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                             120 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 7.005 A de-novo factor VIII (F8) mutation creates a challenge for PGD Laurie, AD
 2008
 16 S3 p. s46-
1 p.
 artikel
2 Advanced maternal age Magli, MC
 2008
 16 S3 p. s6-
1 p.
 artikel
3 Aneuploidy preimplantation genetic screening for patients presenting with recurrent pregnancy loss Leigh, DA
 2008
 16 S3 p. s24-
1 p.
 artikel
4 5.002 Aneuploidy rates in blood cells and oocytes Zotova, N
 2008
 16 S3 p. s39-s40
nvt p.
 artikel
5 7.006 Application of PGD for single gene disorders Ismailoglu, B
 2008
 16 S3 p. s46-s47
nvt p.
 artikel
6 Author Index 2008
 16 S3 p. s57-s59
nvt p.
 artikel
7 Beneficial effects of preimplantation genetic diagnosis in patients with repeated implantation failures Beyazyurek, C
 2008
 16 S3 p. s24-
1 p.
 artikel
8 Benefit of preimplantation genetic screening is related to improved laboratory practice Beyer, C
 2008
 16 S3 p. s17-
1 p.
 artikel
9 Beta-thalassaemia with human leukocyte antigen typing for PGD Ozgon, G
 2008
 16 S3 p. s29-
1 p.
 artikel
10 9.001 Blastocyst biopsy: evaluation of data 4 years on Leigh, D
 2008
 16 S3 p. s51-
1 p.
 artikel
11 15.001 Blastocyst biopsy in PGD practice: laboratory considerations Traversa, M
 2008
 16 S3 p. s55-s56
nvt p.
 artikel
12 Blastocysts derived from low- and high-quality embryos are equally potential sources of human embryonic stem cell lines Borges Jr, E
 2008
 16 S3 p. s34-s35
nvt p.
 artikel
13 0.001 Canada's national citizen deliberation on preimplantation genetic diagnosis Nisker, J
 2008
 16 S3 p. s37-
1 p.
 artikel
14 Can high magnification morphological selection of spermatozoa be effective reducing chromosomal risk for patients carrying translocations? Vialard, F
 2008
 16 S3 p. s27-
1 p.
 artikel
15 6.002 Case report: meiotic segregation pattern and preimplantation diagnosis in a Robertsonian translocation (13;21) Fernández, S
 2008
 16 S3 p. s43-
1 p.
 artikel
16 Characterizations of the post-PGD embryo—the laws and policies of four countries van Wagner, E
 2008
 16 S3 p. s32-
1 p.
 artikel
17 Choosing disability and regulating the use of PGD in Australia, the UK and Europe Karpin, I
 2008
 16 S3 p. s12-
1 p.
 artikel
18 Chromosomes from embryonic cells: a cytogenetic analysis Leigh, D
 2008
 16 S3 p. s34-
1 p.
 artikel
19 Clinical outcome of newborn and child development follow-up: IVF versus IVF-PGD cycles Velilla, E
 2008
 16 S3 p. s32-
1 p.
 artikel
20 Clinical outcome of PGD Tur–Kaspa, I
 2008
 16 S3 p. s13-
1 p.
 artikel
21 5.007 Clinical outcome of preimplantation genetic diagnosis for aneuploidy screening in couples with recurrent miscarriage: the Mexican experience Rodriguez, R
 2008
 16 S3 p. s41-s42
nvt p.
 artikel
22 5.006 Clinical pregnancy and live birth rates in women ≥38 years old undergoing IVF with and without PGD Kumbak, B
 2008
 16 S3 p. s41-
1 p.
 artikel
23 Comprehensive microarray genetic analyses on single cells from human embryos Kearns, WG
 2008
 16 S3 p. s28-
1 p.
 artikel
24 Cytogenetic studies of first-trimester spontaneous miscarriage: what relevance to PGD? Hardy, K
 2008
 16 S3 p. s24-s25
nvt p.
 artikel
25 Derivation and characterization of the first abnormal human embryonic stem cell carrying a mutated von Hippel Lindau allele De Vos, J
 2008
 16 S3 p. s34-
1 p.
 artikel
26 11.003 Developmental competence of fresh and frozen–thawed embryos after biopsy of two blastomeres in preimplantation genetic diagnosis Kim, MJ
 2008
 16 S3 p. s54-
1 p.
 artikel
27 5.008 Development of a single cell PCR protocol for the detection of myotonic dystrophy, sex and chromosome 21 copy number Rueda, Bravo L
 2008
 16 S3 p. s42-
1 p.
 artikel
28 Diagnosis of the male factor: an important step towards optimizing pregnancy rates in art Fernández, S
 2008
 16 S3 p. s21-s22
nvt p.
 artikel
29 Dilemmas in male factor: role of aneuploidy analysis in male infertility Gianaroli, L
 2008
 16 S3 p. s9-
1 p.
 artikel
30 DNA fragmentation and aneuploidy rates in the sperm of infertile men before and after density gradient centrifugation Christopikou, D
 2008
 16 S3 p. s19-s20
nvt p.
 artikel
31 Double factor preimplantation genetic diagnosis applied to Angelman Syndrome Obradors, A
 2008
 16 S3 p. s29-
1 p.
 artikel
32 10.001 Elucidation of abnormal fertilization by single cell analysis using FISH and PCR haplotype analysis Yaron, Y
 2008
 16 S3 p. s53-
1 p.
 artikel
33 Embryo cryopreservation in preimplantation genetic diagnosis Boada, M
 2008
 16 S3 p. s5-
1 p.
 artikel
34 11.002 Embryo development and aneuploidy rate of multinucleated embryos from a donor egg IVF programme Fernández, S
 2008
 16 S3 p. s53-s54
nvt p.
 artikel
35 Embryo transfer in biopsied embryo Coroleu, B
 2008
 16 S3 p. s14-
1 p.
 artikel
36 Epigenetics and male infertility Camprubí, C
 2008
 16 S3 p. s13-
1 p.
 artikel
37 6.003 FISH analysis of chromosome segregation in spermatozoa of a t(1;15)(q21;p12) carrier: predictive test for PGD Loginova, J
 2008
 16 S3 p. s43-s44
nvt p.
 artikel
38 French national cohort of children born after PGD Foix-L’Hélias, L
 2008
 16 S3 p. s33-
1 p.
 artikel
39 7.008 Fully informative PGD for cystic fibrosis in a couple with an unknown maternal mutation using microsatellite markers Tazon-Vega, B
 2008
 16 S3 p. s47-
1 p.
 artikel
40 4.002 Genetic aspects of male infertility in assisted reproduction Cinar, C
 2008
 16 S3 p. s38-
1 p.
 artikel
41 Genetics and ‘omics’ Fragkouli,, E
 2008
 16 S3 p. s10-s11
nvt p.
 artikel
42 How to prepare an IVF–PGD cycle Sánchez, M
 2008
 16 S3 p. s6-
1 p.
 artikel
43 Human susceptibility to aneuploidy and the link to infertility Mantzouratou, A
 2008
 16 S3 p. s20-s21
nvt p.
 artikel
44 Impact of sperm chromosomal abnormalities on the chromosomal constitution of preimplantation embryos Rodrigo, L
 2008
 16 S3 p. s22-s23
nvt p.
 artikel
45 5.004 Improvement of chances by preimplantation genetic screening Schmutzler, AG
 2008
 16 S3 p. s40-s41
nvt p.
 artikel
46 Incidence of embryo aneuploidies in two hormonal stimulation protocols Mercader, A
 2008
 16 S3 p. s21-
1 p.
 artikel
47 11.001 Influence of the fertilization procedure on PGD cycle outcome in absence of male factor Esbert, M
 2008
 16 S3 p. s53-
1 p.
 artikel
48 Interchromosomal effects: studies on sperm Tempest, HG
 2008
 16 S3 p. s9-
1 p.
 artikel
49 Is preimplantation genetic screening useful in repeated IVF failure group? Gordts, S
 2008
 16 S3 p. s23-s24
nvt p.
 artikel
50 Male factor Kahraman, S
 2008
 16 S3 p. s7-s8
nvt p.
 artikel
51 Meiotic studies in testicular biopsy Sarrate, Z
 2008
 16 S3 p. s9-s10
nvt p.
 artikel
52 Merging ART and stem cells Cram, D
 2008
 16 S3 p. s14-s15
nvt p.
 artikel
53 7.015 Molecular analysis of spinal muscular atrophy for preimplantation genetic diagnosis Demir, S
 2008
 16 S3 p. s50-
1 p.
 artikel
54 Molecular diagnostics of Down syndrome using quantitative apex microarrays Oitmaa, E
 2008
 16 S3 p. s27-
1 p.
 artikel
55 Monosomy rescue in preimplantation genetic diagnosis of aneuploidy Colls, P
 2008
 16 S3 p. s18-s19
nvt p.
 artikel
56 5.005 Morphological embryo selection: do we work correctly with recurrent miscarriage couples? del Río, F
 2008
 16 S3 p. s41-
1 p.
 artikel
57 Mosaicism and error rates in PGD Munné, S
 2008
 16 S3 p. s5-s6
nvt p.
 artikel
58 Multiple displacement amplification in preimplantation genetic diagnosis: Bernabeu Institute experience Lledó, B
 2008
 16 S3 p. s31-
1 p.
 artikel
59 4.004 New approaches in polar body analysis Klehr-Martinelli, M
 2008
 16 S3 p. s39-
1 p.
 artikel
60 7.007 New approach for haplotyping single gene PGD in couples with de-novo mutations Lledó, B
 2008
 16 S3 p. s47-
1 p.
 artikel
61 7.016 Newborn children after PGD in an affected couple with X-linked adrenoleukodystrophy: case report Cabello, Y
 2008
 16 S3 p. s50-
1 p.
 artikel
62 6.004 Normal birth after PGD by FISH in a couple with a balanced translocation der(15)t(Y;15)(p12;p11.1) associated with severe oligoasthenozoospermia and testicular seminoma in the male partner: case report Hernández, J
 2008
 16 S3 p. s44-
1 p.
 artikel
63 Number of oocytes retrieved and cycle outcome in preimplantation genetic diagnosis (PGD) patients for aneuploidy screening Santana, A
 2008
 16 S3 p. s21-
1 p.
 artikel
64 14.002 Oligohydramnios diagnosis, treatment and consequences in term and post-term pregnancies Brandi, A
 2008
 16 S3 p. s55-
1 p.
 artikel
65 7.001 One-step multiplex PCR for preimplantation genetic diagnosis of Huntington's disease Peciña, A
 2008
 16 S3 p. s45-
1 p.
 artikel
66 Optimizing ovarian stimulation for IVF with PGD Tur–Kaspa, I
 2008
 16 S3 p. s22-s23
nvt p.
 artikel
67 5.001 Origin of autosomal monosomy in early stages of preimplantation embryo development Artukhova, VG
 2008
 16 S3 p. s39-
1 p.
 artikel
68 7.012 Outcome of preimplantation genetic diagnosis for genetic disease Gordts, S
 2008
 16 S3 p. s49-
1 p.
 artikel
69 Outcomes of preimplantation genetic diagnosis cycles for translocation carriers: 8-year experience Beyazyurek, C
 2008
 16 S3 p. s26-
1 p.
 artikel
70 7.018 Outcomes of preimplantation genetic diagnosis for single gene disorders Ercelen, N
 2008
 16 S3 p. s51-
1 p.
 artikel
71 Patients’ experiences of preimplantation genetic diagnosis in Sweden Malmgren, H
 2008
 16 S3 p. s31-s32
nvt p.
 artikel
72 PGD for gene defects in blastocyst stage Kokkali, G
 2008
 16 S3 p. s12-
1 p.
 artikel
73 PGD for recurrent implantation failure Wilton, L
 2008
 16 S3 p. s7-
1 p.
 artikel
74 7.014 PGD is a valuable reproductive option for couples at risk of transmitting autosomal dominant disorders with high clinical variability Gigarel, N
 2008
 16 S3 p. s49-s50
nvt p.
 artikel
75 PGD registries: ESHRE PGD Consortium Harper, J
 2008
 16 S3 p. s12-s13
nvt p.
 artikel
76 PND or PGD: the place of PGD in human medicine Simpson, JL
 2008
 16 S3 p. s5-
1 p.
 artikel
77 Predictive value of embryo morphology on day 3 and day 5 in chromosomal abnormalities of older patients Florensa, M
 2008
 16 S3 p. s27-s28
nvt p.
 artikel
78 11.004 Pregnancy of transgenic-clone goat using mammary gland epithelial cells as donor cells Liu, LJ
 2008
 16 S3 p. s55-
1 p.
 artikel
79 Preimplantation diagnosis for mitochondrial DNA disorders: contribution to understanding mitochondrial DNA segregation during early human embryonic development Steffann, J
 2008
 16 S3 p. s30-
1 p.
 artikel
80 9.003 Preimplantation genetic aneuploidy screening in women older than 42 years Guillén, A
 2008
 16 S3 p. s52-
1 p.
 artikel
81 Preimplantation genetic diagnosis as a source of human embryonic stem cell lines Verlinsky, Y
 2008
 16 S3 p. s15-
1 p.
 artikel
82 7.013 Preimplantation genetic diagnosis for familial hypercholesterolaemia Dhanjal, S
 2008
 16 S3 p. s49-
1 p.
 artikel
83 7.002 Preimplantation genetic diagnosis for hypophosphatasia Sharapova, T
 2008
 16 S3 p. s41-
1 p.
 artikel
84 Preimplantation genetic diagnosis for late-onset diseases Spits, C
 2008
 16 S3 p. s11-
1 p.
 artikel
85 7.004 Preimplantation genetic diagnosis for non-syndromic deafness by polar body and blastomere biopsy Altarescu, G
 2008
 16 S3 p. s46-
1 p.
 artikel
86 Preimplantation genetic diagnosis for reciprocal translocations—the Japanese experience Roche, M
 2008
 16 S3 p. s27-
1 p.
 artikel
87 Preimplantation genetic diagnosis for Zellweger syndrome Barsky, I
 2008
 16 S3 p. s29-s30
nvt p.
 artikel
88 Preimplantation genetic diagnosis in a highly recombinant region: when crossover between the TSC2 gene and linked markers makes accurate diagnosis extremely difficult Renbaum, P
 2008
 16 S3 p. s30-
1 p.
 artikel
89 9.004 Preimplantation genetic diagnosis in a public hospital in Spain: an alternative to prenatal diagnosis Polo, A
 2008
 16 S3 p. s52-s53
nvt p.
 artikel
90 Preimplantation genetic diagnosis in translocations carriers Parriego, M
 2008
 16 S3 p. s26-s27
nvt p.
 artikel
91 7.010 Preimplantation genetic diagnosis of cytochrome c oxidase deficiency Liss, J
 2008
 16 S3 p. s48-
1 p.
 artikel
92 Preimplantation genetic diagnosis of single gene disorders: outcome from over 200 cases Sánchez, J
 2008
 16 S3 p. s30-s31
nvt p.
 artikel
93 0.002 Preimplantation genetic diagnosis on the social determinants of the ‘health’ of embryos Nisker, J
 2008
 16 S3 p. s37-
1 p.
 artikel
94 Preimplantation genetic diagnosis significantly reduces pregnancy loss and increases take-home baby rate in poor prognosis patients Kavrut, M
 2008
 16 S3 p. s23-
1 p.
 artikel
95 6.005 Preimplantation genetic testing outcomes for poor prognosis cryptic translocation carrier couples Ercelen, N
 2008
 16 S3 p. s44-s45
nvt p.
 artikel
96 Preimplantation HLA typing Rechitsky, S
 2008
 16 S3 p. s11-s12
nvt p.
 artikel
97 5.003 Prognosis of preimplantation genetic diagnosis in oncological patients Mollá, M
 2008
 16 S3 p. s40-
1 p.
 artikel
98 Public awareness and regulation of preimplantation genetic diagnosis in Australia van Leeuwen, BH
 2008
 16 S3 p. s32-s33
nvt p.
 artikel
99 Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR: large scale clinical application and future implications Cirigliano, V
 2008
 16 S3 p. s17-s18
nvt p.
 artikel
100 Relationship between sperm aneuploidy and PGD Sánchez, M
 2008
 16 S3 p. s22-
1 p.
 artikel
101 Repeated pregnancy loss Rubio, C
 2008
 16 S3 p. s7-
1 p.
 artikel
102 Reproductive relevance of chromosomal aberrations in male karyotypes Bronet, F
 2008
 16 S3 p. s25-s26
nvt p.
 artikel
103 Results and follow-up: preimplantation genetic diagnosis (PGD) for structural chromosomal aberrations Fischer, J
 2008
 16 S3 p. s8-
1 p.
 artikel
104 Review of blastocyst biopsy outcomes from routine clinical application in over 1100 cycles Traversa, M
 2008
 16 S3 p. s18-
1 p.
 artikel
105 Screening of 24 chromosomes in single cells using microarray comparative genomic hybridization methods: implications for preimplantation genetic diagnosis Steuerwald, NM
 2008
 16 S3 p. s28-s29
nvt p.
 artikel
106 6.001 Sperm FISH analysis of a familial complex chromosome rearrangement: predictive value on the outcome of PGD Loup, V
 2008
 16 S3 p. s43-
1 p.
 artikel
107 Sperm genetic analysis in patient with altered karyotype Blanco, J
 2008
 16 S3 p. s10-
1 p.
 artikel
108 Structural reorganizations and male infertility Anton, E
 2008
 16 S3 p. s8-s9
nvt p.
 artikel
109 7.003 Successful outcomes in 36 cycles of preimplantation genetic diagnosis for 12 kinds of single gene disorders Lee, HS
 2008
 16 S3 p. s45-s46
nvt p.
 artikel
110 7.011 Successful preimplantation genetic diagnosis for Duchenne muscular dystrophy using multiple displacement amplification Ren, Z
 2008
 16 S3 p. s48-s49
nvt p.
 artikel
111 Survival of frozen-thawed blastocysts after preimplantation genetic diagnosis: pregnancy and delivery Hernández, J
 2008
 16 S3 p. s20-
1 p.
 artikel
112 7.009 Term pregnancies after PGD for Portuguese familial amyloidotic polyneuropathy Carvalho, F
 2008
 16 S3 p. s47-s48
nvt p.
 artikel
113 The ethics of using embryos in research Pennings, G
 2008
 16 S3 p. s14-
1 p.
 artikel
114 The European Human Embryonic Stem Cell registry: hESCreg Aran, B
 2008
 16 S3 p. s33-s34
nvt p.
 artikel
115 The meiotic segregation of paracentric inversions: how breakpoint mapping can make the difference Pellestor, F
 2008
 16 S3 p. s25-
1 p.
 artikel
116 4.003 The use of fastFISH for preimplantation genetic screening Al Farawati, SF
 2008
 16 S3 p. s38-s39
nvt p.
 artikel
117 The use of telomeric probes in PGS–selecting categories for which they have the biggest benefit Baborova, P
 2008
 16 S3 p. s32-
1 p.
 artikel
118 4.001 Twin pregnancy after double factor PGD analysis: diagnosis of Von Hippel-Lindau disease and aneuploidy screening Obradors, A
 2008
 16 S3 p. s37-s38
nvt p.
 artikel
119 9.002 Vitrification of biopsied blastocysts using a closed method Lozano, MD
 2008
 16 S3 p. s51-s52
nvt p.
 artikel
120 7.017 Y chromosome microdeletions in Iranian infertile men Mirfakhraie, R
 2008
 16 S3 p. s50-s51
nvt p.
 artikel
                             120 gevonden resultaten
 
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