Tel.: +34 91 736 2385
LOCAL TIME
Contact: Katarina Gluic
Hours: Mon-Thu 8:30-17:00 Fri 8:30-15:00
22:45
For help with a poster, please specify the poster number, the first author and the congress and we will reply shortly.
Poster no.
Contact name
E-mail
Telephone
Congress
Comments

50th ERA-EDTA Congress

 

May 18-21 2013 Istanbul
FAQs
   
Discussion forum - 50th ERA-EDTA Congress
    Topic - Genetic diseases and molecular genetics

If you are already registered in PosterSessionOnline, enter your e-mail and click on LOGIN. Otherwise click on REGISTER
  
 Thread / Poster  Author  Replies  Last reply
CORRELATION BETWEEN ANTI-PHOSPHOLIPASE A2 RECEPTOR AND ANTI-SOLUBLE PHOSPHOLIPASE A2 ANTIBODIES IN IDIOPATHIC MEMBRANOUS NEPHROPATHY  Nikou Fotouhi 1      4/26/2013 6:33:00 AM  
RESEQUENCING STUDY OF 40 CANDIDATE GENES IN 960 INDIVIDUALS WITH VARYING DEGREES OF URINARY CALCIUM EXCRETION SUGGESTS ASSOCIATION WITH CLAUDIN14  Hakan Toka 1      4/25/2013 9:51:00 PM  
CARDIAC VARIANT OF FABRY DISEASE RESPONDING TO DOUBLE DOSE OF AGALSIDASE ALFA  Christos Paliouras 1      4/25/2013 2:23:00 PM  
ONTOGENY OF THE CIRCADIAN MOLECULAR CLOCKWORK IN THE RAT KIDNEY  Krisztina Meszaros 1      4/25/2013 1:58:00 PM  
THE FABRAZYME, ANGIOTENSIN RECEPTOR BLOCKER AND ACE INHIBITOR TREATMENT STUDY FOR FABRY NEPHROPATHY (FOR THE FAACET INVESTIGATORS)  David G Warnock 1      4/25/2013 12:31:00 PM  
SYNERGY BETWEEN THE PHARMACOLOGICAL CHAPERONE 1-DEOXYGALACTONOJIRIMYCIN AND AGALSIDASE ALPHA IN CULTURED FIBROBLASTS FROM PATIENTS WITH FABRY DISEASE  Antonio Pisani 1      4/24/2013 10:25:00 PM  
MTHFR (C677T AND A1298C) POLYMORPHISMS AND DIABETIC NEPHROPATHY  Anis Baffoun 1      4/24/2013 6:05:00 PM  
PATHOPHYSIOLOGY OF FAMILIAL MICROSCOPIC HEMATURIA (FMH) WITH THIN BASEMENT MEMBRANES AND/OR PROGRESSIVE KIDNEY DISEASE. COL4A3/A4 HETEROZYGOUS MUTATIONS ARE THE COMMONEST CAUSE BUT ALPORT COL4A5 HYPOMORPHIC, MISSENCE MUTATIONS ARE ALSO A POSSIBILITY  Alkis Pierides 1      4/24/2013 4:15:00 PM  
THIN BASEMENT MEMBRANE NEPHROPATHY DUE TO HETEROZYGOUS COL4A3/COL4A4 MUTATIONS IS A MORE FREQUENT CAUSE OF ESKD COMPARED TO ALPORT SYNDROME  Maria Arsali 1      4/24/2013 4:10:00 PM  
STUDY OF THE COL4A3 GENE AND DESCRIPTION OF NEW MUTATIONS RESPONSIBLE FOR AUTOSOMAL DOMINANT ALPORT SYNDROME  Consolación Rosado 1      4/23/2013 12:36:00 PM  
IDENTIFICATION OF QUANTITATIVE TRAIT LOCI FOR DEGLYCOSYLATED IgA1 SERUM LEVELS IN FAMILIAL IgA NEPHROPATHY  Francesco Pesce 1      4/23/2013 12:36:00 PM  
STUDY OF THE COL4A4 GENE AND DESCRIPTION OF NEW MUTATIONS RESPONSIBLE FOR ALPORT SYNDROME  Consolación Rosado 1      4/23/2013 12:36:00 PM  
DIFFERENTIALLY EXPRESSED GENES AND THEIR ASSOCIATED NETWORKS IN CLEAR-CELL RENAL CELL CARCINOMA (RCC)  APOSTOLOS ZARAVINOS 1      4/23/2013 12:36:00 PM  
HEMOLYSIS: A FATAL COMPLICATION OF ALKAPTONURIA IN SEVERE RENAL FAILURE PATIENTS.  Stanislas BATAILLE 1      4/23/2013 12:36:00 PM  
       




Most viewed poster for this congress
Poster: 15
Visits: 822
Title: EFFECTS OF UREMIC TOXIN P-CRESOL ON PROLIFERATION, APOPTOSIS, DIFFERENTIATION AND GLUCOSE UPTAKE IN 3T3-L1 CELLS
Authors: Sayuri Tanaka , Sayuri Tanaka,1 Shozo Yano,2 Toshitsugu Sugimoto.1
Centre: Shimane University Faculty of Medicine

Poster most viewed in this topic
Poster: 33
Visits: 172
Title: DIFFERENTIALLY EXPRESSED GENES AND THEIR ASSOCIATED NETWORKS IN CLEAR-CELL RENAL CELL CARCINOMA (RCC)
Authors: APOSTOLOS ZARAVINOS , Apostolos Zaravinos,1 Constantinos C Deltas.1
Centre: University of Cyprus


 






PosterSessionOnline
Logo Draft
 
Logo Cert