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Adverse childhood experiences of persons at risk for Huntington's disease or BRCA1/2 hereditary breast/ovarian cancerVAN DER MEER, L. B; VAN DUIJN, E; WOLTERBEEK, R et al.Clinical genetics. 2012, Vol 81, Num 1, pp 18-23, issn 0009-9163, 6 p.Article

Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the NetherlandsVAN RIJ, M C; DE DIE-SMULDERS, C.E.M; BIJLSMA, E. K et al.Clinical genetics. 2013, Vol 83, Num 2, pp 118-124, issn 0009-9163, 7 p.Article

Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks?LODDER, L. N; FRETS, P. G; CORNELISSE, C. J et al.Journal of medical genetics. 1999, Vol 36, Num 12, pp 906-913, issn 0022-2593Article

Screening and diagnosis for the fragile X syndrome among the mentally retarded : An epidemiological and psychological surveyDE VRIES, B. B. A; VAN DEN OUWELAND, A. M. W; TIBBEN, A et al.American journal of human genetics. 1997, Vol 61, Num 3, pp 660-667, issn 0002-9297Article

Presymptomatic DNA-testing for Huntington disease : pretest attitudes and expectations of applicants and their partners in the Dutch programTIBBEN, A; FRETS, P. G; VAN DE KAMP, J. J. P et al.American journal of medical genetics. 1993, Vol 48, Num 1, pp 10-16, issn 0148-7299Article

Impact of screening for breast cancer in high-risk women on health-related quality of lifeRIJNSBURGER, A. J; ESSINK-BOT, M. L; VAN DOOREN, S et al.British journal of cancer. 2004, Vol 91, Num 1, pp 69-76, issn 0007-0920, 8 p.Article

Behavioural complaints in participants who underwent predictive testing for Huntington's diseaseWITJES-ANE, M-N W; ZWINDERMAN, A. H; TIBBEN, A et al.Journal of medical genetics. 2002, Vol 39, Num 11, pp 857-862, issn 0022-2593, 6 p.Article

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutationWAGNER, A; TOPS, C; MEIJERS-HEIJBOER, H et al.Journal of medical genetics. 2002, Vol 39, Num 11, pp 833-837, issn 0022-2593, 5 p.Article

BRCA1 in the family : A case description of the psychological implicationsDUDOKDEWIT, A. C; TIBBEN, A; FRETS, P. G et al.American journal of medical genetics. 1997, Vol 71, Num 1, pp 63-71, issn 0148-7299Article

DNA testing for fragile X syndrome : implications for parents and familyVAN RIJN, M. A; DE VRIES, B. B. A; TIBBEN, A et al.Journal of medical genetics. 1997, Vol 34, Num 11, pp 907-911, issn 0022-2593Article

Early cognitive and Motor symptoms in identified carriers of the gene for Huntington diseaseDE BOO, G. M; TIBBEN, A; LANSER, J. B. K et al.Archives of neurology (Chicago). 1997, Vol 54, Num 11, pp 1353-1357, issn 0003-9942Article

Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?HELDERMAN-VAN DEN ENDEN, Atjm; VAN DEN BERGEN, J. C; BREUNING, M. H et al.Clinical genetics. 2011, Vol 79, Num 3, pp 236-242, issn 0009-9163, 7 p.Article

Who is prone to high levels of distress after prophylactic mastectomy and/or salpingo-ovariectomy?BRESSER, P. J. C; VAN GOOL, A. R; SEYNAEVE, C et al.Annals of oncology. 2007, Vol 18, Num 10, pp 1641-1645, issn 0923-7534, 5 p.Article

Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testingVAN OOSTROM, I; MEIJERS-HEIJBOER, H; DUIVENVOORDEN, H. J et al.Annals of oncology. 2006, Vol 17, Num 7, pp 1090-1095, issn 0923-7534, 6 p.Article

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsRIZZU, P; VAN SWIETEN, J. C; GOEDERT, M et al.American journal of human genetics. 1999, Vol 64, Num 2, pp 414-421, issn 0002-9297Article

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22 : A genetic and clinicopathological study of three Dutch familiesHEUTINK, P; STEVENS, M; RIZZU, P et al.Annals of neurology. 1997, Vol 41, Num 2, pp 150-159, issn 0364-5134Article

Predictive testing for Huntington disease : nonparticipants compared with participants in the Dutch programVAN DER STEENSTRATEN, I. M; TIBBEN, A; ROOS, R. A. C et al.American journal of human genetics. 1994, Vol 55, Num 4, pp 618-625, issn 0002-9297Article

Attitudes of Dutch general practitioners towards presymptomatic DNA-testing for Huntington diseaseTHOMASSEN, R; TIBBEN, A; NIERMEIJER, M. F et al.Clinical genetics. 1993, Vol 43, Num 2, pp 63-68, issn 0009-9163Article

Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA1/2-test resultsVOS, J; OOSTERWIJK, J. C; GOMEZ-GARCIA, E et al.Clinical genetics. 2011, Vol 79, Num 3, pp 207-218, issn 0009-9163, 12 p.Article

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing : a prospective studyVAN OOSTROM, I; MEIJERS-HEIJBOER, H; DUIVENVOORDEN, H. J et al.Clinical genetics. 2007, Vol 71, Num 1, pp 35-42, issn 0009-9163, 8 p.Article

The course of distress in women at increased risk of breast and ovarian cancer due to an (identified) genetic susceptibility who opt for prophylactic mastectomy and/or salpingo -oophorectomyBRESSER, P. J. C; SEYNAEUE, C; VAN GOOL, A. R et al.European journal of cancer (1990). 2007, Vol 43, Num 1, pp 95-103, issn 0959-8049, 9 p.Article

Screening for the fragile X syndrome among the mentally retarded: a clinical studyDE VRIES, B. B. A; MOHKAMSING, S; NIERMEIJER, M. F et al.Journal of medical genetics. 1999, Vol 36, Num 6, pp 467-470, issn 0022-2593Article

Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders : Comparing questionnaire results with in-depth interviewsDUDOKDEWIT, A. C; TIBBEN, A; DUIVENVOORDEN, H. J et al.American journal of medical genetics. 1998, Vol 75, Num 1, pp 62-74, issn 0148-7299Article

Predicting adaptation to presymptomatic DNA testing for late onset disorders : Who will experience distress?WIT, A. C. D; TIBBEN, A; DUIVENVOORDEN, H. J et al.Journal of medical genetics. 1998, Vol 35, Num 9, pp 745-754, issn 0022-2593Article

Presymptomatic DNA testing for Huntington disease : identifying the need for psychological interventionTIBBEN, A; DUIVENVOORDEN, H. J; VEGTER-VAN DER VLIS, M et al.American journal of medical genetics. 1993, Vol 48, Num 3, pp 137-144, issn 0148-7299Article

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