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Page 1
The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing.
Levaillant L, Bouhours-Nouet N, Illouz F, Amsellem Jager J, Bachelot A, Barat P, Baron S, Bensignor C, Brac De La Perriere A, Braik Djellas Y, Caillot M, Caldagues E, Campas MN, Caquard M, Cartault A, Cheignon J, Decrequy A, Delemer B, Dieckmann K, Donzeau A, Doye E, Fradin M, Gaudillière M, Gatelais F, Gorce M, Hazart I, Houcinat N, Houdon L, Ister-Salome M, Jozwiak L, Jeannoel P, Labarthe F, Lacombe D, Lambert AS, Lefevre C, Leheup B, Leroy C, Maisonneuve B, Marchand I, Marquant E, Muszlak M, Pantalone L, Pochelu S, Quelin C, Radet C, Renoult-Pierre P, Reynaud R, Rouleau S, Teinturier C, Thevenon J, Turlotte C, Valle A, Vierge M, Villanueva C, Ziegler A, Dieu X, Bouzamondo N, Rodien P, Prunier-Mirebeau D, Coutant R. Levaillant L, et al. Among authors: bouzamondo n. J Clin Endocrinol Metab. 2023 Aug 18;108(9):e779-e788. doi: 10.1210/clinem/dgad119. J Clin Endocrinol Metab. 2023. PMID: 36884306 Free PMC article.
Congenital hypothyroidism and hearing loss without inner ear malformation: Think TPO.
Ziegler A, Denommé-Pichon AS, Boucher S, Bouzamondo N, Colin E, Dieu X, Jean Yves T, Bouhours N, Rouleau S, Coutant R, Rodien P, Prunier D, Bonneau D. Ziegler A, et al. Among authors: bouzamondo n. Clin Genet. 2021 Apr;99(4):604-606. doi: 10.1111/cge.13902. Epub 2020 Dec 27. Clin Genet. 2021. PMID: 33368191 No abstract available.
Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity.
Dieu X, Bouzamondo N, Briet C, Illouz F, Moal V, Boux de Casson F, Bouhours-Nouet N, Reynier P, Coutant R, Rodien P, Mirebeau-Prunier D. Dieu X, et al. Among authors: bouzamondo n. J Clin Med. 2020 Jul 3;9(7):2105. doi: 10.3390/jcm9072105. J Clin Med. 2020. PMID: 32635414 Free PMC article.
Apparent resistance to thyroid hormones: From biological interference to genetics.
Dieu X, Sueur G, Moal V, Boux de Casson F, Bouzamondo N, Bouhours N, Briet C, Illouz F, Reynier P, Coutant R, Rodien P, Mirebeau-Prunier D. Dieu X, et al. Among authors: bouzamondo n. Ann Endocrinol (Paris). 2019 Nov;80(5-6):280-285. doi: 10.1016/j.ando.2019.06.005. Epub 2019 Jul 26. Ann Endocrinol (Paris). 2019. PMID: 31590893
Metabolomics signatures of a subset of RET variants according to their oncogenic risk level.
Veyrat-Durebex C, Bouzamondo N, Le Mao M, Chao de la Barca JM, Bris C, Dieu X, Simard G, Gadras C, Tessier L, Drui D, Borson-Chazot F, Barlier A, Reynier P, Prunier-Mirebeau D. Veyrat-Durebex C, et al. Among authors: bouzamondo n. Endocr Relat Cancer. 2019 Mar 1;26(3):379-389. doi: 10.1530/ERC-18-0314. Endocr Relat Cancer. 2019. PMID: 30653460
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
Lebeault M, Pinson S, Guillaud-Bataille M, Gimenez-Roqueplo AP, Carrie A, Barbu V, Pigny P, Bezieau S, Rey JM, Delvincourt C, Giraud S, Veyrat-Durebex C, Saulnier P, Bouzamondo N, Chabbert M, Blin J, Mohamed A, Romanet P, Borson-Chazot F, Rohmer V, Barlier A, Mirebeau-Prunier D. Lebeault M, et al. Among authors: bouzamondo n. Thyroid. 2017 Dec;27(12):1511-1522. doi: 10.1089/thy.2016.0399. Epub 2017 Nov 3. Thyroid. 2017. PMID: 28946813