Lista de obras - Nelly Frydman - Dominio Público Uruguay

Adequate ovarian follicular status does not prevent the decrease in pregnancy rates associated with high sperm DNA fragmentation

artículo científico publicado en 2007

Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination

artículo científico publicado en 2002

Data from artificial models of mitochondrial DNA disorders are not always applicable to humans

artículo científico publicado en 2014

Dexamethasone induces germ cell apoptosis in the human fetal ovary

artículo científico publicado en 2012

Dynamics of serum anti-Müllerian hormone levels during the luteal phase of controlled ovarian hyperstimulation

artículo científico publicado en 2004

First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency

artículo científico publicado en 2000

Genome Editing and Dialogic Responsibility: "What's in a Name?".

artículo científico publicado en 2015

Human foetal ovary shares meiotic preventing factors with the developing testis

artículo científico publicado en 2017

Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophy

artículo científico publicado en 2005

In vitro fertilization and embryo transfer in seminatural cycles for patients with ovarian aging

artículo científico publicado en 2005

Levels of follicular G-CSF and interleukin-15 appear as noninvasive biomarkers of subsequent successful birth in modified natural in vitro fertilization/intracytoplasmic sperm injection cycles.

artículo científico publicado en 2010

Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.

artículo científico publicado en 2013

Optimal reproductive competence of oocytes retrieved through follicular flushing in minimal stimulation IVF.

artículo científico publicado en 2008

Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.

artículo científico publicado en 2011

Preimplantation genetic diagnosis: state of the art.

artículo científico publicado en 2009

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system

artículo científico publicado en 2011

Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.

artículo científico publicado en 2003

Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR

artículo científico publicado en 2004

The 3D vascular status of the follicle after HCG administration is qualitatively rather than quantitatively associated with its reproductive competence

artículo científico publicado en 2006

[Preimplantation genetic diagnosis: update of the Parisian group]

artículo científico publicado en 2002

[Prenatal and preimplantation genetic diagnosis: decision tree, new practices?].

artículo científico publicado en 2005

[Ten years' experience of preimplantation genetic diagnosis in Paris: remaining obstacles and potential solutions]

artículo científico publicado en 2011

[The French experience with preimplantation genetic diagnosis (PGD)]

artículo científico publicado en 2003

Lista de obras de Nelly Frydman

Adequate ovarian follicular status does not prevent the decrease in pregnancy rates associated with high sperm DNA fragmentation

Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination

Data from artificial models of mitochondrial DNA disorders are not always applicable to humans

Dexamethasone induces germ cell apoptosis in the human fetal ovary

Dynamics of serum anti-Müllerian hormone levels during the luteal phase of controlled ovarian hyperstimulation

First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency

Genome Editing and Dialogic Responsibility: "What's in a Name?".

Human foetal ovary shares meiotic preventing factors with the developing testis

Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophy

In vitro fertilization and embryo transfer in seminatural cycles for patients with ovarian aging

Levels of follicular G-CSF and interleukin-15 appear as noninvasive biomarkers of subsequent successful birth in modified natural in vitro fertilization/intracytoplasmic sperm injection cycles.

Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.

Optimal reproductive competence of oocytes retrieved through follicular flushing in minimal stimulation IVF.

Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.

Preimplantation genetic diagnosis: state of the art.

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system

Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.

Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR

The 3D vascular status of the follicle after HCG administration is qualitatively rather than quantitatively associated with its reproductive competence

[Preimplantation genetic diagnosis: update of the Parisian group]

[Prenatal and preimplantation genetic diagnosis: decision tree, new practices?].

[Ten years' experience of preimplantation genetic diagnosis in Paris: remaining obstacles and potential solutions]

[The French experience with preimplantation genetic diagnosis (PGD)]