Detalhe da pesquisa
1.
Exploring formal and informal learning opportunities during morning report: a qualitative study.
BMC Med Educ
; 24(1): 184, 2024 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38395817
2.
Survival, surveillance, and genetics in patients with Peutz-Jeghers syndrome: A nationwide study.
Clin Genet
; 104(1): 81-89, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37017260
3.
Feasibility and early clinical impact of precision medicine for late-stage cancer patients in a regional public academic hospital.
Acta Oncol
; 62(3): 261-271, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36905645
4.
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.
Hered Cancer Clin Pract
; 21(1): 19, 2023 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821984
5.
When to consult a geneticist specialising in gestational trophoblastic disease.
Gynecol Obstet Invest
; 2023 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37245506
6.
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
Hered Cancer Clin Pract
; 20(1): 36, 2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36182917
7.
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Genet Med
; 23(4): 705-712, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257847
8.
Danish guidelines for management of non-APC-associated hereditary polyposis syndromes.
Hered Cancer Clin Pract
; 19(1): 41, 2021 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34620187
9.
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Genet Med
; 22(9): 1569, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32690931
10.
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Genet Med
; 22(1): 15-25, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31337882
11.
Maternally contributed Nlrp9b expressed in human and mouse ovarian follicles contributes to early murine preimplantation development.
J Assist Reprod Genet
; 37(6): 1355-1365, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32399794
12.
The pivotal roles of the NOD-like receptors with a PYD domain, NLRPs, in oocytes and early embryo development.
Biol Reprod
; 101(2): 284-296, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31201414
13.
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome.
Genet Med
; 21(12): 2706-2712, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204389
14.
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.
Hered Cancer Clin Pract
; 17: 28, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31636762
15.
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.
Gut
; 67(7): 1306-1316, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28754778
16.
Choroid plexus hyperplasia and chromosome 9p gains.
Am J Med Genet A
; 176(6): 1416-1422, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29663640
17.
Prognosis for pregnancies with trisomy 16 confined to the placenta: A Danish cohort study.
Prenat Diagn
; 38(13): 1103-1110, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30328629
18.
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database.
Gut
; 66(3): 464-472, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657901
19.
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database.
Gut
; 66(9): 1657-1664, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27261338
20.
Infants with prenatally diagnosed kidney anomalies have an increased risk of urinary tract infections.
Acta Paediatr
; 106(11): 1875-1881, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28793177