Personnier C - Search Results

Year	Number of Results
2011	1
2014	1
2015	1
2016	3
2017	1
2019	2
2025	0

1

Erratum à l'article « Un programme d'éducation thérapeutique centré sur la transition des patients, avec endocrinopathie chronique, entre les services d'endocrinologie pédiatrique et adulte » [Presse Med. 45 (5) (2016) e119-e129].

Malivoir S, Courtillot C, Bachelot A, Chakhtoura Z, Téjédor I, Touraine P; Les référents pédiatres. Malivoir S, et al. Presse Med. 2016 Jul-Aug;45(7-8P1):718. doi: 10.1016/j.lpm.2016.06.012. Epub 2016 Jul 27. Presse Med. 2016. PMID: 27476021 French. No abstract available.

2

11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.

Abi Habib W, Brioude F, Azzi S, Salem J, Das Neves C, Personnier C, Chantot-Bastaraud S, Keren B, Le Bouc Y, Harbison MD, Netchine I. Abi Habib W, et al. Among authors: personnier c. Hum Mutat. 2017 Jan;38(1):105-111. doi: 10.1002/humu.23131. Epub 2016 Oct 26. Hum Mutat. 2017. PMID: 27701793

3

Clinical features and treatment of pediatric somatotropinoma: case study of an aggressive tumor due to a new AIP mutation and extensive literature review.

Personnier C, Cazabat L, Bertherat J, Gaillard S, Souberbielle JC, Habrand JL, Dufour C, Clauser E, SainteRose C, Polak M. Personnier C, et al. Horm Res Paediatr. 2011;75(6):392-402. doi: 10.1159/000327831. Epub 2011 May 6. Horm Res Paediatr. 2011. PMID: 21546764 Review.

4

Prevalence of pituitary dysfunction after severe traumatic brain injury in children and adolescents: a large prospective study.

Personnier C, Crosnier H, Meyer P, Chevignard M, Flechtner I, Boddaert N, Breton S, Mignot C, Dassa Y, Souberbielle JC, Piketty M, Laborde K, Jais JP, Viaud M, Puget S, Sainte-Rose C, Polak M. Personnier C, et al. J Clin Endocrinol Metab. 2014 Jun;99(6):2052-60. doi: 10.1210/jc.2013-4129. Epub 2014 Mar 17. J Clin Endocrinol Metab. 2014. PMID: 24635130

5

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

6

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

7

Pituitary deficiency and precocious puberty after childhood severe traumatic brain injury: a long-term follow-up prospective study.

Dassa Y, Crosnier H, Chevignard M, Viaud M, Personnier C, Flechtner I, Meyer P, Puget S, Boddaert N, Breton S, Polak M. Dassa Y, et al. Among authors: personnier c. Eur J Endocrinol. 2019 May 1;180(5):281-290. doi: 10.1530/EJE-19-0034. Eur J Endocrinol. 2019. PMID: 30884465

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