Hereditary polycystic kidney disease is characterized by lymphopenia across all stages of kidney dysfunction: an observational study

Author:

Van Laecke Steven1,Kerre Tessa2,Nagler Evi V1,Maes Bart3,Caluwe Rogier4,Schepers Eva1,Glorieux Griet1,Van Biesen Wim1,Verbeke Francis1

Affiliation:

1. Renal Division, Ghent University Hospital, Ghent, Belgium

2. Department of Haematology and Clinical Chemistry, Microbiology and Immunology, Faculty of Medicine and Health Sciences, Ghent University Hospital, Ghent, Belgium

3. Department of Nephrology, AZ Delta, Roeselare, Belgium

4. Division of Nephrology, OLVZ, Aalst, Belgium

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference36 articles.

1. Polycystic kidney disease;Wilson;N Engl J Med,2004

2. Autosomal dominant polycystic kidney disease: risk factor for nonmelanoma skin cancer following kidney transplantation;Bretagnol;Transpl Int,2010

3. Cyst infections in patients with autosomal dominant polycystic kidney disease;Sallée;Clin J Am Soc Nephrol,2009

4. Risk and prognosis of hospitalization for pneumonia among individuals with and without functioning renal transplants in Denmark: a population-based study;Nielsen;Clin Infect Dis,2012

5. Radiologic and clinical bronchiectasis associated with autosomal dominant polycystic kidney disease;Moua;PLoS One,2014

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