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

171 related items for PubMed ID: 19754869

  • 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. [Trichothiodystrophy: a morphological and biochemical study].
    Van Neste D, Boré P.
    Ann Dermatol Venereol; 1983; 110(5):409-17. PubMed ID: 6625462
    [Abstract] [Full Text] [Related]

  • 25. Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex.
    Price VH, Odom RB, Ward WH, Jones FT.
    Arch Dermatol; 1980 Dec; 116(12):1375-84. PubMed ID: 7458366
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Analysis of mutations in the XPD gene in a patient with brittle hair.
    Shin S, Kim J, Kim Y, Sun JY, Yoo JH, Lee KA.
    Ann Clin Lab Sci; 2013 Dec; 43(3):323-7. PubMed ID: 23884229
    [Abstract] [Full Text] [Related]

  • 28. Hair diagnoses and signs: the use of dermatoscopy.
    Wallace MP, de Berker DA.
    Clin Exp Dermatol; 2010 Jan; 35(1):41-6. PubMed ID: 19549236
    [Abstract] [Full Text] [Related]

  • 29. Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.
    Theil AF, Botta E, Raams A, Smith DEC, Mendes MI, Caligiuri G, Giachetti S, Bione S, Carriero R, Liberi G, Zardoni L, Swagemakers SMA, Salomons GS, Sarasin A, Lehmann A, van der Spek PJ, Ogi T, Hoeijmakers JHJ, Vermeulen W, Orioli D.
    Am J Hum Genet; 2019 Aug 01; 105(2):434-440. PubMed ID: 31374204
    [Abstract] [Full Text] [Related]

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

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

  • 32. [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].
    Poissonnier M, Blanc A, Bat P.
    J Genet Hum; 1988 Aug 01; 36(4):361-5. PubMed ID: 3221211
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. "Curly" wood and tiger tails: an explanation for light and dark banding with polarization in trichothiodystrophy.
    Sperling LC, DiGiovanna JJ.
    Arch Dermatol; 2003 Sep 01; 139(9):1189-92. PubMed ID: 12975162
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Diagnosis of trichothiodystrophy in 2 siblings.
    Bracun R, Hemmer W, Wolf-Abdolvahab S, Focke M, Botzi C, Killian W, Götz M, Jarisch R.
    Dermatology; 1997 Sep 01; 194(1):74-6. PubMed ID: 9031799
    [Abstract] [Full Text] [Related]

  • 37. DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.
    Takayama K, Danks DM, Salazar EP, Cleaver JE, Weber CA.
    Hum Mutat; 1997 Sep 01; 9(6):519-25. PubMed ID: 9195225
    [Abstract] [Full Text] [Related]

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

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

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.