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Items: 1 to 50 of 134

1.

American Funding Cutback to East Jerusalem Hospitals: A Blow to the Health of the City.

Clarfield AM, Skorecki K, Paltiel O, Glick SM, Beyar R, Ben Yehuda D, Carmi R, Gil Z, Billan S, Azzam Z, Basis F, Levy-Lahad E, Lahad A, Izraeli S, Turner D, Halevy Y.

Am J Public Health. 2018 Dec;108(12):1624-1625. doi: 10.2105/AJPH.2018.304792. No abstract available.

2.

The Task Force for the Promotion of the Status of Women in Medicine in Israel.

Borow M, Levi B, Carmi R.

Isr Med Assoc J. 2018 Apr;20(4):254-259. Review.

3.

Women and health in Israel.

Granek L, Nakash O, Carmi R.

Lancet. 2017 Jun 24;389(10088):2575-2578. doi: 10.1016/S0140-6736(17)30563-9. Epub 2017 May 8. No abstract available.

PMID:
28495110
4.

FDG PET/CT early dynamic blood flow and late standardized uptake value determination in hepatocellular carcinoma.

Bernstine H, Braun M, Yefremov N, Lamash Y, Carmi R, Stern D, Steinmetz A, Sosna J, Groshar D.

Radiology. 2011 Aug;260(2):503-10. doi: 10.1148/radiol.11102350. Epub 2011 May 9.

PMID:
21555347
5.

Dual-energy based spectral electronic cleansing in non-cathartic computed tomography colonography: an emerging novel technique.

Eliahou R, Azraq Y, Carmi R, Mahgerefteh SY, Sosna J.

Semin Ultrasound CT MR. 2010 Aug;31(4):309-14. doi: 10.1053/j.sult.2010.05.005. Review.

PMID:
20691931
6.

Quantifying center bias of observers in free viewing of dynamic natural scenes.

Tseng PH, Carmi R, Cameron IG, Munoz DP, Itti L.

J Vis. 2009 Jul 9;9(7):4. doi: 10.1167/9.7.4.

PMID:
19761319
7.

Congenital glaucoma: CYP1B1 mutations in Israeli Bedouin kindreds.

Bar-Yosef U, Levy J, Elbedour K, Ofir R, Carmi R, Birk OS.

J Glaucoma. 2010 Jan;19(1):35-8. doi: 10.1097/IJG.0b013e3181a98b6f.

PMID:
19593207
8.

A targeted population carrier screening program for severe and frequent genetic diseases in Israel.

Zlotogora J, Carmi R, Lev B, Shalev SA.

Eur J Hum Genet. 2009 May;17(5):591-7. doi: 10.1038/ejhg.2008.241. Epub 2008 Dec 24.

9.

Attitudes toward the acceptability of reasons for pregnancy termination due to fetal abnormalities among prenatal care providers and consumers in Israel.

Mishori Dery A, Carmi R, Shoham Vardi I.

Prenat Diagn. 2008 Jun;28(6):518-24. doi: 10.1002/pd.2017.

PMID:
18509872
10.

Deletion of the first pair of fibronectin type III repeats of the integrin beta-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients.

Birnbaum RY, Landau D, Elbedour K, Ofir R, Birk OS, Carmi R.

Am J Med Genet A. 2008 Apr 15;146A(8):1063-6. doi: 10.1002/ajmg.a.31903. No abstract available.

PMID:
18348258
11.

Different perceptions and attitudes regarding prenatal testing among service providers and consumers in Israel.

Mishori Dery A, Carmi R, Shoham Vardi I.

Community Genet. 2007;10(4):242-51.

PMID:
17895630
12.

Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example.

Hanein S, Perrault I, Gerber S, Delphin N, Benezra D, Shalev S, Carmi R, Feingold J, Dufier JL, Munnich A, Kaplan J, Rozet JM, Jeanpierre M.

Eur J Hum Genet. 2008 Jan;16(1):115-23. Epub 2007 Aug 8.

13.

Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.

Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS.

Invest Ophthalmol Vis Sci. 2007 May;48(5):2208-13.

PMID:
17460281
14.

The role of memory in guiding attention during natural vision.

Carmi R, Itti L.

J Vis. 2006 Aug 10;6(9):898-914.

PMID:
17083283
15.

Visual causes versus correlates of attentional selection in dynamic scenes.

Carmi R, Itti L.

Vision Res. 2006 Dec;46(26):4333-45. Epub 2006 Oct 18.

16.

Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).

Chiang AP, Beck JS, Yen HJ, Tayeh MK, Scheetz TE, Swiderski RE, Nishimura DY, Braun TA, Kim KY, Huang J, Elbedour K, Carmi R, Slusarski DC, Casavant TL, Stone EM, Sheffield VC.

Proc Natl Acad Sci U S A. 2006 Apr 18;103(16):6287-92. Epub 2006 Apr 10.

17.

CAM in medical education: has the time come?

Oberbaum M, Shuval J, Haramati A, Singer SR, Halevi J, Lumpkin MD, Carmi R.

Isr Med Assoc J. 2005 Sep;7(9):607-10. No abstract available.

18.

Promoting Arab and Israeli cooperation: peacebuilding through health initiatives.

Skinner H, Abdeen Z, Abdeen H, Aber P, Al-Masri M, Attias J, Avraham KB, Carmi R, Chalin C, El Nasser Z, Hijazi M, Jebara RO, Kanaan M, Pratt H, Raad F, Roth Y, Williams AP, Noyek A.

Lancet. 2005 Apr 2-8;365(9466):1274-7.

PMID:
15811462
19.
20.

Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome.

Héon E, Westall C, Carmi R, Elbedour K, Panton C, Mackeen L, Stone EM, Sheffield VC.

Am J Med Genet A. 2005 Jan 30;132A(3):283-7.

PMID:
15690372
21.

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.

Nishimura DY, Fath M, Mullins RF, Searby C, Andrews M, Davis R, Andorf JL, Mykytyn K, Swiderski RE, Yang B, Carmi R, Stone EM, Sheffield VC.

Proc Natl Acad Sci U S A. 2004 Nov 23;101(47):16588-93. Epub 2004 Nov 11.

22.

Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13.

Narkis G, Landau D, Manor E, Elbedour K, Tzemach A, Fishelson M, Geiger D, Ofir R, Carmi R, Birk OS.

Am J Med Genet A. 2004 Oct 15;130A(3):272-6.

PMID:
15378541
23.

Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3).

Chiang AP, Nishimura D, Searby C, Elbedour K, Carmi R, Ferguson AL, Secrist J, Braun T, Casavant T, Stone EM, Sheffield VC.

Am J Hum Genet. 2004 Sep;75(3):475-84. Epub 2004 Jul 16.

24.

Lowering the burden of hereditary diseases in a traditional, inbred community: ethical aspects of genetic research and its application.

Carmi R, Elbedour K, Wietzman D, Sheffield V, Shoham-Vardi I.

Sci Context. 1998 Autumn-Winter;11(3-4):391-95.

PMID:
15168669
25.

[A comprehensive program for prevention of genetic diseases among Arabs in Israel].

Shalev SA, Carmi R, Leventhal A, Zlotogora J.

Harefuah. 2003 Nov;142(11):792-4, 804. Hebrew.

PMID:
14631914
26.
27.

A new autosomal recessive congenital contractural syndrome in an Israeli Bedouin kindred.

Landau D, Mishori-Dery A, Hershkovitz R, Narkis G, Elbedour K, Carmi R.

Am J Med Genet A. 2003 Feb 15;117A(1):37-40.

PMID:
12548738
28.

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).

Mykytyn K, Nishimura DY, Searby CC, Beck G, Bugge K, Haines HL, Cornier AS, Cox GF, Fulton AB, Carmi R, Iannaccone A, Jacobson SG, Weleber RG, Wright AF, Riise R, Hennekam RC, Lüleci G, Berker-Karauzum S, Biesecker LG, Stone EM, Sheffield VC.

Am J Hum Genet. 2003 Feb;72(2):429-37. Epub 2003 Jan 10.

29.

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.

Mykytyn K, Nishimura DY, Searby CC, Shastri M, Yen HJ, Beck JS, Braun T, Streb LM, Cornier AS, Cox GF, Fulton AB, Carmi R, Lüleci G, Chandrasekharappa SC, Collins FS, Jacobson SG, Heckenlively JR, Weleber RG, Stone EM, Sheffield VC.

Nat Genet. 2002 Aug;31(4):435-8. Epub 2002 Jul 15.

PMID:
12118255
30.

HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease.

Neuhausen SL, Weizman Z, Camp NJ, Elbedour K, Sheffield VC, Zone JJ, Carmi R.

Hum Immunol. 2002 Jun;63(6):502-7.

PMID:
12039527
31.

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.

Walder RY, Landau D, Meyer P, Shalev H, Tsolia M, Borochowitz Z, Boettger MB, Beck GE, Englehardt RK, Carmi R, Sheffield VC.

Nat Genet. 2002 Jun;31(2):171-4. Epub 2002 May 28.

PMID:
12032570
32.

Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C.

Meiner V, Shpitzen S, Mandel H, Klar A, Ben-Neriah Z, Zlotogora J, Sagi M, Lossos A, Bargal R, Sury V, Carmi R, Leitersdorf E, Zeigler M.

Genet Med. 2001 Sep-Oct;3(5):343-8.

PMID:
11545687
33.

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, Riise R, Baldi A, Raas-Rothschild A, Gorman SW, Duhl DM, Jacobson SG, Casavant T, Stone EM, Sheffield VC.

Nat Genet. 2001 Jun;28(2):188-91.

PMID:
11381270
34.

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).

Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, Heon E, Iannaccone A, Bonneau D, Biesecker LG, Jacobson SG, Stone EM, Sheffield VC.

Hum Mol Genet. 2001 Apr 1;10(8):865-74.

PMID:
11285252
35.

Osteopetrosis: a single centre experience of stem cell tranisplantation and prenatal diagnosis.

Kapelushnik J, Shalev C, Yaniv I, Aker M, Carmi R, Cohen Z, Mozer A, Schulman C, Stein G, Or R.

Bone Marrow Transplant. 2001 Jan;27(2):129-32.

36.

Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysis.

Shalev H, Mishori-Dery A, Kapelushnik J, Moser A, Sheffield VC, McClain A, Carmi R.

Prenat Diagn. 2001 Mar;21(3):183-6.

PMID:
11260604
37.

Observation of spontaneous flux generation in a multi-josephson-junction loop

Carmi R, Polturak E, Koren G.

Phys Rev Lett. 2000 May 22;84(21):4966-9.

PMID:
10990843
38.

Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterization.

Falik-Zaccai TC, Shachak E, Abeliovitch D, Lerer I, Shefer R, Carmi R, Ries L, Friedman M, Shohat M, Borochowitz Z.

Isr Med Assoc J. 2000 Aug;2(8):601-4.

39.

Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta)

Carmi R, Polturak E, Koren G, Auerbach A.

Nature. 2000 Apr 20;404(6780):853-5.

PMID:
10786787
40.

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2.

Scott DA, Drury S, Sundstrom RA, Bishop J, Swiderski RE, Carmi R, Ramesh A, Elbedour K, Srikumari Srisailapathy CR, Keats BJ, Sheffield VC, Smith RJ.

Gene. 2000 Apr 4;246(1-2):265-74.

PMID:
10767548
41.

Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency.

Leiberman E, Pesler D, Parvari R, Elbedour K, Abdul-Latif H, Brown MR, Parks JS, Carmi R.

Am J Med Genet. 2000 Jan 31;90(3):188-92.

PMID:
10678654
43.

Growth hormone deficiency type IB caused by cryptic splicing of the GH-1 gene.

Abdul-Latif H, Leiberman E, Brown MR, Carmi R, Parks JS.

J Pediatr Endocrinol Metab. 2000 Jan;13(1):21-8.

PMID:
10689634
44.

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC.

Nat Genet. 2000 Feb;24(2):127-31.

PMID:
10655056
45.

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

Ying L, Katz Y, Schlesinger M, Carmi R, Shalev H, Haider N, Beck G, Sheffield VC, Landau D.

Am J Hum Genet. 1999 Dec;65(6):1538-46.

46.

The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.

Gorman SW, Haider NB, Grieshammer U, Swiderski RE, Kim E, Welch JW, Searby C, Leng S, Carmi R, Sheffield VC, Duhl DM.

Genomics. 1999 Jul 15;59(2):150-60.

PMID:
10409426
47.

Maternal factors associated with severity of birth defects.

Sheiner E, Shoham-Vardi I, Sheiner EK, Mazor M, Katz M, Carmi R.

Int J Gynaecol Obstet. 1999 Mar;64(3):227-32.

PMID:
10366043
48.

Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth.

Parvari R, Mumm S, Galil A, Manor E, Bar-David Y, Carmi R.

Am J Med Genet. 1999 Apr 2;83(4):302-7.

PMID:
10208166
49.

Use of isolated inbred human populations for identification of disease genes.

Sheffield VC, Stone EM, Carmi R.

Trends Genet. 1998 Oct;14(10):391-6.

PMID:
9820027
50.

Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H.

Ohali M, Shalev H, Schlesinger M, Katz Y, Kachko L, Carmi R, Sofer S, Landau D.

Pediatr Nephrol. 1998 Oct;12(8):619-24.

PMID:
9811382

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