Digitale Bibliotheek
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                             98 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Accessibility to the preimplantation genetic screening Mugica, Amaia
2018
36 S1 p. e32
artikel
2 Administration of canestan prior to frozen embryo transfer (FET) of euploid blastocysts may improve clinical outcomeadministration of canestan prior to frozen embryo transfer (FET) of euploid blastocysts may improve clinical outcome Lee, Colin Soon Soo
2018
36 S1 p. e31-e32
artikel
3 Aneuploidy as both a cause and a cure for cancer Depamphilis, Melvin
2018
36 S1 p. e1-e2
artikel
4 Aneuploidy rates are associated with the blasotcyst biopsy technique Whitney, John B.
2018
36 S1 p. e12-e13
artikel
5 Aneuploidy rates of next-generation sequencing in preimplantation genetic diagnosis for balanced translocation carriers Ozer, Leyla
2018
36 S1 p. e39
artikel
6 Aneuploidy status is associated with the length of time that the pronuclei are visible Gould, Rebecca L.
2018
36 S1 p. e26-e27
artikel
7 A novel algorithm for determining the level of mosaicism in preimplantation genetic screening (PGS) with next-generation sequencing (NGS) Castejon Fernandez, Natalia
2018
36 S1 p. e16
artikel
8 Are metabolic disorder carries subject to poor ovarian response in PGD cycles? Baltaci, Volkan
2018
36 S1 p. e32
artikel
9 Aseptic vitrification of blastocysts after trophectoderm (TE) biopsy Wirleitner, Barbara
2018
36 S1 p. e31
artikel
10 A single blastocyst biopsy resulting in a mosaic and euploid profile: a case report Jones, Amy
2018
36 S1 p. e25
artikel
11 Carrier screening. Disease prevention vs cost effectiveness Franasiak, Jason
2018
36 S1 p. e6-e7
artikel
12 Cattle karyomapping to optimise food production and delivery of superior genetics: the first liveborn calves Turner, Kara
2018
36 S1 p. e20
artikel
13 Challenges in interpreting the relevance of segmental mosaicism detected by NGS Grkovic, Steve
2018
36 S1 p. e10-e11
artikel
14 Chromosomal polymorphic variations in females significantly affects clinical outcomes following an in vitro fertilization cycle Cruz, María
2018
36 S1 p. e41
artikel
15 Clinical significance of undiagnosed mosaicism in IVF embryos Perry, Emma
2018
36 S1 p. e14
artikel
16 Combined PGD and PGS by NGS on the same biopsy using a single index Jasper, Melinda
2018
36 S1 p. e16-e17
artikel
17 Combined PGS and PGD for thalassemia Brockman, Matthew
2018
36 S1 p. e8-e9
artikel
18 Common variants associated with mitotic-origin of aneuploidy in human embryos McCoy, Rajiv
2018
36 S1 p. e1
artikel
19 Concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy testing without whole genome amplification Zimmerman, Rebekah
2018
36 S1 p. e6
artikel
20 Custom NGS algorithm for consistent and accurate diagnosis of mosaicism in trophectoderm biopsies Vera-Rodriguez, Maria
2018
36 S1 p. e12
artikel
21 Detection limit of partial insertions and deletions for PGS in terms of NGS by analyzing 242 embryos of couples with balanced translocations Blanca, Helena
2018
36 S1 p. e17
artikel
22 Detection of segmental aneuploidy and mosaicism in preimplantation embryo model by next generation sequencing methodologies Biricik, Anil
2018
36 S1 p. e15
artikel
23 Development of a 5 hour PGS protocol for a day 5 fresh transfer Proptopsaltis, Sandra
2018
36 S1 p. e18-e19
artikel
24 Differences in euploidy rates between the main indications for PGS Tagliani-Ribeiro, Alice
2018
36 S1 p. e40-e41
artikel
25 Does the change of technology from acgh to NGS impact aneuploidy rates? Coprerski, Bruno
2018
36 S1 p. e19
artikel
26 Embryo and paternal factors associated with blastocyst chromosomal mosaicism Lledo Bosch, Belen
2018
36 S1 p. e11-e12
artikel
27 Embryo culture conditions and more De los Santos, María José
2018
36 S1 p. e2
artikel
28 Environmentally induced epigenetic inheritance of sperm epimutations and disease: exposure and disease diagnostics in sperm Skinner, Michael K.
2018
36 S1 p. e6
artikel
29 Euploidy rate of day 7 blastocysts derived from in vitro fertilisation (IVF) Yap, Wei Yuan
2018
36 S1 p. e30
artikel
30 Evaluation of reproductive laboratorial parameters of patients with X chromosome mosaic karyotype Christofolini, Denise
2018
36 S1 p. e27
artikel
31 Evidence to suggest a unique 3D organization of chromosomes within the sperm nucleus: implications for fertilization and early embryonic development Tempest, Helen
2018
36 S1 p. e15-e16
artikel
32 Excellent ongoing pregnancy rate with combined use of PCR for monogenic disease and NGS for aneuploidy screening Lee, Vivian Chi Yan
2018
36 S1 p. e28-e29
artikel
33 From prenatal diagnosis of fetal abnormality to preimplantation genetic diagnosis for skeletal dysplasia using next-generation-sequencing technologies Penacho, Vanessa
2018
36 S1 p. e9-e10
artikel
34 Haplotyping and copy-number profiling of single cells by massive parallel sequencing Masset, Heleen
2018
36 S1 p. e9
artikel
35 Higher than expected reproductive risk for autosomal paracentric inversion carriers Garcia-Guixé, Elena
2018
36 S1 p. e33-e34
artikel
36 How are we perceived by our clinical fellows? Critical review of SART and ESHRE data Xu, Kangpu
2018
36 S1 p. e7
artikel
37 How to choose prenatal testing options for pregnant women after preimplantation genetic screening: genetic counseling challenges Tamura, Chieko
2018
36 S1 p. e14-e15
artikel
38 Impact of application of next generation technologies on the outcome of preimplantation genetic testing for structural rearrangements (PGT-SR) Maithripala, Savanie
2018
36 S1 p. e38-e39
artikel
39 Implementation of the next generation sequencing based preimplantation genetic screening in clinical practice: challenges and benefits Marinova, Elena
2018
36 S1 p. e24-e25
artikel
40 Incidence of chromosomal aneuploidies at embryonic level with comparison based on type of biopsy and maternal age: first indian experience Khajuria, Rajni
2018
36 S1 p. e22
artikel
41 Introduction of a novel, universal NGS-based research Method for preimplantation genetic diagnosis and screening Devogelaere, Benoit
2018
36 S1 p. e21
artikel
42 Investigation of the relationship between embryo ploidy, nuclear mitochondrial mismatch and embryo morphology Jawdat, Razan Saeed
2018
36 S1 p. e25-e26
artikel
43 It's a mosaic result- what do I say now? Leigh, Don
2018
36 S1 p. e2
artikel
44 Laboratory conditions/biopsy strategies Rienzi, Laura
2018
36 S1 p. e3
artikel
45 Maternal age has no influence on mitochondrial DNA (mtDNA) content in chromosomally normal embryos Ogur, Cagri
2018
36 S1 p. e17
artikel
46 Maternal age triggers the formation of chromosomal losses more than gains and/or segmental aneuploidies in preimplantation embryos Ogur, Cagri
2018
36 S1 p. e19-e20
artikel
47 Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants Ghevaria, Harita
2018
36 S1 p. e33
artikel
48 Mitochondrial assessment in day 3 biopsy, a prognostic factor for positive pregnancy Eibes Peteiro, Paula
2018
36 S1 p. e27
artikel
49 Mitochondrial DNA copy number measured by mitoscore is associated to trophectoderm quality De Los Santos, Maria José
2018
36 S1 p. e13
artikel
50 Mitochondrial genome coverage for copy number determination and detection of disease; the impact of WGA Fraser, Michelle
2018
36 S1 p. e25
artikel
51 Mitoscore values are not affected by atmospheric oxygen concentration during embryo culture Mifsud, Amparo
2018
36 S1 p. e14
artikel
52 Morphological blastocyst grade is not a determinant for implantation of euploid embryos Abramov, Rina
2018
36 S1 p. e32-e33
artikel
53 Mosaicism and segmentals in POCs and prenatal diagnosis Cram, David
2018
36 S1 p. e2-e3
artikel
54 New all-in-one protocol for 24-chromosome aneuploidies and monogenic diseases detection by next- generation sequencing: first-year experience González-Reig, Santiago
2018
36 S1 p. e34-e35
artikel
55 Next generation sequencing (NGS) methodology reliable detects segmental aneuploidies with mosaic patterns Fiorentino, Francesco
2018
36 S1 p. e17-e18
artikel
56 Next generation sequencing to detect low grade mosaicism and its effect on the live birth rate Morales, Ruth
2018
36 S1 p. e18
artikel
57 NGS-analysis of chorionic villi of miscarriages and conforming trophectoderm cells of transferred blastocysts Mykytenko, Dmytro
2018
36 S1 p. e22-e23
artikel
58 NGS aneuploidy screening in embryo cells and miscarriage material Glinkina, Zhanna
2018
36 S1 p. e23-e24
artikel
59 Non invasive analysis of the embryonic genome: a critical review of non invasive approaches for PGD and PGS Capalbo, Antonio
2018
36 S1 p. e7-e8
artikel
60 Off the street phasing (OTSP): free no hassle haplotype phasing for molecular PGD applications Altarescu, Gheona
2018
36 S1 p. e34
artikel
61 Ovarian rejuvenation. Is that for real? Herraiz, Sonia
2018
36 S1 p. e5-e6
artikel
62 Patients undergoing preimplantation genetic screening may benefit from artificial oocyte activation Nagorny, Viktor
2018
36 S1 p. e28
artikel
63 PGD-A in advanced maternal age: final results of a day-3 biopsy RCT Rubio, Carmen
2018
36 S1 p. e8
artikel
64 PGD by FISH for a reciprocal translocation-first baby from South India Hari, Ritu
2018
36 S1 p. e37-e38
artikel
65 PGD for de novo mutation: when mosaicism prevents PGD setup and leads to genetic counselling revision Kieffer, Emmanuelle
2018
36 S1 p. e37
artikel
66 PGD for HLA (ESHRE study) Kakourou, Georgia
2018
36 S1 p. e4-e5
artikel
67 PGS diagnosis increases implantation and clinical pregnancy rate Rueda, Ricardo
2018
36 S1 p. e30-e31
artikel
68 Prediction of mendelian disorders risk in assisted reproductive technology patients of middle eastern ethnicity based on detection of germline variants using an expanded preconception carrier genetic screening test Martin, Julio
2018
36 S1 p. e10
artikel
69 Preimplantation genetic diagnosis allows to correct karyotype of a patient and to change risk calculation Musatova, Elizaveta
2018
36 S1 p. e36
artikel
70 Preimplantation genetic diagnosis for achondroplasia by two haplotyping system: short tandem repeats (STRs) and single nucleotide polymorphism (SNP) Shen, Xiaoting
2018
36 S1 p. e36-e37
artikel
71 Preimplantation genetic diagnosis for translocations and interchromosomal effect assessed by array CGH Mateu, Emilia
2018
36 S1 p. e20-e21
artikel
72 Preimplantation genetic diagnosis in families with high risk for spinal muscular atrophy (SMA) Orlova, Anna
2018
36 S1 p. e36
artikel
73 Preimplantation genetic diagnosis of α- and β-double thalassemia combined with aneuploidy screening by next generation sequencing Shen, Xiaoting
2018
36 S1 p. e35-e36
artikel
74 Pre-implantation genetic screening for discrimination of carrier and non-carrier reciprocal translocation with array-CGH and PGD Pingsuthiwong, Sarinee
2018
36 S1 p. e38
artikel
75 Preimplantation genetic testing (PGT) for borderline indications – PGT for cancer Rechistky, Svetlana
2018
36 S1 p. e5
artikel
76 Prenatalis® NIPT: accredited high resolution non-invasive prenatal testing by using massive parallel ultra- deep sequencing Harasim, Thomas
2018
36 S1 p. e40
artikel
77 Re-analysis of aneuploid embryos after TE-biopsy and acgh by NGS on inner cell mass biopsy Hruba, Martina
2018
36 S1 p. e23
artikel
78 Review of the clinical evidence of mtDNA for embryo viability Gianaroli, Luca
2018
36 S1 p. e3-e4
artikel
79 Segmental aneuploidies in PGD cycles for single gene conditions by karyomapping Vesela, Katerina
2018
36 S1 p. e10
artikel
80 Single embryo transfer as an imperative choice for patients over 38 years old in autologous IVF PGS cycles Barash, Oleksii
2018
36 S1 p. e29-e30
artikel
81 Sperm DNA quality correlates with PGD results Zhylkova, Ievgeniia
2018
36 S1 p. e40
artikel
82 Strategies and clinical outcome of preimplantation genetic diagnosis for polycystic kidney disease Berckmoes, Veerle
2018
36 S1 p. e39
artikel
83 Successful preimplantation genetic diagnosis of α-and β-double thalassemia combined with HLA typing by next generation sequencing Shen, Xiaoting
2018
36 S1 p. e35
artikel
84 The effects of laser manipulation on biopsy karyotype in PGS Victor, Andrea
2018
36 S1 p. e29
artikel
85 The extent of chromosomal mosaicism influences the clinical outcome of in vitro fertilization treatments Spinella, Francesca
2018
36 S1 p. e11
artikel
86 The incidence and origin of segmental chromosome abnormalities in human IVF embryos detected during PGD and PGS Hornak, Miroslav
2018
36 S1 p. e13-e14
artikel
87 The likelihood of transferring a euploid embryo after PGD-aneuploidy cycles depends not only on female age but also on the number of oocytes collected Cetinkaya, Murat
2018
36 S1 p. e27-e28
artikel
88 Therapeutic success of HSCT by preimplantation haplotyping, follow-up of 520 cycles Cetinkaya, Murat
2018
36 S1 p. e8
artikel
89 The structure and location gradation of oocyte meiotic spindle and its relationship to embryos' quality and euploidy Gontar, Julia
2018
36 S1 p. e26
artikel
90 The use of low oxygen concentration during embryo culture seems not to affect blastocyst aneuploidy rate Mercader, Amparo
2018
36 S1 p. e30
artikel
91 Transfer of aneuploid embryos following preimplantation genetic diagnosis: the added value of a haplotyping-based genome-wide approach Melotte, Cindy
2018
36 S1 p. e23
artikel
92 Uniparental disomy testing in robertsonian translocation carriers Trková, Marie
2018
36 S1 p. e39-e40
artikel
93 Validating PGS by probing the karyotypic concordance between ICM and TE Viotti, Manuel
2018
36 S1 p. e28
artikel
94 Validation of embryocellecttm with sureplex amplified embryo biopsies Robinson, Christine
2018
36 S1 p. e19
artikel
95 Validation of two whole genome amplification methods for PGD on monogenetic diseases and aneuploidy screening Chow, Judy F.C.
2018
36 S1 p. e21-e22
artikel
96 What about the maternal endometrium. The search for the personalized WOI and microbiota Simon, Carlos
2018
36 S1 p. e4
artikel
97 What next generation sequencing brings to preimplantation genetic testing Unsal, Evrim
2018
36 S1 p. e24
artikel
98 When to transfer? Fresh vs. deferred transfer Kahraman, Semra
2018
36 S1 p. e3
artikel
                             98 gevonden resultaten
 
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