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kw.\*:("autosomal recessive polycystic kidney disease")

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Autosomal recessive polycystic kidney disease: The Clinical experience in North AmericaGUAY-WOODFORD, Lisa M; DESMOND, Renee A.Pediatrics (Evanston). 2003, Vol 111, Num 5, pp 1072-1080, issn 0031-4005, 9 p., 1Article

Does TNF-α enhance cystogenesis in ADPKD?PIRSON, Yves.Nephrology, dialysis, transplantation (Print). 2008, Vol 23, Num 12, pp 3773-3775, issn 0931-0509, 3 p.Article

New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 geneZERRES, K; SENDEREK, J; BERGMANN, C et al.Clinical genetics. 2004, Vol 66, Num 1, pp 53-57, issn 0009-9163, 5 p.Article

Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric studyCHAPAL, Marion; DEBOUT, Agnes; HOURMANT, Maryvonne et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 5, pp 2083-2088, issn 0931-0509, 6 p.Article

Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)FISCHER, Dagmar-Christiane; JACOBY, Ulrike; BERGMANN, Carsten et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 6, pp 1819-1827, issn 0931-0509, 9 p.Article

Comparative proteomic analysis suggests that mitochondria are involved in autosomal recessive polycystic kidney diseaseLI, Qing-Wei; LU, Xiao-Yan; WEI, Yu-Quan et al.Proteomics (Weinheim. Print). 2012, Vol 12, Num 15-16, pp 2556-2570, issn 1615-9853, 15 p.Article

Delayed cystogenesis and increased ciliogenesis associated with the re-expression of polaris in Tg737 mutant miceBROWN, Nicole E; MURCIA, Noel S.Kidney international. 2003, Vol 63, Num 4, pp 1220-1229, issn 0085-2538, 10 p.Article

Successful transplantation in a child with rapid progression of autosomal recessive polycystic kidney disease associated with a novel mutationPRELOG, Martina; BERGMANN, Carsten; BERND ZIMMERHACKL, Lothar et al.Pediatric transplantation. 2006, Vol 10, Num 3, pp 362-366, issn 1397-3142, 5 p.Article

Murine models of polycystic kidney disease: molecular and therapeutic insightsGUAY-WOODFORD, Lisa M.American journal of physiology. Renal physiology. 2003, Vol 54, Num 6, pp F1034-F1049, issn 1931-857XArticle

Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk miceWEN LIU; MURCIA, Noel S; YI DUAN et al.American journal of physiology. Renal physiology. 2005, Vol 58, Num 5, pp F978-F988, issn 1931-857XArticle

Protein composition of liver cyst fluid from the BALB/ c-cpk/+ mouse model of autosomal recessive polycystic kidney diseaseXIANYIN LAI; BLAZER- YOST, Bonnie L; GATTONE, Vincent H et al.Proteomics (Weinheim. Print). 2009, Vol 9, Num 14, pp 3775-3782, issn 1615-9853, 8 p.Article

Haplotype analysis improves molecular diagnostics of Autosomal recessive polycystic kidney diseaseCONSUGAR, Mark B; ANDERSON, Sarah A; HILDEBRANDT, Friedhelm et al.American journal of kidney diseases. 2005, Vol 45, Num 1, pp 77-87, issn 0272-6386, 11 p.Article

Polycystic kidney disease : genes, proteins, animal models, disease mechanisms and therapeutic opportunitiesTORRES, V. E; HARRIS, P. C.Journal of internal medicine. 2007, Vol 261, Num 1, pp 17-31, issn 0954-6820, 15 p.Conference Paper

Inhibition of mTOR with sirolimus does not attenuate progression of liver and kidney disease in PCK ratsRENKEN, Catharina; FISCHER, Dagmar-Christiane; KUNDT, Günther et al.Nephrology, dialysis, transplantation (Print). 2011, Vol 26, Num 1, pp 92-100, issn 0931-0509, 9 p.Article

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney diseaseDENAMUR, Erick; DELEZOIDE, Anne-Lise; MISSY, Pascale et al.Kidney international. 2010, Vol 77, Num 4, pp 350-358, issn 0085-2538, 9 p.Article

Combination treatment of PKD utilizing dual inhibition of EGF-receptor activity and ligand bioavailabilitySWEENEY, William E; HAMAHIRA, Kiyoshi; SWEENEY, Jennifer et al.Kidney international. 2003, Vol 64, Num 4, pp 1310-1319, issn 0085-2538, 10 p.Article

Abnormal EGF-dependent regulation of sodium absorption in ARPKD collecting duct cellsVEIZIS, I. Elias; COTTON, Calvin U.American journal of physiology. Renal physiology. 2005, Vol 57, Num 3, pp F474-F482, issn 1931-857XArticle

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)BERGMANN, Carsten; SENDEREK, Jan; SEEMAN, Tomas et al.Kidney international. 2005, Vol 67, Num 3, pp 829-848, issn 0085-2538, 20 p.Article

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney DiseaseO'BRIEN, Kevin; FONT-MONTGOMERY, Esperanza; MOHAN, Parvathi et al.Journal of pediatric gastroenterology and nutrition. 2012, Vol 54, Num 1, pp 83-89, issn 0277-2116, 7 p.Article

Adrenal insufficiency due to isolated adrenocorticotropin deficiency complicated by autosomal recessive polycystic kidney diseaseYONEMURA, Katushiko; YASUDA, Hideo; FUJIGAKI, Yoshihide et al.Renal failure. 2003, Vol 25, Num 3, pp 485-492, issn 0886-022X, 8 p.Article

Autosomal recessive polycystic kidney disease: outcomes from a single-center experienceCAPISONDA, Rhona; PHAN, Veronique; TRAUBUCI, Jeffrey et al.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 2, pp 119-126, issn 0931-041X, 8 p.Article

Recombinant human growth hormone therapy in autosomal recessive polycystic kidney diseaseLILOVA, Marusia; KAPLAN, Bernard S; MEYERS, Kevin E. C et al.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 1, pp 57-61, issn 0931-041X, 5 p.Article

The place of liver transplantation in Caroli's disease and syndromeDE KERCKHOVE, Laurent; DE MEYER, Martine; VERBAANDERT, Catherine et al.Transplant international. 2006, Vol 19, Num 5, pp 381-388, issn 0934-0874, 8 p.Article

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