Search Results - "Smulders, C."

Control and Impact of Metal Loading Heterogeneities at the Nanoscale on the Performance of Pt/Zeolite Y Catalysts for Alkane Hydroconversion by van der Wal, Lars I, Oenema, Jogchum, Smulders, Luc C. J, Samplonius, Nonne J, Nandpersad, Karan R, Zečević, Jovana, de Jong, Krijn P

“…The preparation of zeolite-based bifunctional catalysts with low noble metal loadings while maintaining optimal performance has been studied. We have deposited…”
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Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas by van der Schoot, V, Dondorp, W, Dreesen, J C F M, Coonen, E, Paulussen, A D C, de Wert, G, de Die-Smulders, C E M

“…Abstract STUDY QUESTION Which clinical and ethical aspects of preimplantation genetic testing for monogenic disorders or structural rearrangements (PGT-M,…”
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Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners by Gietel-Habets, J.J.G., de Die-Smulders, C.E.M., Derks-Smeets, I.A.P., Tibben, A., Tjan-Heijnen, V.C.G., van Golde, R., Gomez-Garcia, E., Kets, C.M., van Osch, L.A.D.M.

“…Abstract STUDY QUESTION To what extent are BRCA mutation carriers and their partners in the Netherlands aware about preimplantation genetic diagnosis (PGD) and…”
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To what extent do decision aids for prenatal screening and diagnosis address involvement of partners in decision-making? - An environmental scan by Severijns, Y., van der Linden, H., de Die-Smulders, C.E.M., Hoving, C., Jansen, J., van Osch, L.A.D.M.

“…•A minority of the DAs about prenatal screening/diagnosis contained content that stimulates or promotes partner involvement.•Most DAs only placed emphasis on…”
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Hereditary diseases and child wish: exploring motives, considerations, and the (joint) decision-making process of genetically at-risk couples by Severijns, Y., de Die-Smulders, C. E. M., Gültzow, T., de Vries, H., van Osch, L. A. D. M.

“…Couples who are at risk of transmitting a genetic disease to their offspring may face difficult challenges regarding reproductive decision-making. Deciding if,…”
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Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists by Reumkens, Kelly, van Oudheusden, A. J. G., Gietel-Habets, J. J. G., Tummers, M. H. E., de Die-Smulders, C. E. M., van Osch, L. A. D. M.

“…For couples at high risk of transmitting a cancer predisposition to offspring, reproductive decision-making can be challenging. As the choice between available…”
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The cognitive and socio-emotional development of 5-year-old children born after PGD by Heijligers, M, Verheijden, L M M, Jonkman, L M, van der Sangen, M, Meijer-Hoogeveen, M, Arens, Y, van der Hoeven, M A, de Die-Smulders, C E M

“…Abstract STUDY QUESTION Does PGD increase the risk on adverse cognitive and socio-emotional development? SUMMARY ANSWER The cognitive and socio-emotional…”
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Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer by Derks-Smeets, I.A.P., Gietel-Habets, J.J.G., Tibben, A., Tjan-Heijnen, V.C.G., Meijer-Hoogeveen, M., Geraedts, J.P.M., van Golde, R., Gomez-Garcia, E., van den Bogaart, E., van Hooijdonk, M., de Die-Smulders, C.E.M., van Osch, L.A.D.M.

“…STUDY QUESTION How do couples with a BRCA1/2 mutation decide on preimplantation genetic diagnosis (PGD) and prenatal diagnosis (PND) for hereditary breast and…”
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Motives and considerations regarding PGT in couples carrying a structural chromosomal abnormality: a qualitative exploration by De Krom, G., Severijns, Y., Vlieg, W. L., Arens, Y. H. J. M., Van Golde, R. J. T., De Die-Smulders, C. E. M., Van Osch, L. A. D. M.

“…Purpose This study aims to describe the motives and considerations of couples carrying a structural chromosomal abnormality deciding on preimplantation genetic…”
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Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 by Mersy, E, Smits, L J M, van Winden, L A A P, de Die-Smulders, C E M, Paulussen, A D C, Macville, M V E, Coumans, A B C, Frints, S G M

“…Research on noninvasive prenatal testing (NIPT) of fetal trisomy 21 is developing fast. Commercial tests have become available. To provide an up-to-date…”
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Hereditary muscular dystrophies and the heart by Hermans, M.C.E, Pinto, Y.M, Merkies, I.S.J, de Die-Smulders, C.E.M, Crijns, H.J.G.M, Faber, C.G

“…Summary Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscular dystrophies. Heart muscle cells as well as…”
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ESHRE PGD Consortium ‘Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)’ by Thornhill, A.R., deDie-Smulders, C.E., Geraedts, J.P., Harper, J.C., Harton, G.L., Lavery, S.A., Moutou, C., Robinson, M.D., Schmutzler, A.G., Scriven, P.N., Sermon, K.D., Wilton, L.

“…Among the many educational materials produced by the European Society of Human Reproduction and Embryology (ESHRE) are guidelines. ESHRE guidelines may be…”
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Counseling young women with early breast cancer on fertility preservation by ter Welle-Butalid, M. E. (Elena), Vriens, I. J. H. (Ingeborg), Derhaag, J. G. (Josien), Leter, E. M. (Edward), de Die-Smulders, C. E. (Christine), Smidt, M. (Marjolein), van Golde, R. J. T. (Ron), Tjan-Heijnen, V. C. G. (Vivianne)

“…Purpose Women with early-stage breast cancer may still have a future child wish, while chemotherapy may impair fertility. To pursue on fertility preservation…”
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Reproductive options for prospective parents in families with Huntington's disease: clinical, psychological and ethical reflections by de Die-Smulders, C E M, de Wert, G M W R, Liebaers, I, Tibben, A, Evers-Kiebooms, G

“…BACKGROUND Huntington's disease (HD) is an autosomal dominant neurodegenerative late onset disorder. This review of reproductive options aims to increase…”
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Support needs of couples with hereditary breast and ovarian cancer during reproductive decision making by Gietel‐Habets, J.J.G., Die‐Smulders, C.E.M., Derks‐Smeets, I.A.P., Tibben, A., Tjan‐Heijnen, V.C.G., Golde, R., Gomez‐Garcia, E., Osch, L.A.D.M.

“…Objective Reproductive decision making for couples with hereditary breast and ovarian cancer (HBOC) is complex and can result in decisional conflict or regret…”
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Recurrent miscarriage in translocation carriers: no differences in clinical characteristics between couples who accept and couples who decline PGD by De Krom, G., Arens, Y.H.J.M., Coonen, E., Van Ravenswaaij-Arts, C.M.A., Meijer-Hoogeveen, M., Evers, J.L.H., Van Golde, R.J.T., De Die-Smulders, C.E.M.

“…STUDY QUESTION Do clinical characteristics of recurrent miscarriage couples with a chromosomal abnormality and who opt for PGD differ from couples that decline…”
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Acute facial nerve palsy in children in a Lyme disease–endemic area in the Netherlands by Bruinsma, R. A., Smulders, C. A., Vermeeren, Y. M., van Kooten, B., Cats, E. A., van Hees, B., van Hensbroek, M. Boele, Hovius, J. W., Zomer, T. P.

“…We assessed the prevalence of Lyme neuroborreliosis in children with acute facial nerve palsy in a Lyme-endemic region and patient characteristics associated…”
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BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD by Derks-Smeets, I. A. P., van Tilborg, T. C., van Montfoort, A., Smits, L., Torrance, H. L., Meijer-Hoogeveen, M., Broekmans, F., Dreesen, J. C. F. M., Paulussen, A. D. C., Tjan-Heijnen, V. C. G., Homminga, I., van den Berg, M. M. J., Ausems, M. G. E. M., de Rycke, M., de Die-Smulders, C. E. M., Verpoest, W., van Golde, R.

“…Purpose The aim of this study was to determine whether BRCA1/2 mutation carriers produce fewer mature oocytes after ovarian stimulation for in vitro…”
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Professionals' knowledge, attitude and referral behaviour of preimplantation genetic diagnosis for hereditary breast and ovarian cancer by Gietel-Habets, J.J.G., de Die-Smulders, C.E.M., Tjan-Heijnen, V.C.G., Derks-Smeets, I.A.P., van Golde, R., Gomez-Garcia, E., van Osch, L.A.D.M.

“…Hereditary breast and ovarian cancer caused by a BRCA1/2 mutation is the most frequent indication for preimplantation genetic diagnosis (PGD) in the…”
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The unfolding clinical spectrum of POLG mutations by Blok, M J, van den Bosch, B J, Jongen, E, Hendrickx, A, de Die-Smulders, C E, Hoogendijk, J E, Brusse, E, de Visser, M, Poll-The, B T, Bierau, J, de Coo, I F, Smeets, H J

“…Mutations in the DNA polymerase-gamma (POLG) gene are a major cause of clinically heterogeneous mitochondrial diseases, associated with mtDNA depletion and…”
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