Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome

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

Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

por Taback, Shayne P, Van Vliet, Guy
Publicado 2011

Growth Hormone Supplementation and Psychosocial Functioning to Adult Height in Turner Syndrome: A Questionnaire Study of Participants in the Canadian Randomized Trial

por Rovet, Joanne F., Van Vliet, Guy
Publicado 2019

Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia

por Grosse, Scott D., Van Vliet, Guy
Publicado 2020

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

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

European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism

por Léger, Juliane, Olivieri, Antonella, Donaldson, Malcolm, Torresani, Toni, Krude, Heiko, van Vliet, Guy, Polak, Michel, Butler, Gary
Publicado 2014

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

Transcriptomic Signature of Human Embryonic Thyroid Reveals Transition From Differentiation to Functional Maturation

por Dom, Geneviève, Dmitriev, Petr, Lambot, Marie-Alexandra, Van Vliet, Guy, Glinoer, Daniel, Libert, Frédérick, Lefort, Anne, Dumont, Jacques E., Maenhaut, Carine
Publicado 2021

Experience With Store-and-Forward Consultations in Providing Access to Pediatric Endocrine Consultations in Low- and Middle-Income Countries

por von Oettingen, Julia E., Craven, Meghan, Duperval, Regina, Sine St. Surin, Florence, Eveillard, Ronald, Saint Fleur, Rony, Van Vliet, Guy, Chanoine, Jean-Pierre, Louis, Renault
Publicado 2019

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

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

por Simonis, Nicolas, Migeotte, Isabelle, Lambert, Nelle, Perazzolo, Camille, de Silva, Deepthi C, Dimitrov, Boyan, Heinrichs, Claudine, Janssens, Sandra, Kerr, Bronwyn, Mortier, Geert, Van Vliet, Guy, Lepage, Philippe, Casimir, Georges, Abramowicz, Marc, Smits, Guillaume, Vilain, Catheline
Publicado 2013

Meeting Report: Measuring Endocrine-Sensitive Endpoints within the First Years of Life

por Arbuckle, Tye E., Hauser, Russ, Swan, Shanna H., Mao, Catherine S., Longnecker, Matthew P., Main, Katharina M., Whyatt, Robin M., Mendola, Pauline, Legrand, Melissa, Rovet, Joanne, Till, Christine, Wade, Mike, Jarrell, John, Matthews, Stephen, Van Vliet, Guy, Bornehag, Carl-Gustaf, Mieusset, Roger
Publicado 2008

Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

por Brue, Thierry, Quentien, Marie-Hélène, Khetchoumian, Konstantin, Bensa, Marco, Capo-Chichi, José-Mario, Delemer, Brigitte, Balsalobre, Aurelio, Nassif, Christina, Papadimitriou, Dimitris T, Pagnier, Anne, Hasselmann, Caroline, Patry, Lysanne, Schwartzentruber, Jeremy, Souchon, Pierre-François, Takayasu, Shinobu, Enjalbert, Alain, Van Vliet, Guy, Majewski, Jacek, Drouin, Jacques, Samuels, Mark E
Publicado 2014