Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF).
about
ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopiesEvidence for a "Pathogenic Triumvirate" in Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney DiseaseTelmisartan ameliorates fibrocystic liver disease in an orthologous rat model of human autosomal recessive polycystic kidney diseasePPAR-gamma agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney diseaseDesign and Implementation of the Hepatorenal Fibrocystic Disease Core Center Clinical Database: A Centralized Resource for Characterizing Autosomal Recessive Polycystic Kidney Disease and Other Hepatorenal Fibrocystic DiseasesCorrelation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease.Magnetic resonance microscopy of renal and biliary abnormalities in excised tissues from a mouse model of autosomal recessive polycystic kidney diseaseGlobal Gene Expression Profiling in PPAR-γ Agonist-Treated Kidneys in an Orthologous Rat Model of Human Autosomal Recessive Polycystic Kidney DiseaseEducational paper: ciliopathies.Beneficial effect of combined treatment with octreotide and pasireotide in PCK rats, an orthologous model of human autosomal recessive polycystic kidney diseaseNew approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.Diagnosis and management of childhood polycystic kidney disease.Postnatal imaging of neonates with prenatally diagnosed genitourinary abnormalities: a practical approach.Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.Magnetic resonance imaging of pancreaticobiliary diseases in children: from technique to practice.Abernethy malformation associated with Caroli's syndrome in a patient with a PKHD1 mutation: a case report.Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.Liver fibrosis in recessive multicystic kidney diseases: transient elastography for early detection.Increased YAP Activation Is Associated With Hepatic Cyst Epithelial Cell Proliferation in ARPKD/CHF.Recent advances in the molecular diagnosis of polycystic kidney disease.Pediatric Hematuria Remains a Clinical Dilemma.Characteristics of Liver Disease in 100 Individuals With Joubert Syndrome Prospectively Evaluated At A Single Center.Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential Diagnoses.Inhibition of mTOR with sirolimus does not attenuate progression of liver and kidney disease in PCK rats.Pleuropulmonary blastoma in a child with autosomal-recessive polycystic kidney disease.
P2860
Q26824716-55E33D71-7CEA-4F49-8BE6-045CBF18186DQ28079756-297877B5-37F5-4CE2-8FC4-B9BA3F49ADF4Q28536366-1E65D76D-E4AB-44FD-B720-4964815A2C78Q28742454-F00D9B52-9106-432A-B109-5382E19A7CA3Q33581306-97C63B12-2C2E-47EE-A9AB-B52246DC0233Q33888356-122B3D80-ED74-49B7-8ED1-9B9962DF68FEQ35206399-39691807-63F4-4890-B56A-D92215508FCDQ35655072-28D6F472-DD2C-4B97-8D9A-BE6942D0E682Q35759778-87EFAD8F-0850-4904-B8F6-00E91ACDFAFAQ35986663-E47BC2C3-22F9-4992-84F2-2205AD9202E6Q36166406-EA66CC08-EA28-4F2A-93B9-42E8155CE0D7Q36380634-EFAD1B7E-BD1E-40EF-B4C3-3B2AF96A6042Q36874632-EF3A8625-5C46-446A-95FB-1FF25B57F1A4Q37806654-D9B83587-0EDF-4DFA-815C-AFB25DFF8274Q37991205-07E3B3A2-B000-497A-B248-D4E05D8134D3Q38151554-C354C67D-A89F-4193-8494-9119D7D68CFCQ38845248-DFEEED92-1870-4D60-BA0B-88D8583E5C80Q40091205-B57B083B-5DE6-44D7-9530-63202BF28B7CQ40981091-43460204-2B8B-41CF-AFBF-967A52767DA1Q44413049-31BE010F-3481-4E11-97FA-84AD41D5208BQ47125278-BAC75A08-3D7A-46DE-8583-0FE69C18989AQ47737330-3E3AA0F6-CFD4-4C2F-8DDF-8B07484716D1Q47809622-1B0B6AF4-8217-4588-BED9-91A1150DC116Q47981846-1CE3BFF8-5516-4F56-BDA9-4C7F1F4791FAQ50301021-DCD02AA1-AB08-4908-96FB-B3550F55D16BQ51554260-BBFE6301-D46E-45F1-963B-CAC95E9C690BQ51862371-6EE7A471-9091-4658-872D-779D717CF58F
P2860
Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF).
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@ast
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@en
type
label
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@ast
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@en
prefLabel
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@ast
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@en
P2093
P2860
P1433
P1476
Autosomal recessive polycystic ...... hepatic fibrosis (ARPKD/CHF).
@en
P2093
Baris Turkbey
Esperanza Font-Montgomery
Iclal Ocak
Joy Bryant
Kailash Daryanani
Linda Lukose
Maya Tuchman
Meral Gunay-Aygun
Parvathi Mohan
Peter L Choyke
P2860
P2888
P304
P356
10.1007/S00247-008-1064-X
P577
2008-12-17T00:00:00Z
P5875
P6179
1023835507