Pinto G - Search Results

1

Identifying patient-related predictors of permanent growth hormone deficiency.

Mericq V, Iñiguez G, Pinto G, Gonzalez-Briceño LG, Samara-Boustani D, Thalassinos C, Flechtner I, Stoupa A, Beltrand J, Besançon A, Brabant S, Ghazal K, Leban M, Touraine P, Cavada G, Polak M, Kariyawasam D. Mericq V, et al. Among authors: pinto g. Front Endocrinol (Lausanne). 2023 Oct 10;14:1270845. doi: 10.3389/fendo.2023.1270845. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37881494 Free PMC article.

2

Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.

Pinto G, Netchine I, Sobrier ML, Brunelle F, Souberbielle JC, Brauner R. Pinto G, et al. J Clin Endocrinol Metab. 1997 Oct;82(10):3450-4. doi: 10.1210/jcem.82.10.4295. J Clin Endocrinol Metab. 1997. PMID: 9329385

3

Idiopathic growth hormone deficiency: presentation, diagnostic and treatment during childhood.

Pinto G, Adan L, Souberbielle JC, Thalassinos C, Brunelle F, Brauner R. Pinto G, et al. Ann Endocrinol (Paris). 1999 Sep;60(3):224-31. Ann Endocrinol (Paris). 1999. PMID: 10520414 Clinical Trial.

4

The use of insulin-like growth factor 1 reference values for the diagnosis of growth hormone deficiency in prepubertal children.

Bussières L, Souberbielle JC, Pinto G, Adan L, Noel M, Brauner R. Bussières L, et al. Among authors: pinto g. Clin Endocrinol (Oxf). 2000 Jun;52(6):735-9. doi: 10.1046/j.1365-2265.2000.00999.x. Clin Endocrinol (Oxf). 2000. PMID: 10848878

5

Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for management.

Pinto G, Tardy V, Trivin C, Thalassinos C, Lortat-Jacob S, Nihoul-Fékété C, Morel Y, Brauner R. Pinto G, et al. J Clin Endocrinol Metab. 2003 Jun;88(6):2624-33. doi: 10.1210/jc.2002-021433. J Clin Endocrinol Metab. 2003. PMID: 12788866

6

Social and psycho-intellectual outcome following radical removal of craniopharyngiomas in childhood. A prospective series.

Pierre-Kahn A, Recassens C, Pinto G, Thalassinos C, Chokron S, Soubervielle JC, Brauner R, Zerah M, Sainte Rose C. Pierre-Kahn A, et al. Among authors: pinto g. Childs Nerv Syst. 2005 Aug;21(8-9):817-24. doi: 10.1007/s00381-005-1205-6. Epub 2005 Jul 28. Childs Nerv Syst. 2005. PMID: 16049724 Clinical Trial.

7

Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Bachelot A, Plu-Bureau G, Thibaud E, Laborde K, Pinto G, Samara D, Nihoul-Fékété C, Kuttenn F, Polak M, Touraine P. Bachelot A, et al. Among authors: pinto g. Horm Res. 2007;67(6):268-76. doi: 10.1159/000098017. Epub 2006 Dec 14. Horm Res. 2007. PMID: 17170529

8

GH deficiency with central precocious puberty: a new rare disorder associated with a developmental defect of the hypothalamic-pituitary area.

Ladjouze A, Soskin S, Garel C, Jullien M, Naud-Saudreau C, Pinto G, Czernichow P, Léger J. Ladjouze A, et al. Among authors: pinto g. Eur J Endocrinol. 2007 Apr;156(4):463-9. doi: 10.1530/EJE-06-0688. Eur J Endocrinol. 2007. PMID: 17389461

9

[The Prader-Willi syndrome].

Diene G, Postel-Vinay A, Pinto G, Polak M, Tauber M. Diene G, et al. Among authors: pinto g. Ann Endocrinol (Paris). 2007 Jun;68(2-3):129-37. doi: 10.1016/j.ando.2007.03.002. Epub 2007 May 17. Ann Endocrinol (Paris). 2007. PMID: 17499572 Review. French.

10

Pamidronate treatment of children with moderate-to-severe osteogenesis imperfecta: a note of caution.

Alharbi M, Pinto G, Finidori G, Souberbielle JC, Guillou F, Gaubicher S, Le Merrer M, Polak M. Alharbi M, et al. Among authors: pinto g. Horm Res. 2009 Jan;71(1):38-44. doi: 10.1159/000173740. Epub 2008 Nov 27. Horm Res. 2009. PMID: 19039235

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