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Irène Netchine

Showing results (1-10 of 83) with videos related to

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Current Opinion in Pediatrics|July 9, 2016
New clinical and molecular insights into Silver-Russell syndromeEloïse Giabicani, Irène Netchine, Frédéric Brioude
Frontiers in Pediatrics|April 19, 2024
Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylationDiane Darneau, Eloïse Giabicani, Irène Netchine, et al.
Pediatric Endocrinology Reviews : PER|January 3, 2018
The Importance of Collaboration in Advancing Understanding of Rare Disorders: US/EU Joint Initiative on Silver-Russell SyndromeJennifer B Salem, Irène Netchine, Madeleine D Harbison
Best Practice & Research. Clinical Endocrinology & Metabolism|June 10, 2008
Epigenetics in Silver-Russell syndromeSylvie Rossignol, Irène Netchine, Yves Le Bouc, et al.
Epigenetics|May 25, 2010
Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseasesSalah Azzi, Sylvie Rossignol, Yves Le Bouc, et al.
Current Pharmaceutical Design|July 30, 2013
Human imprinting anomalies in fetal and childhood growth disorders: clinical implications and molecular mechanismsSalah Azzi, Fréderic Brioude, Yves Le Bouc, et al.
Nestle Nutrition Institute Workshop Series|March 19, 2013
Epigenetic anomalies in childhood growth disordersIrène Netchine, Sylvie Rossignol, Salah Azzi, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|August 9, 2018
Diagnosis and management of postnatal fetal growth restrictionEloïse Giabicani, Aurélie Pham, Frédéric Brioude, et al.
Archives of Disease in Childhood|February 21, 2015
Prevalence and management of gastrointestinal manifestations in Silver-Russell syndromeCéline Marsaud, Sylvie Rossignol, Patrick Tounian, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain developmentIrène Netchine, Salah Azzi, Yves Le Bouc, et al.
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Current Opinion in Pediatrics|July 9, 2016
New clinical and molecular insights into Silver-Russell syndromeEloïse Giabicani, Irène Netchine, Frédéric Brioude
Frontiers in Pediatrics|April 19, 2024
Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylationDiane Darneau, Eloïse Giabicani, Irène Netchine, et al.
Pediatric Endocrinology Reviews : PER|January 3, 2018
The Importance of Collaboration in Advancing Understanding of Rare Disorders: US/EU Joint Initiative on Silver-Russell SyndromeJennifer B Salem, Irène Netchine, Madeleine D Harbison
Best Practice & Research. Clinical Endocrinology & Metabolism|June 10, 2008
Epigenetics in Silver-Russell syndromeSylvie Rossignol, Irène Netchine, Yves Le Bouc, et al.
Epigenetics|May 25, 2010
Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseasesSalah Azzi, Sylvie Rossignol, Yves Le Bouc, et al.
Current Pharmaceutical Design|July 30, 2013
Human imprinting anomalies in fetal and childhood growth disorders: clinical implications and molecular mechanismsSalah Azzi, Fréderic Brioude, Yves Le Bouc, et al.
Nestle Nutrition Institute Workshop Series|March 19, 2013
Epigenetic anomalies in childhood growth disordersIrène Netchine, Sylvie Rossignol, Salah Azzi, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|August 9, 2018
Diagnosis and management of postnatal fetal growth restrictionEloïse Giabicani, Aurélie Pham, Frédéric Brioude, et al.
Archives of Disease in Childhood|February 21, 2015
Prevalence and management of gastrointestinal manifestations in Silver-Russell syndromeCéline Marsaud, Sylvie Rossignol, Patrick Tounian, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain developmentIrène Netchine, Salah Azzi, Yves Le Bouc, et al.
Pageof 9