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Page 1
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population.
El Allali Y, Hermetet C, Bacchetta J, Amouroux C, Rothenbuhler A, Porquet-Bordes V, Champigny MA, Baron S, Barat P, Bony-Trifunovic H, Bourdet K, Busiah K, Cartigny-Maciejewski M, Compain F, Coutant R, Amsellem-Jager J, De Kerdanet M, Magontier N, Mignot B, Richard O, Rossignol S, Soskin S, Berot A, Naud-Saudreau C, Salles JP, Linglart A, Edouard T, Lienhardt-Roussie A. El Allali Y, et al. Among authors: amouroux c. Eur J Endocrinol. 2021 Feb;184(2):347-355. doi: 10.1530/EJE-20-1119. Eur J Endocrinol. 2021. PMID: 33361469
Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.
Boros E, Ertl DA, Berkenou J, Audrain C, Lecoq AL, Kamenicky P, Briot K, Amouroux C, Zhukouskaya V, Gueorguieva I, Mignot B, Girerd B, Porquet Bordes V, Salles JP, Edouard T, Coutant R, Bacchetta J, Linglart A, Rothenbuhler A. Boros E, et al. Among authors: amouroux c. Eur J Endocrinol. 2023 Oct 17;189(4):469-475. doi: 10.1093/ejendo/lvad144. Eur J Endocrinol. 2023. PMID: 37831782
ENPP1 deficiency: almost ready for prime time!
Bacchetta J, Amouroux C. Bacchetta J, et al. Among authors: amouroux c. Arch Pediatr. 2024 Sep;31(4S1):4S1-4S2. doi: 10.1016/S0929-693X(24)00150-7. Arch Pediatr. 2024. PMID: 39343467 No abstract available.
Endocrine management of transgender adolescents: Expert consensus of the french society of pediatric endocrinology and diabetology working group.
Brezin F, Busiah K, Leroy C, Fiot E, Bensignor C, Amouroux C, Caquard M, Cartault A, Castets S, Delcour C, Devernay M, Feigerlova E, Hoarau M, Lebon-Labich B, Lambert AS, Rouleau S, Trouvin MA, Vautier V, Martinerie L. Brezin F, et al. Among authors: amouroux c. Arch Pediatr. 2024 Nov 16:S0929-693X(24)00176-3. doi: 10.1016/j.arcped.2024.08.003. Online ahead of print. Arch Pediatr. 2024. PMID: 39551654 Free article.
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in France.
Bonnet E, Winter M, Mallet D, Plotton I, Bouvattier C, Cartigny M, Martinerie L, Polak M, Bachelot A, Huet F, Baron S, Houang M, Soskin S, Lienhardt A, Bertherat J, Amouroux C, Bouty A, Duranteau L, Besson R, El Ghoneimi A, Samara-Boustani D, Becmeur F, Kalfa N, Paris F, Medjkane F, Brac de la Perrière A, Bretones P, Lejeune H, Nicolino M, Mouriquand P, Gorduza DB, Gay CL. Bonnet E, et al. Among authors: amouroux c. Endocr Connect. 2023 Feb 14;12(3):e220227. doi: 10.1530/EC-22-0227. Print 2023 Mar 1. Endocr Connect. 2023. PMID: 36606580 Free PMC article.
Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephaly.
Sabbagh Q, Tharreau M, Cenni C, Sanchez E, Ruiz-Pallares N, Alkar F, Amouroux C, David S, Prodhomme O, Leboucq N, Meunier I, Bessis D, Theron A, Barat-Houari M, Willems M. Sabbagh Q, et al. Among authors: amouroux c. Eur J Med Genet. 2023 May;66(5):104733. doi: 10.1016/j.ejmg.2023.104733. Epub 2023 Feb 25. Eur J Med Genet. 2023. PMID: 36842471
40 results