Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

Quiz Page JUNE 2013

(2013) Badria Al Ghaithi et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Two Patients With History of STEC-HUS, Posttransplant Recurrence and Complement Gene Mutations

(2013) M. Alberti et al.   AMERICAN JOURNAL OF TRANSPLANTATION

Outcomes of kidney allograft in recipients with kidney disease of unknown etiology

(2013) Hyo Jin Kim et al.   CLINICAL TRANSPLANTATION

Renal Complications of Fabry Disease

(2013) Nikolina Basic-Jukic et al.   CURRENT PHARMACEUTICAL DESIGN

Long-term enzyme replacement therapy is associated with reduced proteinuria and preserved proximal tubular function in women with Fabry disease

(2013) T. Prabakaran et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Hereditary causes of kidney stones and chronic kidney disease

(2013) Vidar O. Edvardsson et al.   PEDIATRIC NEPHROLOGY

Adenine Phosphoribosyltransferase Deficiency

(2012) G. Bollee et al.   Clinical Journal of the American Society of Nephrology

Kidney transplantation and enzyme replacement therapy in patients with Fabry disease

(2012) Markus Cybulla et al.   JOURNAL OF NEPHROLOGY

2,8-Dihydroxyadeninuria disease

(2012) Shree G. Sharma et al.   KIDNEY INTERNATIONAL

Fabry nephropathy: indications for screening and guidance for diagnosis and treatment by the European Renal Best Practice

(2012) Wim Terryn et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Senior–Løken syndrome: A syndromic form of retinal dystrophy associated with nephronophthisis

(2012) C.C. Ronquillo et al.   VISION RESEARCH

Phenotype and Outcome in Hereditary Tubulointerstitial Nephritis Secondary to UMOD Mutations

(2011) G. Bollee et al.   Clinical Journal of the American Society of Nephrology

Kidney biopsy in patients with diabetes mellitus

(2011) D.G. Haider et al.   CLINICAL NEPHROLOGY

Hyperuricemia, gout and the kidney

(2011) Terence Gibson   CURRENT OPINION IN RHEUMATOLOGY

Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis

(2011) O. Boyer et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

(2011) Stanislas Faguer et al.   KIDNEY INTERNATIONAL

The rediscovery of uromodulin (Tamm–Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease

(2011) Luca Rampoldi et al.   KIDNEY INTERNATIONAL

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

(2011) Rasheed A. Gbadegesin et al.   KIDNEY INTERNATIONAL

Unexpected Fabry Disease in a Renal Allograft Kidney: An Underrecognized Cause of Poor Allograft Function

(2011) Olga Kochar et al.   ULTRASTRUCTURAL PATHOLOGY

Decreased Kidney Function and Crystal Deposition in the Tubules After Kidney Transplant

(2010) Piero Stratta et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Crystalline nephropathy due to 2,8-dihydroxyadeninuria: an under-recognized cause of irreversible renal failure

(2010) S. H. Nasr et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Uromodulin-Associated Kidney Disease

(2010) Anthony J. Bleyer et al.   NEPHRON CLINICAL PRACTICE

Mechanisms of Nephronophthisis and Related Ciliopathies

(2010) Toby W. Hurd et al.   NEPHRON EXPERIMENTAL NEPHROLOGY

Variable renal phenotype in a family with an INF2 mutation

(2010) Hyun Kyung Lee et al.   PEDIATRIC NEPHROLOGY

Nephronophthisis

(2010) Matthias T. F. Wolf et al.   PEDIATRIC NEPHROLOGY