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Choni Rinat

Research Profile

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Kidneys

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Israel

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Amino Acid Sequences

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Publications

TOP 3
Rachel Becker-Cohen; Efrat Ben-Shalom; Sofia Feinstein; Heftziba Ivgi; Choni Rinat; Yaacov Frishberg
Vitamin A deficiency associated with urinary retinol binding protein wasting in Dent's disease.
Choni Rinat; Amiram Nir; Nurit Algur; Rachel Becker-Cohen; Efrat Ben-Shalom; Benjamin Farber; Sofia Feinstein; Yaacov Frishberg
B-type natriuretic peptides are reliable markers of cardiac strain in CKD pediatric patients.
Ruth Belostotsky; Efrat Ben-Shalom; Choni Rinat; Rachel Becker-Cohen; Sofia Feinstein; Sharon Zeligson; Reeval Segel; Orly Elpeleg; Suheir Nassar; Yaacov Frishberg
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

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All Publications

2012: Rachel Becker-Cohen; Efrat Ben-Shalom; Sofia Feinstein; Heftziba Ivgi; Choni Rinat; Yaacov Frishberg
Vitamin A deficiency associated with urinary retinol binding protein wasting in Dent's disease.
Pediatric nephrology (Berlin, Germany) 2012;27(7):1097-102.
2012: Choni Rinat; Amiram Nir; Nurit Algur; Rachel Becker-Cohen; Efrat Ben-Shalom; Benjamin Farber; Sofia Feinstein; Yaacov Frishberg
B-type natriuretic peptides are reliable markers of cardiac strain in CKD pediatric patients.
Pediatric nephrology (Berlin, Germany) 2012;27(4):617-25.
2011: Ruth Belostotsky; Efrat Ben-Shalom; Choni Rinat; Rachel Becker-Cohen; Sofia Feinstein; Sharon Zeligson; Reeval Segel; Orly Elpeleg; Suheir Nassar; Yaacov Frishberg
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;88(2):193-200.
2010: Ruth Belostotsky; Eric Seboun; Gregory H Idelson; Dawn S Milliner; Rachel Becker-Cohen; Choni Rinat; Carla G Monico; Sofia Feinstein; Efrat Ben-Shalom; Daniella Magen; Irith Weissman; Celine Charon; Yaacov Frishberg
Mutations in DHDPSL are responsible for primary hyperoxaluria type III.
American journal of human genetics 2010;87(3):392-9.
2010: Choni Rinat; Rachel Becker-Cohen; Amiram Nir; Sofia Feinstein; David Shemesh; Nurit Algur; Efrat Ben-Shalom; Benjamin Farber; Yaacov Frishberg
A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failure.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010;25(3):785-93.
2009: Yaacov Frishberg; Dganit Dinour; Ruth Belostotsky; Rachel Becker-Cohen; Choni Rinat; Sofia Feinstein; Paulina Navon-Elkan; Efrat Ben-Shalom
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?
Pediatric nephrology (Berlin, Germany) 2009;24(12):2369-73.
2008: Rachel Becker-Cohen; Amiram Nir; Efrat Ben-Shalom; Choni Rinat; Sofia Feinstein; Benjamin Farber; Yaacov Frishberg
Improved left ventricular mass index in children after renal transplantation.
Pediatric nephrology (Berlin, Germany) 2008;23(9):1545-50.
2008: Sofia Feinstein; Choni Rinat; Rachel Becker-Cohen; Efrat Ben-Shalom; Shepard B Schwartz; Yaacov Frishberg
The outcome of chronic dialysis in infants and toddlers--advantages and drawbacks of haemodialysis.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008;23(4):1336-45.
2007: Yaacov Frishberg; Ziva Ben-Neriah; Maija Suvanto; Choni Rinat; Minna Männikkö; Sofia Feinstein; Rachel Becker-Cohen; Hannu Jalanko; Joël Zlotogora; Marjo Kestilä
Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(3):180-4.
2007: Asif Ali; Paul T Christie; Irina V Grigorieva; Brian Harding; Hilde Van Esch; S Faisal Ahmed; Maria Bitner-Glindzicz; Eberhard Blind; Catherine Bloch; Patricia Christin; Peter Clayton; Jozef Gecz; Brigitte Gilbert-Dussardier; Encarna Guillen-Navarro; Anna Hackett; Isil Halac; Geoffrey N Hendy; Fiona Lalloo; Christoph J Mache; Zulf Mughal; Albert C M Ong; Choni Rinat; Nicholas Shaw; Sarah F Smithson; John Tolmie; Jacques Weill; M Andrew Nesbit; Rajesh V Thakker
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.
Human molecular genetics 2007;16(3):265-75.
2007: Yaacov Frishberg; Nobuaki Ito; Choni Rinat; Yuji Yamazaki; Sofia Feinstein; Itaru Urakawa; Paulina Navon-Elkan; Rachel Becker-Cohen; Takeyoshi Yamashita; Kaori Araya; Takashi Igarashi; Toshiro Fujita; Seiji Fukumoto
Hyperostosis-hyperphosphatemia syndrome: a congenital disorder of O-glycosylation associated with augmented processing of fibroblast growth factor 23.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2007;22(2):235-42.
2007: Rachel Becker-Cohen; Maurizio Bruschi; Choni Rinat; Sofia Feinstein; Cristina Zennaro; Gian Marco Ghiggeri; Yaacov Frishberg
Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2007;7(1):256-60.
2006: Rachel Becker-Cohen; Amiram Nir; Choni Rinat; Sofia Feinstein; Nurit Algur; Benjamin Farber; Yaacov Frishberg
Risk factors for cardiovascular disease in children and young adults after renal transplantation.
Clinical journal of the American Society of Nephrology : CJASN 2006;1(6):1284-92.
2006: Sofia Feinstein; Rachel Becker-Cohen; Choni Rinat; Yaacov Frishberg
Hyperphosphatemia is prevalent among children with nephrotic syndrome and normal renal function.
Pediatric nephrology (Berlin, Germany) 2006;21(10):1406-12.
2006: Choni Rinat; Esther Zoref-Shani; Ziva Ben-Neriah; Yael Bromberg; Rachel Becker-Cohen; Sofia Feinstein; Oded Sperling; Yaacov Frishberg
Molecular, biochemical, and genetic characterization of a female patient with Lesch-Nyhan disease.
Molecular genetics and metabolism 2006;87(3):249-52.
2006: Yaacov Frishberg; Sofia Feinstein; Choni Rinat; Rachel Becker-Cohen; Israela Lerer; Annick Raas-Rothschild; Benjamin Ferber; Amiram Nir
The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?
Journal of the American Society of Nephrology : JASN 2006;17(1):227-31.
2005: Yaacov Frishberg; Choni Rinat; Adel Shalata; Ihab Khatib; Sofia Feinstein; Rachel Becker-Cohen; Irit Weismann; Ronald J A Wanders; Gill Rumsby; Frank Roels; Hanna Mandel
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in Israel.
American journal of nephrology 2005;25(3):269-75.
2005: Sofia Feinstein; Rami Keich; Rachel Becker-Cohen; Choni Rinat; Shepard B Schwartz; Yaacov Frishberg
Is noncompliance among adolescent renal transplant recipients inevitable?
Pediatrics 2005;115(4):969-73.
2003: Alfred Drukker; Sofia Feinstein; Choni Rinat; Anat Rotem-Braun; Yaacov Frishberg
Cadaver-donor renal transplantation of children in Israel (1990-2001): racial disparities in health care delivery?
Pediatrics 2003;112(2):341-4.
2003: Yaacov Frishberg; Choni Rinat; Sofia Feinstein; Rachel Becker-Cohen; Orli Megged; Yechiel Schlesinger
Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2003;18(3):273-5.
2002: Danko Milosevic; Choni Rinat; Drago Batinic; Yaacov Frishberg
Genetic analysis--a diagnostic tool for primary hyperoxaluria type I.
Pediatric nephrology (Berlin, Germany) 2002;17(11):896-8.
2002: Yaacov Frishberg; Choni Rinat; Orli Megged; Eli Shapira; Sofia Feinstein; Annick Raas-Rothschild
Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.
Journal of the American Society of Nephrology : JASN 2002;13(2):400-5.
2001: Choni Rinat; A Farkas; Yaacov Frishberg
Familial inheritance of crossed fused renal ectopia.
Pediatric nephrology (Berlin, Germany) 2001;16(3):269-70.
2000: Yaacov Frishberg; Sofia Feinstein; Choni Rinat; Alfred Drukker
Hypothyroidism in primary hyperoxaluria type 1.
The Journal of pediatrics 2000;136(2):255-7.
1999: Choni Rinat; Ronald J A Wanders; Alfred Drukker; David Halle; Yaacov Frishberg
Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic group.
Journal of the American Society of Nephrology : JASN 1999;10(11):2352-8.