Terkko Navigator / Pediatric Nephrology

Iohexol-measured glomerular filtration rate in children and adolescents with chronic kidney disease: a pilot study comparing venous and finger stick methods: response to comments from Dr. Luis-Lima

Correction to: Neonatal hypertension: cases, causes, and clinical approach

Comments on Tașdemir et al.: A rare cause of AA amyloidosis and end-stage kidney failure

A child with bilateral multiple renal cysts presenting with ascites and pleural effusion: Questions

A rare cause of AA amyloidosis and end-stage kidney failure: Questions

Caplacizumab for relapsing thrombotic thrombocytopenic purpura

Comments on the letter of Galland et al. on“A rare cause of AA amyloidosis and end-stage kidney failure”

A rare cause of AA amyloidosis and end-stage kidney failure: Answers

A child with bilateral multiple renal cysts presenting with ascites and pleural effusion: Answers

Response to“Iohexol-measured glomerular filtration rate in children and adolescents with chronic kidney disease: a pilot study comparing venous and finger stick methods”

Association of low birth weight and prematurity with clinical outcomes of childhood nephrotic syndrome: a prospective cohort study

Should ACE inhibitors and ARBs be used in combination in children?

Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

Estimating glomerular filtration rate in youth with obesity and type 2 diabetes: the iCARE study equation

Endoplasmic reticulum stress and monogenic kidney diseases in precision nephrology

Relationship between food insecurity and high blood pressure in a national sample of children and adolescents

Acute pancreatitis in children on chronic maintenance dialysis

Depression and neurocognitive dysfunction in pediatric and young adult chronic kidney disease

Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children

Association between BMI changes and mortality risk in children with end-stage renal disease

An adolescent patient presenting with hyponatremic seizure: Questions

Nephrotic syndrome and mitochondrial disorders: answers

Correction to: Predictors of patency for arteriovenous fistulae and grafts in pediatric hemodialysis patients

Proteinuria in a patient with Graves’ disease: Questions

Writing a paper for publication

Nephrotic syndrome and mitochondrial disorders: Questions

An adolescent patient presenting with hyponatremic seizure: Answers

Proteinuria in a patient with Graves’ disease: Answers

The role of properdin in complement-mediated renal diseases: a new player in complement-inhibiting therapy?

Extra-renal manifestations of atypical hemolytic uremic syndrome

Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study

Phthalate-associated hypertension in premature infants: a prospective mechanistic cohort study

Treatment of infant formula with patiromer dose dependently decreases potassium concentration

Epidemiology and clinical features of childhood-onset anti-neutrophil cytoplasmic antibody–associated vasculitis: a clinicopathological analysis

Association between the clinical presentation of congenital anomalies of the kidney and urinary tract (CAKUT) and gene mutations: an analysis of 66 patients at a single institution

New insights into the role of HNF-1β in kidney (patho)physiology

Methylprednisolone or cyclosporine a in the treatment of Henoch-Schönlein nephritis: a nationwide study

Hemolytic uremic syndrome in a developing country: Consensus guidelines

Autoimmune abnormalities of the alternative complement pathway in membranoproliferative glomerulonephritis and C3 glomerulopathy

Cardiovascular disease risk among children with focal segmental glomerulosclerosis: a report from the chronic kidney disease in children study

Why 0.9% saline is isotonic: understanding the aqueous phase of plasma and the difference between osmolarity and osmolality

The unusual suspects: a curious case of acute kidney injury—Questions

Renal stone and chronic kidney failure associated with hypouricemia: Questions

Response to“Predictors of rituximab-related neutropenia in Japanese children with steroid-dependent nephrotic syndrome”

A child with anemia, thrombocytopenia, renal failure and elevated amylase, and lipase enzymes: Answers

Iodine excess in children with kidney disease: are we missing hypothyroidism?

Voiding cystography: an unusual route of induced hypothyroidism by iodine overdose in two newborns with chronic kidney disease

Predictors of rituximab-related neutropenia in Japanese children with steroid-dependent nephrotic syndrome

The unusual suspects: a curious case of acute kidney injury—Answers

A child with anemia, thrombocytopenia, renal failure and elevated amylase, and lipase enzymes: Questions