Research Topics
| Giovanni M FrascàSummaryAffiliation: University of Bologna Country: Italy Publications
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Detail Information
Publications
Thin basement membrane disease in patients with familial IgA nephropathyGiovanni M Frascà
Nephrology, Dialysis and Renal Transplantation Unit, St Orsola University Hospital, Bologna, Italy
J Nephrol 17:778-85. 2004..The familial form of IgAN has been increasingly recognized, supporting the suggestion that genetic factors could be involved in the disease pathogenesis, although it remains unclear whether the familial form is itself heterogeneous...
Thin glomerular basement membrane diseaseG M Frasca
Nephrology and Dialysis Unit, St Orsola Hospital, Bologna, Italy
J Nephrol 13:15-9. 2000..TBMD may arise with other glomerular diseases, most frequently IgA nephropathy, and it remains to be established whether these cases are a casual occurrence or whether a thinner than normal GBM predisposes to immune complex deposition...
Two different glomerular diseases in the same patient at an interval of 7 yearsGiovanni M Frascà
Nephrology, Dialysis and Renal Transplantation Unit, Pathology Department, St Orsola University Hospital, Bologna, Italy
Nephrol Dial Transplant 17:2014-6. 2002
[Recurrence of glomerulonephritis in transplanted kidney]G M Frasca
U O di Nefrologia, Dialisi e Trapianto Renale, Ospedale S Orsola Malpighi, Bologna, Italy
G Ital Nefrol 20:400-13. 2003..Finally, the risk of disease recurrence should always be included among the parameters used in evaluating a possible transplantation from living donor...
Plasma exchange treatment improves prognosis of antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis: a case-control study in 26 patients from a single centerGiovanni M Frascà
Nephrology, Dialysis and Renal Transplantation Unit, St Orsola University Hospital, Bologna, Italy
Ther Apher Dial 7:540-6. 2003..These data suggest that PE may significantly improve the prognosis of patients with ANCA-associated crescentic GN even if they are not dialysis-dependent at the time of diagnosis...
A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT geneGiovanni M Frascà
Nephrology, Dialysis and Renal Transplantation Unit, St Orsola University Hospital, Via Massarenti 9, 40137 Bologna, Italy
Nephrol Dial Transplant 19:1622-4. 2004
Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology GroupGiovanni M Frascà
Nephrology, Dialysis and Renal Transplantation Unit, St Orsola University Hospital, V Massarenti 9, 40137 Bologna, Italy
Nephrol Dial Transplant 20:545-51. 2005..This study investigated 51 patients with the morphological diagnosis of TBMD lacking any sign of ATS, with the aim of defining the prevalence of type IV collagen mutations and the course of the disease...
