Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1992 3
1993 1
1994 1
1995 2
1996 1
1997 1
1998 1
1999 1
2001 2
2002 1
2003 1
2004 1
2006 3
2007 3
2008 1
2009 1
2010 2
2011 3
2012 2
2013 2
2014 4
2015 6
2016 5
2017 7
2018 10
2019 4
2020 7
2021 4
2022 5
2023 8
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

85 results

Results by year

Filters applied: . Clear all
Page 1
Arterial Spin Labeling and Central Precocious Puberty.
Denis J, Dangouloff-Ros V, Pinto G, Flechtner I, Piketty M, Samara D, Levy R, Grévent D, Millischer AE, Brunelle F, Prevot V, Polak M, Boddaert N. Denis J, et al. Clin Neuroradiol. 2020 Mar;30(1):137-144. doi: 10.1007/s00062-018-0738-5. Epub 2018 Nov 5. Clin Neuroradiol. 2020. PMID: 30397727
PURPOSE: To evaluate a non-invasive method to assess the progressivity of idiopathic central precocious puberty (CPP) by quantifying perfusion of the pituitary stalk with arterial spin labeling (ASL) and using the gonadotropin-releasing hormone (GnRH) …
PURPOSE: To evaluate a non-invasive method to assess the progressivity of idiopathic central precocious puberty
Differentiation of Idiopathic Central Precocious Puberty From Premature Thelarche Using Principal Component Analysis.
Cleemann Wang A, Hagen CP, Johannsen TH, Madsen AG, Cleemann LH, Christiansen P, Main KM, Juul A, Jensen RB. Cleemann Wang A, et al. J Clin Endocrinol Metab. 2024 Jan 18;109(2):370-379. doi: 10.1210/clinem/dgad535. J Clin Endocrinol Metab. 2024. PMID: 37698163
CONTEXT: Nonprogressive premature thelarche (PT) is a self-limiting variant of early puberty, while idiopathic central precocious puberty (ICPP) is a disorder that causes progressive development of secondary sexual characteristics and often requires tr …
CONTEXT: Nonprogressive premature thelarche (PT) is a self-limiting variant of early puberty, while idiopathic central prec
A Clinical Study of Girls With Idiopathic Central Precocious Puberty and Psychological Behavior Problems.
Xie LL, Yang Y, Xiong XY, Yang L, Wu X, Zhang DG. Xie LL, et al. Clin Pediatr (Phila). 2023 Sep;62(8):914-918. doi: 10.1177/00099228221149551. Epub 2023 Jan 20. Clin Pediatr (Phila). 2023. PMID: 36661073
To understand the psychological effects on behavior of girls with idiopathic central precocious puberty (ICPP) and to explore the role of gonadotropin-releasing hormone analog (GnRHa) in the reversal or blocking of the negative psychological effects on …
To understand the psychological effects on behavior of girls with idiopathic central precocious puberty (ICPP) a …
Gonadotropin-releasing hormone analogue and recombinant human growth hormone treatment for idiopathic central precocious puberty in girls.
Shi Y, Ma Z, Yang X, Ying Y, Luo X, Hou L. Shi Y, et al. Front Endocrinol (Lausanne). 2022 Dec 14;13:1085385. doi: 10.3389/fendo.2022.1085385. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36589818 Free PMC article.
PURPOSE: To investigate the effectiveness and safety of gonadotropin-releasing hormone analogue (GnRHa) in combination with recombinant human growth hormone (rhGH) in girls with central precocious puberty (CPP). METHODS: Clinical data of 80 girls diagnosed with idiopathic
PURPOSE: To investigate the effectiveness and safety of gonadotropin-releasing hormone analogue (GnRHa) in combination with recombinant huma …
Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.
Lin WD, Cheng CF, Wang CH, Liang WM, Chen CH, Hsieh AR, Chiu ML, Lin TH, Liao CC, Huang SM, Tsai CH, Chang CY, Lin YJ, Tsai FJ. Lin WD, et al. Eur J Endocrinol. 2021 Aug 27;185(4):441-451. doi: 10.1530/EJE-21-0424. Eur J Endocrinol. 2021. PMID: 34288885
OBJECTIVE, To investigate the genetic characteristics of idiopathic central precocious puberty (ICPP) and validate its polygenic risk for early puberty. ...A validation group was also investigated for the weighted polygenic risk score (wPRS) of …
OBJECTIVE, To investigate the genetic characteristics of idiopathic central precocious puberty (ICPP) and valida …
Noninvasive radiomics-based method for evaluating idiopathic central precocious puberty in girls.
Jiang H, Shu Z, Luo X, Wu M, Wang M, Feng Q, Chen J, Lin C, Ding Z. Jiang H, et al. J Int Med Res. 2021 Feb;49(2):300060521991023. doi: 10.1177/0300060521991023. J Int Med Res. 2021. PMID: 33596690 Free PMC article.
We investigated the use of a more accurate method using texture analysis to evaluate idiopathic central precocious puberty (ICPP) by MRI. METHODS: In total, 352 texture features of the pituitary were extracted from 12 healthy girls and 18 girls with IC …
We investigated the use of a more accurate method using texture analysis to evaluate idiopathic central precocious p
Impact of COVID-19 lockdown on idiopathic central precocious puberty - experience from an Indian centre.
Mondkar SA, Oza C, Khadilkar V, Shah N, Gondhalekar K, Kajale N, Khadilkar A. Mondkar SA, et al. J Pediatr Endocrinol Metab. 2022 Jun 3;35(7):895-900. doi: 10.1515/jpem-2022-0157. Print 2022 Jul 26. J Pediatr Endocrinol Metab. 2022. PMID: 35658967
OBJECTIVES: Owing to increase in referrals for precocity observed during COVID-19 lockdown, this study was conducted to estimate the proportion of patients referred for precocity and within these, those with idiopathic central precocious puberty
OBJECTIVES: Owing to increase in referrals for precocity observed during COVID-19 lockdown, this study was conducted to estimate the …
Serum Nesfatin-1 Levels in Girls with Idiopathic Central Precocious Puberty.
Altıncık A, Sayın O. Altıncık A, et al. J Clin Res Pediatr Endocrinol. 2018 Mar 1;10(1):8-12. doi: 10.4274/jcrpe.4677. Epub 2017 Jul 24. J Clin Res Pediatr Endocrinol. 2018. PMID: 28739555 Free PMC article.
METHODS: The aim of this study was to investigate the following: i) the role of nesfatin-1 in puberty, and ii) relationship between nesfatin-1 and anthropometric measurements and gonadotropin levels in girls with idiopathic central precocious puberty ( …
METHODS: The aim of this study was to investigate the following: i) the role of nesfatin-1 in puberty, and ii) relationship between nesfatin …
Development and validation of a model for predicting the adult height of girls with idiopathic central precocious puberty.
Wu W, Zhu X, Chen Y, Yang X, Zhang Y, Chen R. Wu W, et al. Eur J Pediatr. 2023 Apr;182(4):1627-1635. doi: 10.1007/s00431-023-04842-3. Epub 2023 Jan 28. Eur J Pediatr. 2023. PMID: 36708384
The aim was to develop a model to predict the adult height (AH) of idiopathic central precocious puberty (ICPP) girls who underwent gonadotropin-releasing hormone analog (GnRHa) treatment. ...Previous models for predicting adult height of …
The aim was to develop a model to predict the adult height (AH) of idiopathic central precocious puberty
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.
Kırkgöz T, Kaygusuz SB, Alavanda C, Helvacıoğlu D, Abalı ZY, Tosun BG, Eltan M, Menevşe TS, Guran T, Arman A, Turan S, Bereket A. Kırkgöz T, et al. J Pediatr Endocrinol Metab. 2023 Mar 9;36(4):401-408. doi: 10.1515/jpem-2022-0645. Print 2023 Apr 25. J Pediatr Endocrinol Metab. 2023. PMID: 36883204
A novel heterozygous c.1A>G (p.Met1Val) mutation, a novel heterozygous c.683_684delCA (p.Ser228*) and a previously reported c.482dupC (Ala162Glyfs*) frameshift variations were detected. The two novel variants are predicted to be pathogenic in silico analyses. CONCLUSION …
A novel heterozygous c.1A>G (p.Met1Val) mutation, a novel heterozygous c.683_684delCA (p.Ser228*) and a previously reported c.482dupC (Al …
85 results