BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 3870940)

  • 1. The Laurence-Moon-Bardet-Biedl-syndrome.
    Luz MF; Marques MN; Jorge E; Jacomini CZ; Ribero Z; Marques J
    Metab Pediatr Syst Ophthalmol (1985); 1985; 8(2-3):15-20. PubMed ID: 3870940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome.
    Green JS; Parfrey PS; Harnett JD; Farid NR; Cramer BC; Johnson G; Heath O; McManamon PJ; O'Leary E; Pryse-Phillips W
    N Engl J Med; 1989 Oct; 321(15):1002-9. PubMed ID: 2779627
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Case report of Laurence-Moon-Bardet-Biedl syndrome].
    Osusky R; Alsaadi AH; Farpour H
    Klin Monbl Augenheilkd; 1991 May; 198(5):445-6. PubMed ID: 1886381
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Laurence-Moon-Bardet-Biedl disease. A clinical contribution (author's transl)].
    Lovisetto P; Biarese V; Trenta N; Rizzi G
    Ann Endocrinol (Paris); 1974; 35(5):547-61. PubMed ID: 4377073
    [No Abstract]   [Full Text] [Related]  

  • 5. Bardet-Biedl syndrome.
    Steiner PA
    J Am Optom Assoc; 1990 Nov; 61(11):852-5. PubMed ID: 2081829
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family.
    Endo M; Tasaka Y; Matsuura N; Matsuda I
    Eur J Pediatr; 1976 Nov; 123(4):269-76. PubMed ID: 991874
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assessment of ophthalmologic, endocrinologic and genetic findings in the Bardet-Biedl syndrome.
    Bergsma DR; Brown KS
    Birth Defects Orig Artic Ser; 1975; 11(2):132-6. PubMed ID: 776244
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Visual function in Laurence-Moon-Bardet-Biedl syndrome. A survey of 26 cases.
    Riise R
    Acta Ophthalmol Suppl (1985); 1987; 182():128-31. PubMed ID: 2837047
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Laurence-Moon syndrome: evaluation of endocrinological function and phenotypic concordance and report of cases.
    Dekaban AS; Parks JS; Ross GT
    Med Ann Dist Columbia; 1972 Nov; 41(11):687-94. PubMed ID: 4508225
    [No Abstract]   [Full Text] [Related]  

  • 10. Laurence-Moon-Biedl-Bardet syndrome: the factor that can blind a family.
    Cowie V
    Nurs Mirror; 1978 Dec; 147(24):36-7. PubMed ID: 252048
    [No Abstract]   [Full Text] [Related]  

  • 11. Laurence-Moon-Bardet-Biedl syndrome: electrophysical and psychophysical findings.
    Katsumi O; Tanino T; Hirose T; Larson EW; Skladzien CJ
    Jpn J Ophthalmol; 1985; 29(3):282-9. PubMed ID: 4079125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Chromosomal aberrations in the Laurence-Moon-Bardet-Biedl syndrome].
    Muchnik SR; Shcherbina AF; Starodubtseva EI
    Oftalmol Zh; 1972; 27(7):517-21. PubMed ID: 4668130
    [No Abstract]   [Full Text] [Related]  

  • 13. [Nosography of the Laurence-Moon-Bardet-Biedl syndrome].
    Argenta G; Sadun D; De Giorgio R
    Riv Neurol; 1976; 46(2):93-101. PubMed ID: 1006077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies.
    Klein D; Ammann F
    J Neurol Sci; 1969; 9(3):479-513. PubMed ID: 5367041
    [No Abstract]   [Full Text] [Related]  

  • 15. [Laurence-Moon-Biedl-Bardet disease].
    Aleksandrov IuS
    Pediatriia; 1976 Aug; (8):89-90. PubMed ID: 1012823
    [No Abstract]   [Full Text] [Related]  

  • 16. Lawrence-Moon-Bardet-Biedl syndrome: a case report.
    Obikili AG
    West Afr J Med; 1990; 9(3):239-41. PubMed ID: 2271440
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
    Rizzo JF; Berson EL; Lessell S
    Ophthalmology; 1986 Nov; 93(11):1452-6. PubMed ID: 3808607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sex chromosome aneuploidy and Bardet-Biedl syndrome.
    Grossniklaus HE; Muir A; Bruner WE; Annable W; Dickerman LL; Johnson WE
    Ophthalmic Paediatr Genet; 1988 Mar; 9(1):37-42. PubMed ID: 3405592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Skeletal anomalies in genetically determined congenital heart disease.
    Poznanski AK; Stern AM; Gall JC
    Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
    [No Abstract]   [Full Text] [Related]  

  • 20. [Laurence-Moon-Bardet-Biedl syndrome, chronic diffuse tubulo-interstitial nephritis and liver involvement].
    Roussel B; Leroux B; Gaillard D; Fandre M
    Helv Paediatr Acta; 1985 Dec; 40(5):405-13. PubMed ID: 4086314
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.