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 *

135 related articles for article (PubMed ID: 19189682)

  • 1. Congenital anodontia in ectodermal dysplasia.
    Pirgon O; Atabek ME; Tanju IA
    J Pediatr Endocrinol Metab; 2008 Dec; 21(12):1111-2. PubMed ID: 19189682
    [No Abstract]   [Full Text] [Related]  

  • 2. A clinico-pathologic presentation. Hereditary hypohidrotic ectodermal dysplasia, or HED.
    Cataldo E; Santis HR
    J Mass Dent Soc; 1996; 45(1):8. PubMed ID: 9520670
    [No Abstract]   [Full Text] [Related]  

  • 3. [Primary anodontia in X-linked hidrotic ectodermal dysplasia].
    Beliakov IuA; Elizarova VM; Smirnova TA; Krotov VA
    Stomatologiia (Mosk); 1998; 77(4):29-31. PubMed ID: 9752735
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial ectodermal dysplasia: a peers' agony.
    Hegde K; Kashyap RR; Nair G; Nair PP
    BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23880572
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
    Nakata M; Koshiba H; Eto K; Nance WE
    Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 'Double trouble': diagnostic challenges in genetic skin disorders.
    Kiritsi D; Valari M; Mileounis K; Bruckner-Tuderman L; Has C
    Br J Dermatol; 2015 Jan; 172(1):276-8. PubMed ID: 24902867
    [No Abstract]   [Full Text] [Related]  

  • 7. [Diagnosis and prosthodontic treatment of congenital ectodermal dysplasia with anodontia].
    Zhou SM
    Zhonghua Kou Qiang Ke Za Zhi; 1983 Sep; 18(3):179-81. PubMed ID: 6581032
    [No Abstract]   [Full Text] [Related]  

  • 8. [Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?].
    Le Marec B; Roussey M; Chevrant-Breton J; Segalen J; Bourdinière J; Sénécal J
    J Genet Hum; 1983 Dec; 31(4):279-93. PubMed ID: 6663288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.
    Spfaer JA
    J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study.
    Bowles B; Ferrer A; Nishimura CJ; Pinto E Vairo F; Rey T; Leheup B; Sullivan J; Schoch K; Stong N; Agolini E; Cocciadiferro D; Williams A; Cummings A; Loddo S; Genovese S; Roadhouse C; McWalter K; ; Wentzensen IM; Li C; Babovic-Vuksanovic D; Lanpher BC; Dentici ML; Ankala A; Hamm JA; Dallapiccola B; Radio FC; Shashi V; Gérard B; Bloch-Zupan A; Smith RJ; Klee EW
    Am J Med Genet A; 2021 Aug; 185(8):2417-2433. PubMed ID: 34042254
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Dental research on patients with anhidrotic ectodermal dysplasia (AED)].
    Hensel E; Hensel S
    Zahn Mund Kieferheilkd Zentralbl; 1988; 76(5):459-64. PubMed ID: 2972135
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
    Issa YA; Kamal L; Rayyan AA; Dweik D; Pierce S; Lee MK; King MC; Walsh T; Kanaan M
    Eur J Hum Genet; 2016 Oct; 24(10):1430-5. PubMed ID: 27049303
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ADULT syndrome: phenotype in a Brazilian family with the R298Q mutation.
    de Almeida HL; van Steensel M; Rocha A; Caspary P; Meijer R
    Int J Dermatol; 2019 Mar; 58(3):e72-e75. PubMed ID: 30656674
    [No Abstract]   [Full Text] [Related]  

  • 14. What syndrome is this? Witkop tooth and nail syndrome.
    Garzon MC; Paller AS
    Pediatr Dermatol; 1996; 13(1):63-4. PubMed ID: 8919531
    [No Abstract]   [Full Text] [Related]  

  • 15. Anhidrotic ectodermal dysplasia.
    Guha PK; Kishore V; Singh G; Rathore BS
    J Assoc Physicians India; 1987 Mar; 35(3):236-8. PubMed ID: 3611009
    [No Abstract]   [Full Text] [Related]  

  • 16. Concomitant hypohydrotic ectodermal dysplasia and Eβ-thalassemia in a child.
    Thapa R; Ghosh A
    J Pediatr Hematol Oncol; 2012 Apr; 34(3):e124-5. PubMed ID: 22441713
    [No Abstract]   [Full Text] [Related]  

  • 17. Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases.
    Vasconcelos Carvalho M; Romero Souto de Sousa J; Paiva Correa de Melo F; Fonseca Faro T; Nunes Santos AC; Carvalho S; Veras Sobral AP
    Dermatol Online J; 2013 Jul; 19(7):18985. PubMed ID: 24010518
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of familial ectodermal dysplasia.
    Yoshinaga T; Miyoshi S; Nishijima S; Yamamura Y
    Z Kinderheilkd; 1973 Aug; 115(1):77-82. PubMed ID: 4757189
    [No Abstract]   [Full Text] [Related]  

  • 19. Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias.
    Whittington A; Stein S; Kenner-Bell B
    Pediatr Dermatol; 2016 Sep; 33(5):e322-6. PubMed ID: 27469932
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Anhidrotic ectodermal dysplasia associated with anodontia and its genetic pattern].
    Nakata M; Koshiba Y
    Kokubyo Gakkai Zasshi; 1976 Jun; 43(2):185-6. PubMed ID: 1069057
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.