BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 3449470)

  • 1. Infantile nephronophthisis.
    Bodaghi E; Honarmand MT; Ahmadi M
    Int J Pediatr Nephrol; 1987; 8(4):207-10. PubMed ID: 3449470
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Nephronophthisis: study of 10 cases. Incidence, natural history and associated pathology (author's transl)].
    Gómez Campderá FJ; Niembro E; López Gómez JM; Canals MJ; Bárcenas MC; Gómez JA; Rengel MA; Luque de Pablos A
    Med Clin (Barc); 1981 Oct; 77(6):230-5. PubMed ID: 7321636
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Juvenile nephronophthisis with calcification of basal ganglia and pancreatic insufficiency.
    Raafat F; Morita M; Lau M; Taylor CM; White RH
    Arch Pathol Lab Med; 1988 Jun; 112(6):630-3. PubMed ID: 3377663
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Juvenile nephronophthisis, congenital hepatic fibrosis and retinal hypoplasia in twins.
    Delaney V; Mullaney J; Bourke E
    Q J Med; 1978 Jul; 47(187):281-90. PubMed ID: 568809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial juvenile nephronophthisis and renal transplantation in two siblings.
    Yoshida A; Morozumi K; Koyama K; Takeda A; Uchida K; Tominaga Y; Oikawa T; Fujinami T; Takagi H
    Nihon Jinzo Gakkai Shi; 1992 Sep; 34(9):1035-9. PubMed ID: 1479732
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Juvenile nephronophthisis and medullary cystic disease--the same disease (report of a large family with medullary cystic disease associated with gout and epilepsy).
    Burke JR; Inglis JA; Craswell PW; Mitchell KR; Emmerson BT
    Clin Nephrol; 1982 Jul; 18(1):1-8. PubMed ID: 7116701
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Retrospective diagnosis of Jeune's syndrome in two patients with chronic renal failure.
    Ring E; Zobel G; Ratschek M; Trop M; Wendler H
    Child Nephrol Urol; 1990; 10(2):88-91. PubMed ID: 2253258
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial juvenile nephronophthisis. Report of cases in two siblings].
    Gekle D; Brunnberg J
    Klin Padiatr; 1972 May; 184(3):213-9. PubMed ID: 5065501
    [No Abstract]   [Full Text] [Related]  

  • 9. Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis.
    Mistry K; Ireland JH; Ng RC; Henderson JM; Pollak MR
    Am J Kidney Dis; 2007 Nov; 50(5):855-64. PubMed ID: 17954299
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Progression of chronic kidney disease in children with vesicoureteral reflux: the North American Pediatric Renal Trials Collaborative Studies Database.
    Novak TE; Mathews R; Martz K; Neu A
    J Urol; 2009 Oct; 182(4 Suppl):1678-81. PubMed ID: 19692051
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Juvenile nephronophthisis with blindness in a three-month-old infant. Senior's syndrome associated with relative parathyroid insufficiency.
    Gruppuso PA; O'Shea PA; Orson JM; Brem AS
    Clin Pediatr (Phila); 1983 Feb; 22(2):114-8. PubMed ID: 6822015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Nephronophthisis, tapeto-retinal degeneration, encephalopathy and vermian agenesis: a new association. Apropos of 3 familial cases].
    Marchal JL; Hehunstre JP; Deminière C; Guérin J; Romanet P
    Ann Pediatr (Paris); 1989 Feb; 36(2):126-31. PubMed ID: 2648941
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Nephronophthisis].
    Loirat C
    Rev Prat; 1997 Sep; 47(14):1541-4. PubMed ID: 9366111
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Nephronophtisis].
    Niaudet P; Salomon R
    Nephrol Ther; 2006 Sep; 2(4):200-6. PubMed ID: 16966065
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Children with chronic renal failure in the Federal Republic of Germany: II. Primary renal diseases, age and intervals from early renal failure to renal death. Arbeitsgemeinschaft für Pädiatrische Nephrologie.
    Pistor K; Schärer K; Olbing H; Tamminen-Möbius T
    Clin Nephrol; 1985 Jun; 23(6):278-84. PubMed ID: 4028524
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetics of kidney diseases and renal fibrosis].
    Grünfeld JP; Chauveau D; Joly D; Oualim Z
    Bull Acad Natl Med; 1999; 183(1):57-63. PubMed ID: 10371765
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.
    Antignac C; Arduy CH; Beckmann JS; Benessy F; Gros F; Medhioub M; Hildebrandt F; Dufier JL; Kleinknecht C; Broyer M
    Nat Genet; 1993 Apr; 3(4):342-5. PubMed ID: 7981755
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early proteinuria and irreversible renal failure after kidney donation in a patient with a family history of renal disease.
    Rubinger D; Silver J; Friedlaender MM; Popovtzer MM
    Isr J Med Sci; 1988; 24(4-5):257-8. PubMed ID: 3288593
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutations of NPHP2 and NPHP3 in infantile nephronophthisis.
    Tory K; Rousset-Rouvière C; Gubler MC; Morinière V; Pawtowski A; Becker C; Guyot C; Gié S; Frishberg Y; Nivet H; Deschênes G; Cochat P; Gagnadoux MF; Saunier S; Antignac C; Salomon R
    Kidney Int; 2009 Apr; 75(8):839-47. PubMed ID: 19177160
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial juvenile nephronophthisis. Experience with eleven cases.
    Lirenman DS; Brianlowry R; Chase WH
    Birth Defects Orig Artic Ser; 1974; 10(4):32-4. PubMed ID: 4470904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.