Detalhe da pesquisa
1.
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT.
J Am Acad Dermatol
; 81(2): 386-394, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30731170
2.
Pembrolizumab for Unresectable or Metastatic Melanoma in Patients Older than 85 Years of Age.
Dermatology
; 235(3): 219-224, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30721908
3.
Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma.
J Med Genet
; 54(9): 607-612, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28592523
4.
Clinical parameters associated with anti-programmed death-1 (PD-1) inhibitors-induced tumor response in melanoma patients.
Invest New Drugs
; 35(6): 842-847, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28569347
5.
Sarcopenic overweight is associated with early acute limiting toxicity of anti-PD1 checkpoint inhibitors in melanoma patients.
Invest New Drugs
; 35(4): 436-441, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28396974
6.
A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants.
Int J Cancer
; 139(9): 2012-20, 2016 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27347659
7.
Germline BAP1 mutations predispose to renal cell carcinomas.
Am J Hum Genet
; 92(6): 974-80, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23684012
8.
Vulvar hidradenoma papilliferum (HP) is located on the sites of mammary-like anogenital glands (MLAGs): Analysis of the photographs of 52 tumors.
J Am Acad Dermatol
; 75(2): 380-4, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26944596
9.
Complete Penetrance and Absence of Intrafamilial Variability in a Large Family with Hereditary Leiomyomatosis and Renal Cell Carcinoma.
Dermatology
; 232(3): 293-7, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27161211
10.
Inflammatory monocytes are potent antitumor effectors controlled by regulatory CD4+ T cells.
Proc Natl Acad Sci U S A
; 110(32): 13085-90, 2013 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23878221
11.
Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma risk.
Int J Cancer
; 137(8): 1901-1909, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25892537
12.
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
Int J Cancer
; 136(6): 1351-60, 2015 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25077817
13.
Sarcoidosis in Patients Treated with Vemurafenib for Metastatic Melanoma: A Paradoxical Autoimmune Activation.
Dermatology
; 231(4): 378-84, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26452227
14.
Malignant Melanoma Arising in Patients with a Large Congenital Melanocytic Naevus: Retrospective Study of 10 Cases with Cytogenetic Analysis.
Acta Derm Venereol
; 95(6): 686-90, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25594732
15.
Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants.
J Med Genet
; 50(4): 264-70, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23384855
16.
[Screening for melanoma, an advanced practice nurse consultation]. / Dépistage du mélanome, pratique collaborative d'une infirmière experte.
Rev Infirm
; (206): 38-40, 2014 Dec.
Artigo
em Francês
| MEDLINE | ID: mdl-25711001
17.
Subacute cutaneous lupus erythematosus induced and exacerbated by proton pump inhibitors.
Dermatology
; 226(2): 119-23, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23548825
18.
Preclinical corrective gene transfer in xeroderma pigmentosum human skin stem cells.
Mol Ther
; 20(4): 798-807, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22068429
19.
Genetic correction of stem cells in the treatment of inherited diseases and focus on xeroderma pigmentosum.
Int J Mol Sci
; 14(10): 20019-36, 2013 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-24113582
20.
Distinct merkel cell polyomavirus molecular features in tumour and non tumour specimens from patients with merkel cell carcinoma.
PLoS Pathog
; 6(8): e1001076, 2010 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20865165