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1964
2025

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

Year Number of Results
1964 1
1968 2
1970 2
1971 5
1972 3
1973 1
1975 2
1977 4
1978 3
1980 2
1983 2
1985 3
1986 1
1987 5
1988 12
1989 12
1990 7
1991 3
1992 12
1993 8
1994 12
1995 13
1996 17
1997 12
1998 10
1999 14
2000 33
2001 43
2002 20
2003 21
2004 28
2005 36
2006 18
2007 23
2008 21
2009 25
2010 35
2011 39
2012 30
2013 35
2014 39
2015 46
2016 43
2017 32
2018 31
2019 31
2020 33
2021 39
2022 31
2023 27
2024 27
2025 0

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871 results

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Page 1
Orthodontic and dentofacial orthopedic treatments in patients with ectodermal dysplasia: a systematic review.
Cerezo-Cayuelas M, Pérez-Silva A, Serna-Muñoz C, Vicente A, Martínez-Beneyto Y, Cabello-Malagón I, Ortiz-Ruiz AJ. Cerezo-Cayuelas M, et al. Orphanet J Rare Dis. 2022 Oct 17;17(1):376. doi: 10.1186/s13023-022-02533-0. Orphanet J Rare Dis. 2022. PMID: 36253866 Free PMC article. Review.
We included articles describing patients with any type of ectodermal dysplasia who received orthodontic or dentofacial orthopedic treatment to facilitate functional and aesthetic oral rehabilitation. ...Thirteen studies were on hypohidrotic and/or anhidrotic ecto
We included articles describing patients with any type of ectodermal dysplasia who received orthodontic or dentofacial orthope …
Noonan syndrome and clinically related disorders.
Tartaglia M, Gelb BD, Zenker M. Tartaglia M, et al. Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):161-79. doi: 10.1016/j.beem.2010.09.002. Best Pract Res Clin Endocrinol Metab. 2011. PMID: 21396583 Free PMC article. Review.
Cardinal features include postnatally reduced growth, distinctive facial dysmorphism, congenital heart defects and hypertrophic cardiomyopathy, variable cognitive deficit and skeletal, ectodermal and hematologic anomalies. Noonan syndrome is transmitted as an autosomal dom …
Cardinal features include postnatally reduced growth, distinctive facial dysmorphism, congenital heart defects and hypertrophic cardiomyopat …
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.
An international advisory group met at the National Institutes of Health in Bethesda, Maryland in 2017, to discuss a new classification system for the ectodermal dysplasias (EDs) that would integrate both clinical and molecular information. We propose the following, a work …
An international advisory group met at the National Institutes of Health in Bethesda, Maryland in 2017, to discuss a new classification syst …
The Cardiofaciocutaneous Syndrome: From Genetics to Prognostic-Therapeutic Implications.
Scorrano G, David E, Calì E, Chimenz R, La Bella S, Di Ludovico A, Di Rosa G, Gitto E, Mankad K, Nardello R, Mangano GD, Leoni C, Ceravolo G. Scorrano G, et al. Genes (Basel). 2023 Nov 22;14(12):2111. doi: 10.3390/genes14122111. Genes (Basel). 2023. PMID: 38136934 Free PMC article. Review.
Cardiofaciocutaneous (CFC) syndrome is one of the rarest RASopathies characterized by multiple congenital ectodermal, cardiac and craniofacial abnormalities with a mild to severe ocular, gastrointestinal and neurological involvement. ...
Cardiofaciocutaneous (CFC) syndrome is one of the rarest RASopathies characterized by multiple congenital ectodermal, cardiac and cra …
Hypohidrotic ectodermal dysplasia: clinical and molecular review.
Reyes-Reali J, Mendoza-Ramos MI, Garrido-Guerrero E, Méndez-Catalá CF, Méndez-Cruz AR, Pozo-Molina G. Reyes-Reali J, et al. Int J Dermatol. 2018 Aug;57(8):965-972. doi: 10.1111/ijd.14048. Epub 2018 May 31. Int J Dermatol. 2018. PMID: 29855039 Review.
Hypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. ...The aim of this review was to update the main clinical characteristics of HED regarding to recent molecular advances in the comprehension of …
Hypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. ...T …
Congenital nail abnormalities.
Nahmani L, Fitoussi F. Nahmani L, et al. Hand Surg Rehabil. 2024 Apr;43S:101527. doi: 10.1016/j.hansur.2023.01.011. Hand Surg Rehabil. 2024. PMID: 38879228 Review.
Nail conditions can be the first sign of nail-patella syndrome, ectodermal dysplasia, dyskeratosis congenita, epidermolysis bullosa, pachyonychia congenita or lung disease. ...
Nail conditions can be the first sign of nail-patella syndrome, ectodermal dysplasia, dyskeratosis congenita, epidermolysis bu …
p63-associated disorders.
Rinne T, Brunner HG, van Bokhoven H. Rinne T, et al. Cell Cycle. 2007 Feb 1;6(3):262-8. doi: 10.4161/cc.6.3.3796. Epub 2007 Feb 3. Cell Cycle. 2007. PMID: 17224651 Free article. Review.
Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics. Different combinations of these features are seen in five different synd …
Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, or …
WNT10A, dermatology and dentistry.
Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. Doolan BJ, et al. Br J Dermatol. 2021 Dec;185(6):1105-1111. doi: 10.1111/bjd.20601. Epub 2021 Sep 7. Br J Dermatol. 2021. PMID: 34184264 Review.
This review focuses on how variants in the WNT10A gene have been associated with various ectodermal disorders and how such changes may have clinical relevance to dermatologists and dentists. Germline mutations in WNT10A underlie several forms of autosomal recessive ecto
This review focuses on how variants in the WNT10A gene have been associated with various ectodermal disorders and how such changes ma …
Ectodermal dysplasias.
Itin PH, Fistarol SK. Itin PH, et al. Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):45-51. doi: 10.1002/ajmg.c.30033. Am J Med Genet C Semin Med Genet. 2004. PMID: 15468153 Review.
The ectodermal dysplasias, as a rule, are not pure "one-layer diseases." Mesodermal and, rarely, endodermal dysplasias coexist. ...In this way, a reclassification of ectodermal dysplasias will be possible according to the function of their involved mutated genes. .. …
The ectodermal dysplasias, as a rule, are not pure "one-layer diseases." Mesodermal and, rarely, endodermal dysplasias coexist. ...In …
871 results