M. Niermeijer

发表

Course of Distress Experienced by Persons at Risk for an Autosomal Dominant Inheritable Disorder Participating in a Predictive Testing Program: An Explorative Study

J. Passchier, H. Duivenvoorden, A. Tibben, 1998, Psychosomatic medicine.

Presymptomatic testing for BRCA1 andBRCA2: how distressing are the pre-test weeks?

P. Devilee, A. Wagner, H. Duivenvoorden, 1999, Journal of medical genetics.

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-oophorectomy.

J. Klijn, C. Seynaeve, H. Duivenvoorden, 2007, European journal of cancer.

Who is prone to high levels of distress after prophylactic mastectomy and/or salpingo-ovariectomy?

J. Klijn, C. Seynaeve, H. Duivenvoorden, 2007, Annals of oncology : official journal of the European Society for Medical Oncology.

Perinatal necropsy by magnetic resonance imaging

M. Niermeijer, 1997, The Lancet.

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

R. Roos, A. Tibben, J. J. van de Kamp, 1994, American journal of human genetics.

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation

H. Meijers-Heijboer, A. Wagner, H. Vasen, 2002, Journal of medical genetics.

On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.

R. Roos, G. van Ommen, A. Tibben, 1993, American journal of medical genetics.

Preliminary experience with predictive testing for insulin-dependent diabetes mellitus

A. Wagner, H. Aanstoot, A. Tibben, 1995, The Lancet.

Effect on a Dutch family of predictive DNA-testing for hereditary breast and ovarian cancer

P. Devilee, A. Tibben, J. Klijn, 1994, The Lancet.

Genetic counselling before intracytoplasmic sperm injection

G. Dohle, M. Niermeijer, P. I. Veld, 1997, The Lancet.

Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.

C. V. van Duijn, J. V. van Swieten, M. Stevens, 1997, Journal of medical genetics.

Psychological studies in Huntington's disease: making up the balance

R. Roos, A. Tibben, R. W. Trijsburg, 2001, Journal of medical genetics.

Testing for Huntington's disease with support for all parties

A. Tibben, R. Roos, F. Verhage, 1990, The Lancet.

DNA testing for fragile X syndrome: implications for parents and family.

B. D. de Vries, A. V. D. van den Ouweland, D. Halley, 1997, Journal of medical genetics.

Caregiver Burden, Health-Related Quality of Life and Coping in Dementia Caregivers: A Comparison of Frontotemporal Dementia and Alzheimer’s Disease

F. Verhey, H. Duivenvoorden, J. V. van Swieten, 2006, Dementia and Geriatric Cognitive Disorders.

Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup.

Rotterdam, J. Passchier, H. Duivenvoorden, 1998, Journal of medical genetics.

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease

G. Ommen, A. Tibben, F. Verhage, 1992, The Lancet.

Psychological effects of presymptomatic DNA testing for Huntington's disease in the Dutch program.

R. Roos, H. Duivenvoorden, A. Tibben, 1994, Psychosomatic medicine.

Psychological consequences of presymptomatic testing for Huntington's disease

A. Tibben, M. Niermeijer, R. Roos, 1997, The Lancet.

Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families

P. Heutink, B. Oostra, C. V. van Duijn, 1997, Annals of neurology.

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

J. Passchier, H. Duivenvoorden, A. van Haeringen, 1997, Journal of medical genetics.

DNA testing for fragile X syndrome: implications for parents and family.

M. Niermeijer, B. de Vries, D. J. Halley, 1997, Journal of medical genetics.