C. Rinat

发表

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

Y. Frishberg, D. Shemesh, Efrat Ben Shalom, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Mutations in DHDPSL are responsible for primary hyperoxaluria type III.

C. Charon, D. Magen, R. Belostotsky, 2010, American journal of human genetics.

Early puberty in end stage renal failure and renal transplant recipients

Y. Frishberg, H. Hirsch, R. Becker-Cohen, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

R. Belostotsky, Y. Frishberg, O. Elpeleg, 2011, American journal of human genetics.

Cadaver-donor renal transplantation of children in Israel (1990-2001): racial disparities in health care delivery?

Y. Frishberg, S. Feinstein, C. Rinat, 2003, Pediatrics.

Hyperphosphatemia is prevalent among children with nephrotic syndrome and normal renal function

Y. Frishberg, S. Feinstein, R. Becker-Cohen, 2006, Pediatric Nephrology.

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

Y. Frishberg, S. Feinstein, R. Becker-Cohen, 2015, Pediatric Nephrology.

Hyperostosis–Hyperphosphatemia Syndrome: A Congenital Disorder of O‐Glycosylation Associated With Augmented Processing of Fibroblast Growth Factor 23

Y. Frishberg, T. Fujita, S. Fukumoto, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hemolytic Uremic Syndrome: A Contemporary Pediatric Experience

D. Landau, Evgenia Gurevich, C. Rinat, 2020, Nephron.

Metabolic alkalosis in infants treated with peritoneal dialysis

Y. Frishberg, L. Shavit, R. Becker-Cohen, 2022, Pediatric Nephrology.

The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?

I. Lerer, Y. Frishberg, A. Nir, 2005, Journal of the American Society of Nephrology : JASN.

Risk factors for cardiovascular disease in children and young adults after renal transplantation.

Y. Frishberg, A. Nir, N. Algur, 2006, Clinical journal of the American Society of Nephrology : CJASN.

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

Y. Frishberg, R. Cytter-Kuint, R. Becker-Cohen, 2021, Pediatric Nephrology.

Intra-Familial Clinical Heterogeneity: Absence of Genotype-Phenotype Correlation in Primary Hyperoxaluria Type 1 in Israel

R. Wanders, H. Mandel, Y. Frishberg, 2005, American Journal of Nephrology.

Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic group.

Y. Frishberg, R. Wanders, D. Halle, 1999, Journal of the American Society of Nephrology : JASN.

Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.

Y. Frishberg, O. Megged, S. Feinstein, 2002, Journal of the American Society of Nephrology : JASN.

Eosinophilia in a peritoneal dialysis patient: Answers

Y. Frishberg, R. Becker-Cohen, C. Rinat, 2018, Pediatric Nephrology.

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

R. Belostotsky, Y. Frishberg, D. Dinour, 2009, Pediatric Nephrology.

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

J. Gécz, M. Bitner-Glindzicz, J. Tolmie, 2006, Human molecular genetics.

Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community

Y. Frishberg, M. Männikkö, J. Zlotogora, 2007, Genetics in Medicine.

Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome

Y. Frishberg, Y. Schlesinger, O. Megged, 2003, Pediatric Nephrology.

The outcome of chronic dialysis in infants and toddlers--advantages and drawbacks of haemodialysis.

Y. Frishberg, S. Schwartz, S. Feinstein, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge

R. Belostotsky, Y. Frishberg, S. Feinstein, 2009, Pediatric Nephrology.

Recurrent Nephrotic Syndrome in Homozygous Truncating NPHS2 Mutation Is Not Due to Anti‐Podocin Antibodies

Y. Frishberg, M. Bruschi, C. Zennaro, 2007, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

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

Y. Frishberg, S. Feinstein, R. Becker-Cohen, 2014, Pediatric Nephrology.

Genetic analysis – a diagnostic tool for primary hyperoxaluria type I

Y. Frishberg, D. Batinic, C. Rinat, 2002, Pediatric Nephrology.

Is Noncompliance Among Adolescent Renal Transplant Recipients Inevitable?

Y. Frishberg, S. Schwartz, S. Feinstein, 2005, Pediatrics.

COVID-19 in children and young adults with kidney disease: risk factors, clinical features and serological response

Y. Frishberg, Efrat Ben Shalom, R. Becker-Cohen, 2021, Journal of Nephrology.

Left ventricular mass and cardiac function in pediatric dialysis patients

Y. Frishberg, A. Nir, C. Rinat, 2016 .

B-type natriuretic peptides are reliable markers of cardiac strain in CKD pediatric patients

Y. Frishberg, A. Nir, N. Algur, 2012, Pediatric Nephrology.