Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome

por Van Vliet*, Guy, Deladoëy*, Johnny
Publicado 2015

From Bioinactive ACTH to ACTH Antagonist: The Clinical Perspective

por Ghaddhab, Chiraz, Vuissoz, Jean-Marc, Deladoëy, Johnny
Publicado 2017

Continuous Subcutaneous Insulin Infusion in Children: A Pilot Study Validating a Protocol to Avoid Hypoglycemia at Initiation

por Manousaki, Despoina, Deladoëy, Johnny, Geoffroy, Louis, Olivier, Patricia
Publicado 2017

Somatic Mutations Are Not Observed by Exome Sequencing of Lymphocyte DNA from Monozygotic Twins Discordant for Congenital Hypothyroidism due to Thyroid Dysgenesis

por Magne, Fabien, Serpa, Roman, Van Vliet, Guy, Samuels, Mark E., Deladoëy, Johnny
Publicado 2014

Transcriptome, Methylome and Genomic Variations Analysis of Ectopic Thyroid Glands

por Abu-Khudir, Rasha, Paquette, Jean, Lefort, Anne, Libert, Frederick, Chanoine, Jean-Pierre, Vassart, Gilbert, Deladoëy, Johnny
Publicado 2010

Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention

por Larrivée-Vanier, Stéphanie, Magne, Fabien, Hamdoun, Elwaseila, Petryk, Anna, Kibar, Zoha, Van Vliet, Guy, Deladoëy, Johnny
Publicado 2020

OR22-01 NF-κB Pathway Is Implicated in Thyroid Embryogenesis

por Vanier, Stéphanie Larrivée, Magne, Fabien, Jean-Louis, Martineau, Samuels, Mark E, Van Vliet, Guy, Deladoey, Johnny Yvan
Publicado 2020

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis

por Larrivée-Vanier, Stéphanie, Jean-Louis, Martineau, Magne, Fabien, Bui, Helen, Rouleau, Guy A., Spiegelman, Dan, Samuels, Mark E., Kibar, Zoha, Van Vliet, Guy, Deladoëy, Johnny
Publicado 2022