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Year Number of Results
1976 1
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1996 1
2002 2
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2006 1
2007 3
2008 2
2009 2
2013 1
2014 1
2015 2
2016 2
2017 1
2018 4
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2022 4
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31 results

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Page 1
Clinical Indications for Growth Hormone Therapy.
Danowitz M, Grimberg A. Danowitz M, et al. Adv Pediatr. 2022 Aug;69(1):203-217. doi: 10.1016/j.yapd.2022.03.005. Epub 2022 Jun 17. Adv Pediatr. 2022. PMID: 35985710 Free PMC article. Review.
Growth hormone (GH) is an injectable medication originally used to replace the deficiency of the hormone, but has expanded to treating conditions that may reduce growth and adult height even when the body maintains endogenous GH production. In the United States, there are 8
Growth hormone (GH) is an injectable medication originally used to replace the deficiency of the hormone, but has expanded to treating condi …
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis.
Farncombe KM, Thain E, Barnett-Tapia C, Sadeghian H, Kim RH. Farncombe KM, et al. BMC Med Genomics. 2022 Jul 15;15(1):160. doi: 10.1186/s12920-022-01304-x. BMC Med Genomics. 2022. PMID: 35840934 Free PMC article. Review.
BACKGROUND: Noonan syndrome (NS) is a genetic disorder characterized by developmental delays, typical facial gestalt and cardiovascular defects. ...CASE PRESENTATION: A female patient was diagnosed with clinical NS at 8 months of age. She presented in adultho …
BACKGROUND: Noonan syndrome (NS) is a genetic disorder characterized by developmental delays, typical facial gestalt and cardi …
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 …
Pectus excavatum and carinatum.
Cobben JM, Oostra RJ, van Dijk FS. Cobben JM, et al. Eur J Med Genet. 2014 Aug;57(8):414-7. doi: 10.1016/j.ejmg.2014.04.017. Epub 2014 May 10. Eur J Med Genet. 2014. PMID: 24821303 Review.
However, the most important and most frequently observed monogenic syndromes with pectus excavatum/carinatum are Marfan Syndrome and Noonan Syndrome....
However, the most important and most frequently observed monogenic syndromes with pectus excavatum/carinatum are Marfan Syndrome and …
Malignant diseases in Noonan syndrome and related disorders.
Hasle H. Hasle H. Horm Res. 2009 Dec;72 Suppl 2:8-14. doi: 10.1159/000243773. Epub 2009 Dec 22. Horm Res. 2009. PMID: 20029231 Review.
The overall risk of cancer in children with Noonan (NS), cardio-facial-cutaneous, Costello or LEOPARD syndrome is high, although no precise estimates are available. ...A review of the literature indicates an increased risk of acute lymphoblastic leukemia and acute m …
The overall risk of cancer in children with Noonan (NS), cardio-facial-cutaneous, Costello or LEOPARD syndrome is high, althou …
Towards better understanding of giant cell granulomas of the oral cavity.
Ahmed A, Naidu A. Ahmed A, et al. J Clin Pathol. 2021 Aug;74(8):483-490. doi: 10.1136/jclinpath-2020-206858. Epub 2021 Apr 15. J Clin Pathol. 2021. PMID: 33858937 Review.
It is important to differentiate them from other giant cell lesions that can occur in the oral cavity, such as giant cell tumour of the bone, aneurysmal bone cyst, brown tumour of hyperparathyroidism, and giant cell lesions of Ramon syndrome, Noonan syndrome, …
It is important to differentiate them from other giant cell lesions that can occur in the oral cavity, such as giant cell tumour of the bone …
Patient engagement in the design of clinical research in Noonan syndrome spectrum disorders: a scoping review.
Tiemens DK, Nugteren J, Leenders E, Wingbermühle E, Pittens CACM, Draaisma JMT. Tiemens DK, et al. Orphanet J Rare Dis. 2021 Oct 26;16(1):449. doi: 10.1186/s13023-021-02083-x. Orphanet J Rare Dis. 2021. PMID: 34702330 Free PMC article. Review.
BACKGROUND: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in several genes of the RAS/MAPK pathway. ...However, this is not automatically followed by patient engagement at higher levels of participation in subsequent research steps. …
BACKGROUND: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in several genes of the RAS/MAPK p …
Laser-assisted thermal capsulorrhaphy.
Noonan TJ, Tokish JM, Briggs KK, Hawkins RJ. Noonan TJ, et al. Arthroscopy. 2003 Oct;19(8):815-9. doi: 10.1016/s0749-8063(03)00737-0. Arthroscopy. 2003. PMID: 14551542 Review.
Of the remaining 42 patients, none underwent further surgery; the average follow-up time was 38.4 months (range, 24 to 66 months); and pain scores improved from 7.8 +/- 2.6 (1-10 scale) to 1.7 +/- 2.6. postoperatively. In addition, 86% of patients reported none or rare epi …
Of the remaining 42 patients, none underwent further surgery; the average follow-up time was 38.4 months (range, 24 to 66 months); and pain …
Senescence in RASopathies, a possible novel contributor to a complex pathophenoype.
Engler M, Fidan M, Nandi S, Cirstea IC. Engler M, et al. Mech Ageing Dev. 2021 Mar;194:111411. doi: 10.1016/j.mad.2020.111411. Epub 2020 Dec 9. Mech Ageing Dev. 2021. PMID: 33309600 Free article. Review.
Here, we consider that in these disorders, senescence induction may result in opposing outcomes, a tumour protective effect and a possible contributor to a premature ageing phenotype identified in Costello syndrome, which belongs to the RASopathy group. In this review, we …
Here, we consider that in these disorders, senescence induction may result in opposing outcomes, a tumour protective effect and a possible c …
Thirty-year outcome in children with hypertrophic cardiomyopathy based on the type.
Tsuda E, Ito Y, Kato Y, Sakaguchi H, Ohuchi H, Kurosaki K. Tsuda E, et al. J Cardiol. 2022 Dec;80(6):557-562. doi: 10.1016/j.jjcc.2022.07.016. Epub 2022 Aug 10. J Cardiol. 2022. PMID: 35961804 Free article. Review.
RESULTS: The age at the time of the diagnosis ranged from 0 to 15 years with a median of 8 years. The number of patients with Noonan syndrome and hypertrophic obstructive cardiomyopathy (HOCM), idiopathic HCM (i-HCM), and secondary HCM (s-HCM) was 13, 13, 65, …
RESULTS: The age at the time of the diagnosis ranged from 0 to 15 years with a median of 8 years. The number of patients with Noon
31 results