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
1983 1
1987 1
1989 1
1990 2
1994 1
1995 1
1998 1
2002 1
2004 1
2005 2
2007 2
2011 1
2013 1
2014 2
2015 2
2016 3
2017 1
2018 1
2019 1
2021 1
2022 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

26 results

Results by year

Filters applied: . Clear all
Page 1
Recent advances in RASopathies.
Aoki Y, Niihori T, Inoue S, Matsubara Y. Aoki Y, et al. J Hum Genet. 2016 Jan;61(1):33-9. doi: 10.1038/jhg.2015.114. Epub 2015 Oct 8. J Hum Genet. 2016. PMID: 26446362 Review.
These disorders include neurofibromatosis type I, Legius syndrome, Noonan syndrome, Noonan syndrome with multiple lentigines (formerly called LEOPARD syndrome), Costello syndrome, cardiofaciocutaneous (CFC) syndrome, Noonan-like syndrome, hereditary gingival fibromatosi
These disorders include neurofibromatosis type I, Legius syndrome, Noonan syndrome, Noonan syndrome with multiple lentigines (formerly calle …
Clinics and genetic background of hereditary gingival fibromatosis.
Strzelec K, Dziedzic A, Łazarz-Bartyzel K, Grabiec AM, Gutmajster E, Kaczmarzyk T, Plakwicz P, Gawron K. Strzelec K, et al. Orphanet J Rare Dis. 2021 Nov 24;16(1):492. doi: 10.1186/s13023-021-02104-9. Orphanet J Rare Dis. 2021. PMID: 34819125 Free PMC article. Review.
BACKGROUND: Hereditary gingival fibromatosis (HGF) is a rare condition characterized by slowly progressive overgrowth of the gingiva. ...The loci related to non-syndromic HGF have been identified on chromosome 2 (GINGF, GINGF3), chromosome 5 (GINGF2), chromosome 11 …
BACKGROUND: Hereditary gingival fibromatosis (HGF) is a rare condition characterized by slowly progressive overgrowth of the g …
Hereditary gingival fibromatosis--a review.
DeAngelo S, Murphy J, Claman L, Kalmar J, Leblebicioglu B. DeAngelo S, et al. Compend Contin Educ Dent. 2007 Mar;28(3):138-43; quiz 144, 152. Compend Contin Educ Dent. 2007. PMID: 17385395 Review.
Hereditary gingival fibromatosis (HGF) is a rare gingival lesion that presents as localized or generalized enlargement of the attached gingiva. ...HGF can present as an isolated feature or as part of a syndrome. Recent findings report a defect in the Son of s …
Hereditary gingival fibromatosis (HGF) is a rare gingival lesion that presents as localized or generalized enlargement …
Modeling RASopathies with Genetically Modified Mouse Models.
Hernández-Porras I, Guerra C. Hernández-Porras I, et al. Methods Mol Biol. 2017;1487:379-408. doi: 10.1007/978-1-4939-6424-6_28. Methods Mol Biol. 2017. PMID: 27924582 Review.
The syndromes included within this classification are neurofibromatosis type 1 (NF1), Noonan syndrome (NS), Noonan syndrome with multiple lentigines (NS-ML, formerly known as LEOPARD syndrome), Costello syndrome (CS), cardio-facio-cutaneous syndrome (CFC), Legius syndrome …
The syndromes included within this classification are neurofibromatosis type 1 (NF1), Noonan syndrome (NS), Noonan syndrome with mult …
Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.
Casas-Alba D, Martínez-Monseny A, Pino-Ramírez RM, Alsina L, Castejón E, Navarro-Vilarrubí S, Pérez-Dueñas B, Serrano M, Palau F, García-Alix A. Casas-Alba D, et al. Hum Mutat. 2018 Dec;39(12):1752-1763. doi: 10.1002/humu.23638. Epub 2018 Sep 17. Hum Mutat. 2018. PMID: 30176098 Review.
Hyaline fibromatosis syndrome (HFS) is the unifying term for infantile systemic hyalinosis and juvenile hyaline fibromatosis. ...Extreme pain at minimal handling in a newborn is the presentation pattern most frequently seen in grade 4 patients (life-limiting disease …
Hyaline fibromatosis syndrome (HFS) is the unifying term for infantile systemic hyalinosis and juvenile hyaline fibromatosis. …
Gingival fibromatosis: clinical, molecular and therapeutic issues.
Gawron K, Łazarz-Bartyzel K, Potempa J, Chomyszyn-Gajewska M. Gawron K, et al. Orphanet J Rare Dis. 2016 Jan 27;11:9. doi: 10.1186/s13023-016-0395-1. Orphanet J Rare Dis. 2016. PMID: 26818898 Free PMC article. Review.
It affects both genders equally. Hereditary, drug-induced, and idiopathic gingival overgrowth have been reported. Hereditary gingival fibromatosis can occur as an isolated condition or as part of a genetic syndrome. ...Mutation in the Son-of-Sevenless-1
It affects both genders equally. Hereditary, drug-induced, and idiopathic gingival overgrowth have been reported. Hereditary gingi
Understanding SOS (Son of Sevenless).
Pierre S, Bats AS, Coumoul X. Pierre S, et al. Biochem Pharmacol. 2011 Nov 1;82(9):1049-56. doi: 10.1016/j.bcp.2011.07.072. Epub 2011 Jul 20. Biochem Pharmacol. 2011. PMID: 21787760 Review.
Essential for normal eye development in Drosophila, SOS has two human homologues, SOS1 and SOS2. The SOS1 gene encodes the Son of Sevenless 1 protein, a Ras and Rac guanine nucleotide exchange factor. This protein is composed of several important domains. ...However, mutat …
Essential for normal eye development in Drosophila, SOS has two human homologues, SOS1 and SOS2. The SOS1 gene encodes the Son of Sevenless …
Pathogenic REST variant causing Jones syndrome and a review of the literature.
Rahikkala E, Julku J, Koskinen S, Keski-Filppula T, Weissgraeber S, Bertoli-Avella AM, Häkli S, Kraatari-Tiri M. Rahikkala E, et al. Eur J Hum Genet. 2023 Apr;31(4):469-473. doi: 10.1038/s41431-022-01258-9. Epub 2022 Dec 13. Eur J Hum Genet. 2023. PMID: 36509837 Free PMC article. Review.
Jones syndrome is a rare dominantly inherited syndrome characterized by gingival fibromatosis and progressive sensorineural hearing loss becoming symptomatic in the second decade of life. ...We review the clinical data from all previously published patients with Jon …
Jones syndrome is a rare dominantly inherited syndrome characterized by gingival fibromatosis and progressive sensorineural he …
Gingival overgrowth in children: epidemiology, pathogenesis, and complications. A literature review.
Doufexi A, Mina M, Ioannidou E. Doufexi A, et al. J Periodontol. 2005 Jan;76(1):3-10. doi: 10.1902/jop.2005.76.1.3. J Periodontol. 2005. PMID: 15830631 Review.
Gingival overgrowth is the enlargement of the attached gingiva due to an increased number of cells. The most prevalent types of gingival overgrowth in children are drug-induced gingival overgrowth, hereditary gingival fibromatosis (HGF), and neu
Gingival overgrowth is the enlargement of the attached gingiva due to an increased number of cells. The most prevalent types of gi
26 results