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
1987 1
1989 1
1992 1
1993 2
1999 1
2003 3
2005 3
2006 1
2008 1
2009 4
2010 2
2011 3
2012 1
2014 4
2015 4
2016 3
2017 3
2018 2
2019 1
2020 1
2021 3
2022 5
2023 4
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

49 results

Results by year

Filters applied: . Clear all
Page 1
Malignancy in Noonan syndrome and related disorders.
Smpokou P, Zand DJ, Rosenbaum KN, Summar ML. Smpokou P, et al. Clin Genet. 2015 Dec;88(6):516-22. doi: 10.1111/cge.12568. Epub 2015 Mar 4. Clin Genet. 2015. PMID: 25683281 Review.
Noonan syndrome (NS) and related disorders, such as NS with multiple lentigines (formerly called LEOPARD syndrome), cardiofaciocutaneous syndrome, and Costello syndrome, constitute an important group of developmental malformation syndromes with
Noonan syndrome (NS) and related disorders, such as NS with multiple lentigines (formerly called LEOPARD syndrome), car
Neurosurgical aspects of Noonan syndrome.
Saragosti E, Fattal-Valevski A, Levin D, Hausman-Kedem M, Constantini S, Mecica N, Zarour S, Roth J. Saragosti E, et al. Childs Nerv Syst. 2023 Apr;39(4):849-856. doi: 10.1007/s00381-023-05888-2. Epub 2023 Feb 27. Childs Nerv Syst. 2023. PMID: 36847963 Review.
PURPOSE: Noonan syndrome (NS) is a rare neurodevelopmental syndrome characterized by dysmorphic features, congenital heart defects, neurodevelopmental delay, and bleeding diathesis. ...
PURPOSE: Noonan syndrome (NS) is a rare neurodevelopmental syndrome characterized by dysmorphic features, congenital he …
Clinical analysis of Noonan syndrome caused by RRAS2 mutations and literature review.
Yu C, Lyn N, Li D, Mei S, Liu L, Shang Q. Yu C, et al. Eur J Med Genet. 2023 Jan;66(1):104675. doi: 10.1016/j.ejmg.2022.104675. Epub 2022 Nov 30. Eur J Med Genet. 2023. PMID: 36460282 Review.
We analyzed the clinical characteristics of all patients with Noonan syndrome caused by RRAS2 variants and reviewed the literature. This discovery expands the genetic and phenotypic spectrum of Noonan syndrome....
We analyzed the clinical characteristics of all patients with Noonan syndrome caused by RRAS2 variants and reviewed the litera …
An approach to familial lymphoedema.
Jones GE, Mansour S. Jones GE, et al. Clin Med (Lond). 2017 Dec;17(6):552-557. doi: 10.7861/clinmedicine.17-6-552. Clin Med (Lond). 2017. PMID: 29196357 Free PMC article. Review.
Common genetic conditions associated with lymphoedema include Turner syndrome and Noonan syndrome; however, there are numerous others that can be classified based on their clinical presentation and associated features. ...
Common genetic conditions associated with lymphoedema include Turner syndrome and Noonan syndrome; however, there are n …
Systematic literature review of lymphatic imaging-guided procedural management of Noonan syndrome.
Cox TP, Vance CJ, Daley SK, Papendieck C, McGregor H, Kuo P, Witte MH. Cox TP, et al. J Vasc Surg Venous Lymphat Disord. 2022 Sep;10(5):1192-1196.e3. doi: 10.1016/j.jvsv.2022.03.017. Epub 2022 May 10. J Vasc Surg Venous Lymphat Disord. 2022. PMID: 35561969 Free PMC article. Review.
OBJECTIVES: To assess through literature case analysis how advances in lymphatic imaging, interventional radiology, and lymphatic vascular microsurgery illuminate and improve the lymphatic-flow status in select patients with Noonan syndrome (NS) who have undergone s …
OBJECTIVES: To assess through literature case analysis how advances in lymphatic imaging, interventional radiology, and lymphatic vascular m …
The efficacy and safety of growth hormone therapy in children with noonan syndrome: a review of the evidence.
Noonan JA, Kappelgaard AM. Noonan JA, et al. Horm Res Paediatr. 2015;83(3):157-66. doi: 10.1159/000369012. Epub 2014 Dec 10. Horm Res Paediatr. 2015. PMID: 25503994 Free article. Review.
Noonan syndrome is a genetic disorder associated with short stature. We reviewed 15 studies in which growth hormone (GH) therapy was used in children with Noonan syndrome. Data show consistent increases in mean height standard deviation score (SDS), wi
Noonan syndrome is a genetic disorder associated with short stature. We reviewed 15 studies in which growth hormone (GH) thera
Noonan syndrome and related disorders: genetics and pathogenesis.
Tartaglia M, Gelb BD. Tartaglia M, et al. Annu Rev Genomics Hum Genet. 2005;6:45-68. doi: 10.1146/annurev.genom.6.080604.162305. Annu Rev Genomics Hum Genet. 2005. PMID: 16124853 Review.
Noonan syndrome is a pleiomorphic autosomal dominant disorder with short stature, facial dysmorphia, webbed neck, and heart defects. ...A mouse model of PTPN11-related Noonan syndrome was recently generated, providing a reagent for studying disease pat
Noonan syndrome is a pleiomorphic autosomal dominant disorder with short stature, facial dysmorphia, webbed neck, and heart de
Chiari I malformation in patients with RASopathies.
Han Y, Chen M, Wang H. Han Y, et al. Childs Nerv Syst. 2021 Jun;37(6):1831-1836. doi: 10.1007/s00381-020-05034-2. Epub 2021 Jan 6. Childs Nerv Syst. 2021. PMID: 33409618 Review.
METHOD AND RESULTS: We reviewed the current knowledge of CIM and RASopathies in the paper. Here, we describe one patient with CIM and Noonan syndrome and three patients with CIM and neurofibromatosis type 1. ...
METHOD AND RESULTS: We reviewed the current knowledge of CIM and RASopathies in the paper. Here, we describe one patient with CIM and Noo
Neurodevelopmental Aspects of RASopathies.
Kim YE, Baek ST. Kim YE, et al. Mol Cells. 2019 Jun 30;42(6):441-447. doi: 10.14348/molcells.2019.0037. Mol Cells. 2019. PMID: 31250618 Free PMC article. Review.
49 results