BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 37646348)

  • 1. The Ectodermal Dysplasias-Burden of Disease Score: Development and Validation of an Ectodermal Dysplasia Family/Parental Burden Score.
    Dufresne H; Maincent O; Taieb C; Bodemer C; Hadj-Rabia S
    Acta Derm Venereol; 2023 Aug; 103():adv5203. PubMed ID: 37646348
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. Quality of life of cutaneous disease in the ectodermal dysplasias.
    Pavlis MB; Rice ZP; Veledar E; Bradley BR; Spraker MK; Chen SC
    Pediatr Dermatol; 2010; 27(3):260-5. PubMed ID: 20609143
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M; Chishti MS; Ali G; Ahmad W
    Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Burden of albinism: development and validation of a burden assessment tool.
    Morice-Picard F; Taïeb C; Marti A; Gliksohn A; Bennani M; Bodemer C; Ezzedine K;
    Orphanet J Rare Dis; 2018 Sep; 13(1):162. PubMed ID: 30227882
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prevalence and Patient Characteristics of Ectodermal Dysplasias in Denmark.
    Herlin LK; Schmidt SAJ; Hermann XB; Rønholt K; Bygum A; Schuster A; Lei U; Mogensen M; Vinding GR; Djursby M; Hove H; Blechingberg J; Graversen L; Mogensen TH; Gjørup H; Langan SM; Sommerlund M
    JAMA Dermatol; 2024 May; 160(5):502-510. PubMed ID: 38477886
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
    Naeem M; John P; Ali G; Ahmad W
    Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment.
    Bergendal B
    Swed Dent J Suppl; 2010; (205):13-78, 7-8. PubMed ID: 20626136
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Incontinentia pigmenti burden scale: designing a family burden questionnaire.
    Taieb C; Hadj-Rabia S; Monnet J; Bennani M; Bodemer C;
    Orphanet J Rare Dis; 2019 Nov; 14(1):271. PubMed ID: 31771608
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update.
    Peschel N; Wright JT; Koster MI; Clarke AJ; Tadini G; Fete M; Hadj-Rabia S; Sybert VP; Norderyd J; Maier-Wohlfart S; Fete TJ; Pagnan N; Visinoni AF; Schneider H
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553593
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ectodermal dysplasia with tetramelic deficiencies and no mutation in p63: odontotrichomelic syndrome or a new entity?
    Zankl A; Scheffer H; Schinzel A
    Am J Med Genet A; 2004 May; 127A(1):74-80. PubMed ID: 15103722
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Family with "pure" hair-nail ectodermal dysplasia.
    Barbareschi M; Cambiaghi S; Crupi AC; Tadini G
    Am J Med Genet; 1997 Oct; 72(1):91-3. PubMed ID: 9295083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hair and sweat glands in families with hypohidrotic ectodermal dysplasia: further characterization.
    Rouse C; Siegfried E; Breer W; Nahass G
    Arch Dermatol; 2004 Jul; 140(7):850-5. PubMed ID: 15262696
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31.
    Habib R; Ansar M; Mattheisen M; Shahid M; Ali G; Ahmad W; Betz RC
    PLoS One; 2015; 10(6):e0129811. PubMed ID: 26115030
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Classifying functional manifestations of ectodermal dysplasias.
    Simeonsson RJ
    Am J Med Genet A; 2009 Sep; 149A(9):2014-9. PubMed ID: 19681156
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.