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

Year Number of Results
1971 1
1973 1
1990 1
1994 3
1995 2
1996 1
1998 1
1999 1
2000 2
2001 3
2002 1
2003 2
2004 2
2005 2
2006 3
2007 1
2008 2
2009 4
2010 4
2011 5
2012 1
2013 4
2014 3
2015 3
2016 4
2017 4
2018 4
2019 4
2020 2
2021 5
2022 4
2023 1
2024 1

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71 results

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Page 1
Periodontal health and gingival diseases and conditions on an intact and a reduced periodontium: Consensus report of workgroup 1 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions.
Chapple ILC, Mealey BL, Van Dyke TE, Bartold PM, Dommisch H, Eickholz P, Geisinger ML, Genco RJ, Glogauer M, Goldstein M, Griffin TJ, Holmstrup P, Johnson GK, Kapila Y, Lang NP, Meyle J, Murakami S, Plemons J, Romito GA, Shapira L, Tatakis DN, Teughels W, Trombelli L, Walter C, Wimmer G, Xenoudi P, Yoshie H. Chapple ILC, et al. J Periodontol. 2018 Jun;89 Suppl 1:S74-S84. doi: 10.1002/JPER.17-0719. J Periodontol. 2018. PMID: 29926944
Periodontal health and gingival diseases and conditions on an intact and a reduced periodontium: Consensus report of workgroup 1 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions.
Chapple ILC, Mealey BL, Van Dyke TE, Bartold PM, Dommisch H, Eickholz P, Geisinger ML, Genco RJ, Glogauer M, Goldstein M, Griffin TJ, Holmstrup P, Johnson GK, Kapila Y, Lang NP, Meyle J, Murakami S, Plemons J, Romito GA, Shapira L, Tatakis DN, Teughels W, Trombelli L, Walter C, Wimmer G, Xenoudi P, Yoshie H. Chapple ILC, et al. J Clin Periodontol. 2018 Jun;45 Suppl 20:S68-S77. doi: 10.1111/jcpe.12940. J Clin Periodontol. 2018. PMID: 29926499
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 …
Syndromes with gingival fibromatosis: A systematic review.
Costa CRR, Braz SV, de Toledo IP, Martelli-Júnior H, Mazzeu JF, Guerra ENS, Coletta RD, Acevedo AC. Costa CRR, et al. Oral Dis. 2021 May;27(4):881-893. doi: 10.1111/odi.13369. Epub 2020 May 25. Oral Dis. 2021. PMID: 32335995 Review.
OBJECTIVE: The aim of systematic review was to describe the phenotypes and molecular profiles of syndromes with gingival fibromatosis (GF). METHODS: A comprehensive search of PubMed, LILACS, Livivo, Scopus, and Web of Science was conducted using key terms relevant t …
OBJECTIVE: The aim of systematic review was to describe the phenotypes and molecular profiles of syndromes with gingival fibromato …
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis.
Chen J, Xu X, Chen S, Lu T, Zheng Y, Gan Z, Shen Z, Ma S, Wang D, Su L, He F, Shang X, Xu H, Chen D, Zhang L, Xiong F. Chen J, et al. Int J Oral Sci. 2023 Sep 26;15(1):46. doi: 10.1038/s41368-023-00244-1. Int J Oral Sci. 2023. PMID: 37752101 Free PMC article.
Hereditary gingival fibromatosis (HGF) is a rare inherited condition with fibromatoid hyperplasia of the gingival tissue that exhibits great genetic heterogeneity. ...Furthermore, a knock-in mouse model confirmed that heterozygous or homozygous mutations within Zfp5 …
Hereditary gingival fibromatosis (HGF) is a rare inherited condition with fibromatoid hyperplasia of the gingival tissue that …
Heterogeneity in gingival fibromatosis.
Witkop CJ Jr. Witkop CJ Jr. Birth Defects Orig Artic Ser. 1971 Jun;7(7):210-21. Birth Defects Orig Artic Ser. 1971. PMID: 4950923 Review.
A review of cases indicated that gingival fibromatosis occurs in a variety of genetic entities. High risk for epilepsy and oligophrenia is associated if hypertrichosis is present. Other entities are symmetrical gingival fibromatosis; Zimmermann-Laband …
A review of cases indicated that gingival fibromatosis occurs in a variety of genetic entities. High risk for epilepsy and oli …
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 (LS, NF …
The syndromes included within this classification are neurofibromatosis type 1 (NF1), Noonan syndrome (NS), Noonan syndrome with multiple le …
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.
Gingival fibromatosis is a rare and heterogeneous group of disorders that develop as slowly progressive, local or diffuse enlargements within marginal and attached gingiva or interdental papilla. ...The pathologic manifestation of gingival fibromatosis …
Gingival fibromatosis is a rare and heterogeneous group of disorders that develop as slowly progressive, local or diffuse enla …
The RASopathies: Biology, genetics and therapeutic options.
Longo JF, Carroll SL. Longo JF, et al. Adv Cancer Res. 2022;153:305-341. doi: 10.1016/bs.acr.2021.07.007. Epub 2021 Aug 7. Adv Cancer Res. 2022. PMID: 35101235
As their causative mutations have been identified, this group of diseases has expanded to include neurofibromatosis type 1 (NF1), Legius syndrome, Noonan syndrome, CBL syndrome, Noonan syndrome-like disorder with loose anagen hair, Noonan syndrome with multiple lentigines, Costel …
As their causative mutations have been identified, this group of diseases has expanded to include neurofibromatosis type 1 (NF1), Legius syn …
Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics.
Hwang J, Kim YL, Kang S, Kim S, Kim SO, Lee JH, Han DH. Hwang J, et al. Oral Dis. 2017 Jan;23(1):102-109. doi: 10.1111/odi.12583. Epub 2016 Oct 10. Oral Dis. 2017. PMID: 27614106
OBJECTIVES: Our study aims to identify genetic variants associated with hereditary gingival fibromatosis (HGF) by applying whole-exome sequencing (WES) and bioinformatics analyses such as gene set enrichment analysis (GSEA) and protein functional network study. ...C …
OBJECTIVES: Our study aims to identify genetic variants associated with hereditary gingival fibromatosis (HGF) by applying who …
71 results