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Dive into the research topics where M. De Rademaeker is active.

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Featured researches published by M. De Rademaeker.


Human Reproduction | 2008

Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis

W. Verpoest; M. De Rademaeker; Karen Sermon; M. De Rycke; Sara Seneca; E.G. Papanikolaou; Claudia Spits; L. Van Landuyt; J. Van der Elst; Patrick Haentjens; Paul Devroey; I. Liebaers

BACKGROUND This study aimed to analyse the reproductive outcome of a large cohort of myotonic dystrophy type 1 (DM1) patients undergoing ICSI and PGD. The secondary outcome parameter of this study was ovarian response as a way to express gonadal function in female DM1 patients. METHODS Prospective cohort study. Real and expected cumulative delivery rates are descriptive. The reproductive outcome per cycle was compared with that of a control group of patients with X-linked recessive disorders. The comparative analysis of ovarian stimulation parameters in the study group versus the control group was carried out using both bivariate (crude) and multivariate (linear regression) analysis. RESULTS Between 1995 and 2005, 205 cycles of ICSI and PGD were carried out for DM1 in 78 couples. The real cumulative delivery rate (max 6 cycles) overall was 46%. The expected overall cumulative delivery rate was 72%. Multivariate analysis did not show a significant difference in total dose of gonadotrophins used for ovarian stimulation between Group A (in which the female partner was affected) and a control group. CONCLUSIONS This study shows that ICSI and PGD for DM1 offer good reproductive outcome, both in cumulative terms and per treatment cycle. There is no evidence of impaired gonadal function in female DM1 patients.


Human Reproduction | 2011

SELECTED ORAL COMMUNICATION SESSION, SESSION 63: PREIMPLANTATION GENETICS Wednesday 6 July 2011 10:00 – 11:45

P. Colls; J. Fischer; T. Escudero; K. Ketterson; G. Harton; S. Munne; A. Capalbo; F. Fiorentino; R. Maggiulli; S. Romano; A. Borsatti; A. Joseph; L. Spizzichino; S. Bono; A. Biricik; S. Colamaria; M.F Ubaldi; L.F Rienzi; P. Rubino; L. Arizzi; M.G Minasi; R. Pena; F. Scarselli; V. Casciani; A. Colasante; S. Ferrero; K. Litwicka; M.T Varricchio; F. Cucinelli; Z.P Nagy


European Journal of Paediatric Neurology | 2017

Complex phenotype associated with mutation in the TANGO2 gene

L. De Meirleir; M. D'Hooghe; M. De Rademaeker; Katrien Stouffs; A. Geldhof; S Seneca


Genetic Counseling | 2016

Evidence from adults with intellectual disability to cnv in prenatal period: how to build penetrance validation and appropriate genetic counselling? an example with 10q11.22 duplication

Yves Sznajer; Claude Bandelier; Marie Ravoet; Joris Vermeesch; Katrien Janssens; Kris Van Den Bogaert; Julie Désir; Annelies Dheedene; Joke Muys; Catherine Staessen; Catheline Vilain; Kathelijn Keymomen; J-S Gatot; Björn Menten; B Grisard; Sonia Rombout; Olivier Vanakker; Bettina Blaumeiser; M. De Rademaeker; Guillaume Smits; A De Leener; Bruno Pichon; A Destree; Thomy de Ravel de l'Argentière; S Gaillez; Jh Caberg; Nicole Revencu; Sandra Janssens; Saskia Bulk; C Melotte


Prenatal Diagnosis | 2015

Belgian MicroArray Prenatal (BEMAPRE) database

Joke Muys; Katrien Janssens; Olivier Vanakker; Catheline Vilain; Guillaume Smits; Claude Bandelier; Saskia Bulk; Jh Caberg; A De Leener; M. De Rademaeker; Thomy de Ravel de l'Argentière; Julie Désir; A Destree; Annelies Dheedene; S Gaillez; B Grisar; Ac Hellin; Sandra Janssens; Kathelijn Keymolen; B Menten; Bruno Pichon; Marie Ravoet; N Rrevency; Sonia Rombout; Catherine Staessen; A. Van Den Bogaert; K. Van Den Bogaert; Joris Vermeesch; Yves Sznajer; Bettina Blaumeiser


Online abstracts | 2015

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens; Frauke Coppieters; J De Zaeytijd; Nicole Weisschuh; Susanne Kohl; Karin Dahan; Fanny Depasse; M. De Rademaeker; B Loeys; Françoise Meire; Thomy de Ravel de l'Argentière; Wouter Steyaert; S De Jaegere; Bp Leroy; E De Baere


Online abstracts | 2015

The Belgian MicroArray Prenatal (BEMAPRE) database

Joke Muys; Katrien Janssens; Olivier Vanakker; Catheline Vilain; Guillaume Smits; Claude Bandelier; Saskia Bulk; Jean-Hubert Caberg; A De Leener; M. De Rademaeker; Thomy de Ravel de l'Argentière; Julie Désir; A Destree; Annelies Dheedene; S Gaillez; Bernard Grisart; Ac Hellin; Sandra Janssens; Kathelijn Keymolen; B Menten; Bruno Pichon; Marie Ravoet; Nicole Revencu; S Rombaut; C. Staessens; A. Van Den Bogaert; K. Van Den Bogaert; Joris Vermeesch; Yves Sznajer; Bettina Blaumeiser


European Journal of Paediatric Neurology | 2015

Two cases of Noonan syndrome. Genotype-phenotype correlation

M. De Rademaeker; An Jansen; I. Gies; Gert Matthijs; Ben Caljon; Katrien Stouffs; Kathelijn Keymolen


European Journal of Paediatric Neurology | 2015

P137 – 2976: Two cases of Noonan syndrome: Genotype–phenotype correlation

M. De Rademaeker; Anna Jansen; I. Gies; G. Matthijs; Ben Caljon; Katrien Stouffs; Kathelijn Keymolen


European Human Genetics Conference 2015 | 2015

The Belgian MicroArray Prenatal (BEMAPRE) database [Online Abstract]

Joke Muys; Katrien Janssens; Olivier Vanakker; Catheline Vilain; Guillaume Smits; Claude Bandelier; Saskia Bulk; Jean-Hubert Caberg; A De Leener; M. De Rademaeker; T. de Ravel de l'Argentière; Julie Désir; A Destree; Annelies Dheedene; S Gaillez; Bernard Grisart; Ac Hellin; Sandra Janssens; Kathelijn Keymolen; B Menten; Bruno Pichon; Marie Ravoet; Nicole Revencu; Sonia Rombout; C. Staessens; A. Van Den Bogaert; K. Van Den Bogaert; J.R. Vermeesch; Yves Sznajer; Bettina Blaumeiser

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Bruno Pichon

Université libre de Bruxelles

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Catheline Vilain

Free University of Brussels

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Claude Bandelier

Université catholique de Louvain

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Guillaume Smits

Université libre de Bruxelles

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Joke Muys

University of Antwerp

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Joris Vermeesch

Katholieke Universiteit Leuven

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