Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L Torri-Tarelli

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Nephron|January 1, 1993
Alport syndrome with type I membranoproliferative glomerulonephritisM Meroni, A Sessa, G Battini, et al.
American Journal of Nephrology|January 1, 1988
Postinfectious glomerulonephritis in the elderlyA Volpi, M Meroni, G Battini, et al.
Nephron|January 1, 1986
Recurrent hemolytic uremic syndrome: case reportM Meroni, A Volpi, G Battini, et al.
Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Tissue Reactions|January 1, 1995
Eliminant effects of calcitonin gene related peptide on the tubular epithelial cells in an isolated and perfused rat kidneyL Giovannini, R Palla, A A Bertelli, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|January 1, 1988
[Long-term captopril therapy of 3 sisters with Bartter's syndrome]A Volpi, M Meroni, G Battini, et al.
Nephron|January 1, 1995
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?A Sessa, A Pietrucci, S Carozzi, et al.
Applied Pathology|January 1, 1989
IgA mesangial nephropathy associated with renal cell carcinomaA Sessa, A Volpi, C Tetta, et al.
Child Nephrology and Urology|January 1, 1988
IgA glomerulonephritis in Wiskott-Aldrich syndromeN G DeSanto, A Sessa, G Capodicasa, et al.
Journal of the American Society of Nephrology : JASN|June 11, 1998
Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlationsG Mazzucco, P Barsotti, A O Muda, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Nephron|January 1, 1993
Alport syndrome with type I membranoproliferative glomerulonephritisM Meroni, A Sessa, G Battini, et al.
American Journal of Nephrology|January 1, 1988
Postinfectious glomerulonephritis in the elderlyA Volpi, M Meroni, G Battini, et al.
Nephron|January 1, 1986
Recurrent hemolytic uremic syndrome: case reportM Meroni, A Volpi, G Battini, et al.
Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Tissue Reactions|January 1, 1995
Eliminant effects of calcitonin gene related peptide on the tubular epithelial cells in an isolated and perfused rat kidneyL Giovannini, R Palla, A A Bertelli, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|January 1, 1988
[Long-term captopril therapy of 3 sisters with Bartter's syndrome]A Volpi, M Meroni, G Battini, et al.
Nephron|January 1, 1995
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?A Sessa, A Pietrucci, S Carozzi, et al.
Applied Pathology|January 1, 1989
IgA mesangial nephropathy associated with renal cell carcinomaA Sessa, A Volpi, C Tetta, et al.
Child Nephrology and Urology|January 1, 1988
IgA glomerulonephritis in Wiskott-Aldrich syndromeN G DeSanto, A Sessa, G Capodicasa, et al.
Journal of the American Society of Nephrology : JASN|June 11, 1998
Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlationsG Mazzucco, P Barsotti, A O Muda, et al.
Pageof 4