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Apparent mineralocorticoid excess in Israel: a case series and literature review

European journal of endocrinology, 2024-05, Vol.190 (5), p.347-353

2024

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TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex

American journal of medical genetics. Part A, 2017-03, Vol.173 (3), p.771-775

2017

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First-week urine beta-2 microglobulin levels in term healthy neonates

Pediatric nephrology (Berlin, West), 2021-06, Vol.36 (6), p.1511-1514

2021

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Post-transplantation lymphoproliferative disorder in pediatric kidney-transplant recipients - A national study

Pediatric transplantation, 2012-09, Vol.16 (6), p.619-626

2012

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Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

American journal of human genetics, 2010-09, Vol.87 (3), p.392-399

2010

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Mutations in the Mitochondrial Seryl-tRNA Synthetase Cause Hyperuricemia, Pulmonary Hypertension, Renal Failure in Infancy and Alkalosis, HUPRA Syndrome

American journal of human genetics, 2011-02, Vol.88 (2), p.193-200

2011

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Contamination of urinary cultures in initial-stream versus later-stream urine in children undergoing bladder catheterization for the diagnosis of urinary tract infection

European journal of emergency medicine, 2017-12, Vol.24 (6), p.e17-e20

2017

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Complications of central venous stenosis due to permanent central venous catheters in children on hemodialysis

Pediatric nephrology (Berlin, West), 2014-11, Vol.29 (11), p.2235-2239

2014

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A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failure

Nephrology, dialysis, transplantation, 2010-03, Vol.25 (3), p.785-793

2010

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N-terminal pro-B-type natriuretic peptide as a marker of bronchopulmonary dysplasia in premature infants

American journal of perinatology, 2010-05, Vol.27 (5), p.381-386

2010

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Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1

The New England journal of medicine, 2021-04, Vol.384 (13), p.1216-1226

2021

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N-acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy

Annals of neurology, 2002-12, Vol.52 (6), p.845-849

2002

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Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial

Clinical journal of the American Society of Nephrology, 2021-07, Vol.16 (7), p.1025-1036

2021

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ACUTE KIDNEY INJURY SECONDARY TO URINARY TRACT OBSTRUCTION - A RARE COMPLICATION OF CIRCUMCISION

הרפואה, 2021-12, Vol.160 (12), p.793

2021

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Acute glomerulonephritis with concurrent suspected bacterial pneumonia – is it the tip of the iceberg?

Pediatric nephrology (Berlin, West), 2024-04, Vol.39 (4), p.1143-1147

2024

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Long-term complications of systemic oxalosis in children—a retrospective single-center cohort study

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.3123-3132

2021

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Eosinophilia in a peritoneal dialysis patient: Answers

Pediatric nephrology (Berlin, West), 2018-09, Vol.33 (9), p.1507-1508

2018

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A non-resolving skin lesion in hemodialysis patient: Answers

Pediatric nephrology (Berlin, West), 2019-04, Vol.34 (4), p.617-618

2019

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Severe neutropenia in children after renal transplantation: incidence, course, and treatment with granulocyte colony-stimulating factor

Pediatric nephrology (Berlin, West), 2015-11, Vol.30 (11), p.2029-2036

2015

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Hypernatremic Dehydration in Young Children: Is There a Solution?

The Israel Medical Association journal, 2016-02, Vol.18 (2), p.95-99

2016

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Dent’s disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Pediatric nephrology (Berlin, West), 2009-12, Vol.24 (12), p.2369-2373

2009

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Vitamin A deficiency associated with urinary retinol binding protein wasting in Dent’s disease

Pediatric nephrology (Berlin, West), 2012-07, Vol.27 (7), p.1097-1102

2012

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Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids

Molecular genetics and metabolism, 2002-11, Vol.77 (3), p.202-208

2002

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Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge

Pediatric nephrology (Berlin, West), 2009-02, Vol.24 (2), p.403-406

2009

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Apparent mineralocorticoid excess in Israel: a case series and literature review

TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex

First-week urine beta-2 microglobulin levels in term healthy neonates

Post-transplantation lymphoproliferative disorder in pediatric kidney-transplant recipients - A national study

Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

Mutations in the Mitochondrial Seryl-tRNA Synthetase Cause Hyperuricemia, Pulmonary Hypertension, Renal Failure in Infancy and Alkalosis, HUPRA Syndrome

Contamination of urinary cultures in initial-stream versus later-stream urine in children undergoing bladder catheterization for the diagnosis of urinary tract infection

Complications of central venous stenosis due to permanent central venous catheters in children on hemodialysis

A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failure

N-terminal pro-B-type natriuretic peptide as a marker of bronchopulmonary dysplasia in premature infants

Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1

N-acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy

Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial

ACUTE KIDNEY INJURY SECONDARY TO URINARY TRACT OBSTRUCTION - A RARE COMPLICATION OF CIRCUMCISION

Acute glomerulonephritis with concurrent suspected bacterial pneumonia – is it the tip of the iceberg?

Long-term complications of systemic oxalosis in children—a retrospective single-center cohort study

Eosinophilia in a peritoneal dialysis patient: Answers

A non-resolving skin lesion in hemodialysis patient: Answers

Severe neutropenia in children after renal transplantation: incidence, course, and treatment with granulocyte colony-stimulating factor

Hypernatremic Dehydration in Young Children: Is There a Solution?

Dent’s disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Vitamin A deficiency associated with urinary retinol binding protein wasting in Dent’s disease

Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids

Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge

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