I. Zelikovic

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Aminoaciduria and Glycosuria

I. Zelikovic, 2009 .

Hereditary Tubulopathies

I. Zelikovic, 2019, Nephrology and Fluid/electrolyte Physiology.

Chapter 18 – Hereditary Tubulopathies

I. Zelikovic, 2012 .

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

Yiping Shen, David T. Miller, O. Platt, 2009, Physiological genomics.

Transcriptional Regulation of the Pendrin Gene

S. Alper, S. L. Carrithers, I. Zelikovic, 2011, Cellular Physiology and Biochemistry.

Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene.

I. Zelikovic, E. Efrati, Lior Adler, 2008, American journal of physiology. Cell physiology.

Low infection rates and prolonged survival times of hemodialysis catheters in infants and children.

A. Engel, D. Magen, Mahdi Tarabeih, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Escherichia coli O 157:H7-associated hemolytic-uremic syndrome after ingestion of contaminated hamburgers.

E. Avner, P. Tarr, L. Fouser, 1994, The Journal of pediatrics.

Hereditary Tubular Disorders of Mineral Handling

D. Magen, I. Zelikovic, 2012 .

Transcriptional Regulation of the Claudin-16 Gene by Mg2+Availability

O. Zinder, I. Zelikovic, E. Efrati, 2006, Cellular Physiology and Biochemistry.

Sodium-coupled amino acid transport in renal tubule.

R. Chesney, I. Zelikovic, 1989, Kidney international.

The human paracellin-1 gene (hPCLN-1): renal epithelial cell-specific expression and regulation.

I. Zelikovic, E. Efrati, Julia Arsentiev-Rozenfeld, 2005, American journal of physiology. Renal physiology.

Molecular pathophysiology of tubular transport disorders

I. Zelikovic, 2001, Pediatric Nephrology.

Cholelithiasis following Escherichia coli O157 : H7-associated hemolytic uremic syndrome

E. Avner, P. Tarr, L. Fouser, 1998, Pediatric Nephrology.

Taurine depletion in very low birth weight infants receiving prolonged total parenteral nutrition: role of renal immaturity.

R. Chesney, C. Ahlfors, A. Friedman, 1990, The Journal of pediatrics.

Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.

Amita Sharma, D. Magen, H. Jüppner, 2012, The Journal of clinical endocrinology and metabolism.

Renal amino acid transport: cellular and molecular events from clearance studies to frog eggs

R. Chesney, Deborah P. Jones, I. Zelikovic, 1993, Pediatric Nephrology.

cAMP-Dependent Protein Kinase Inhibits Proline Transport Across the Rat Renal Tubular Brush Border Membrane

J. Wager-Miller, I. Zelikovic, 2001, Bioscience reports.

Proline transport in MDCK cells expressing a mutant regulatory subunit of cAMP-dependent protein kinase.

J. Wager-Miller, I. Zelikovic, 2001, Molecular genetics and metabolism.

Cl- and membrane potential dependence of amino acid transport across the rat renal brush border membrane.

I. Zelikovic, A. Budreau-Patters, 1999, Molecular genetics and metabolism.

Developmental maturation of Na(+)-H+ exchange in rat renal tubular brush-border membrane.

R. Chesney, I. Zelikovic, P. Lohstroh, 1991, The American journal of physiology.

Chloride and membrane potential dependence of sodium ion-proline symport.

R. Chesney, I. Zelikovic, A. Budreau, 1991, Journal of the American Society of Nephrology : JASN.

Increased Na+‐taurine symporter in rat renal brush border membranes: preformed or newly synthesized?

R. Chesney, I. Zelikovic, P. Lohstroh, 1989, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Development of renal amino acid transport systems.

R. Chesney, I. Zelikovic, 1989, Seminars in nephrology.

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

D. Magen, K. Skorecki, S. Selig, 2010, The New England journal of medicine.

The claudin‐16 channel gene is transcriptionally inhibited by 1,25‐dihydroxyvitamin D

I. Zelikovic, E. Efrati, Julia Rozenfeld, 2015, Experimental physiology.

Plasmapheresis in a very young infant with atypical hemolytic uremic syndrome

D. Magen, R. Elhasid, G. Bar-Joseph, 2001, Pediatric Nephrology.

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

D. Behar, M. Indelman, R. Bergman, 2004, Nature Genetics.

Pendrin Function and Regulation in Xenopus Oocytes

D. Vandorpe, S. Alper, J. Heneghan, 2011, Cellular Physiology and Biochemistry.

Aminoaciduria and Glycosuria in Children

I. Zelikovic, 2015, Pediatric Nephrology.

The role of protein phosphorylation in renal amino acid transport

I. Zelikovic, J. Przekwas, 1993, Pediatric Nephrology.

Good outcome in prune-belly syndrome despite associated severe anomalies

R. Chesney, D. Uehling, A. Friedman, 1988, Pediatric Nephrology.

The taurine transporter: mechanisms of regulation

A. Patters, R. Chesney, D. P. Jones, 2006, Acta physiologica.

Mysterious hyperkalemia and cardiac arrest in a newborn infant undergoing continuous veno-venous hemofiltration dialysis: answer

M. Halberthal, G. Bar-Joseph, I. Zelikovic, 2008, Pediatric Nephrology.

Mysterious hyperkalemia and cardiac arrest in a newborn infant undergoing continuous veno-venous hemofiltration dialysis: question

M. Halberthal, G. Bar-Joseph, I. Zelikovic, 2008, Pediatric Nephrology.

Natural history of fetal simple renal cysts detected in early pregnancy.

E. Zimmer, S. Blazer, Z. Blumenfeld, 1999, The Journal of urology.

Transcriptional Regulation and Epigenetics of Pendrin

S. Alper, C. Nofziger, I. Zelikovic, 2017 .

Pendrin, a Novel Transcriptional Target of the Uroguanylin System

S. Alper, S. L. Carrithers, I. Zelikovic, 2013, Cellular Physiology and Biochemistry.

The pendrin anion exchanger gene is transcriptionally regulated by uroguanylin: a novel enterorenal link.

S. Alper, S. L. Carrithers, I. Zelikovic, 2012, American journal of physiology. Renal physiology.

Human SLC26A4/Pendrin STAS domain is a nucleotide-binding protein: Refolding and characterization for structural studies

Alok K. Sharma, S. Alper, A. C. Rigby, 2016, Biochemistry and biophysics reports.

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.

R. Szargel, V. Labay, N. Cohen, 2003, Kidney international.

Early performance of voiding cystourethrogram after urinary tract infection in children.

D. Magen, I. Kassis, D. Berkowitz, 2008, The Israel Medical Association journal : IMAJ.

Urinary tract infections in children. An update.

I. Zelikovic, R. Adelman, P. A. Nancarrow, 1992, The Western journal of medicine.

Peritonitis in childhood renal disease.

R. Chesney, E. Feinstein, I. Zelikovic, 1988, American journal of nephrology.

Acute hemodialysis therapy in neonates with inborn errors of metabolism

H. Mandel, D. Magen, D. Eytan, 2022, Pediatric Nephrology.

Precordial pain and electrocardiographic abnormalities simulating myocardial infarction associated with increased intracranial pressure in a child.

I. Varsano, M. Aygen, M. Shalit, 1981, Helvetica paediatrica acta.

Long-term hemodialysis therapy in neonates and infants with end-stage renal disease: a 16-year experience and outcome

D. Magen, Mahdi Tarabeih, S. Pollack, 2016, Pediatric Nephrology.

Autosomal recessive renal proximal tubulopathy and hypercalciuria: a new syndrome.

D. Magen, I. Zelikovic, E. Efrati, 2004, American journal of kidney diseases : the official journal of the National Kidney Foundation.

A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.

E. Sprecher, D. Magen, K. Skorecki, 2005, Kidney international.

Anion dependence of taurine transport by rat renal brush-border membrane vesicles.

R. Chesney, I. Zelikovic, P. Lohstroh, 1989, The American journal of physiology.

Renal taurine transport--recent developments.

R. Chesney, S. Lippincott, A. Friedman, 1987, Advances in experimental medicine and biology.

Practical Algorithms in Pediatric Nephrology: (Practical Algorithms in Pediatrics. Series Editor: Z. Hochberg)

I. Zelikovic, I. Eisenstein, I. Eisenstein, 2008 .

Severe renal osteodystrophy without elevated serum immunoreactive parathyroid hormone concentrations in hypomagnesemia due to renal magnesium wasting.

R. Chesney, A. Friedman, I. Zelikovic, 1987, Pediatrics.

Renal failure in renal magnesium wasting: recurrence of disease in a renal transplant

R. Chesney, A. Friedman, I. Zelikovic, 1995, Pediatric Nephrology.

Pre- and postoperative fluid management in infancy.

R. Chesney, I. Zelikovic, 1989, Pediatrics in review.

Outbreak of respiratory syncytial virus infection in a neonatal intensive care unit.

N. Varsano, I. Zelikovic, L. Rannon, 1984, Israel journal of medical sciences.

Renal adaptation to dietary amino acid alteration is expressed in immature renal brush border membranes

R. Chesney, N. Gusowski, I. Zelikovic, 2004, Pediatric nephrology (Berlin, West).

Developmental Aspects of Renal β-Amino Acid Transport. VI. The Role of Membrane Fluidity and Phospholipid Composition in the Renal Adaptive Response in Nursing Animals

R. Chesney, N. Gusowski, I. Zelikovic, 1987, Pediatric Research.

Studies on renal adaptation to altered dietary amino acid intake: tissue taurine responses in nursing and adult rats.

R. Chesney, S. Lippincott, N. Gusowski, 1986, The Journal of nutrition.

Membrane Fluidity and Phospholipid Composition in Relation to Sulfur Amino Acid Intake in Brush Border Membranes of Rat Kidney

R. Chesney, N. Gusowski, I. Zelikovic, 1986, Pediatric Research.

Hypokalaemic salt-losing tubulopathies: an evolving story.

I. Zelikovic, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

MPGN type I induced by granulocyte colony stimulating factor

M. Berant, D. Magen, O. Ben‐Izhak, 2002, Pediatric Nephrology.

Molecular Dynamics Simulations of the STAS Domains of Rat Prestin and Human Pendrin Reveal Conformational Motions in Conserved Flexible Regions

Alok K. Sharma, S. Alper, I. Zelikovic, 2014, Cellular Physiology and Biochemistry.

The renal transport of taurine and the regulation of renal sodium-chloride-dependent transporter activity

R. Chesney, Deborah P. Jones, I. Zelikovic, 1990, Pediatric Nephrology.

Ionic and voltage requirements for tubular taurine transport.

R. Chesney, I. Zelikovic, P. Lohstroh, 1990, Progress in clinical and biological research.

An infant with polydactyly and renal anomalies: early diagnosis of a rare syndrome.

D. Magen, A. Khoury, A. Lorber, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Respiratory Arrest Precipitated by Codeine in a Child with Chronic Renal Failure

A. Lynn, F. Levy, I. Zelikovic, 1997, Clinical pediatrics.

Transcriptional Regulation of the Pendrin Gene

S. Alper, S. L. Carrithers, I. Zelikovic, 2011, Cellular Physiology and Biochemistry.

Acetylcysteine for severe atelectasis in premature infants.

E. Wilunsky, I. Zelikovic, S. Reisner, 1985, Clinical Pharmacist.

Neonatal transient renal failure with renal medullary hyperechogenicity: clinical and laboratory features

M. Epelman, M. Soudack, I. Makhoul, 2005, Pediatric Nephrology.

Renal tubular disorders

I. Zelikovic, 2005 .

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

D. Magen, K. Skorecki, S. Selig, 2010, The New England journal of medicine.