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Literature DB >> 3974779

Morphological transition in minimal change nephrotic syndrome.

A Tejani.

Abstract

Entities: Disease

Mesh：

Year: 1985 PMID： 3974779 DOI： 10.1159/000183363

Source DB: PubMed Journal: Nephron ISSN： 1660-8151 Impact factor: 2.847

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17 in total

Review 1. Minimal change disease and idiopathic FSGS: manifestations of the same disease.

Authors: Rutger J Maas; Jeroen K Deegens; Bart Smeets; Marcus J Moeller; Jack F Wetzels
Journal: Nat Rev Nephrol Date: 2016-10-17 Impact factor: 28.314

2. The renal functional and structural consequences of corticosteroid and angiotensin-converting enzyme inhibitor therapy in chronic puromycin aminonucleoside nephropathy.

Authors: H Trachtman; R Del Pizzo; E Valderrama; B Gauthier
Journal: Pediatr Nephrol Date: 1990-09 Impact factor: 3.714

3. Idiopathic nephrotic syndrome in Polish children - its variants and associations with HLA.

Authors: Aleksandra Krasowska-Kwiecień; Krystyna Sancewicz-Pach; Anna Moczulska
Journal: Pediatr Nephrol Date: 2006-09-12 Impact factor: 3.714

4. Steroid-resistant nephrotic syndrome: long-term evolution after sequential therapy.

Authors: Antonia Peña; Juan Bravo; Marta Melgosa; Carlota Fernandez; Carmen Meseguer; Laura Espinosa; Angel Alonso; M Luz Picazo; Mercedes Navarro
Journal: Pediatr Nephrol Date: 2007-09-18 Impact factor: 3.714

5. Sodium dodecyl sulphate polyacrylamide gel electrophoresis of urinary proteins in steroid-responsive and steroid-resistant nephrotic syndrome in children.

Authors: G Ramjee; H M Coovadia; M Adhikari
Journal: Pediatr Nephrol Date: 1994-12 Impact factor: 3.714

Morphological transition in minimal change nephrotic syndrome.

Review 1. Minimal change disease and idiopathic FSGS: manifestations of the same disease.

2. The renal functional and structural consequences of corticosteroid and angiotensin-converting enzyme inhibitor therapy in chronic puromycin aminonucleoside nephropathy.

3. Idiopathic nephrotic syndrome in Polish children - its variants and associations with HLA.

4. Steroid-resistant nephrotic syndrome: long-term evolution after sequential therapy.

5. Sodium dodecyl sulphate polyacrylamide gel electrophoresis of urinary proteins in steroid-responsive and steroid-resistant nephrotic syndrome in children.

6. Focal sclerosing glomerulopathy. Risk factors of progression and optimal mode of treatment.

7. Alternative treatment to corticosteroids in steroid sensitive idiopathic nephrotic syndrome.

8. Immunopathological findings in idiopathic nephrosis: clinical significance of glomerular "immune deposits".

9. Racial differences in the incidence and renal outcome of idiopathic focal segmental glomerulosclerosis in children.

10. Kidney biopsy prior to cyclophosphamide therapy in primary nephrotic syndrome.