132 related articles for article (PubMed ID: 9572384)
1. Sonographic findings in familial juvenile nephronophthisis-medullary cystic disease complex.
Chuang YF; Tsai TC
J Clin Ultrasound; 1998 May; 26(4):203-6. PubMed ID: 9572384
[TBL] [Abstract][Full Text] [Related]
2. Familial juvenile nephronophthisis. An ultrasonographic follow-up of seven patients.
Ala-Mello S; Jääskeläinen J; Koskimies O
Acta Radiol; 1998 Jan; 39(1):84-9. PubMed ID: 9498877
[TBL] [Abstract][Full Text] [Related]
3. Juvenile nephronophthisis-medullary cystic disease complex: a family study.
Tsai JD; Lin SP; Huang FY; Hsu HC; Tsai TC
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(2):116-20. PubMed ID: 9151464
[TBL] [Abstract][Full Text] [Related]
4. Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood.
Avni FE; Guissard G; Hall M; Janssen F; DeMaertelaer V; Rypens F
Pediatr Radiol; 2002 Mar; 32(3):169-74. PubMed ID: 12164348
[TBL] [Abstract][Full Text] [Related]
5. Sonographic pattern of recessive polycystic kidney disease in young adults. Differences from the dominant form.
Nicolau C; Torra R; Badenas C; Pérez L; Oliver JA; Darnell A; Brú C
Nephrol Dial Transplant; 2000 Sep; 15(9):1373-8. PubMed ID: 10978393
[TBL] [Abstract][Full Text] [Related]
6. Ultrasound findings in juvenile nephronophthisis.
Blowey DL; Querfeld U; Geary D; Warady BA; Alon U
Pediatr Nephrol; 1996 Feb; 10(1):22-4. PubMed ID: 8611349
[TBL] [Abstract][Full Text] [Related]
7. Sonographic findings in renal parenchymal malacoplakia.
Venkatesh SK; Mehrotra N; Gujral RB
J Clin Ultrasound; 2000 Sep; 28(7):353-7. PubMed ID: 10934335
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive polycystic kidney disease: long-term sonographic findings in patients surviving the neonatal period.
Blickman JG; Bramson RT; Herrin JT
AJR Am J Roentgenol; 1995 May; 164(5):1247-50. PubMed ID: 7717240
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus.
Scolari F; Ghiggeri GM; Casari G; Amoroso A; Puzzer D; Caridi GL; Valzorio B; Tardanico R; Vizzardi V; Savoldi S; Viola BF; Bossini N; Prati E; Gusmano R; Maiorca R
Nephrol Dial Transplant; 1998 Oct; 13(10):2536-46. PubMed ID: 9794556
[TBL] [Abstract][Full Text] [Related]
10. Imaging features of tuberous sclerosis complex with autosomal-dominant polycystic kidney disease: a contiguous gene syndrome.
Back SJ; Andronikou S; Kilborn T; Kaplan BS; Darge K
Pediatr Radiol; 2015 Mar; 45(3):386-95. PubMed ID: 25355409
[TBL] [Abstract][Full Text] [Related]
11. Multiple unilateral renal cysts in two children.
Dugougeat F; Navarro O; Soares Souza AS; Geary D; Daneman A
Pediatr Radiol; 2000 May; 30(5):346-8. PubMed ID: 10836602
[TBL] [Abstract][Full Text] [Related]
12. Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1.
Stavrou C; Pierides A; Zouvani I; Kyriacou K; Antignac C; Neophytou P; Christodoulou K; Deltas CC
Am J Med Genet; 1998 May; 77(2):149-54. PubMed ID: 9605289
[TBL] [Abstract][Full Text] [Related]
13. Late occurrence of cysts in autosomal dominant medullary cystic kidney disease.
Neumann HP; Zäuner I; Strahm B; Bender BU; Schollmeyer P; Blum U; Rohrbach R; Hildebrandt F
Nephrol Dial Transplant; 1997 Jun; 12(6):1242-6. PubMed ID: 9198059
[TBL] [Abstract][Full Text] [Related]
14. Clinical, pathological and genetic aspects of a form of cystic disease of the renal medulla: familial juvenile nephronophthisis (FJN).
van Collenburg JJ; Thompson MW; Huber J
Clin Nephrol; 1978 Feb; 9(2):55-62. PubMed ID: 639367
[TBL] [Abstract][Full Text] [Related]
15. Renal medullary cystic disease. Findings at urography and ultrasonography.
Olsen A; Hansen Højhus J; Steffensen G
Acta Radiol; 1988; 29(5):527-9. PubMed ID: 3048348
[TBL] [Abstract][Full Text] [Related]
16. Renal involvement in children with HNF1β mutation: early sonographic appearances and long-term follow-up.
Avni FE; Lahoche A; Langlois C; Garel C; Hall M; Vivier PH
Eur Radiol; 2015 May; 25(5):1479-86. PubMed ID: 25638216
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Pyramidal hyperechogenicity in autosomal recessive polycystic kidney disease resembling medullary nephrocalcinosis.
Herman TE; Siegel MJ
Pediatr Radiol; 1991; 21(4):270-1. PubMed ID: 1870923
[TBL] [Abstract][Full Text] [Related]
19. Abnormal integrin receptor expression in two cases of familial nephronophthisis.
Rahilly MA; Fleming S
Histopathology; 1995 Apr; 26(4):345-9. PubMed ID: 7607623
[TBL] [Abstract][Full Text] [Related]
20. [Renal failure and cystic kidney diseases].
Correas JM; Joly D; Chauveau D; Richard S; Hélénon O
J Radiol; 2011 Apr; 92(4):308-22. PubMed ID: 21549887
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
