Detalhe da pesquisa
1.
Wnt/ß-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders.
Mol Psychiatry
; 26(7): 3572-3585, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33867523
2.
Changes in serum PSA after endoscopic enucleation of the prostate are predictive for the future diagnosis of prostate cancer.
World J Urol
; 39(7): 2621-2626, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32997261
3.
Coverage determinants of breast cancer screening in Flanders: an evaluation of the past decade.
Int J Equity Health
; 19(1): 212, 2020 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246477
4.
Pain-related fear in adolescents with chronic musculoskeletal pain: process evaluation of an interdisciplinary graded exposure program.
BMC Health Serv Res
; 20(1): 213, 2020 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32171308
5.
Flemish breast cancer screening programme: 15 years of key performance indicators (2002-2016).
BMC Cancer
; 19(1): 1012, 2019 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660890
6.
Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial.
Qual Life Res
; 27(8): 2027-2033, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29603114
7.
Practitioner review: evidence-based practice guidelines on alcohol and drug misuse among adolescents: a systematic review.
J Child Psychol Psychiatry
; 55(1): 3-21, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24117606
8.
Quantifying independent risk factors for failing to rescreen in a breast cancer screening program in Flanders, Belgium.
Prev Med
; 69: 280-6, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25456812
9.
Antimicrobial resistance to benzylpenicillin in invasive pneumococcal disease in Belgium, 2003-2010: the effect of altering clinical breakpoints.
Epidemiol Infect
; 141(3): 490-5, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22677465
10.
A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.
Nat Genet
; 3(4): 327-32, 1993 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-7526933
11.
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
12.
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.
Nat Genet
; 25(2): 182-6, 2000 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-10835633
13.
SOX10 mutations in patients with Waardenburg-Hirschsprung disease.
Nat Genet
; 18(2): 171-3, 1998 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-9462749
14.
Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility.
Reprod Biomed Online
; 24(1): 72-82, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22116069
15.
Physiotherapists' knowledge, attitude and practice behavior to prevent chronification in patients with non-specific, non-traumatic, acute- and subacute neck pain: A qualitative study.
Musculoskelet Sci Pract
; 57: 102493, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34922256
16.
Irregular screening participation increases advanced stage breast cancer at diagnosis: A population-based study.
Breast
; 65: 61-66, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35820298
17.
Determinants of Non-Participation in Population-Based Breast Cancer Screening: A Systematic Review and Meta-Analysis.
Front Oncol
; 12: 817222, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35311110
18.
Contacts between general practitioners and migrants without a residence permit and the use of "urgent" medical care.
Scand J Public Health
; 39(6): 649-55, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21719529
19.
Reduced humoral immune response after BNT162b2 coronavirus disease 2019 messenger RNA vaccination in cancer patients under antineoplastic treatment.
ESMO Open
; 6(5): 100274, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34597941
20.
The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.
J Med Genet
; 46(11): 752-8, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19880712