:  Publisher English Wikipedia <ref>{{Cite pmid|16952054}}</ref> Nephropedia Template TP ( {{tp|p=16952054|t=Focal and segmental glomerulosclerosis |pdf=|usr=|}} Twit Text Focal and segmental glomerulosclerosis http://www.kidney.de/pget.php?&tw=1&pmid=16952054 DeepDyve Pubget Overpricing

lüll Focal and segmental glomerulosclerosis Daskalakis N; Winn MP Cell Mol Life Sci 2006[Nov]; 63 (21): 2506-11 An increasing cause of end-stage renal disease is the pathological lesion focal and segmental glomerulosclerosis (FSGS). FSGS is characterized by proteinuria and frequently nephrotic syndrome with ensuing renal failure. The etiology remains unknown in the majority of individuals. The idiopathic form of FSGS is most common; however, secondary forms of FSGS do exist. There is a form of FSGS that is fulminant that frequently recurs after renal transplantation with an estimated frequency of approximately 30%, suggesting that the pathogenesis is not solely a result of intrinsic kidney disease. Recently, hereditary forms of the disease were recognized as well as those associated with other congenital syndromes. Known genetic causes of the hereditary form of this disease have been suggested to account for upwards of 18% of cases. This review will address recent discoveries of the genetic mechanisms of hereditary FSGS and the current interpretations of their interactions at the slit diaphragm. |Genome, Human/genetics[MESH] |Glomerulosclerosis, Focal Segmental/*pathology[MESH] |Humans[MESH] |Intracellular Signaling Peptides and Proteins/genetics[MESH] |Membrane Proteins/genetics[MESH] |Mutation/genetics[MESH] |TRPV Cation Channels/genetics[MESH]

*{{pmid16952054}}
*<b>[http://www.kidney.de/mlpefetch.php?search=16952054 Focal and segmental glomerulosclerosis ]</b> Cell Mol Life Sci 2006; 63(21) ; 2506-11 Daskalakis N; Winn MP

    *16952054*

Nephropedia PMID record
{{recpmid|pmid=16952054|ti=Focal and segmental glomerulosclerosis |au=Daskalakis N; Winn MP|so=Cell Mol Life Sci 2006; 63 (21): 2506-11|ab=An increasing cause of end-stage renal disease is the pathological lesion focal and segmental glomerulosclerosis (FSGS). FSGS is characterized by proteinuria and frequently nephrotic syndrome with ensuing renal failure. The etiology remains unknown in the majority of individuals. The idiopathic form of FSGS is most common; however, secondary forms of FSGS do exist. There is a form of FSGS that is fulminant that frequently recurs after renal transplantation with an estimated frequency of approximately 30%, suggesting that the pathogenesis is not solely a result of intrinsic kidney disease. Recently, hereditary forms of the disease were recognized as well as those associated with other congenital syndromes. Known genetic causes of the hereditary form of this disease have been suggested to account for upwards of 18% of cases. This review will address recent discoveries of the genetic mechanisms of hereditary FSGS and the current interpretations of their interactions at the slit diaphragm.}}
Deutsche Wikipedia - im Artikel
<ref>{{BibPMID|16952054}}</ref>
Hier den unten stehenden Textblock hineinkopieren
{{BibRecord | Autor = Daskalakis N; Winn MP | Titel = Focal and segmental glomerulosclerosis | Band = 63 | Nummer = 21 | Jahr = 2006 | Monat = Nov | Sprache = eng | DOI = | Seite = 2506-11 | PMID = 16952054 | Typ= {{{Typ|}}} | Kommentar = {{{Kommentar|}}} | format = {{{format|}}} | record = {{{record|}}} }}

Cell Mol Life Sci