Search Results - "Kemper, Markus J."
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New therapies in steroid-sensitive and steroid-resistant idiopathic nephrotic syndrome
Published in Pediatric nephrology (Berlin, West) (01-06-2011)“…Although many children with idiopathic nephrotic syndrome (INS) respond initially to steroid therapy, repeated courses for patients with relapses often cause…”
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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome
Published in Clinical journal of the American Society of Nephrology (05-02-2016)“…Treatment of congenital nephrotic syndrome (CNS) and steroid-resistant nephrotic syndrome (SRNS) is demanding, and renal prognosis is poor. Numerous causative…”
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Early-Childhood Membranous Nephropathy Due to Cationic Bovine Serum Albumin
Published in The New England journal of medicine (02-06-2011)“…BSA ingested in food can escape the intestinal barrier and induce antibovine serum albumin antibodies. The authors of this study identified circulating BSA in…”
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Chest configuration in children and adolescents with infantile nephropathic cystinosis compared with other chronic kidney disease entities and its clinical determinants
Published in Pediatric nephrology (Berlin, West) (01-12-2023)“…Background Infantile nephropathic cystinosis (INC) is a systemic lysosomal storage disease causing intracellular cystine accumulation, resulting in renal…”
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Human factor H-related protein 2 (CFHR2) regulates complement activation
Published in PloS one (18-11-2013)“…Mutations and deletions within the human CFHR gene cluster on chromosome 1 are associated with diseases, such as dense deposit disease, CFHR nephropathy or…”
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The influence of gender and sexual hormones on incidence and outcome of chronic kidney disease
Published in Pediatric nephrology (Berlin, West) (01-08-2012)“…It has long been known that the female sex is associated with a better clinical outcome in chronic renal diseases. Although many experimental, clinical, and…”
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Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Published in American journal of human genetics (06-08-2015)“…Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease in the first three decades of life…”
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The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
Published in Nature genetics (01-06-2006)“…The molecular basis of nephronophthisis, the most frequent genetic cause of renal failure in children and young adults, and its association with retinal…”
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Treatment of Genetic Forms of Nephrotic Syndrome
Published in Frontiers in pediatrics (26-03-2018)“…Idiopathic steroid-resistant nephrotic syndrome (SRNS) is most frequently characterized by focal segmental glomerulosclerosis (FSGS) but also other…”
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Immunohistochemical and serological characterization of membranous nephropathy in children and adolescents
Published in Pediatric nephrology (Berlin, West) (01-03-2018)“…Background Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults, but is less frequent in children. Antibodies against four antigens…”
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Epidemiology and Morbidity of Epstein-Barr Virus Infection in Pediatric Renal Transplant Recipients: A Multicenter, Prospective Study
Published in Clinical infectious diseases (01-01-2013)“…Background. The epidemiology and morbidity of Epstein-Barr virus (EBV) infection in pediatric renal transplant recipients have been characterized…”
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Response to cyclosporine in steroid-resistant nephrotic syndrome: discontinuation is possible
Published in Pediatric nephrology (Berlin, West) (01-09-2015)“…Background Steroid-resistant nephrotic syndrome (SRNS) is still regarded as a serious disease although treatment with cyclosporine (CSA) has improved outcome…”
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Transmission of Glomerular Permeability Factor Soluble Urokinase Plasminogen Activator Receptor (suPAR) From a Mother to Child
Published in American journal of kidney diseases (01-02-2013)Get full text
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Long-term outcome after combined or sequential liver and kidney transplantation in children with infantile and juvenile primary hyperoxaluria type 1
Published in Frontiers in pediatrics (17-03-2023)“…Combined or sequential liver and kidney transplantation (CLKT/SLKT) restores kidney function and corrects the underlying metabolic defect in children with…”
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Long-Term Transplantation Outcomes in Patients With Primary Hyperoxaluria Type 1 Included in the European Hyperoxaluria Consortium (OxalEurope) Registry
Published in Kidney international reports (01-02-2022)“…In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney stones, nephrocalcinosis, and kidney failure. As PH1 is caused by a…”
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Urinary tract infections in children after renal transplantation
Published in Pediatric nephrology (Berlin, West) (01-06-2009)“…Urinary tract infections (UTI) after pediatric kidney transplantation (KTX) are an important clinical problem and occur in 15–33% of patients. Febrile UTI,…”
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Clinical and Laboratory Consequences of Platelet Transfusion in Shiga Toxin–Mediated Hemolytic Uremic Syndrome
Published in Transfusion medicine reviews (01-01-2017)“…Recent studies suggest that platelet transfusions are harmful in patients with thrombotic thrombocytopenic purpura, an entity of thrombotic microangiopathies…”
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Effect of the Dialysis Fluid Buffer on Peritoneal Membrane Function in Children
Published in Clinical journal of the American Society of Nephrology (01-01-2013)“…Double-chamber peritoneal dialysis fluids exert less toxicity by their neutral pH and reduced glucose degradation product content. The role of the buffer…”
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Pathogenesis, diagnosis and management of hyperkalemia
Published in Pediatric nephrology (Berlin, West) (01-03-2011)“…Hyperkalemia is a potentially life-threatening condition in which serum potassium exceeds 5.5 mmol/l. It can be caused by reduced renal excretion, excessive…”
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CTLA4 Polymorphisms in Minimal Change Nephrotic Syndrome in Children: A Case-Control Study
Published in American journal of kidney diseases (01-06-2014)Get full text
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