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New Horizons in Short Children Born Small for Gestational Age
Irène Netchine
,
Manouk van Der Steen
,
Abel López-Bermejo
,
Ekaterina Koledova
,
Mohamad Maghnie
Journal articles
hal-03244959v1
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11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome
Walid Abi Habib
,
Frederic Brioude
,
Salah Azzi
,
Jennifer Salem
,
Cristina das Neves
,
et al.
Journal articles
hal-04026539v1
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Quality of life and mental health of adolescents and adults with Silver-Russell syndrome
Mélissa Burgevin
,
Agnès Lacroix
,
Karine Bourdet
,
Régis Coutant
,
Bruno Donadille
,
et al.
Journal articles
hal-03629998v1
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A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome
Salah Azzi
,
Jennifer Salem
,
Nathalie Thibaud
,
Sandra Chantot-Bastaraud
,
Eli Lieber
,
et al.
Journal articles
hal-01293084v1
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National cohort on imprinting disorders and their metabolic consequences (RaDiCo-IDMet)
Eve Klising-Sireul
,
Radico Team
,
Irène Netchine
,
Agnès Linglart
,
Laure Jamot
4th ID school of the Imprinting disorder network, Mar 2017, Behoust, France
Conference papers
inserm-04059036v1
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Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network
Thomas Eggermann
,
Justin H Davies
,
Maithé Tauber
,
Erica van den Akker
,
Anita Hokken-Koelega
,
et al.
Journal articles
hal-03215322v1
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Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells
A Pham
,
C Selenou
,
E Giabicani
,
V Fontaine
,
S Marteau
,
et al.
Journal articles
hal-03933584v1
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11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome
Walid Abi Habib
,
Frederic Brioude
,
Salah Azzi
,
Jennifer Salem
,
Cristina das Neves
,
et al.
Journal articles
inserm-04032178v1
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Clinical characteristics, puberty pattern and adult or near-adult-height data in a group of patients with growth failure due to severe primary IGF-1 deficiency (GROWPATI study).
Athanasia Stoupa
,
Christine Lorraud
,
Isabelle Flechtner
,
Magali Viaud
,
Graziella Pinto
,
et al.
European Society for Paediatric Endocrinology 58th Annual Meeting, Sep 2019, Vienna, Austria
Conference poster
inserm-04163446v1
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Fetal and post-natal growth are impaired in children with deletions of the GH1 gene: description of a cohort of 14 patients. European Society for Paediatric
E Darvish
,
Marie Legendre
,
Irène Netchine
,
Serge Amselem
,
Frédéric Brioude
Endocrinology 58th Annual Meeting, Sep 2019, Vienna, Austria
Conference poster
inserm-04159171v1
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IGF2: Development, Genetic and Epigenetic Abnormalities
Céline Sélénou
,
Frédéric Brioude
,
Eloïse Giabicani
,
Marie-Laure Sobrier
,
Irène Netchine
Journal articles
hal-03711849v1
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Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth
Aurelie Pham
,
Delphine Mitanchez
,
Anne Forhan
,
Laurence Perin
,
Yves Le Bouc
,
et al.
Journal articles
hal-04026820v1
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Increasing knowledge in IGF1R defects: lessons from 35 new patients
Eloïse Giabicani
,
Marjolaine Willems
,
Virginie Steunou
,
Sandra Chantot-Bastaraud
,
Nathalie Thibaud
,
et al.
Journal articles
hal-02435128v1
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