Bony H - Search Results

Year	Number of Results
1993	1
2004	2
2011	2
2015	1
2016	2
2017	1
2019	2
2020	1
2023	1
2024	0

1

Evaluation of catch-up growth in severe pediatric Hashimoto's hypothyroidism.

Vincent A, Bouvattier C, Teinturier C, Rodrigue D, Busiah K, Olivier-Petit I, Bony H, Barat P, Cammas B, Coutant R, Lienhardt A, Linglart A, Lambert AS. Vincent A, et al. Among authors: bony h. Arch Pediatr. 2023 Apr;30(3):142-148. doi: 10.1016/j.arcped.2023.01.001. Epub 2023 Mar 10. Arch Pediatr. 2023. PMID: 36907727

2

[Adolescent obesity: guidelines for the management].

Boudailliez B, Fremaux MP, Jeanne F, Escoffier I, Bony H. Boudailliez B, et al. Among authors: bony h. Arch Pediatr. 2004 Oct;11(10):1274-6. doi: 10.1016/j.arcped.2004.04.012. Arch Pediatr. 2004. PMID: 15475292 French.

3

Should We Assess Pituitary Function in Children After a Mild Traumatic Brain Injury? A Prospective Study.

Briet C, Braun K, Lefranc M, Toussaint P, Boudailliez B, Bony H. Briet C, et al. Among authors: bony h. Front Endocrinol (Lausanne). 2019 Mar 19;10:149. doi: 10.3389/fendo.2019.00149. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 30941101 Free PMC article.

4

Differences in the prescribing of potentially inappropriate medicines in older Australians: comparison of community dwelling and residential aged care residents.

Bony H, Lloyd RA, Hotham ED, Corre LJ, Corlis ME, Loffler HA, Scarlett GK, Tsimbinos JM, Todd IP, Suppiah V. Bony H, et al. Sci Rep. 2020 Jun 23;10(1):10170. doi: 10.1038/s41598-020-66991-x. Sci Rep. 2020. PMID: 32576947 Free PMC article.

5

X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome.

Fiot E, Zenaty D, Boizeau P, Haigneré J, Dos Santos S, Léger J; French Turner Syndrome Study Group. Fiot E, et al. Eur J Endocrinol. 2016 Mar;174(3):281-8. doi: 10.1530/EJE-15-1000. Epub 2015 Dec 14. Eur J Endocrinol. 2016. PMID: 26744895

6

Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B (HNF1B) molecular defects.

Dubois-Laforgue D, Bellanné-Chantelot C, Charles P, Jacquette A, Larger E, Ciangura C, Saint-Martin C, Rastel C, Keren B, Timsit J; Monogenic Diabetes Study Group of the Société Francophone du Diabète (SFD). Dubois-Laforgue D, et al. Diabetes Metab. 2017 Feb;43(1):89-92. doi: 10.1016/j.diabet.2016.10.003. Epub 2016 Nov 10. Diabetes Metab. 2017. PMID: 27838256 No abstract available.

7

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood.

Fiot E, Zénaty D, Boizeau P, Haignere J, Dos Santos S, Léger J; French Turner Syndrome Study Group. Fiot E, et al. Eur J Endocrinol. 2019 Jun 1;180(6):397-406. doi: 10.1530/EJE-18-0878. Eur J Endocrinol. 2019. PMID: 30991358

8

Subtle health impairment and socioeducational attainment in young adult patients with congenital hypothyroidism diagnosed by neonatal screening: a longitudinal population-based cohort study.

Léger J, Ecosse E, Roussey M, Lanoë JL, Larroque B; French Congenital Hypothyroidism Study Group. Léger J, et al. J Clin Endocrinol Metab. 2011 Jun;96(6):1771-82. doi: 10.1210/jc.2010-2315. Epub 2011 Mar 9. J Clin Endocrinol Metab. 2011. PMID: 21389139

9

[Prospective study at 1 week of life of thyroid function in 97 consecutive pre-term newborns under 32 weeks of gestation].

Goissen C, Fontaine C, Braun K, Bony H, Al-Hosri J, Ramadan-Ghostine G, Léké A, Boudailliez B, Tourneux P. Goissen C, et al. Among authors: bony h. Arch Pediatr. 2011 Mar;18(3):253-60. doi: 10.1016/j.arcped.2010.12.018. Epub 2011 Feb 2. Arch Pediatr. 2011. PMID: 21292456 French.

10

[Megaesophagus associated with growth hormone deficiency in a 14-year-old adolescent].

Djeddi D, Seryer K, Delcenserie R, Ribeiro L, Bony H, Lenaerts C, Boudailliez B. Djeddi D, et al. Among authors: bony h. Arch Pediatr. 2004 Aug;11(8):973-4. doi: 10.1016/j.arcped.2004.04.016. Arch Pediatr. 2004. PMID: 15288093 French. No abstract available.

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