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Attributs	Valeurs
type	Person
name	Sermon K. Sermon Karen Sermon K.D. Sermon K
personal mailbox	karen.sermon@uzbrussel.be karen.sermon@az.vub.ac.be Karen.Sermon@uzbrussel.be
familyName	Sermon
Given name	K. Karen K K.D.
is relates of	http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_11/101093humrepdep266/authorship/5 http://hub.abes.fr/oup/periodical/humrep/1992/volume_7/issue_suppl1/101093humrep7suppl1107/authorship/2 http://hub.abes.fr/oup/periodical/humrep/2005/volume_21/issue_2/101093humrepdei345/authorship/5 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_5/101093humrepden488/authorship/4 http://hub.abes.fr/oup/periodical/humrep/2010/volume_25/issue_1/101093humrepdep298/authorship/6 http://hub.abes.fr/oup/periodical/molehr/2003/volume_9/issue_9/101093molehrgag065/authorship/2 http://hub.abes.fr/oup/periodical/humupd/2000/volume_6/issue_4/101093humupd64364/authorship/3 http://hub.abes.fr/oup/periodical/nar/2006/volume_34/issue_9/101093nargkl336/authorship/3 http://hub.abes.fr/oup/periodical/molehr/1998/volume_4/issue_8/101093molehr48791/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_3/101093humrepdem327/authorship/11 http://hub.abes.fr/oup/periodical/humrep/2005/volume_21/issue_1/101093humrepdei292/authorship/14 http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_12/101093humrepden238/authorship/6 http://hub.abes.fr/oup/periodical/molehr/2006/volume_13/issue_1/101093molehrgal091/authorship/4 http://hub.abes.fr/oup/periodical/molehr/1999/volume_5/issue_7/101093molehr57691/authorship/2 http://hub.abes.fr/oup/periodical/molehr/2003/volume_9/issue_7/101093molehrgag054/authorship/2 http://hub.abes.fr/oup/periodical/molehr/2005/volume_11/issue_5/101093molehrgah170/authorship/10 http://hub.abes.fr/oup/periodical/humrep/1998/volume_13/issue_suppl1/101093humrep13suppl1186/authorship/2 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_10/101093humrepdep234/authorship/6 http://hub.abes.fr/oup/periodical/molehr/2008/volume_14/issue_3/101093molehrgan001/authorship/5 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_7/101093humrepdep062/authorship/1 http://hub.abes.fr/oup/periodical/molehr/2000/volume_6/issue_12/101093molehr6121165/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_3/101093humrepdem424/authorship/2 http://hub.abes.fr/oup/periodical/humrep/1995/volume_10/issue_8/101093oxfordjournalshumrepa136270/authorship/1 http://hub.abes.fr/oup/periodical/humrep/1997/volume_12/issue_8/101093humrep1281756/authorship/2 http://hub.abes.fr/oup/periodical/humrep/2004/volume_19/issue_3/101093humrepdeh153/authorship/5 http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_4/101093humrepdem354/authorship/13 http://hub.abes.fr/oup/periodical/humrep/2008/volume_23/issue_7/101093humrepden105/authorship/3 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_1/101093humrepden351/authorship/3 http://hub.abes.fr/oup/periodical/humrep/1992/volume_7/issue_9/101093oxfordjournalshumrepa137842/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2003/volume_18/issue_2/101093humrepdeg065/authorship/1 http://hub.abes.fr/oup/periodical/humrep/1991/volume_6/issue_2/101093oxfordjournalshumrepa137322/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2005/volume_20/issue_1/101093humrepdeh579/authorship/11 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_11/101093humrepdep262/authorship/3 http://hub.abes.fr/oup/periodical/molehr/1996/volume_2/issue_3/101093molehr23209/authorship/1 http://hub.abes.fr/oup/periodical/molehr/2005/volume_11/issue_1/101093molehrgah128/authorship/3 http://hub.abes.fr/oup/periodical/humupd/2002/volume_8/issue_1/101093humupd8111/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2005/volume_20/issue_1/101093humrepdeh552/authorship/1 http://hub.abes.fr/oup/periodical/humrep/2002/volume_17/issue_11/101093humrep17112807/authorship/2 http://hub.abes.fr/oup/periodical/humrep/2007/volume_22/issue_4/101093humrepdel470/authorship/6 http://hub.abes.fr/oup/periodical/humrep/1998/volume_13/issue_11/101093humrep13113169/authorship/3 http://hub.abes.fr/oup/periodical/humrep/2007/volume_22/issue_2/101093humrepdel402/authorship/1 http://hub.abes.fr/oup/periodical/molehr/1998/volume_4/issue_10/101093molehr410978/authorship/2 http://hub.abes.fr/oup/periodical/molehr/2008/volume_14/issue_7/101093molehrgan034/authorship/7 http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_11/101093humrepdep272/authorship/5
is Author of	Preimplantation diagnosis ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006 What next for preimplantation genetic screening? Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders Single embryo transfer in preimplantation genetic diagnosis cycles for women <36 years does not reduce delivery rate ESHRE PGD Consortium data collection IV: May-December 2001 Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis The Brussels' experience of more than 5 years of clinical preimplantation genetic diagnosis ESHRE PGD Consortium data collection V: Cycles from January to December 2002 with pregnancy follow-up to October 2003 Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency Preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions β-N-acetylhexosaminidase activity in human oocytes and preimplantation embryos ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004 Clinical experience with preimplantation genetic diagnosis and intracytoplasmic sperm injection Preimplantation genetic diagnosis for neurofibromatosis type 1 Characterization of CD30 expression in human embryonic stem cell lines cultured in serum-free media and passaged mechanically Cumulative reproductive outcome after preimplantation genetic diagnosis: a report on 1498 couples Simultaneous amplification of the two most frequent mutations of infantile Tay-Sachs disease in single blastomeres Preimplantation genetic diagnosis for fragile Xa syndrome: difficult but not impossible Novel universal approach for preimplantation genetic diagnosis of β-thalassaemia in combination with HLA matching of embryos ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005 Report on a consecutive series of 581 children born after blastomere biopsy for preimplantation genetic diagnosis Improving clinical preimplantation genetic diagnosis for cystic fibrosis by duplex PCR using two polymorphic markers or one polymorphic marker in combination with the detection of the ΔF508 mutation Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease). Markers that define stemness in ESC are unable to identify the totipotent cells in human preimplantation embryos The causes of misdiagnosis and adverse outcomes in PGD Preimplantation genetic diagnosis: current status and new developments. Sex selection by preimplantation genetic diagnosis: should it be carried out for social purposes? β-N-Acetythexosaminidase activity in mouse oocytes and preimplantation embryos ESHRE PGD Consortium ‘Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)’ Single-cell chromosomal imbalances detection by array CGH Human embryonic stem cell lines derived from single blastomeres of two 4-cell stage embryos Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A. Successful preimplantation genetic diagnosis is related to the number of available cumulus-oocyte complexes. Adaptation of the primer extension preamplification (PEP) reaction for preimplantation diagnosis: single blastomere analysis using short PEP protocols CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation PGD for autosomal dominant polycystic kidney disease type 1 Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions Fluorescent PCR and automated fragment analysis in preimplantation genetic diagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia Current concepts in preimplantation genetic diagnosis (PGD): a molecular biologist’s view

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