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 *

140 related articles for article (PubMed ID: 7141791)

  • 41. Laurence-Moon-Biedl-Bardet syndrome in four kindreds.
    Penchaszadeh V; Walker BA
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):185-8. PubMed ID: 5173140
    [No Abstract]   [Full Text] [Related]  

  • 42. [Clinical aspects of the Laurence-Moon-Bardet-Biedl syndrome in Panama].
    Díaz E; Ward J
    Rev Med Panama; 1983 May; 8(2):156-9. PubMed ID: 6878759
    [No Abstract]   [Full Text] [Related]  

  • 43. Nail-patella syndrome.
    Sabnis SG; Antonovych TT; Argy WP; Rakowski TA; Gandy DR; Salcedo JR
    Clin Nephrol; 1980 Sep; 14(3):148-53. PubMed ID: 7418282
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Renal lipidosis associated with arteriohepatic dysplasia (Alagille's syndrome).
    Chung-Park M; Petrelli M; Tavill AS; Hall PW; Henoch MS; Dahms BB
    Clin Nephrol; 1982 Dec; 18(6):314-20. PubMed ID: 7151349
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The renal lesion of the Laurence-Moon-Biedl syndrome.
    Hurley RM; Dery P; Norady MB; Drummond KN
    J Pediatr; 1975 Aug; 87(2):206-9. PubMed ID: 1151560
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Hypokalemic paralysis and megaloblastic anaemia in Laurence-Moon-Bardet-Biedl syndrome.
    Abbasi A; Butt N; Sultan B; Munir SM
    J Coll Physicians Surg Pak; 2009 Mar; 19(3):186-8. PubMed ID: 19268021
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Urographic findings in the Bardet-Biedl syndrome, formerly the Laurence-Moon-Biedl syndrome.
    Alton DJ; McDonald P
    Radiology; 1973 Dec; 109(3):659-63. PubMed ID: 4772182
    [No Abstract]   [Full Text] [Related]  

  • 48. Renal diseases: a 27-year renal biopsy study.
    Carvalho E; do Sameiro Faria M; Nunes JP; Sampaio S; Valbuena C
    J Nephrol; 2006; 19(4):500-7. PubMed ID: 17048208
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinico-pathological profile of 22 cases of cystic renal dysplasia.
    Singh S; Gupta R; Nigam S; Khurana N; Aggarwal SK; Chaturvedi KU; Mandal AK
    Indian J Pathol Microbiol; 2007 Jan; 50(1):6-10. PubMed ID: 17474245
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Bardet-Biedl syndrome. Apropos of a family].
    Guízar-Vázquez JJ; Escobar-Morales BG; Valdés de Fromow ML; Salamanca-Gómez F
    Bol Med Hosp Infant Mex; 1984 Aug; 41(8):442-6. PubMed ID: 6477712
    [No Abstract]   [Full Text] [Related]  

  • 51. Laurence-Moon-Bardet-Biedl syndrome in combination with Cotard's syndrome. Case report.
    Lerner V; Bergman J; Greenberg D; Bar-El Y
    Isr J Psychiatry Relat Sci; 1995; 32(4):291-4. PubMed ID: 8641859
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A familial syndrome of growth retardation, severe Fanconi-type renal disease and glomerular changes--a new entity?
    Bartsocas CS; Bernstein J; Orloff S; Chandra R; Schulman JD
    Int J Pediatr Nephrol; 1986; 7(2):101-6. PubMed ID: 3721723
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome.
    Katsanis N; Beales PL; Woods MO; Lewis RA; Green JS; Parfrey PS; Ansley SJ; Davidson WS; Lupski JR
    Nat Genet; 2000 Sep; 26(1):67-70. PubMed ID: 10973251
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Clinicopathologic characteristics of 1,316 children with renal disease].
    Dang XQ; Yi ZW; He XJ; Wu XC; Cao Y; Mo SH; He QN; Guan FJ; Huang DL
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Apr; 9(2):117-21. PubMed ID: 17448305
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
    Slavotinek AM; Searby C; Al-Gazali L; Hennekam RC; Schrander-Stumpel C; Orcana-Losa M; Pardo-Reoyo S; Cantani A; Kumar D; Capellini Q; Neri G; Zackai E; Biesecker LG
    Hum Genet; 2002 Jun; 110(6):561-7. PubMed ID: 12107442
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Early sonographic aspects of kidney morphology in Bardet-Biedl syndrome.
    Dippell J; Varlam DE
    Pediatr Nephrol; 1998 Sep; 12(7):559-63. PubMed ID: 9761354
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Familial juvenile nephronophthisis--a cause of chronic renal failure in childhood].
    Vergesslich KA; Ponhold W; Balzar E; Syrè G; Ulrich W
    Wien Klin Wochenschr; 1986 May; 98(11):351-5. PubMed ID: 3524015
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Clinical aspects of bilateral renal dysplasia in children.
    Gur A; Siegel NJ; Davis DA; Kashgarian MK; Hayslett JP
    Nephron; 1975; 15(1):50-61. PubMed ID: 236522
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Phenotypic overlap of McKusick-Kaufman syndrome with bardet-biedl syndrome: a literature review.
    Slavotinek AM; Biesecker LG
    Am J Med Genet; 2000 Nov; 95(3):208-15. PubMed ID: 11102925
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Clinical and histopathological characteristics of biopsy-proven renal diseases in Croatia].
    Batinić D; Sćukanec-Spoljar M; Milosević D; Subat-Dezulović M; Saraga M; Delmis J; Puretić Z; Cvitkovic-Kuzmić A; Skitarelić N; Spajic M; Nizić L; Vrljicak K; Matković M; Kniewald H; Batinić D; Grković L; Borojević I; Flajsman S; Kosuljandić-Vukić D; Marić S; Ljubanović D
    Acta Med Croatica; 2007 Sep; 61(4):361-4. PubMed ID: 18044469
    [TBL] [Abstract][Full Text] [Related]  

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