238 related articles for article (PubMed ID: 30703280)
1. 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
Am J Med Genet A; 2019 Mar; 179(3):442-447. PubMed ID: 30703280
[TBL] [Abstract][Full Text] [Related]
2. Ectodermal dysplasias: a new clinical-genetic classification.
Priolo M; Laganà C
J Med Genet; 2001 Sep; 38(9):579-85. PubMed ID: 11546825
[TBL] [Abstract][Full Text] [Related]
3. Gene Mutations of the Three Ectodysplasin Pathway Key Players (
Ahmed HA; El-Kamah GY; Rabie E; Mostafa MI; Abouzaid MR; Hassib NF; Mehrez MI; Abdel-Kader MA; Mohsen YH; Zada SK; Amr KS; Sayed ISM
Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573371
[TBL] [Abstract][Full Text] [Related]
4. Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanisms.
Priolo M
Am J Med Genet A; 2009 Sep; 149A(9):2003-13. PubMed ID: 19504607
[TBL] [Abstract][Full Text] [Related]
5. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
Martínez-Romero MC; Ballesta-Martínez MJ; López-González V; Sánchez-Soler MJ; Serrano-Antón AT; Barreda-Sánchez M; Rodriguez-Peña L; Martínez-Menchon MT; Frías-Iniesta J; Sánchez-Pedreño P; Carbonell-Meseguer P; Glover-López G; Guillén-Navarro E;
Orphanet J Rare Dis; 2019 Dec; 14(1):281. PubMed ID: 31796081
[TBL] [Abstract][Full Text] [Related]
6. Ectodermal dysplasias: clinical and molecular review.
Visinoni AF; Lisboa-Costa T; Pagnan NA; Chautard-Freire-Maia EA
Am J Med Genet A; 2009 Sep; 149A(9):1980-2002. PubMed ID: 19681154
[TBL] [Abstract][Full Text] [Related]
7. Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias.
Maier-Wohlfart S; Aicher C; Willershausen I; Peschel N; Meißner U; Gölz L; Schneider H
Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421794
[TBL] [Abstract][Full Text] [Related]
8. [Ectodermal dysplasias – molecular mechanisms responsible for occurrence of most frequent syndroms].
Grabarczyk A; Wertheim-Tysarowska K; Bal J
Postepy Biochem; 2021 Sep; 67(3):248-258. PubMed ID: 34894390
[TBL] [Abstract][Full Text] [Related]
9. WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).
Guazzarotti L; Tadini G; Mancini GE; Sani I; Pisanelli S; Galderisi F; D'Auria E; Secondi R; Bottero A; Zuccotti GV
Clin Genet; 2018 Mar; 93(3):693-698. PubMed ID: 28976000
[TBL] [Abstract][Full Text] [Related]
10. Ectodermal dysplasias.
Itin PH; Fistarol SK
Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):45-51. PubMed ID: 15468153
[TBL] [Abstract][Full Text] [Related]
11. Towards a unified classification of the ectodermal dysplasias: opportunities outweigh challenges.
Irvine AD
Am J Med Genet A; 2009 Sep; 149A(9):1970-2. PubMed ID: 19681131
[TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia.
Burger K; Schneider AT; Wohlfart S; Kiesewetter F; Huttner K; Johnson R; Schneider H
Am J Med Genet A; 2014 Oct; 164A(10):2424-32. PubMed ID: 24715423
[TBL] [Abstract][Full Text] [Related]
13. Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families.
Güven Y; Bal E; Altunoglu U; Yücel E; Hadj-Rabia S; Koruyucu M; Bahar Tuna E; Çıldır Ş; Aktören O; Bodemer C; Uyguner ZO; Smahi A; Kayserili H
Cytogenet Genome Res; 2019; 157(4):189-196. PubMed ID: 30974434
[TBL] [Abstract][Full Text] [Related]
14. Update on ectodermal dysplasias clinical classification.
Pagnan NA; Visinoni ÁF
Am J Med Genet A; 2014 Oct; 164A(10):2415-23. PubMed ID: 25098893
[TBL] [Abstract][Full Text] [Related]
15. What the future holds for ectodermal dysplasias: future research and treatment directions.
Slavkin HC
Am J Med Genet A; 2009 Sep; 149A(9):2071-4. PubMed ID: 19681133
[TBL] [Abstract][Full Text] [Related]
16. Rationale and background as basis for a new classification of the ectodermal dysplasias.
Itin PH
Am J Med Genet A; 2009 Sep; 149A(9):1973-6. PubMed ID: 19353583
[TBL] [Abstract][Full Text] [Related]
17. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Plaisancié J; Bailleul-Forestier I; Gaston V; Vaysse F; Lacombe D; Holder-Espinasse M; Abramowicz M; Coubes C; Plessis G; Faivre L; Demeer B; Vincent-Delorme C; Dollfus H; Sigaudy S; Guillén-Navarro E; Verloes A; Jonveaux P; Martin-Coignard D; Colin E; Bieth E; Calvas P; Chassaing N
Am J Med Genet A; 2013 Apr; 161A(4):671-8. PubMed ID: 23401279
[TBL] [Abstract][Full Text] [Related]
18. Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II).
Wright JT; Morris C; Clements SE; D'Souza R; Gaide O; Mikkola M; Zonana J
Am J Med Genet A; 2009 Sep; 149A(9):2062-7. PubMed ID: 19681147
[TBL] [Abstract][Full Text] [Related]
19. Second International Conference on a classification of ectodermal dysplasias: development of a multiaxis model.
Salinas CF; Irvine AD; Itin PH; Di Giovanna JJ; Schneider H; Clarke AJ; McGovern LS; Fete M
Am J Med Genet A; 2014 Oct; 164A(10):2482-9. PubMed ID: 24700551
[TBL] [Abstract][Full Text] [Related]
20. Ectodermal dysplasias: not only 'skin' deep.
Priolo M; Silengo M; Lerone M; Ravazzolo R
Clin Genet; 2000 Dec; 58(6):415-30. PubMed ID: 11149610
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
