Static Var Compensator and Active Power Filter With Power Injection Capability, Using 27-Level Inverters and Photovoltaic Cells von Flores, P., Dixon, J., Ortuzar, M., Carmi, R., Barriuso, P., Moran, L.

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TU‐E‐210A‐03: A Double‐Layer Detector, Dual‐Energy CT — Principles, Advantages and Applications von Altman, A, Carmi, R

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Voltage-source active power filter based on multilevel converter and ultracapacitor DC link von Ortuzar, M.E., Carmi, R.E., Dixon, J.W., Moran, L.

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Perineal Biodegradable Balloon Is Effective for Both Sparing the Rectum and as a Fiducial Marker in Prostate Cancer Patients Treated With Mild Hypofractionation von Ben-Yosef, R, Heres, T, Berniger, A, Carmi, R, I. lvovich, Genesin, Y

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Dynamic Versus Quasi Static Fracture Toughness of Additively Manufactured AlSi10Mg Alloy by Selective Laser Melting Technique von Chakotay, E., Carmi, R., Alon, I., Shneck, R., Pinkas, M., Stern, A., Bussiba, A.

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A comparison of the minimum canal wall thickness remaining following preparation using two nickel-titanium rotary systems von Garala, M., Kuttler, S., Hardigan, P., Steiner-Carmi, R., Dorn, S.

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Quantifying center bias of observers in free viewing of dynamic natural scenes von Tseng, Po-He, Carmi, Ran, Cameron, Ian G M, Munoz, Douglas P, Itti, Laurent

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Familial aggregation in the fibromyalgia syndrome von BUSKILA, D, NEUMANN, L, HAZANOV, I, CARMI, R

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EP-2337: Comparison between two frameless immobilization techniques for Brain stereotactic radiosurgery von Lvovich, I., Kaidar-Person, O., Bar-Deroma, R., Carmi, R.

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EP-2393: The influence of raising patient awareness of physical activity during radiation treatment von Webster, H., Carmi, R., Bar-Deroma, R., Bar-Sela, G.

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Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta) von Carmi, R, Polturak, E, Koren, G, Auerbach, A

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss von Scott, DA, Kraft, ML, Carmi, R, Ramesh, A, Elbedour, K, Yairi, Y, Srisailapathy, C. R. Srikumari, Rosengren, SS, Markham, AF, Mueller, RF, Lench, NJ, Van Camp, G, Smith, RJH, Sheffield, VC

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Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O7-δ von Carmi, R., Polturak, E., Koren, G., Auerbach, A.

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Homozygosity Mapping with SNP Arrays Identifies TRIM32, an E3 Ubiquitin Ligase, as a Bardet-Biedl Syndrome Gene (BBS11) von Chiang, Annie P., Beck, John S., Yen, Hsan-Jan, Tayeh, Marwan K., Scheetz, Todd E., Swiderski, Ruth E., Nishimura, Darryl Y., Braun, Terry A., Kim, Kwang-Youn A., Huang, Jian, Elbedour, Khalil, Carmi, Rivka, Slusarski, Diane C., Casavant, Thomas L., Stone, Edwin M., Sheffield, Val C.

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Bbs2-Null Mice Have Neurosensory Deficits, a Defect in Social Dominance, and Retinopathy Associated with Mislocalization of Rhodopsin von Nishimura, Darryl Y., Fath, Melissa, Mullins, Robert F., Searby, Charles, Andrews, Michael, Davis, Roger, Andorf, Jeaneen L., Mykytyn, Kirk, Swiderski, Ruth E., Yang, Baoli, Carmi, Rivka, Stone, Edwin M., Sheffield, Val C., Nathans, Jeremy

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Clinical presentation and outcome in primary familial hypomagnesaemia von Shalev, Hanna, Phillip, Moshe, Galil, Aharon, Carmi, Rivka, Landau, Daniel

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Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15 von Carmi, Rivka, Rokhlina, Tatiana, Kwitek-Black, Anne E., Elbedour, Khalil, Nishimura, Darryl, Stone, Edwin M., Sheffield, Val C.

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia von Sheffield, Val C, Walder, Roxanne Y, Landau, Daniel, Meyer, Peter, Shalev, Hanna, Tsolia, Maria, Borochowitz, Zvi, Boettger, Melanie Barbara, Beck, Gretel E, Englehardt, Richard K, Carmi, Rivka

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Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3) von Chiang, Annie P., Nishimura, Darryl, Searby, Charles, Elbedour, Khalil, Carmi, Rivka, Ferguson, Amanda L., Secrist, Jenifer, Braun, Terry, Casavant, Thomas, Stone, Edwin M., Sheffield, Val C.

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Familial Hypomagnesemia Maps to Chromosome 9q, not to the X Chromosome: Genetic Linkage Mapping and Analysis of a Balanced Translocation Breakpoint von Walder, R.Y., Shalev, H., Brennan, T.M.H., Carmi, R., Elbedour, K., Scott, D.A., Hanauer, A., Mark, A.L., Patil, S., Stone, E.M., Sheffield, V.C.

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