S
Saskia M. Imhof
Researcher at VU University Medical Center
Publications - 56
Citations - 2336
Saskia M. Imhof is an academic researcher from VU University Medical Center. The author has contributed to research in topics: Retinoblastoma & Medicine. The author has an hindex of 25, co-authored 43 publications receiving 2222 citations. Previous affiliations of Saskia M. Imhof include VU University Amsterdam & University of Amsterdam.
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Journal ArticleDOI
Incidence of retinoblastoma in children born after in-vitro fertilisation.
Annette C. Moll,Saskia M. Imhof,Johannes R. M. Cruysberg,Antoinette Y. N. Schouten-van Meeteren,Maarten Boers,Flora E van Leeuwen,Flora E van Leeuwen +6 more
TL;DR: This study diagnosed retinoblastoma in five patients born after IVF in the Netherlands between November, 2000, and February, 2002, to calculate the relative risk of the disease and found a possible association with an increased risk in a population-based study.
Journal ArticleDOI
Risk of Second Malignancies in Survivors of Retinoblastoma: More Than 40 Years of Follow-up
T. Marees,Annette C Moll,Saskia M. Imhof,Michiel R. de Boer,Peter J. Ringens,Flora E. van Leeuwen +5 more
TL;DR: Risks of second malignancies in middle-aged hereditary retinoblastoma survivors suggests that these individuals have an excess risk of epithelial cancer.
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Second primary tumors in hereditary retinoblastoma: a register-based study, 1945-1997: is there an age effect on radiation-related risk?
Annette C. Moll,Saskia M. Imhof,Antoinette Y. N. Schouten-van Meeteren,Dirk J. Kuik,Pieter Hofman,Maarten Boers +5 more
TL;DR: In this article, the influence of age at external beam irradiation (EBRT) on the occurrence of second primary tumors (SPTs) inside and outside the irradiation field in hereditary retinoblastoma patients was evaluated.
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Incidence and survival of retinoblastoma in The Netherlands: a register based study 1862-1995.
Annette C. Moll,Dirk J. Kuik,Lex M. Bouter,den W. Otter,P.D. Bezemer,J. W. Koten,Saskia M. Imhof,B.P. Kuyt,K.E.W.P. Tan +8 more
TL;DR: Although survival for retinoblastoma was significantly better after 1945 than before, in comparison with the Dutch population the mortality between 1900 and 1990 increased for the hereditary and decreased for the non-hereditary retinOBlastoma patients.
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Second primary tumors in patients with retinoblastoma: a review of the literature
TL;DR: SPT is a serious problem for the survivors of hereditary retinoblastoma and its importance should be recognized in (genetic) counseling of patients.