1. A model to characterize psychopathological features in adults with Prader‐Willi syndrome. Issue 1 (17th November 2017) Authors: Thuilleaux, Denise; Laurier, Virginie; Copet, Pierre; Tricot, Julie; Demeer, Geneviève; Mourre, Fabien; Tauber, Maithé; Jauregi, Joseba Journal: American journal of medical genetics Issue: Volume 176:Issue 1(2018) Page Start: 41 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bridging the gap: metabolic and endocrine care of patients during transition. Issue 6 (November 2016) Authors: Hokken-Koelega, Anita; van der Lely, Aart-Jan; Hauffa, Berthold; Häusler, Gabriele; Johannsson, Gudmundur; Maghnie, Mohamad; Argente, Jesús; DeSchepper, Jean; Gleeson, Helena; Gregory, John W; Höybye, Charlotte; Keleştimur, Fahrettin; Luger, Anton; Müller, Hermann L; Neggers, Sebastian; Popovic-B... Journal: Endocrine connections Issue: Volume 5:Issue 6(2016) Page Start: R44 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction. Issue 4 (April 2021) Authors: Tauber, Maithé; Hoybye, Charlotte Journal: Lancet Issue: Volume 9:Issue 4(2021) Page Start: 235 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Growth patterns of patients with Noonan syndrome: correlation with age and genotype. Issue 5 (May 2016) Authors: Cessans, Catie; Ehlinger, Virginie; Arnaud, Catherine; Yart, Armelle; Capri, Yline; Barat, Pascal; Cammas, Benoit; Lacombe, Didier; Coutant, Régis; David, Albert; Baron, Sabine; Weill, Jacques; Leheup, Bruno; Nicolino, Marc; Salles, Jean-Pierre; Verloes, Alain; Tauber, Maithé; Cavé, Hélène; Edoua... Journal: European journal of endocrinology Issue: Volume 174:Issue 5(2016) Page Start: 641 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome. Issue 1 (December 2016) Authors: Beauloye, Veronique; Diene, Gwenaelle; Kuppens, Renske; Zech, Francis; Winandy, Coralie; Molinas, Catherine; Faye, Sandy; Kieffer, Isabelle; Beckers, Dominique; Nergårdh, Ricard; Hauffa, Berthold; Derycke, Christine; Delhanty, Patrick; Hokken-Koelega, Anita; Tauber, Maithé Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Letter regarding "Prevalence of growth hormone deficiency in previously GH‐treated young adults with Prader‐Willi syndrome" by Donze et al. (26th June 2019) Authors: Höybye, Charlotte; Tauber, Maithé; Angulo, Moris A.; Eiholzer, Urs; Driscoll, Daniel J.; Cassidy, Suzanne B.; Holland, Antony J. Journal: Clinical endocrinology Issue: Volume 91:Number 4(2019) Page Start: 578 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype. (14th May 2015) Authors: Haine, Elsa; Salles, Jean‐Pierre; Khau Van Kien, Philippe; Conte‐Auriol, Françoise; Gennero, Isabelle; Plancke, Aurélie; Julia, Sophie; Dulac, Yves; Tauber, Maithé; Edouard, Thomas Journal: Journal of bone and mineral research Issue: Volume 30:Number 8(2015:Aug.) Page Start: 1369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. New candidate loci identified by array‐CGH in a cohort of 100 children presenting with syndromic obesity. Issue 8 (29th April 2014) Authors: Vuillaume, Marie‐Laure; Naudion, Sophie; Banneau, Guillaume; Diene, Gwenaelle; Cartault, Audrey; Cailley, Dorothée; Bouron, Julie; Toutain, Jérôme; Bourrouillou, Georges; Vigouroux, Adeline; Bouneau, Laurence; Nacka, Fabienne; Kieffer, Isabelle; Arveiler, Benoit; Knoll‐Gellida, Anja; Babin, Patri... Journal: American journal of medical genetics Issue: Volume 164:Issue 8(2014.) Page Start: 1965 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Noonan syndrome males display Sertoli cell-specific primary testicular insufficiency. Issue 6 (December 2018) Authors: Moniez, Sophie; Pienkowski, Catherine; Lepage, Benoit; Hamdi, Safouane; Daudin, Myriam; Oliver, Isabelle; Jouret, Béatrice; Cartault, Audrey; Diene, Gwenaelle; Verloes, Alain; Cavé, Hélène; Salles, Jean-Pierre; Tauber, Maithé; Yart, Armelle; Edouard, Thomas Journal: European journal of endocrinology Issue: Volume 179:Issue 6(2018) Page Start: 409 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growth. (12th April 2018) Authors: Tajan, Mylène; Pernin-Grandjean, Julie; Beton, Nicolas; Gennero, Isabelle; Capilla, Florence; Neel, Benjamin G; Araki, Toshiyuki; Valet, Philippe; Tauber, Maithé; Salles, Jean-Pierre; Yart, Armelle; Edouard, Thomas Journal: Human molecular genetics Issue: Volume 27:Number 13(2018:Jul. 01) Page Start: 2276 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗