These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 20078794)

  • 1. Dental abnormalities associated with X-linked hypohidrotic ectodermal dysplasia in dogs.
    Lewis JR; Reiter AM; Mauldin EA; Casal ML
    Orthod Craniofac Res; 2010 Feb; 13(1):40-7. PubMed ID: 20078794
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-Linked Hypohidrotic Ectodermal Dysplasia-General Features and Dental Abnormalities in Affected Dogs Compared With Human Dental Abnormalities.
    Moura E; Rotenberg IS; Pimpão CT
    Top Companion Anim Med; 2019 Jun; 35():11-17. PubMed ID: 31122682
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The prevalence of X-linked hypohidrotic ectodermal dysplasia (XLHED) in Denmark, 1995-2010.
    Nguyen-Nielsen M; Skovbo S; Svaneby D; Pedersen L; Fryzek J
    Eur J Med Genet; 2013 May; 56(5):236-42. PubMed ID: 23416623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Significant correction of disease after postnatal administration of recombinant ectodysplasin A in canine X-linked ectodermal dysplasia.
    Casal ML; Lewis JR; Mauldin EA; Tardivel A; Ingold K; Favre M; Paradies F; Demotz S; Gaide O; Schneider P
    Am J Hum Genet; 2007 Nov; 81(5):1050-6. PubMed ID: 17924345
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review.
    Anbouba GM; Carmany EP; Natoli JL
    Am J Med Genet A; 2020 Apr; 182(4):831-841. PubMed ID: 31981414
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Orofacial features of hypohidrotic ectodermal dysplasia.
    de Aquino SN; Paranaíba LM; Swerts MS; Martelli DR; de Barros LM; Martelli Júnior H
    Head Neck Pathol; 2012 Dec; 6(4):460-6. PubMed ID: 22421994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.
    Wohlfart S; Meiller R; Hammersen J; Park J; Menzel-Severing J; Melichar VO; Huttner K; Johnson R; Porte F; Schneider H
    Orphanet J Rare Dis; 2020 Jan; 15(1):7. PubMed ID: 31924237
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dental Findings and Functional Prosthesis use in Child with Hypohidrotic Ectodermal Dysplasia: A Case Report.
    Cyrkin E; Zemnick C; Yoon RK
    N Y State Dent J; 2016 Nov; 82(6):39-42. PubMed ID: 30512258
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A frameshift variant in the EDA gene in Dachshunds with X-linked hypohidrotic ectodermal dysplasia.
    Hadji Rasouliha S; Bauer A; Dettwiler M; Welle MM; Leeb T
    Anim Genet; 2018 Dec; 49(6):651-654. PubMed ID: 30276836
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Anomalies of tooth formation in hypohidrotic ectodermal dysplasia.
    Lexner MO; Bardow A; Hertz JM; Nielsen LA; Kreiborg S
    Int J Paediatr Dent; 2007 Jan; 17(1):10-8. PubMed ID: 17181574
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Upper cervical spine and craniofacial morphology in hypohidrotic ectodermal dysplasia.
    Sonnesen L; Jasemi A; Gjørup H; Daugaard-Jensen J
    Eur Arch Paediatr Dent; 2018 Oct; 19(5):331-336. PubMed ID: 30128696
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dental Implant Therapy for a Child with X-linked Hypohidrotic Ectodermal Dysplasia--Three Decades of Managed Care.
    Bergendal B; Bjerklin K; Bergendal T; Koch G
    Int J Prosthodont; 2015; 28(4):348-56. PubMed ID: 26218015
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.
    Zhang J; Han D; Song S; Wang Y; Zhao H; Pan S; Bai B; Feng H
    Eur J Med Genet; 2011; 54(4):e377-82. PubMed ID: 21457804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
    Schneider H; Hammersen J; Preisler-Adams S; Huttner K; Rascher W; Bohring A
    J Med Genet; 2011 Jun; 48(6):426-32. PubMed ID: 21357618
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reliability of prenatal detection of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography.
    Hammersen J; Wohlfart S; Goecke TW; Köninger A; Stepan H; Gallinat R; Morris S; Bücher K; Clarke A; Wünsche S; Beckmann MW; Schneider H; Faschingbauer F
    Prenat Diagn; 2019 Aug; 39(9):796-805. PubMed ID: 30394555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.
    Clauss F; Chassaing N; Smahi A; Vincent MC; Calvas P; Molla M; Lesot H; Alembik Y; Hadj-Rabia S; Bodemer C; Manière MC; Schmittbuhl M
    Clin Genet; 2010 Sep; 78(3):257-66. PubMed ID: 20236127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation.
    Zeng B; Lu H; Xiao X; Zhou L; Lu J; Zhu L; Yu D; Zhao W
    Oral Dis; 2015 Nov; 21(8):994-1000. PubMed ID: 26411740
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnosis of X-Linked Hypohidrotic Ectodermal Dysplasia by Meibography and Infrared Thermography of the Eye.
    Kaercher T; Dietz J; Jacobi C; Berz R; Schneider H
    Curr Eye Res; 2015 Sep; 40(9):884-90. PubMed ID: 25310457
    [TBL] [Abstract][Full Text] [Related]  

  • 20. No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
    Körber L; Schneider H; Fleischer N; Maier-Wohlfart S
    Orphanet J Rare Dis; 2021 Feb; 16(1):98. PubMed ID: 33622384
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.