Literature DB >> 15539444

ESHRE PGD Consortium 'Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)'.

A R Thornhill1, C E deDie-Smulders, J P Geraedts, J C Harper, G L Harton, S A Lavery, C Moutou, M D Robinson, A G Schmutzler, P N Scriven, K D Sermon, L Wilton.   

Abstract

Among the many educational materials produced by the European Society of Human Reproduction and Embryology (ESHRE) are guidelines. ESHRE guidelines may be developed for many reasons but their intent is always to promote best quality practices in reproductive medicine. In an era in which preimplantation genetic diagnosis (PGD) has become a reality, we must strive to maintain its efficacy and credibility by offering the safest and most effective treatment available. The dominant motivators for the development of current comprehensive guidelines for best PGD practice were (i) the absence of guidelines and/or regulation for PGD in many countries and (ii) the observation that no consensus exists on many of the clinical and technical aspects of PGD. As a consequence, the ESHRE PGD Consortium undertook to draw up guidelines aimed at giving information, support and guidance to potential, fledgling and established PGD centres. The success of a PGD treatment cycle is the result of great attention to detail. We have strived to provide a similar level of detail in this document and hope that it will assist staff in achieving the best clinical outcome for their patients.

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Year:  2004        PMID: 15539444     DOI: 10.1093/humrep/deh579

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  64 in total

1.  Singling out genetic disorders and disease.

Authors:  Martine De Rycke
Journal:  Genome Med       Date:  2010-10-06       Impact factor: 11.117

2.  Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.

Authors:  Maartje C Van Rij; Marjan De Rademaeker; Céline Moutou; Jos C F M Dreesen; Martine De Rycke; Inge Liebaers; Joep P M Geraedts; Christine E M De Die-Smulders; Stéphane Viville
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

3.  Case report: birth of healthy twins after preimplantation genetic diagnosis of propionic acidemia.

Authors:  Trinitat M Alberola; Rosa Bautista-Llácer; Xavier Vendrell; Elena García-Mengual; Merche Pardo; Maria Vila; Carmen Calatayud
Journal:  J Assist Reprod Genet       Date:  2010-12-03       Impact factor: 3.412

Review 4.  Recurrent implantation failure: definition.

Authors:  John Rinehart
Journal:  J Assist Reprod Genet       Date:  2007-08-03       Impact factor: 3.412

5.  Dermatology in the postgenomic era: harnessing human variation for personalized medicine.

Authors:  Anthony E Oro
Journal:  Arch Dermatol       Date:  2008-03

6.  Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.

Authors:  Els Dequeker; Manfred Stuhrmann; Michael A Morris; Teresa Casals; Carlo Castellani; Mireille Claustres; Harry Cuppens; Marie des Georges; Claude Ferec; Milan Macek; Pier-Franco Pignatti; Hans Scheffer; Marianne Schwartz; Michal Witt; Martin Schwarz; Emmanuelle Girodon
Journal:  Eur J Hum Genet       Date:  2008-08-06       Impact factor: 4.246

7.  Quality management system in PGD/PGS: now is the time.

Authors:  Xavier Vendrell; Raquel Carrero; Trinitat Alberola; Rosa Bautista-Llácer; Elena García-Mengual; Reyes Claramunt; Manuel Pérez-Alonso
Journal:  J Assist Reprod Genet       Date:  2009-03-06       Impact factor: 3.412

8.  Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy.

Authors:  Gheona Altarescu; Talia Eldar-Geva; Baruch Brooks; Edith Zylber-Haran; Irit Varshaver; Ehud J Margalioth; Ephrat Levy-Lahad; Paul Renbaum
Journal:  J Assist Reprod Genet       Date:  2009-07       Impact factor: 3.412

9.  New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?

Authors:  Mouna Barat-Houari; Karine Nguyen; Rafaëlle Bernard; Céline Fernandez; Catherine Vovan; Corinne Bareil; Philippe Khau Van Kien; Delphine Thorel; Sylvie Tuffery-Giraud; Francis Vasseur; Shahram Attarian; Jean Pouget; Anne Girardet; Nicolas Lévy; Mireille Claustres
Journal:  Eur J Hum Genet       Date:  2009-11-25       Impact factor: 4.246

10.  Pregnancy and Birth After a Two-Step PGD: Polar Body Diagnosis for Hemophilia A and Array CGH on Trophectoderm Cells for Chromosomal Aberrations.

Authors:  W Würfel; R Suttner; D Shakeshaft; V Mayer; U Schoen; K Sendelbach; M Locher; U Koehler; K Fiedler; G Krüsmann; E Holinski-Feder
Journal:  Geburtshilfe Frauenheilkd       Date:  2013-08       Impact factor: 2.915

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