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 *

100 related articles for article (PubMed ID: 3813407)

  • 1. [The FLOTCH syndrome. Familial occurrence of total LeukOnychia, Trichilemmal cysts and Ciliary dystrophy with dominant autosomal Heredity].
    Friedel J; Heid E; Grosshans E
    Ann Dermatol Venereol; 1986; 113(6-7):549-53. PubMed ID: 3813407
    [No Abstract]   [Full Text] [Related]  

  • 2. Leukonychia totalis associated with multiple pilar cysts: report of a five-generation family: FLOTCH syndrome?
    Rodríguez-Lojo R; Del Pozo J; Sacristán F; Barja J; Piñeyro-Molina F; Pérez-Varela L
    Eur J Dermatol; 2011; 21(4):484-6. PubMed ID: 21659070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FLOTCH Syndrome: A Case of Leukonychia Totalis and Multiple Pilar Cysts.
    Mansour M; Brothers R; Brothers R
    Cutis; 2023 Oct; 112(4):200-202. PubMed ID: 37988304
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Hereditary leukonychia totalis, acanthosis-nigricans-like lesions and hair dysplasia: a new syndrome?
    Le Corre Y; Steff M; Croue A; Filmon R; Verret JL; Le Clech C
    Eur J Med Genet; 2009; 52(4):229-33. PubMed ID: 19401242
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetics of hereditary hair and nail disease.
    van Steensel MA; van Geel M; Steijlen PM
    Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):52-60. PubMed ID: 15468149
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A syndrome: uncombable hair. Observation of 6 members of a family with pili canaliculi, associated with pili torti, progressive alopecia, atopic eczema and hamartomas].
    Braun-Falco O; Ryckmanns F; Heilgemeir GP; Ring J
    Hautarzt; 1982 Jul; 33(7):366-72. PubMed ID: 7107281
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heritable nail disorders.
    Kucirka SJ; Scher RK
    Dermatol Clin; 1987 Jan; 5(1):179-91. PubMed ID: 3030593
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Monilethrix: exclusive involvement of body hair].
    Hamm H; Echternacht-Happle K; Happle R
    Z Hautkr; 1984 Sep; 59(17):1177-8. PubMed ID: 6485460
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dominant dystrophic epidermolysis bullosa presenting as familial nail dystrophy.
    Dharma B; Moss C; McGrath JA; Mellerio JE; Ilchyshyn A
    Clin Exp Dermatol; 2001 Jan; 26(1):93-6. PubMed ID: 11260188
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Monilethrix].
    Zimmermann R
    Dermatol Monatsschr; 1983; 169(10):638-45. PubMed ID: 6642030
    [No Abstract]   [Full Text] [Related]  

  • 12. [Colobomatous microphthalmos with cyst and 4 P- syndrome].
    Baudet D; Defawe G; Le Marec B; Picard F; Nicaise A; Urvoy M
    Bull Soc Ophtalmol Fr; 1984 Jan; 84(1):67-8. PubMed ID: 6529828
    [No Abstract]   [Full Text] [Related]  

  • 13. Pili trianguli canaliculi: uncombable hair syndrome in a family with apparent autosomal dominant inheritance.
    de Luna MM; Rubinson R; de Kohan ZB
    Pediatr Dermatol; 1985 Jul; 2(4):324-7. PubMed ID: 4011511
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.
    Nagy N; Wedgeworth E; Hamada T; White JM; Hashimoto T; McGrath JA
    J Dermatol Sci; 2010 Jun; 58(3):220-2. PubMed ID: 20418069
    [No Abstract]   [Full Text] [Related]  

  • 15. Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia.
    Boulé S; Fressart V; Laux D; Mallet A; Simon F; de Groote P; Bonnet D; Klug D; Charron P
    Int J Cardiol; 2012 Nov; 161(1):50-2. PubMed ID: 22795705
    [No Abstract]   [Full Text] [Related]  

  • 16. Werner's syndrome.
    Duvic M; Lemak NA
    Dermatol Clin; 1995 Jan; 13(1):163-8. PubMed ID: 7712642
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
    Stoll C; Roth MP; Hessemann H; Paira M
    Arch Fr Pediatr; 1983 Dec; 40(10):763-6. PubMed ID: 6673680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic hair and nail disorders.
    Sprecher E
    Clin Dermatol; 2005; 23(1):47-55. PubMed ID: 15708289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial trichomegaly.
    Harrison DA; Mullaney PB
    Arch Ophthalmol; 1997 Dec; 115(12):1602-3. PubMed ID: 9400804
    [No Abstract]   [Full Text] [Related]  

  • 20. [Schopf-Schulz-Passarge syndrome: 2 cases].
    Gkolfinopoulos T; Ingen-Housz-Oro S; Cavelier-Balloy B; Blanchet-Bardon C
    Ann Dermatol Venereol; 2001 Dec; 128(12):1330-3. PubMed ID: 11908136
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.