BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 1476579)

  • 1. Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia.
    Gyure KA; Kurczynski TW; Gunning W; French BN
    Pediatr Neurol; 1992; 8(6):469-72. PubMed ID: 1476579
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Restrictive dermopathy].
    Gross C; Hausser I; von der Wense A; Langner C; Simoens W; Bau O; Rompel R; Meyer W; Rüschoff J
    Pathologe; 1999 Nov; 20(6):365-70. PubMed ID: 10591957
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis.
    Argenziano G; Monsurrò MR; Pazienza R; Delfino M
    J Am Acad Dermatol; 1998 Feb; 38(2 Pt 2):344-8. PubMed ID: 9486713
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital anhidrotic ectodermal dysplasia in a female infant].
    Riedler J
    Monatsschr Kinderheilkd; 1992 Jul; 140(7):398-400. PubMed ID: 1501613
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters.
    Stoll C; Alembik Y; Finck S; Janser B
    Genet Couns; 1992; 3(1):35-9. PubMed ID: 1590979
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trichorrhexis nodosa and lip pits in autosomal dominant ectodermal dysplasia--central nervous system malformation syndrome.
    Silengo M; Pietragalla A; Jarre L
    Am J Med Genet; 1997 Aug; 71(2):226-8. PubMed ID: 9217228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Autosomal recessive ectodermal dysplasia--a special nosologic entity? (author's transl)].
    Lelis J
    Dermatol Monatsschr; 1979 Aug; 165(8):587-92. PubMed ID: 159839
    [No Abstract]   [Full Text] [Related]  

  • 8. Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
    Ohdo S; Madokoro H; Sonoda T; Takei M; Yasuda H; Mori N
    J Med Genet; 1987 Oct; 24(10):609-12. PubMed ID: 3681906
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
    Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
    Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Comèl-Netherton syndrome].
    Blaschke S; Möller R; Hausser I; Anton-Lamprecht I; Paul E
    Hautarzt; 1998 Jun; 49(6):499-504. PubMed ID: 9675580
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hidrotic ectodermal dysplasia].
    Altmeyer P; Schindera I
    Hautarzt; 1975 Dec; 26(12):631-7. PubMed ID: 1213883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].
    Costet C; Betis F; Bérard E; Tsimaratos M; Sigaudy S; Antignac C; Gastaud P
    J Fr Ophtalmol; 2000 Feb; 23(2):158-60. PubMed ID: 10705117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition.
    Hay RJ; Wells RS
    Br J Dermatol; 1976 Mar; 94(3):277-89. PubMed ID: 946410
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cutaneous findings in a new syndrome of autosomal recessive ectodermal dysplasia with corkscrew hairs.
    Abramovits-Ackerman W; Bustos T; Simosa-Leon V; Fernandez L; Ramella M
    J Am Acad Dermatol; 1992 Dec; 27(6 Pt 1):917-21. PubMed ID: 1479096
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Netherton's syndrome. Ichthyosis-like changes in the skin and trichorrhexis invaginata. Demonstration of pathologically changed cortex keratin in the hair].
    Orfanos CE; Mahrle G; Salamon T
    Hautarzt; 1971 Sep; 22(9):397-409. PubMed ID: 5172063
    [No Abstract]   [Full Text] [Related]  

  • 16. A distinct type of hidrotic ectodermal dysplasia.
    Halal F; Setton N; Wang NS
    Am J Med Genet; 1991 Mar; 38(4):552-6. PubMed ID: 2063897
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Infantile progressive striato-thalamic degeneration in two siblings: a new syndrome.
    Gieron MA; Gilbert-Barness E; Vonsattel JP; Korthals JK
    Pediatr Neurol; 1995 Apr; 12(3):260-3. PubMed ID: 7619197
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alopecia: syndromes of genetic significance.
    Muller SA
    J Invest Dermatol; 1973 Jun; 60(6):475-92. PubMed ID: 4581946
    [No Abstract]   [Full Text] [Related]  

  • 19. Black hair follicular dysplasia, an autosomal recessive condition in dogs.
    Schmutz SM; Moker JS; Clark EG; Shewfelt R
    Can Vet J; 1998 Oct; 39(10):644-6. PubMed ID: 9789677
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome-McKusick 10030): further suggestion of autosomal recessive inheritance.
    Sybert VP
    Am J Med Genet; 1989 Feb; 32(2):266-7. PubMed ID: 2929669
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.