RAAS-deficient organoids indicate delayed angiogenesis as a possible cause for autosomal recessive renal tubular dysgenesis von Pode-Shakked, Naomi, Slack, Megan, Sundaram, Nambirajan, Schreiber, Ruth, McCracken, Kyle W., Dekel, Benjamin, Helmrath, Michael, Kopan, Raphael

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SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome von Perez, Yonatan, Shorer, Zamir, Liani-Leibson, Keren, Chabosseau, Pauline, Kadir, Rotem, Volodarsky, Michael, Halperin, Daniel, Barber-Zucker, Shiran, Shalev, Hanna, Schreiber, Ruth, Gradstein, Libe, Gurevich, Evgenia, Zarivach, Raz, Rutter, Guy A, Landau, Daniel, Birk, Ohad S

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Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children von Vivante, Asaf, Chacham, Orna Staretz, Shril, Shirlee, Schreiber, Ruth, Mane, Shrikant M., Pode-Shakked, Ben, Soliman, Neveen A., Koneth, Irene, Schiffer, Mario, Anikster, Yair, Hildebrandt, Friedhelm

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Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center von David, Odeya, Agur, Rotem, Novoa, Rosa, Shaki, David, Walker, Dganit, Carmon, Lior, Eskin-Schwartz, Marina, Birk, Ohad S., Ling, Galina, Schreiber, Ruth, Loewenthal, Neta, Haim, Alon, Hershkovitz, Eli

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Pediatric chronic kidney disease rates in Southern Israel are higher than reported von Landau, Daniel, Schreiber, Ruth, Kleinman, Anya, Vodonos, Alina, Shalev, Hannah

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X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome von Hadar, Noam, Schreiber, Ruth, Eskin-Schwartz, Marina, Kristal, Eyal, Shubinsky, George, Ling, Galina, Cohen, Idan, Geylis, Michael, Nahum, Amit, Yogev, Yuval, Birk, Ohad S

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Glomerular involvement in children with H syndrome von David, Odeya, Geylis, Michael, Kristal, Eyal, Ling, Galina, Schreiber, Ruth

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Listeria Meningitis in an Immunocompetent Adolescent von Hassin, Ori, Danino, Dana, Schreiber, Ruth, Leibovitz, Eugene, Amit, Nahum

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FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases von Kagan, Maayan, Ben Moshe, Yishay, Shlomovitz, Omer, Atias-Varon, Danit, Haskin, Orly, Ben-Shalom, Efrat, Magen, Daniella, Schreiber, Ruth, Volovelsky, Oded, Shasha-Lavsky, Hadas, Davidovits, Miriam, Borovitz, Yael, Mor, Nofar, Khavkin, Yulia, Tzvi Behr, Shimrit, Pollack, Shirley, Geylis, Michael, Schnapp, Aviad, Weissman, Irith, Barel, Ortal, Vivante, Asaf

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Dominant PAX2 mutations may cause steroid resistant neprotic syndrome and FSGS in children von Vivante, Asaf, Chacham, Orna, Shril, Shirlee, Schreiber, Ruth, Soliman, Neveen A., Koneth, Irene, Schiffer, Mario, Anikster, Yair, Hildebrandt, Friedhelm

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A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I von Halperin, Daniel, Dolgin, Vadim, Geylis, Michael, Drabkin, Max, Yogev, Yuval, Wormser, Ohad, Schreiber, Ruth, Shalev, Hanna, Landau, Daniel, Birk, Ohad S.

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Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure von Ben-Moshe, Yishay, Shlomovitz, Omer, Atias-Varon, Danit, Haskin, Orly, Ben-Shalom, Efrat, Shasha Lavsky, Hadas, Volovelsky, Oded, Mane, Shrikant, Ben-Ruby, Dror, Chowers, Guy, Skorecki, Karl, Borovitz, Yael, Kagan, Maayan, Mor, Nofar, Khavkin, Yulia, Tzvi-Behr, Shimrit, Pollack, Shirley, Toder, Moran Plonsky, Geylis, Michael, Schnapp, Aviad, Becker-Cohen, Rachel, Weissman, Irith, Schreiber, Ruth, Davidovits, Miriam, Frishberg, Yaacov, Magen, Daniella, Barel, Ortal, Vivante, Asaf

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Determinants of Aciclovir-Induced Nephrotoxicity in Children von Schreiber, Ruth, Wolpin, Jacob, Koren, Gideon

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Inherited renal tubular dysgenesis may not be universally fatal von Schreiber, Ruth, Gubler, Marie-Claire, Gribouval, Olivier, Shalev, Hanna, Landau, Daniel

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Meconium stained amniotic fluid in preterm delivery is an independent risk factor for perinatal complications von Mazor, Moshe, Hershkovitz, Reli, Bashiri, Asher, Maymon, Eli, Ruth Schreiber, Dukler, Doron, Katz, Miriam, Shoham-Vardi, Ilana

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Nerve growth factor-tyrosine kinase A pathway is involved in thermoregulation and adaptation to stress: studies on patients with hereditary sensory and autonomic neuropathy type IV von Loewenthal, Neta, Levy, Jacov, Schreiber, Ruth, Pinsk, Vered, Perry, Zvi, Shorer, Zamir, Hershkovitz, Eli

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Hemolytic Uremic Syndrome After Pediatric Liver Transplantation von Turner, Dan, Schreiber, Ruth, Grant, David, Hebert, Diane, Sherman, Philip M.

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The .PI. and .SIGMA.N electronic states of the succinimidyl radical. Can nitrogen-centered radicals have .SIGMA.N ground states? An ab initio study von Apeloig, Yitzhak, Schreiber, Ruth

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Electrophoretic Deposition of Phosphors: I. Conductivity and Zeta Potential Measurements von Shane, Michael J., Talbot, Jan B., Schreiber, Ruth D., Ross, Colette L., Sluzky, Esther, Hesse, K.R.

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Pediatric chronic kidney disease rates in Southern Israel von Landau, Daniel, Schreiber, Ruth, Kleinman, Anya, Vodonos, Alina, HannaHannah Shalev

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