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 *

120 related articles for article (PubMed ID: 21220888)

  • 21. Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions.
    Djabali K; Zlotogorski A; Metzker A; Ben-Amitai D; Christiano AM
    Exp Dermatol; 2004 Apr; 13(4):251-6. PubMed ID: 15086341
    [TBL] [Abstract][Full Text] [Related]  

  • 22. JAAD Grand rounds quiz. Cicatricial alopecia.
    Berlin JM; Wang AL; McDuffie BC; Leeman DR
    J Am Acad Dermatol; 2010 Sep; 63(3):547-8. PubMed ID: 20708483
    [No Abstract]   [Full Text] [Related]  

  • 23. Electrophysiology extends the phenotypic spectrum of X-linked myopathy with excessive autophagy.
    Munteanu I; Ackerley CA; Mnatzakanian GN; Kissel JT; Minassian BA
    Neurology; 2005 Mar; 64(5):927-8. PubMed ID: 15753448
    [No Abstract]   [Full Text] [Related]  

  • 24. Preimplantation genetic diagnosis.
    Braude P; Pickering S; Flinter F; Ogilvie CM
    Nat Rev Genet; 2002 Dec; 3(12):941-53. PubMed ID: 12459724
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene: A lesson for differential diagnosis of alopecia universalis.
    Henn W; Zlotogorski A; Lam H; Martinez-Mir A; Zaun H; Christiano AM
    J Am Acad Dermatol; 2002 Oct; 47(4):519-23. PubMed ID: 12271294
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a new mutation in the gene coding for hairless protein responsible for alopecia universalis: The importance of direct gene sequencing.
    Nucara S; Colao E; Mangone G; Baudi F; Fabiani F; Nocera D; Passafaro G; Longo T; Laria AE; Malatesta P; Amato R; Trapasso F; Perrotti N
    Dermatol Online J; 2011 Jan; 17(1):3. PubMed ID: 21272494
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.
    Wali A; Ansar M; Khan MN; Ahmad W
    Clin Exp Dermatol; 2006 Sep; 31(5):695-8. PubMed ID: 16901311
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Atrichia with papular lesions resulting from novel compound heterozygous mutations in the human hairless gene.
    Michailidis E; Theos A; Zlotogorski A; Martinez-Mir A; Christiano AM
    Pediatr Dermatol; 2007; 24(5):E79-82. PubMed ID: 17958788
    [TBL] [Abstract][Full Text] [Related]  

  • 29. X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease.
    Isoardo G; Di Vito N; Nobile M; Benetton G; Fassio F
    Neurology; 2005 Nov; 65(10):1672-3. PubMed ID: 16301507
    [No Abstract]   [Full Text] [Related]  

  • 30. Papular elastorrhexis, a distinctive entity?
    Del Pozo J; Martínez W; Sacristán F; Fernández-Jorge B; Fonseca E
    Am J Dermatopathol; 2008 Apr; 30(2):188-90. PubMed ID: 18360129
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Five years' experience of preimplantation genetic diagnosis in the Parisian Center: outcome of the first 441 started cycles.
    Feyereisen E; Steffann J; Romana S; Lelorc'h M; Ray P; Kerbrat V; Tachdjian G; Frydman R; Frydman N
    Fertil Steril; 2007 Jan; 87(1):60-73. PubMed ID: 17074325
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pinpoint white dots in the scalp: dermoscopic and histopathologic correlation.
    Abraham LS; Piñeiro-Maceira J; Duque-Estrada B; Barcaui CB; Sodré CT
    J Am Acad Dermatol; 2010 Oct; 63(4):721-2. PubMed ID: 20846575
    [No Abstract]   [Full Text] [Related]  

  • 33. Conradi-Hünermann-Happle syndrome.
    Hartman RD; Molho-Pessach V; Schaffer JV
    Dermatol Online J; 2010 Nov; 16(11):4. PubMed ID: 21163155
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of a recurrent mutation in the human hairless gene underlying atrichia with papular lesions.
    Massé M; Martinez-Mir A; Lam H; Geraghty MT; Christiano AM
    Clin Exp Dermatol; 2005 Jul; 30(4):363-5. PubMed ID: 15953070
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [X-linked hypogammaglobulinemia with growth hormone deficiency].
    Okada S; Miyagawa S; Nishimura S; Kobayashi M; Nishi Y
    Nihon Rinsho; 2006 May; Suppl 1():67-9. PubMed ID: 16776095
    [No Abstract]   [Full Text] [Related]  

  • 36. Familial localized connective tissue nevus of the scalp with alopecia (report of a very unusual case).
    Aroni K; Kyriazi E; Aivaliotis M; Davaris P
    J Eur Acad Dermatol Venereol; 2004 May; 18(3):340-1. PubMed ID: 15096150
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Atrichia with papular lesions and mental retardation in two sisters.
    del Castillo V; Ruiz-Maldonado R; Carnevale A
    Int J Dermatol; 1974; 13(5):261-5. PubMed ID: 4418335
    [No Abstract]   [Full Text] [Related]  

  • 38. A hairy paradox: congenital triangular alopecia with a central hair tuft.
    Assouly P; Happle R
    Dermatology; 2010; 221(2):107-9. PubMed ID: 20587991
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Superimposed linear lichen planopilaris: another polygenic disorder exemplifying a new genetic concept.
    Bussmann C; Happle R; Baar W; Bieber T; Haidl G; Novak N
    Eur J Dermatol; 2010; 20(3):269-70. PubMed ID: 20483712
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Reticulate Pigmentation with Systemic Manifestations in a Child.
    Duman N; Ersoy-Evans S; Gököz Ö
    Pediatr Dermatol; 2015; 32(6):871-2. PubMed ID: 26584697
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.