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Salah Azzi

Showing results (1-10 of 27) with videos related to

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Current Opinion in Endocrinology, Diabetes, and Obesity|December 11, 2013
Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulationSalah Azzi, Walid Abi Habib, Irene Netchine
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|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.
Endocrine Development|November 28, 2012
Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromesIrène Netchine, Sylvie Rossignol, Salah Azzi, et al.
Bulletin De L'Academie Nationale De Medecine|December 21, 2010
[Epigenetics, genomic imprinting and developmental disorders]Yves Le Bouc, Sylvie Rossignol, Salah Azzi, et al.
Journal of Medical Genetics|May 9, 2015
A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndromeSalah Azzi, Jennifer Salem, Nathalie Thibaud, et al.
Human Mutation|February 1, 2011
Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromesSalah Azzi, Virginie Steunou, Alexandra Rousseau, et al.
Epigenetics|December 10, 2013
Degree of methylation of ZAC1 (PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohortSalah Azzi, Theo C J Sas, Yves Koudou, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Current Opinion in Endocrinology, Diabetes, and Obesity|December 11, 2013
Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulationSalah Azzi, Walid Abi Habib, Irene Netchine
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|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.
Endocrine Development|November 28, 2012
Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromesIrène Netchine, Sylvie Rossignol, Salah Azzi, et al.
Bulletin De L'Academie Nationale De Medecine|December 21, 2010
[Epigenetics, genomic imprinting and developmental disorders]Yves Le Bouc, Sylvie Rossignol, Salah Azzi, et al.
Journal of Medical Genetics|May 9, 2015
A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndromeSalah Azzi, Jennifer Salem, Nathalie Thibaud, et al.
Human Mutation|February 1, 2011
Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromesSalah Azzi, Virginie Steunou, Alexandra Rousseau, et al.
Epigenetics|December 10, 2013
Degree of methylation of ZAC1 (PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohortSalah Azzi, Theo C J Sas, Yves Koudou, et al.
Pageof 3