Commonality and Variation in Social Fluidity in Industrial Nations. Part I: A Model for Evaluating the 'FJH Hypothesis'Erikson et al. · European Sociological Review1987PDF995 KB
Genome-wide Study of Familial Juvenile Hyperuricaemic (gouty) Nephropathy (FJHN) Indicates a New Locus, FJHN3, Linked to Chromosome 2p22.1-p21Piret · Human Genetics2011PDF403 KB
Homozygosity for Uromodulin Disorders: FJHN and MCKD-type 2REZENDE-LIMA · Kidney International2004PDF153 KB
Familial Juvenile Hyperuricaemic Nephropathy (FJHN): Linkage Analysis in 15 Families, Physical and Transcriptional Characterisation of the FJHN Critical Region on Chromosome 16p11.2 and the Analysis of Seven Candidate GenesStibůrková · European Journal of Human Genetics2003PDF153 KB
Allelism of MCKD, FJHN and GCKD Caused by Impairment of Uromodulin Export DynamicsRampoldi · Human Molecular Genetics2003PDF818 KB
Alterations of Uromodulin Biology: a Common Denominator of the Genetically Heterogeneous FJHN/MCKD SyndromeVylet'al · Kidney International2006PDF840 KB
Wild-type Uromodulin Prevents NFkB Activation in Kidney Cells, While Mutant Uromodulin, Causing FJHU Nephropathy, Does NotDinour · Wichtig Editore2014PDF2.6 MB
Early Treatment with Allopurinol in Familial Juvenile Hyerpuricaemic Nephropathy (FJHN) Ameliorates the Long-term Progression of Renal DiseaseFAIRBANKS · QJM2002PDF120 KB
First Report of Familial Juvenile Hyperuricemic Nephropathy (FJHN) in Iran Caused By a Novel De Novo Mutation (E197X) in UMODMalakoutian · Journal of Molecular and Genetic Medicine2016PDF690 KB
Efficacy of Allopurinol in Ameliorating the Progressive Renal Disease in Familial Juvenile Hyperuricaemic Nephropathy (FJHN): A Six Year UpdateBride · Clinical Biochemistry1997PDF128 KB
The Uromodulin C744G Mutation Causes MCKD2 and FJHN in Children and Adults and May Be Due to a Possible Founder EffectWolf · Kidney International2007PDF210 KB
