Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome

Por Van Vliet*, Guy, Deladoëy*, Johnny
Publicado no F1000Prime Rep (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 em 2011

Variation by Ethnicity in the Prevalence of Congenital Hypothyroidism Due to Thyroid Dysgenesis

Por Stoppa-Vaucher, Sophie, Van Vliet, Guy, Deladoëy, Johnny
Publicado em 2011

Quality of referral of short children to the paediatric endocrinologist and impact of a fax communication system

Por Chiniara, Lyne, Perry, Rebecca J, Van Vliet, Guy, Huot, Céline, Deal, Cheri
Publicado em 2013

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 no Horm Res Paediatr (2014)

Role for Tissue-Dependent Methylation Differences in the Expression of FOXE1 in Nontumoral Thyroid Glands

Por Abu-Khudir, Rasha, Magne, Fabien, Chanoine, Jean-Pierre, Deal, Cheri, Van Vliet, Guy, Deladoëy, Johnny
Publicado no J Clin Endocrinol Metab (2014)

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 em 2014

Conserved Telomere Length in Human Ectopic Thyroids: An Argument Against Premature Differentiation Causing Arrested Migration

Por Larrivée-Vanier, Stéphanie, Magne, Fabien, Patey, Natalie, Chanoine, Jean-Pierre, Vuissoz, Jean-Marc, Van Vliet, Guy, Deladoëy, Johnny
Publicado no Thyroid (2015)

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 em 2013

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Por Pulichino, Anne-Marie, Vallette-Kasic, Sophie, Couture, Catherine, Gauthier, Yves, Brue, Thierry, David, Michel, Malpuech, Georges, Deal, Cheri, Van Vliet, Guy, De Vroede, Monique, Riepe, Felix G., Partsch, Carl-Joachim, Sippell, Wolfgang G., Berberoglu, Merih, Atasay, Begüm, Drouin, Jacques
Publicado em 2003

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

Por Tornberg, Janne, Sykiotis, Gerasimos P., Keefe, Kimberly, Plummer, Lacey, Hoang, Xuan, Hall, Janet E., Quinton, Richard, Seminara, Stephanie B., Hughes, Virginia, Van Vliet, Guy, Van Uum, Stan, Crowley, William F., Habuchi, Hiroko, Kimata, Koji, Pitteloud, Nelly, Bülow, Hannes E.
Publicado em 2011

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 em 2008

Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Por Raivio, Taneli, Sidis, Yisrael, Plummer, Lacey, Chen, Huaibin, Ma, Jinghong, Mukherjee, Abir, Jacobson-Dickman, Elka, Quinton, Richard, Van Vliet, Guy, Lavoie, Helene, Hughes, Virginia A., Dwyer, Andrew, Hayes, Frances J., Xu, Shuyun, Sparks, Susan, Kaiser, Ursula B., Mohammadi, Moosa, Pitteloud, Nelly
Publicado em 2009

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Por Raivio, Taneli, Sidis, Yisrael, Plummer, Lacey, Chen, Huaibin, Ma, Jinghong, Mukherjee, Abir, Jacobson-Dickman, Elka, Quinton, Richard, Van Vliet, Guy, Lavoie, Helene, Hughes, Virginia A., Dwyer, Andrew, Hayes, Frances J., Xu, Shuyun, Sparks, Susan, Kaiser, Ursula B., Mohammadi, Moosa, Pitteloud, Nelly
Publicado no Mol Endocrinol (2009)

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 no BMC Med Genet (2014)

Mutations in Prokineticin 2 and Prokineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

Por Cole, Lindsay W., Sidis, Yisrael, Zhang, ChengKang, Quinton, Richard, Plummer, Lacey, Pignatelli, Duarte, Hughes, Virginia A., Dwyer, Andrew A., Raivio, Taneli, Hayes, Frances J., Seminara, Stephanie B., Huot, Celine, Alos, Nathalie, Speiser, Phyllis, Takeshita, Akira, VanVliet, Guy, Pearce, Simon, Crowley, William F., Zhou, Qun-Yong, Pitteloud, Nelly
Publicado em 2008

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism

Por Miraoui, Hichem, Dwyer, Andrew A., Sykiotis, Gerasimos P., Plummer, Lacey, Chung, Wilson, Feng, Bihua, Beenken, Andrew, Clarke, Jeff, Pers, Tune H., Dworzynski, Piotr, Keefe, Kimberley, Niedziela, Marek, Raivio, Taneli, Crowley, William F., Seminara, Stephanie B., Quinton, Richard, Hughes, Virginia A., Kumanov, Philip, Young, Jacques, Yialamas, Maria A., Hall, Janet E., Van Vliet, Guy, Chanoine, Jean-Pierre, Rubenstein, John, Mohammadi, Moosa, Tsai, Pei-San, Sidis, Yisrael, Lage, Kasper, Pitteloud, Nelly
Publicado em 2013