Collapsing glomerulopathy associated with inherited mitochondrial injury.
Publication
, Journal Article
Barisoni, L; Diomedi-Camassei, F; Santorelli, FM; Caridi, G; Thomas, DB; Emma, F; Piemonte, F; Ghiggeri, GM
Published in: Kidney international
July 2008
Duke Scholars
Published In
Kidney international
DOI
EISSN
1523-1755
ISSN
0085-2538
Publication Date
July 2008
Volume
74
Issue
2
Start / End Page
237 / 243
Related Subject Headings
- Urology & Nephrology
- Mutation
- Mitochondrial Diseases
- Male
- Infant
- Humans
- Glomerulosclerosis, Focal Segmental
- Genetic Diseases, Inborn
- 3202 Clinical sciences
- 1103 Clinical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Barisoni, L., Diomedi-Camassei, F., Santorelli, F. M., Caridi, G., Thomas, D. B., Emma, F., … Ghiggeri, G. M. (2008). Collapsing glomerulopathy associated with inherited mitochondrial injury. Kidney International, 74(2), 237–243. https://doi.org/10.1038/sj.ki.5002767
Barisoni, Laura, Francesca Diomedi-Camassei, Filippo M. Santorelli, Gianluca Caridi, David B. Thomas, Francesco Emma, Fiorella Piemonte, and Gian Marco Ghiggeri. “Collapsing glomerulopathy associated with inherited mitochondrial injury.” Kidney International 74, no. 2 (July 2008): 237–43. https://doi.org/10.1038/sj.ki.5002767.
Barisoni L, Diomedi-Camassei F, Santorelli FM, Caridi G, Thomas DB, Emma F, et al. Collapsing glomerulopathy associated with inherited mitochondrial injury. Kidney international. 2008 Jul;74(2):237–43.
Barisoni, Laura, et al. “Collapsing glomerulopathy associated with inherited mitochondrial injury.” Kidney International, vol. 74, no. 2, July 2008, pp. 237–43. Epmc, doi:10.1038/sj.ki.5002767.
Barisoni L, Diomedi-Camassei F, Santorelli FM, Caridi G, Thomas DB, Emma F, Piemonte F, Ghiggeri GM. Collapsing glomerulopathy associated with inherited mitochondrial injury. Kidney international. 2008 Jul;74(2):237–243.
Published In
Kidney international
DOI
EISSN
1523-1755
ISSN
0085-2538
Publication Date
July 2008
Volume
74
Issue
2
Start / End Page
237 / 243
Related Subject Headings
- Urology & Nephrology
- Mutation
- Mitochondrial Diseases
- Male
- Infant
- Humans
- Glomerulosclerosis, Focal Segmental
- Genetic Diseases, Inborn
- 3202 Clinical sciences
- 1103 Clinical Sciences