Search Results - "Carmi, R."

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  1. 1

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

    Published in Medical Physics (01-06-2009)
    “…The emerging of fast‐rotating MDCT scanners, and the recent approach of the, so called, “Slice War” to its saturation, opened new opportunities for CT…”
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    Conference Proceeding Journal Article
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    Static Var Compensator and Active Power Filter With Power Injection Capability, Using 27-Level Inverters and Photovoltaic Cells by Flores, P., Dixon, J., Ortuzar, M., Carmi, R., Barriuso, P., Moran, L.

    “…An active power filter and static var compensator with active power generation capability has been implemented using a 27-level inverter. Each phase of this…”
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    Journal Article
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    A comparison of the minimum canal wall thickness remaining following preparation using two nickel-titanium rotary systems by Garala, M., Kuttler, S., Hardigan, P., Steiner-Carmi, R., Dorn, S.

    Published in International endodontic journal (01-09-2003)
    “…Aim  To examine in vitro whether Profile or Hero 642 nickel–titanium rotary instrument systems substantially reduce the minimum canal wall thickness present…”
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    Journal Article
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    Voltage-source active power filter based on multilevel converter and ultracapacitor DC link by Ortuzar, M.E., Carmi, R.E., Dixon, J.W., Moran, L.

    “…A new topology for active power filters (APF) using an 81-level converter is analyzed. Each phase of the converter is composed of four three-state converters,…”
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    Journal Article
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    Familial aggregation in the fibromyalgia syndrome by BUSKILA, D, NEUMANN, L, HAZANOV, I, CARMI, R

    Published in Seminars in arthritis and rheumatism (01-12-1996)
    “…The authors studied the familial occurrence of fibromyalgia (FMS) to determine a possible role of genetic and familial factors in this syndrome. Fifty-eight…”
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    Journal Article
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    Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta) by Carmi, R, Polturak, E, Koren, G, Auerbach, A

    Published in Nature (London) (20-04-2000)
    “…A noteworthy feature of the high-temperature superconductors is the unconventional symmetry of the superconducting order parameter. Several experiments have…”
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    Journal Article
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    Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O7-δ by CARMI, R, POLTURAK, E, KOREN, G, AUERBACH, A

    Published in Nature (London) (20-04-2000)
    “…A noteworthy feature of the high-temperature superconductors is the unconventional symmetry of the superconducting order parameter. Several experiments have…”
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    Journal Article
  9. 9

    Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss by 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

    Published in Human mutation (1998)
    “…Mutations in the Cx26 gene have been shown to cause autosomal recessive nonsyndromic hearing loss (ARNSHL) at the DFNB1 locus on chromosome 13q12. Using direct…”
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    Journal Article
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    Clinical presentation and outcome in primary familial hypomagnesaemia by Shalev, Hanna, Phillip, Moshe, Galil, Aharon, Carmi, Rivka, Landau, Daniel

    Published in Archives of disease in childhood (01-02-1998)
    “…The clinical presentation and long term outcome (mean follow up eight years, range 0.25 to 21) of 15 patients with autosomal recessive primary familial…”
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    Journal Article
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    Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15 by Carmi, R, Rokhlina, T, Kwitek-Black, A E, Elbedour, K, Nishimura, D, Stone, E M, Sheffield, V C

    Published in Human molecular genetics (01-01-1995)
    “…Bardet-Biedl syndrome is a heterogeneous autosomal recessive disorder characterized by obesity, mental retardation, polydactyly, retinitis pigmentosa and…”
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    Journal Article
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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 by 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.

    Published in Human molecular genetics (01-09-1997)
    “…Familial hypomagnesemia with secondary hypocalcemia (HSH) (MIM 307600) was studied in three inbred Bedouin kindreds from Israel. The three kindreds, one…”
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    Journal Article
  13. 13

    An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred bedouin kindreds by SCOTT, D. A, CARMI, R, ELBEDOUR, K, YOSEFSBERG, S, STONE, E. M, SHEFFIELD, V. C

    Published in American journal of human genetics (01-08-1996)
    “…Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of severe inherited childhood deafness. We present the linkage analysis of two…”
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    Journal Article
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    Quantifying center bias of observers in free viewing of dynamic natural scenes by Tseng, Po-He, Carmi, Ran, Cameron, Ian G M, Munoz, Douglas P, Itti, Laurent

    Published in Journal of vision (Charlottesville, Va.) (09-07-2009)
    “…Human eye-tracking studies have shown that gaze fixations are biased toward the center of natural scene stimuli ("center bias"). This bias contaminates the…”
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    Journal Article
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    Osteopetrosis : a single centre experience of stem cell transplantation and prenatal diagnosis by KAPELUSHNIK, J, SHALEV, C, YANIV, I, AKER, M, CARMI, R, COHEN, Z, MOZER, A, SCHULMAN, C, STEIN, G, OR, R

    Published in Bone marrow transplantation (Basingstoke) (01-01-2001)
    “…Malignant osteopetrosis (MOP) is an autosomal recessive disease in which osteoclast dysfunction results in excessive bone deposition and early infant death…”
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    Journal Article
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    Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22 by ZVULUNOV, A, KACHKO, L, MANOR, E, SHINWELL, E, CARMI, R

    Published in British journal of dermatology (1951) (01-06-1998)
    “…A distinct form of aplasia cutis congenita presenting as linear facial skin defects has been described under a variety of names as Xp deletion syndrome, MIDAS…”
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    Journal Article
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    Refining the DFNB7–DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2 by Scott, D.A., Drury, S., Sundstrom, R.A., Bishop, J., Swiderski, R.E., Carmi, R., Ramesh, A., Elbedour, K., Srikumari Srisailapathy, C.R., Keats, B.J., Sheffield, V.C., Smith, R.J.H.

    Published in Gene (04-04-2000)
    “…The combined DFNB7–DFNB11 deafness locus maps to chromosome 9q13–q21 between markers D9S1806 and D9S769. We have determined the cDNA sequence and genomic…”
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    Journal Article
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    Resolution enhancement of X-ray CT by spatial and temporal MLEM deconvolution correction by Carmi, R., Shapiro, O., Braunstein, D.

    “…In multi-slice CT, there is an ongoing trend to use smaller slice thickness and faster rotation time, leading to smaller detector pixel size and shorter…”
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    Conference Proceeding