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                             125 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Author index 2010
20 S1 p. S43-S46
4 p.
artikel
2 C25 AMH in human follicular fluid Dewailly, D.
2010
20 S1 p. S7-
1 p.
artikel
3 C9 Can we build a human cell based model: SMA Di Giorgio, F.P.
2010
20 S1 p. S3-
1 p.
artikel
4 C36 Cervical washing Dupont-Bernabé, C.
2010
20 S1 p. S11-
1 p.
artikel
5 C30 Clinical relevance of male meiosis and sperm aneuploidy Martin, R.H.
2010
20 S1 p. S9-
1 p.
artikel
6 C37 Clinical validation of a non-invasive test for prenatal diagnosis of cystic fibrosis and spinal muscular atrophy based on genetic analysis of circulating trophoblastic cells Paterlini-Brechot, P.
2010
20 S1 p. S11-S12
2 p.
artikel
7 C32 Comprehensive microarray genetic analyses on single cell(s) from polar bodies or embryos to determine 23-chromosome aneuploidy, structural chromosome aberrations and genome-wide scans using single nucleotide polymorphisms (SNPs); to identify what partner provided the extra chromosome in aneuploid embryos; and to determine what embryo implanted following an in vitro fertilization (IVF) cycle Kearns, W.G.
2010
20 S1 p. S9-
1 p.
artikel
8 C31 Controlled ovarian stimulation: today and tomorrow Frydman, R.
2010
20 S1 p. S9-
1 p.
artikel
9 C16 Day 3 or Day 5 embryo biopsy: what is the best? Cohen, J.
2010
20 S1 p. S5-
1 p.
artikel
10 C17 Effect of embryo biopsy on subsequent development Frydman, N.
2010
20 S1 p. S5-
1 p.
artikel
11 C35 Effects of ovarian stimulation on endometrial gene expression profile Pellicer, A.
2010
20 S1 p. S10-S11
2 p.
artikel
12 C4 Emerging issues: Cost-effective PGD Renwick, P.
2010
20 S1 p. S2-
1 p.
artikel
13 C26 Follicular G-CSF appears as a non invasive biomarker of subsequent birth Lédée, N.
2010
20 S1 p. S8-
1 p.
artikel
14 C38 Future approach for testing of circulating fetal DNA Costa, J.M.
2010
20 S1 p. S12-
1 p.
artikel
15 C21 Genomic imprinting: about germ cells and maintenance of epigenetic information Feil, R.
2010
20 S1 p. S6-
1 p.
artikel
16 C20 Germ cells from stem cells and reprogrammed somatic cells Nayernia, K.
2010
20 S1 p. S6-
1 p.
artikel
17 C10 hESc and IPSc as models for genetic defects Viville, S.
2010
20 S1 p. S3-
1 p.
artikel
18 C23 Imaging Ebner, T.
2010
20 S1 p. S6-S7
2 p.
artikel
19 C34 Is there a particular COS for patients having genetic diseases? Verpoest, W.
2010
20 S1 p. S10-
1 p.
artikel
20 C18 Lessons from human embryo Van de Velde, H.
2010
20 S1 p. S5-S6
2 p.
artikel
21 C24 Non-invasive assessments of oocytes and embryos: Genomics of cumulus cells Hamamah, S.
2010
20 S1 p. S7-
1 p.
artikel
22 C3 Novel indications for preimplantation genetic diagnosis Rechitsky, S.
2010
20 S1 p. S1-S2
2 p.
artikel
23 C13 Oncogenetics and PND Hughes, M.
2010
20 S1 p. S4-
1 p.
artikel
24 C15 One vs two cell biopsy for PGD Braude, P.
2010
20 S1 p. S5-
1 p.
artikel
25 C43 PGD and children follow-up Bonduelle, M.
2010
20 S1 p. S13-
1 p.
artikel
26 C39 PGD and ethics: What limits should be assigned to the indications? Simpson, J.L.
2010
20 S1 p. S12-
1 p.
artikel
27 C19 PGD and PGS: which perspectives? Liebaers, I.
2010
20 S1 p. S6-
1 p.
artikel
28 C42 PGD and PND: Which and why for who? Cordier, A.G.
2010
20 S1 p. S12-S13
2 p.
artikel
29 C6 PGD and translocations Pellestor, F.
2010
20 S1 p. S2-
1 p.
artikel
30 C28 PGD for aneuploidy: CGH Gianaroli, L.
2010
20 S1 p. S8-
1 p.
artikel
31 C2 PGD for monogenic diseases: Molecular aspects De Rycke, M.
2010
20 S1 p. S1-
1 p.
artikel
32 C7 Preconception diagnosis for chromosomal abnormalities Kuliev, A.
2010
20 S1 p. S2-S3
2 p.
artikel
33 C14 Preimplantation aneuploidy testing outcome Munné, S.
2010
20 S1 p. S4-S5
2 p.
artikel
34 C8 Preimplantation genetic diagnosis and male infertility Kahraman, S.
2010
20 S1 p. S3-
1 p.
artikel
35 C12 Preimplantation genetic diagnosis for BRCA 1/2 SenGupta, S.
2010
20 S1 p. S4-
1 p.
artikel
36 C41 Preimplantation genetic diagnosis: the recommendations of French Committee of Ethics Le Coz, P.
2010
20 S1 p. S12-
1 p.
artikel
37 C5 Quality control for PGD Moutou, C.
2010
20 S1 p. S2-
1 p.
artikel
38 C11 Report on prenatal diagnosis, pregnancy termination and preimplantation genetic diagnosis in inherited cancers in France Stoppa-Lyonnet, D.
2010
20 S1 p. S4-
1 p.
artikel
39 C40 Reprogenetics between science, medicine, and society: Socio-ethical reflections based on the practice of preimplantation genetic diagnosis in France Bouffard, C.
2010
20 S1 p. S12-
1 p.
artikel
40 C22 Stem cells and the IVF clinic Murdoch, A.
2010
20 S1 p. S6-
1 p.
artikel
41 C33 The management of poor responder for IVF with PGD Tur-Kaspa, I.
2010
20 S1 p. S10-
1 p.
artikel
42 C29 The origin of aneuploidy in humans: where we've been, where we're going Hassold, T.
2010
20 S1 p. S8-S9
2 p.
artikel
43 C1 Twenty years of designer babies Handyside, A.H.
2010
20 S1 p. S1-
1 p.
artikel
44 C27 What is an invasive technique or not in embryo selection? Cohen, J.
2010
20 S1 p. S8-
1 p.
artikel
45 Editorial Board 2010
20 S1 p. i-
1 p.
artikel
46 O12 Chromosome length correlates proportionally and negatively with aneuploidy and proportionally and positively with chromatid maldistribution Schmutzler, A.G.
2010
20 S1 p. S19-
1 p.
artikel
47 O16 Comparative genomic hybridisation (aCGH) to identify unbalanced products associated with specific chromosomal rearrangements Thornhill, A.
2010
20 S1 p. S20-
1 p.
artikel
48 O18 Comparison of differential gene expression profile between human embryo on day 3 and trophoblast of blastocyst on day 5: Molecular signature specific for each Assou, S.
2010
20 S1 p. S21-
1 p.
artikel
49 O15 Extended culture is a poor tool for selecting chromosomally normal embryos: Comparison of day-3 and day-5 embryos analyzed using comprehensive chromosome screening methods Munné, S.
2010
20 S1 p. S20-
1 p.
artikel
50 O4 First clinical application of karyomapping for PGD of Gaucher disease combined with 24 chromosome screening Handyside, A.
2010
20 S1 p. S16-
1 p.
artikel
51 O9 First report of hematopoietic cell transplantation for sickle cell disease from in-vitro fertilization-selected donor Del Toro, G.
2010
20 S1 p. S18-
1 p.
artikel
52 O19 Gene expression profile of apoptosis regulators of the Bcl-2 family during early embryonic development Boumela, I.
2010
20 S1 p. S21-
1 p.
artikel
53 O11 Human embryonic stem cells harboring an unbalanced reciprocal translocation t(11;22) as a valuable model for studying single gene dosage effects Frumkin, T.
2010
20 S1 p. S18-
1 p.
artikel
54 O2 Outcomes of 303 cycles on preimplantation Human Leukocyte Antigen typing with or without mutation analysis Ekmekci, C.G.
2010
20 S1 p. S15-
1 p.
artikel
55 O5 PGS by polar body biopsy – High aneuploidy rate independent of age Acar-Perk, B.
2010
20 S1 p. S16-
1 p.
artikel
56 O3 Preimplantation genetic diagnosis as a strategy to prevent a fetomaternal incompatibility for a highly immunogenic platelet antigen causing severe Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT) Freixa, L.
2010
20 S1 p. S15-S16
2 p.
artikel
57 O13 Preimplantation Genetic Diagnosis (PGD) for an apparently sporadic TSC2 mutation confirms the presence of germline mosaicism of paternal origin Traversa, M.
2010
20 S1 p. S19-
1 p.
artikel
58 O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism Altarescu, G.
2010
20 S1 p. S15-
1 p.
artikel
59 O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible Renbaum, P.
2010
20 S1 p. S17-
1 p.
artikel
60 O7 Quantitative analysis of DNA methylation at multiple imprinted genes in single human preimplantation embryos by pyrosequencing Huntriss, J.
2010
20 S1 p. S17-
1 p.
artikel
61 O6 Reanalysis of day 5 embryos following preimplantation genetic screening (PGS) for chromosomal abnormalities by fluorescence in situ hybridization on a single blastomere among different indication groups Christopikou, D.
2010
20 S1 p. S17-
1 p.
artikel
62 O10 Self correction of aneuploid embryos during hESC culture Candan, Z.N.
2010
20 S1 p. S18-
1 p.
artikel
63 O14 Trophectoderm biopsy and array CGH to detect unbalanced forms of t(9;15)(q22.2;q11.1) after failed FISH Lynch, C.
2010
20 S1 p. S19-S20
2 p.
artikel
64 O17 Whole genome profiling of early blocked embryos using customised genomic micro array Benkhalifa, M.
2010
20 S1 p. S20-S21
2 p.
artikel
65 P56 Acquisition of a trisomy 20 in the human embryonic stem cell line HD90 Pellestor, F.
2010
20 S1 p. S41-
1 p.
artikel
66 P22 Aggressive ovarian stimulation may affect IVF outcome after PGD for reciprocal translocation carriers Okutman-Emonts, O.
2010
20 S1 p. S30-
1 p.
artikel
67 P38 Aneuploidy screening in single cells using microarray comparative genomic hybridization for preimplantational genetic diagnosis purposes Martinez-Fresno, M.
2010
20 S1 p. S35-
1 p.
artikel
68 P4 A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues Iourov, I.Y.
2010
20 S1 p. S24-
1 p.
artikel
69 P57 A new technique for polar body biopsy with laser tweezers and femtosecond laser zona pellucida drilling Sergeev, S.A.
2010
20 S1 p. S41-S42
2 p.
artikel
70 P9 A rapid hybridization method to detect chromosomes 15, 17, X and Y in the second hybridization round in a PGD cycle Pérez, N.
2010
20 S1 p. S25-S26
2 p.
artikel
71 P52 A rapid prenatal screening assay to simultaneously detect aneuploidies for all chromosomes from single CVS and amniocentesis samples using BACs on Beads™ Walker, R.K.
2010
20 S1 p. S40-
1 p.
artikel
72 P27 Attempt to devise new, non-invasive prenatal diagnosis method based on fetal genetic material isolation from maternal blood Grabowska, A.
2010
20 S1 p. S32-
1 p.
artikel
73 P42 Can array CGH lead us to a non-invasive selection tool? Cater, E.
2010
20 S1 p. S37-
1 p.
artikel
74 P8 Case report: high polar bodies aneuploidy rate in a patient with severe ovarian hyperstimulation syndrome Diblík, J.
2010
20 S1 p. S25-
1 p.
artikel
75 P3 24 chromosome PGS: Position not quantity Ioannou, D.
2010
20 S1 p. S23-S24
2 p.
artikel
76 P39 Clinical results of array CGH for PGS Munné, S.
2010
20 S1 p. S36-
1 p.
artikel
77 P55 Comparison of obstetrical and neonatal outcomes of pregnancies obtained after preimplantation diagnosis versus intracytoplasmic injection Lamazou, F.
2010
20 S1 p. S41-
1 p.
artikel
78 P14 Complete or partial correction of aneuploidic embryos on day 3 forming hatching/hatched blastocysts on day 5 Altin, G.
2010
20 S1 p. S27-
1 p.
artikel
79 P41 Comprehensive embryo analysis of AMA-related aneuploidies and mosaicism by Short-CGH Rius, M.
2010
20 S1 p. S36-
1 p.
artikel
80 P5 Correlation between preimplantation genetic screening for chromosomal aneuploidies and amount of embryos in IVF cycles Kremenskoy, M.
2010
20 S1 p. S24-
1 p.
artikel
81 P12 Efficacy of 24 chromosome FISH analysis in preimplantation embryos Fernández, S.
2010
20 S1 p. S26-S27
2 p.
artikel
82 P20 Embryo chromosome abnormalities of robertsonian translocation and the relashionship with the sex of the carrier and the size of the chromosomes involved Oter, M.
2010
20 S1 p. S29-
1 p.
artikel
83 P45 Ethical and legal aspects of surrogate pregnancy: opinion of French women on surrogate pregnancy Alouini, S.
2010
20 S1 p. S38-
1 p.
artikel
84 P58 Familial frameshift SRY mutation inherited from a mosaic father with hypospadias and cryptorchidy Le Caignec, C.
2010
20 S1 p. S42-
1 p.
artikel
85 P60 FSH-R polymorphism in severe types of OHSS Macek Sr., M.
2010
20 S1 p. S42-
1 p.
artikel
86 P51 High rate of chromosomal mosaicism in spontaneously aborted fetuses: Analysis of 715 consecutive cases with special emphasis to IVF Vorsanova, S.G.
2010
20 S1 p. S40-
1 p.
artikel
87 P43 Impact of slow-freezing-thawing on the gene expression profile of human metaphase II oocytes: transcriptomic study Monzo, C.
2010
20 S1 p. S37-
1 p.
artikel
88 P10 Molecular cytogenetic diagnosis in 591 married couples with reproductive failures: application for genetic counseling, IVF and PGD Vorsanova, S.G.
2010
20 S1 p. S26-
1 p.
artikel
89 P47 Nondisclosure PGD for late onset autosomal dominant diseases: revised ethical considerations Tur-Kaspa, I.
2010
20 S1 p. S38-S39
2 p.
artikel
90 P26 Ongoing pregnancy after PGD for cystic fibrosis and blastomere aneuploidy screening by Short-CGH Daina, G.
2010
20 S1 p. S31-S32
2 p.
artikel
91 P21 Outcomes of 252 preimplantation genetic diagnosis cycles for chromosomal rearrangements Beyazyurek, C.
2010
20 S1 p. S29-S30
2 p.
artikel
92 P34 Parthenogenetic activation of human oocytes as a model for PB-PGD Paracchini, V.
2010
20 S1 p. S34-
1 p.
artikel
93 P54 PGD activity in France: the French specificities Di Costanzo, S.
2010
20 S1 p. S40-S41
2 p.
artikel
94 P18 PGD for a woman carrier of a balanced reciprocal translocation (11;22) and a man with high expression of 16q22 fragile site Martinez-Pasarell, O.
2010
20 S1 p. S28-S29
2 p.
artikel
95 P13 PGD for gender selection: What is the percentage of embryos not available? Aboujaoude, I.
2010
20 S1 p. S27-
1 p.
artikel
96 P7 PGS program: coculture versus sequential culture system in advanced maternal age Nogales, C.
2010
20 S1 p. S25-
1 p.
artikel
97 P32 Pitfalls of preimplantation genetic diagnosis for mitochondrial DNA mutations by using polar body analysis Gigarel, N.
2010
20 S1 p. S33-
1 p.
artikel
98 P6 Polar body analysis by FISH: Evaluation of hybridisation efficiency Woeck, M.
2010
20 S1 p. S24-S25
2 p.
artikel
99 P19 Polar body based preimplantation genetic diagnosis for female translocation carriers in a public hospital in Austria Maurer, M.
2010
20 S1 p. S29-
1 p.
artikel
100 P35 Preimplantation diagnosis of monogenic diseases in GENNET Putzova, M.
2010
20 S1 p. S34-
1 p.
artikel
101 P1 Preimplantation genetic diagnosis and maternal age: the effect of embryo cohort size Ercelen, N.
2010
20 S1 p. S23-
1 p.
artikel
102 P24 Preimplantation genetic diagnosis for cystic fibrosis: The Montpellier center experience Fernandez, C.
2010
20 S1 p. S30-S31
2 p.
artikel
103 P29 Preimplantation genetic diagnosis for detection of the CAG repeat expansion in spinocerebellar ataxia type 6 Hung, C-C.
2010
20 S1 p. S32-S33
2 p.
artikel
104 P23 Preimplantation genetic diagnosis for Fragile X syndrome Fernandez, C.
2010
20 S1 p. S30-
1 p.
artikel
105 P28 Preimplantation genetic diagnosis of enlarged vestibular aqueduct using GenomiPhi technology and primer extension mini-sequencing Hung, C-C.
2010
20 S1 p. S32-
1 p.
artikel
106 P30 Preimplantation genetic diagnosis of β-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes Lin, S-Y.
2010
20 S1 p. S33-
1 p.
artikel
107 P16 Preimplantation Genetic Diagnosis (PGD) cycles for translocations carriers. Results in a public hospital López, O.
2010
20 S1 p. S28-
1 p.
artikel
108 P36 Pre-implantation Genetic Haplotyping; KFSHRC experience Qubbaj, W.
2010
20 S1 p. S34-S35
2 p.
artikel
109 P44 Profile of genes differentially expressed in human cumulus cells according to oocyte nuclear maturation stages under in vivo conditions: Clinical applications Ouandaogo, G.
2010
20 S1 p. S37-
1 p.
artikel
110 Programme 2010
20 S1 p. v-ix
nvt p.
artikel
111 P37 Routine use of PCR for PGD in translocation carriers: New developments to differentiate balanced carriers from non-carriers Traversa, M.V.
2010
20 S1 p. S35-
1 p.
artikel
112 P46 “Seriousness” and the regulation of preimplantation genetic diagnosis: the case of Down's syndrome Krahn, T.
2010
20 S1 p. S38-
1 p.
artikel
113 P2 Sex chromosome abnormalities in embryos from women undergoing PGS: Focus on meiotic errors involving the X-chromosome Ghevaria, H.
2010
20 S1 p. S23-
1 p.
artikel
114 P40 Short-CGH in a PGD for a reciprocal translocation: first clinical application Rius, M.
2010
20 S1 p. S36-
1 p.
artikel
115 P17 Sperm and lymphocyte aneuploidy in patients with translocations Zotova, N.
2010
20 S1 p. S28-
1 p.
artikel
116 P11 Sperm aneuploidy: When to stop counting? Tempest, H.G.
2010
20 S1 p. S26-
1 p.
artikel
117 P15 Sperm-FISH analysis revealed normal sperm cells for 14;14 homologous robertsonian translocation in a male carrier: A case report Çinar, Ç.
2010
20 S1 p. S27-S28
2 p.
artikel
118 P59 Sperm transcriptome profiling and spermatogenesis decays in normal and oligozoospermic patients Montjean, D.
2010
20 S1 p. S42-
1 p.
artikel
119 P49 Stem cell compliance on consent: rules and reality Wallwork, T.
2010
20 S1 p. S39-
1 p.
artikel
120 P31 Successful preimplantation genetic diagnosis (PGD) test for Hirschsprung disease Burlet, P.
2010
20 S1 p. S33-
1 p.
artikel
121 P25 The importance of genetic counseling of the men enrolled in ICSI program Glinkina, Zh.
2010
20 S1 p. S31-
1 p.
artikel
122 P33 The interest in preimplantation genetic diagnosis in late-onset monogenic diseases carriers Krutílková, V.
2010
20 S1 p. S34-
1 p.
artikel
123 P50 Travel to obtain reprogenetic services: Global and social trends Couture, V.
2010
20 S1 p. S39-
1 p.
artikel
124 P48 When to offer PGD for HLA typing to parents of a sick child: Suggested clinical guidelines Tur-Kaspa, I.
2010
20 S1 p. S39-
1 p.
artikel
125 P53 Widespread chromosome instability in different fetal tissues provides additional biological basis for the low success rate: implications for preimplantation genetic diagnosis Yurov, Y.B.
2010
20 S1 p. S40-
1 p.
artikel
                             125 gevonden resultaten
 
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