Patrakka J - Search Results

1

The number of podocyte slit diaphragms is decreased in minimal change nephrotic syndrome.

Patrakka J, Lahdenkari AT, Koskimies O, Holmberg C, Wartiovaara J, Jalanko H. Patrakka J, et al. Pediatr Res. 2002 Sep;52(3):349-55. doi: 10.1203/00006450-200209000-00007. Pediatr Res. 2002. PMID: 12193666

2

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

Patrakka J, Ruotsalainen V, Reponen P, Qvist E, Laine J, Holmberg C, Tryggvason K, Jalanko H. Patrakka J, et al. Transplantation. 2002 Feb 15;73(3):394-403. doi: 10.1097/00007890-200202150-00013. Transplantation. 2002. PMID: 11884936

3

Tissue expression of nephrin in human and pig.

Kuusniemi AM, Kestilä M, Patrakka J, Lahdenkari AT, Ruotsalainen V, Holmberg C, Karikoski R, Salonen R, Tryggvason K, Jalanko H. Kuusniemi AM, et al. Among authors: patrakka j. Pediatr Res. 2004 May;55(5):774-81. doi: 10.1203/01.PDR.0000117842.10241.2C. Epub 2004 Feb 5. Pediatr Res. 2004. PMID: 14764915

4

Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria.

Lahdenkari AT, Lounatmaa K, Patrakka J, Holmberg C, Wartiovaara J, Kestilä M, Koskimies O, Jalanko H. Lahdenkari AT, et al. Among authors: patrakka j. J Am Soc Nephrol. 2004 Oct;15(10):2611-8. doi: 10.1097/01.ASN.0000139478.03463.D9. J Am Soc Nephrol. 2004. PMID: 15466265

5

Expression of nephrin in pediatric kidney diseases.

Patrakka J, Ruotsalainen V, Ketola I, Holmberg C, Heikinheimo M, Tryggvason K, Jalanko H. Patrakka J, et al. J Am Soc Nephrol. 2001 Feb;12(2):289-296. doi: 10.1681/ASN.V122289. J Am Soc Nephrol. 2001. PMID: 11158218

6

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations.

Patrakka J, Martin P, Salonen R, Kestilä M, Ruotsalainen V, Männikkö M, Ryynänen M, Rapola J, Holmberg C, Tryggvason K, Jalanko H. Patrakka J, et al. Lancet. 2002 May 4;359(9317):1575-7. doi: 10.1016/S0140-6736(02)08504-5. Lancet. 2002. PMID: 12047969

7

Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

Kuusniemi AM, Qvist E, Sun Y, Patrakka J, Rönnholm K, Karikoski R, Jalanko H. Kuusniemi AM, et al. Among authors: patrakka j. Transplantation. 2007 May 27;83(10):1316-23. doi: 10.1097/01.tp.0000262569.27890.64. Transplantation. 2007. PMID: 17519780

8

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.

Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H. Patrakka J, et al. Kidney Int. 2000 Sep;58(3):972-80. doi: 10.1046/j.1523-1755.2000.00254.x. Kidney Int. 2000. PMID: 10972661 Free article.

9

Role of nephrin in cell junction formation in human nephrogenesis.

Ruotsalainen V, Patrakka J, Tissari P, Reponen P, Hess M, Kestilä M, Holmberg C, Salonen R, Heikinheimo M, Wartiovaara J, Tryggvason K, Jalanko H. Ruotsalainen V, et al. Among authors: patrakka j. Am J Pathol. 2000 Dec;157(6):1905-16. doi: 10.1016/S0002-9440(10)64829-8. Am J Pathol. 2000. PMID: 11106563 Free PMC article.

10

Genetic kidney diseases disclose the pathogenesis of proteinuria.

Jalanko H, Patrakka J, Tryggvason K, Holmberg C. Jalanko H, et al. Among authors: patrakka j. Ann Med. 2001 Nov;33(8):526-33. doi: 10.3109/07853890108995962. Ann Med. 2001. PMID: 11730159 Free article. Review.

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