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Items: 1 to 20 of 315

1.

Fibronectin glomerulopathy with nephrotic syndrome in a 3-year-old male.

Niimi K, Tsuru N, Uesugi N, Takebayashi S.

Pediatr Nephrol. 2002 May;17(5):363-6.

PMID:
12042895
2.

Fibronectin glomerulopathy in a 34-year-old man: a case report.

Brcić I, Brcić L, Kuzmanić D, Corić M, Corić M.

Ultrastruct Pathol. 2010 Aug;34(4):240-2. doi: 10.3109/01913121003783209.

PMID:
20594046
3.

Immunotactoid glomerulopathy.

Korbet SM, Schwartz MM, Rosenberg BF, Sibley RK, Lewis EJ.

Medicine (Baltimore). 1985 Jul;64(4):228-43.

PMID:
4010500
4.

Fibronectin non-amyloid glomerulopathy.

Yong JL, Killingsworth MC, Spicer ST, Wu XJ.

Int J Clin Exp Pathol. 2009 Nov 20;3(2):210-6.

5.

Idiopathic membranous glomerulopathy in Canadian children: a clinicopathologic study.

Latham P, Poucell S, Koresaar A, Arbus G, Baumal R.

J Pediatr. 1982 Nov;101(5):682-5.

PMID:
7131140
6.

Familial lobular glomerulopathy.

Abt AB, Wassner SJ, Moran JJ.

Hum Pathol. 1991 Aug;22(8):825-9.

PMID:
1869266
7.

Familial glomerulopathy with giant fibrillar (fibronectin-positive) deposits: 15-year follow-up in a large kindred.

Gemperle O, Neuweiler J, Reutter FW, Hildebrandt F, Krapf R.

Am J Kidney Dis. 1996 Nov;28(5):668-75.

PMID:
9158203
8.

[Diagnostic pathway of an unusual case of nephrotic syndrome: immunotactoid glomerulopathy].

Manganelli R, Iannaccone S, Ferbo U, De Simone W.

G Ital Nefrol. 2010 Nov-Dec;27(6):668-73. Italian.

PMID:
21132650
9.

Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease.

Strøm EH, Banfi G, Krapf R, Abt AB, Mazzucco G, Monga G, Gloor F, Neuweiler J, Riess R, Stosiek P, et al.

Kidney Int. 1995 Jul;48(1):163-70.

10.

Long-term follow-up of a paediatric case of lipoprotein glomerulopathy.

Koitabashi Y, Ikoma M, Miyahira T, Fujita R, Mio H, Ishida M, Shimizu K, Sakaguchi H.

Pediatr Nephrol. 1990 Mar;4(2):122-8.

PMID:
2397177
11.

Renal biopsy studies in 150 children with non-specific glomerulopathy.

Van Acker KJ, Vanden Brande J, Holvoet H.

Acta Paediatr Scand. 1975 Mar;64(2):345-54.

PMID:
1130193
12.

Familial glomerular disease with asymptomatic proteinuria and nephrotic syndrome: a new clinical entity.

Mathis BJ, Calabrese KE, Slick GL.

J Am Osteopath Assoc. 1992 Jul;92(7):875-80, 883-4.

PMID:
1429048
13.

Newer glomerular diseases.

Abt AB, Cohen AH.

Semin Nephrol. 1996 Nov;16(6):501-10. Review.

PMID:
9125794
14.

Focal and segmental hyalinosis.

Saint-Hillier Y, Morel-Maroger L, Woodrow D, Richet G.

Adv Nephrol Necker Hosp. 1975;5:67-88. No abstract available.

PMID:
811095
15.

Progressive glomerulopathy with unusual deposits of striated structures: a new disease entity?

Ohtani H, Wakui H, Komatsuda A, Goto H, Tada M, Ozawa M, Kobayashi R, Sawada K.

Nephrol Dial Transplant. 2010 Jun;25(6):2016-9. doi: 10.1093/ndt/gfq037.

16.

Immunotactoid glomerulopathy in sickle cell anemia.

Aviles DH, Craver R, Warrier RP.

Pediatr Nephrol. 2001 Jan;16(1):82-4.

PMID:
11198611
17.

Glomerulopathies with organized deposits.

Iskandar SS, Herrera GA.

Semin Diagn Pathol. 2002 Aug;19(3):116-32. Review.

PMID:
12180633
18.

Thin basement membrane nephropathy associated with minimal change disease in a 15-year-old boy.

Fujinaga S, Kaneko K, Ohtomo Y, Murakami H, Takemoto M, Takada M, Shimizu T, Yamashiro Y.

Pediatr Nephrol. 2006 Feb;21(2):277-80.

PMID:
16362391
19.

The Cockayne syndrome: an evaluation of hypertension and studies of renal pathology.

Higginbottom MC, Griswold WR, Jones KL, Vasquez MD, Mendoza SA, Wilson CB.

Pediatrics. 1979 Dec;64(6):929-34.

PMID:
514720
20.

Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants.

Liapis H, Gökden N, Hmiel P, Miner JH.

Hum Pathol. 2002 Aug;33(8):836-45.

PMID:
12203217
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