IGF2: Development, Genetic and Epigenetic Abnormalities von Sélénou, Céline, Brioude, Frédéric, Giabicani, Eloïse, Sobrier, Marie-Laure, Netchine, Irène

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Models for predicting the adult height and age at first menstruation of girls with idiopathic central precocious puberty von Giabicani, Eloïse, Lemaire, Pierre, Brauner, Raja

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Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome von Giabicani, Éloïse, Boulé, Michèle, Aubertin, Guillaume, Galliani, Eva, Brioude, Frédéric, Dubern, Béatrice, Netchine, Irène

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Overgrowth syndromes — clinical and molecular aspects and tumour risk von Brioude, Frédéric, Toutain, Annick, Giabicani, Eloise, Cottereau, Edouard, Cormier-Daire, Valérie, Netchine, Irene

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Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome von Geoffron, Sophie, Abi Habib, Walid, Chantot-Bastaraud, Sandra, Dubern, Béatrice, Steunou, Virginie, Azzi, Salah, Afenjar, Alexandra, Busa, Tiffanny, Pinheiro Canton, Ana, Chalouhi, Christel, Dufourg, Marie-Noëlle, Esteva, Blandine, Fradin, Mélanie, Geneviève, David, Heide, Solveig, Isidor, Bertrand, Linglart, Agnès, Morice Picard, Fanny, Naud-Saudreau, Catherine, Oliver Petit, Isabelle, Philip, Nicole, Pienkowski, Catherine, Rio, Marlène, Rossignol, Sylvie, Tauber, Maithé, Thevenon, Julien, Vu-Hong, Thuy-Ai, Harbison, Madeleine D, Salem, Jennifer, Brioude, Frédéric, Netchine, Irène, Giabicani, Eloïse

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Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants von Pham, Aurélie, Sobrier, Marie-Laure, Giabicani, Eloïse, Le Jules Fernandes, Marilyne, Mitanchez, Delphine, Brioude, Fréderic, Netchine, Irène

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Diagnosis and management of postnatal fetal growth restriction von Giabicani, Eloïse, Pham, Aurélie, Brioude, Frédéric, Mitanchez, Delphine, Netchine, Irène

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Dental pulp stem cells as a promising model to study imprinting diseases von Giabicani, Eloïse, Pham, Aurélie, Sélénou, Céline, Sobrier, Marie-Laure, Andrique, Caroline, Lesieur, Julie, Linglart, Agnès, Poliard, Anne, Chaussain, Catherine, Netchine, Irène

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Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylation von Darneau, Diane, Giabicani, Eloïse, Netchine, Irène, Pham, Aurélie

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Imprinted disorders and growth von Giabicani, Éloïse, Brioude, Frédéric, Le Bouc, Yves, Netchine, Irène

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Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders von Abi Habib, Walid, Brioude, Frédéric, Azzi, Salah, Rossignol, Sylvie, Linglart, Agnès, Sobrier, Marie-Laure, Giabicani, Éloïse, Steunou, Virginie, Harbison, Madeleine D, Le Bouc, Yves, Netchine, Irène

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Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment von Lokulo‐Sodipe, Oluwakemi, Giabicani, Eloïse, Canton, Ana P. M., Ferrand, Nawfel, Child, Jenny, Wakeling, Emma L., Binder, Gerhard, Netchine, Irène, Mackay, Deborah J. G., Inskip, Hazel M., Byrne, Christopher D., Temple, I. Karen, Davies, Justin H.

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Demographic Characteristics, Risk Factors, and Presenting Features of Children with Symptomatic Nutritional Rickets: A French Series von Flot, Claire, Porquet-Bordes, Valérie, Bacchetta, Justine, Rothenbuhler, Anya, Lienhardt-Roussie, Anne, Giabicani, Eloise, Gueorguieva, Iva, Storey, Caroline, Linglart, Agnès, Salles, Jean-Pierre, Edouard, Thomas

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Roles of Type 1 Insulin-Like Growth Factor (IGF) Receptor and IGF-II in Growth Regulation: Evidence From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion von Giabicani, Eloïse, Chantot-Bastaraud, Sandra, Bonnard, Adeline, Rachid, Myriam, Whalen, Sandra, Netchine, Irène, Brioude, Frédéric

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New clinical and molecular insights into Silver-Russell syndrome von Giabicani, Eloïse, Netchine, Irène, Brioude, Frédéric

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Imprinting disorders von Eggermann, Thomas, Monk, David, de Nanclares, Guiomar Perez, Kagami, Masayo, Giabicani, Eloïse, Riccio, Andrea, Tümer, Zeynep, Kalish, Jennifer M., Tauber, Maithé, Duis, Jessica, Weksberg, Rosanna, Maher, Eamonn R., Begemann, Matthias, Elbracht, Miriam

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Presentation of 493 consecutive girls with idiopathic central precocious puberty: a single-center study von Giabicani, Eloïse, Allali, Slimane, Durand, Adélaïde, Sommet, Julie, Couto-Silva, Ana-Claudia, Brauner, Raja

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Diagnosis and management of Silver–Russell syndrome: first international consensus statement von Wakeling, Emma L., Brioude, Frédéric, Lokulo-Sodipe, Oluwakemi, O'Connell, Susan M., Salem, Jennifer, Bliek, Jet, Canton, Ana P. M., Chrzanowska, Krystyna H., Davies, Justin H., Dias, Renuka P., Dubern, Béatrice, Elbracht, Miriam, Giabicani, Eloise, Grimberg, Adda, Grønskov, Karen, Hokken-Koelega, Anita C. S., Jorge, Alexander A., Kagami, Masayo, Linglart, Agnes, Maghnie, Mohamad, Mohnike, Klaus, Monk, David, Moore, Gudrun E., Murray, Philip G., Ogata, Tsutomu, Petit, Isabelle Oliver, Russo, Silvia, Said, Edith, Toumba, Meropi, Tümer, Zeynep, Binder, Gerhard, Eggermann, Thomas, Harbison, Madeleine D., Temple, I. Karen, Mackay, Deborah J. G., Netchine, Irène

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Premature pubarche before one year of age: distinguishing between mini-puberty variants and precocious puberty von Bourayou, Rafik, Giabicani, Eloïse, Pouillot, Monique, Brailly-Tabard, Sylvie, Brauner, Raja

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Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis von Mackay, Deborah J G, Gazdagh, Gabriella, Monk, David, Brioude, Frederic, Giabicani, Eloise, Krzyzewska, Izabela M, Kalish, Jennifer M, Maas, Saskia M, Kagami, Masayo, Beygo, Jasmin, Kahre, Tiina, Tenorio-Castano, Jair, Ambrozaitytė, Laima, Burnytė, Birutė, Cerrato, Flavia, Davies, Justin H, Ferrero, Giovanni Battista, Fjodorova, Olga, Manero-Azua, Africa, Pereda, Arrate, Russo, Silvia, Tannorella, Pierpaola, Temple, Karen I, Õunap, Katrin, Riccio, Andrea, de Nanclares, Guiomar Perez, Maher, Eamonn R, Lapunzina, Pablo, Netchine, Irène, Eggermann, Thomas, Bliek, Jet, Tümer, Zeynep

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