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 *

125 related articles for article (PubMed ID: 7735410)

  • 21. Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.
    Winter H; Rogers MA; Langbein L; Stevens HP; Leigh IM; Labrèze C; Roul S; Taieb A; Krieg T; Schweizer J
    Nat Genet; 1997 Aug; 16(4):372-4. PubMed ID: 9241275
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1.
    Winter H; Labrèze C; Chapalain V; Surlève-Bazeille JE; Mercier M; Rogers MA; Taieb A; Schweizer J
    J Invest Dermatol; 1998 Jul; 111(1):169-72. PubMed ID: 9665406
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Localized monilethrix with improvement after treatment of iron deficiency anaemia.
    Karaman GC; Sendur N; Basar H; Bozkurt Savk E
    J Eur Acad Dermatol Venereol; 2001 Jul; 15(4):362-4. PubMed ID: 11730057
    [No Abstract]   [Full Text] [Related]  

  • 24. Hair loss in a 6-month-old child. Monilethrix.
    Amichai B; Metzker A
    Arch Dermatol; 1996 May; 132(5):574-5, 577-8. PubMed ID: 8624158
    [No Abstract]   [Full Text] [Related]  

  • 25. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
    Schaffer JV; Bazzi H; Vitebsky A; Witkiewicz A; Kovich OI; Kamino H; Shapiro LS; Amin SP; Orlow SJ; Christiano AM
    J Invest Dermatol; 2006 Jun; 126(6):1286-91. PubMed ID: 16543896
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Congenital and hereditary hair abnormalities.
    Dawber R
    Exp Dermatol; 1999 Aug; 8(4):296-7. PubMed ID: 10439227
    [No Abstract]   [Full Text] [Related]  

  • 27. Review and new case reports on scanning electron microscopy of pili annulati, Monilethrix and Trichothiodystrophy.
    Meyvisch K; Song M; Dourov N
    Scanning Microsc; 1992 Jun; 6(2):537-41. PubMed ID: 1462138
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Keratosis pilaris and hereditary koilonychia without monilethrix.
    Thai KE; Sinclair RD
    J Am Acad Dermatol; 2001 Oct; 45(4):627-9. PubMed ID: 11568761
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hair casts: a clinical and morphologic control study.
    Shieh X; Yi X
    Arch Dermatol; 1992 Nov; 128(11):1553-4. PubMed ID: 1444518
    [No Abstract]   [Full Text] [Related]  

  • 30. Trichothiodystrophic hair reveals an abnormal pattern of viscoelastic parameters.
    Tsambaos D; Nikiforidis G; Balas C; Marinoni S
    Skin Pharmacol; 1994; 7(5):257-61. PubMed ID: 8054207
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ancient observations of "uncombable hair syndrome".
    Zanca A; Zanca A
    Int J Dermatol; 1993 Oct; 32(10):707. PubMed ID: 8225707
    [No Abstract]   [Full Text] [Related]  

  • 32. Picture of the month. Uncombable hair (pili trianguli et canaliculi).
    Navarini AA; Kaufmann F; Kaech A; Trüeb RM; Weibel L
    Arch Pediatr Adolesc Med; 2010 Dec; 164(12):1165-6. PubMed ID: 21135347
    [No Abstract]   [Full Text] [Related]  

  • 33. Monilethrix: an electron microscopic and electron histochemical study.
    Gummer CL; Dawber RP; Swift JA
    Br J Dermatol; 1981 Nov; 105(5):529-41. PubMed ID: 7295569
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial multiple trichodiscomas.
    Camarasa JG; Calderon P; Moreno A
    Acta Derm Venereol; 1988; 68(2):163-5. PubMed ID: 2453999
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndrome.
    Silengo MC; Davi GF; Bianco R; Costa M; DeMarco A; Verona R; Franceschini P
    Clin Genet; 1982 May; 21(5):297-300. PubMed ID: 7116674
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Changes in the hair in a case of biotinidase deficiency].
    Calvieri S; Giustini S; Camplone G; Innocenzi D
    Ann Dermatol Venereol; 1989; 116(11):802-4. PubMed ID: 2619167
    [No Abstract]   [Full Text] [Related]  

  • 37. [Monilethrix--rare syndrome of structural hair abnormalities].
    Brzezińska-Wcisło L; Bogdanowski T; Szeremeta-Bazylewicz G; Pierzchała E
    Pol Merkur Lekarski; 1999 Nov; 7(41):226-8. PubMed ID: 10680457
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Hair dysplasia in oculo-dento-digital syndrome. Apropos of a mother-daughter case].
    Adamski H; Chevrant-Breton J; Odent S; Patoux-Pibouin M; Le Marec B; Laudren A; Urvoy M
    Ann Dermatol Venereol; 1994; 121(10):694-9. PubMed ID: 7793757
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The heat shrink tube technology--a simple method for making hair cross sections.
    Wagner G; Heine M; Sachse MM
    J Dtsch Dermatol Ges; 2015 Jan; 13(1):55-7. PubMed ID: 25640500
    [No Abstract]   [Full Text] [Related]  

  • 40. [Hair cylinders].
    Rüdlinger R; Vogel A; Meyer J; Zisiadis S; Wüthrich B
    Hautarzt; 1984 Feb; 35(2):88-91. PubMed ID: 6706582
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.