
; 116(52): 26846-26852, 2019 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31818947
3.
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.
Clin Chem
; 67(6): 876-888, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33969388
4.
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry.
Am J Med Genet A
; 185(11): 3390-3400, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34435747
5.
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families.
BMC Public Health
; 21(1): 692, 2021 04 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888076
6.
Bullosis Diabeticorum: A Neglected Bullous Dermatosis.
Skinmed
; 16(1): 77-79, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29551123
7.
Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth.
PLoS Genet
; 10(5): e1004333, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24831815
8.
Type VII collagen regulates expression of OATP1B3, promotes front-to-rear polarity and increases structural organisation in 3D spheroid cultures of RDEB tumour keratinocytes.
J Cell Sci
; 127(Pt 4): 740-51, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24357722
9.
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.
Genet Med
; 18(7): 727-36, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26681309
10.
The Importance of Esophagography in Patients With Recessive Dystrophic Epidermolysis Bullosa.
AJR Am J Roentgenol
; 207(4): 778-781, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27384758
11.
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.
Proc Natl Acad Sci U S A
; 110(19): 7790-5, 2013 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23603273
12.
Fatal Outcome from Brain Vascular Lesions in a Neonate with Blue Rubber Bleb Nevus Syndrome.
Pediatr Dermatol
; 33(1): e29-31, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26608350
13.
Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 Mutation.
Rev Invest Clin
; 68(3): 143-6, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27409001
14.
[Sjögren's syndrome (SS), a review of the subject and saliva as a diagnostic method]. / Síndrome de Sjögren (SS), revisión del tema y saliva como método diagnóstico.
Gac Med Mex
; 152(3): 371-80, 2016.
Artigo
em Espanhol
| MEDLINE | ID: mdl-27335194
15.
Multidisciplinary care of epidermolysis bullosa during the COVID-19 pandemic-Consensus: Recommendations by an international panel of experts.
J Am Acad Dermatol
; 83(4): 1222-1224, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32682031
16.
Chromoblastomycosis by Cladophialophora carrionii associated with squamous cell carcinoma and review of published reports.
Mycopathologia
; 179(1-2): 153-7, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344197
17.
Evaluation of internal consistency of the epidermolysis bullosa oropharyngeal severity score (EBOS).
Acta Odontol Scand
; 73(2): 156-60, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25598172
18.
Hypertrichosis lanuginosa congenita treated with diode laser epilation during infancy.
Pediatr Dermatol
; 31(4): 529-30, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23025656
19.
Pseudoxanthoma elasticum: Dermoscopy and mutation analysis.
Australas J Dermatol
; 60(2): e156-e158, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30229859
20.
[Primary cutaneous coccidioidomycosis in an infant]. / Coccidioidomicosis cutánea primaria en infante.
Gac Med Mex
; 150(2): 175-6, 2014.
Artigo
em Espanhol
| MEDLINE | ID: mdl-24603999