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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

413 related items for PubMed ID: 15719880

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia.
    Lin TK, Huang CY, Lin MH, Chao SC.
    Clin Exp Dermatol; 2004 Sep; 29(5):536-8. PubMed ID: 15347342
    [Abstract] [Full Text] [Related]

  • 26. Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia.
    Yapijakis C, Douka A, Gintoni I, Agiannitopoulos K, Vlachakis D, Chrousos GP.
    Adv Exp Med Biol; 2023 Sep; 1423():181-186. PubMed ID: 37525042
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. [Ectodermal dysplasia syndrome].
    Mortier K, Wackens G.
    Ned Tijdschr Tandheelkd; 2003 May; 110(5):190-2. PubMed ID: 12784514
    [Abstract] [Full Text] [Related]

  • 29. Ectodermal dysplasia: otolaryngologic manifestations and management.
    Daniel E, McCurdy EA, Shashi V, McGuirt WF.
    Laryngoscope; 2002 Jun; 112(6):962-7. PubMed ID: 12160292
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Hypohidrotic ectodermal dysplasia (HED).
    Ahmed B, Yazdanie N.
    J Coll Physicians Surg Pak; 2006 Jan; 16(1):61-3. PubMed ID: 16441993
    [Abstract] [Full Text] [Related]

  • 33. Hypohidrotic ectodermal dysplasia--a case report.
    Gopinath VK, Manoj KM, Mahesh K.
    J Indian Soc Pedod Prev Dent; 1999 Sep; 17(3):90-2. PubMed ID: 10863497
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
    Azeem Z, Naqvi SK, Ansar M, Wali A, Naveed AK, Ali G, Hassan MJ, Tariq M, Basit S, Ahmad W.
    Arch Dermatol Res; 2009 Sep; 301(8):625-9. PubMed ID: 19551394
    [Abstract] [Full Text] [Related]

  • 36. Familial ectodermal dysplasia: a peers' agony.
    Hegde K, Kashyap RR, Nair G, Nair PP.
    BMJ Case Rep; 2013 Jul 23; 2013():. PubMed ID: 23880572
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Bibi N, Ahmad S, Ahmad W, Naeem M.
    Australas J Dermatol; 2011 Feb 23; 52(1):37-42. PubMed ID: 21332691
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 21.