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Items: 1 to 50 of 69

1.

Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy.

Backenroth D, Zahdeh F, Kling Y, Peretz A, Rosen T, Kort D, Zeligson S, Dror T, Kirshberg S, Burak E, Segel R, Levy-Lahad E, Zangen D, Altarescu G, Carmi S, Zeevi DA.

Genet Med. 2019 Jun;21(6):1390-1399. doi: 10.1038/s41436-018-0351-7. Epub 2018 Nov 19.

PMID:
30449887
2.

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.

Sagi-Dain L, Maya I, Reches A, Frumkin A, Grinshpun-Cohen J, Segel R, Manor E, Khayat M, Tenne T, Banne E, Shalata A, Yonath H, Berger R, Singer A, Ben-Shachar S.

Obstet Gynecol. 2018 Dec;132(6):1368-1375. doi: 10.1097/AOG.0000000000002975.

PMID:
30399107
3.

An immune tolerance approach using transient low-dose methotrexate in the ERT-naïve setting of patients treated with a therapeutic protein: experience in infantile-onset Pompe disease.

Kazi ZB, Desai AK, Troxler RB, Kronn D, Packman S, Sabbadini M, Rizzo WB, Scherer K, Abdul-Rahman O, Tanpaiboon P, Nampoothiri S, Gupta N, Feigenbaum A, Niyazov DM, Sherry L, Segel R, McVie-Wylie A, Sung C, Joseph AM, Richards S, Kishnani PS.

Genet Med. 2019 Apr;21(4):887-895. doi: 10.1038/s41436-018-0270-7. Epub 2018 Sep 14.

4.

Essential Role of BRCA2 in Ovarian Development and Function.

Weinberg-Shukron A, Rachmiel M, Renbaum P, Gulsuner S, Walsh T, Lobel O, Dreifuss A, Ben-Moshe A, Zeligson S, Segel R, Shore T, Kalifa R, Goldberg M, King MC, Gerlitz O, Levy-Lahad E, Zangen D.

N Engl J Med. 2018 Sep 13;379(11):1042-1049. doi: 10.1056/NEJMoa1800024.

5.

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.

Sagi-Dain L, Singer A, Frumkin A, Shalata A, Koifman A, Segel R, Benyamini L, Rienstein S, Kahyat M, Sharony R, Maya I, Ben Shachar S.

J Perinat Med. 2018 Dec 19;47(1):30-34. doi: 10.1515/jpm-2017-0321.

PMID:
29813032
6.

Mitochondrial PITRM1 peptidase loss-of-function in childhood cerebellar atrophy.

Langer Y, Aran A, Gulsuner S, Abu Libdeh B, Renbaum P, Brunetti D, Teixeira PF, Walsh T, Zeligson S, Ruotolo R, Beeri R, Dweikat I, Shahrour M, Weinberg-Shukron A, Zahdeh F, Baruffini E, Glaser E, King MC, Levy-Lahad E, Zeviani M, Segel R.

J Med Genet. 2018 Sep;55(9):599-606. doi: 10.1136/jmedgenet-2018-105330. Epub 2018 May 15.

PMID:
29764912
7.

Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 Deletion.

Gilboa T, Segel R, Zeligson S, Alterescu G, Ben-Pazi H.

J Child Neurol. 2018 Jun;33(7):482-486. doi: 10.1177/0883073818767036. Epub 2018 Apr 24.

PMID:
29687738
8.

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.

Sagi-Dain L, Singer A, Hadid Y, Sharony R, Vinkler C, Bar-Shira A, Segel R, Ben Shachar S, Maya I.

J Matern Fetal Neonatal Med. 2019 Aug;32(16):2643-2648. doi: 10.1080/14767058.2018.1443070. Epub 2018 Feb 28.

PMID:
29455582
9.

Brain calcifications and PCDH12 variants.

Nicolas G, Sanchez-Contreras M, Ramos EM, Lemos RR, Ferreira J, Moura D, Sobrido MJ, Richard AC, Lopez AR, Legati A, Deleuze JF, Boland A, Quenez O, Krystkowiak P, Favrole P, Geschwind DH, Aran A, Segel R, Levy-Lahad E, Dickson DW, Coppola G, Rademakers R, de Oliveira JRM.

Neurol Genet. 2017 Jul 26;3(4):e166. doi: 10.1212/NXG.0000000000000166. eCollection 2017 Aug.

10.

Adenosine Deaminase 2 Deficiency: More Than Monogenic Vasculitis.

Berkun Y, Segel R, Navon-Elkan P.

Isr Med Assoc J. 2017 Jul;19(7):435-437. Review. No abstract available.

11.

Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.

Vivante A, Ityel H, Pode-Shakked B, Chen J, Shril S, van der Ven AT, Mann N, Schmidt JM, Segel R, Aran A, Zeharia A, Staretz-Chacham O, Bar-Yosef O, Raas-Rothschild A, Landau YE, Lifton RP, Anikster Y, Hildebrandt F.

Pediatr Nephrol. 2017 Dec;32(12):2273-2282. doi: 10.1007/s00467-017-3755-8. Epub 2017 Aug 5.

12.

Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia.

Zambonin JL, Bellomo A, Ben-Pazi H, Everman DB, Frazer LM, Geraghty MT, Harper AD, Jones JR, Kamien B, Kernohan K, Koenig MK, Lines M, Palmer EE, Richardson R, Segel R, Tarnopolsky M, Vanstone JR, Gibbons M, Collins A, Fogel BL; Care4Rare Canada Consortium, Dudding-Byth T, Boycott KM.

Orphanet J Rare Dis. 2017 Jun 28;12(1):121. doi: 10.1186/s13023-017-0672-7. Review.

13.

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Meyer E, Carss KJ, Rankin J, Nichols JME, Grozeva D, Joseph AP, Mencacci NE, Papandreou A, Ng J, Barral S, Ngoh A, Ben-Pazi H, Willemsen MA, Arkadir D, Barnicoat A, Bergman H, Bhate S, Boys A, Darin N, Foulds N, Gutowski N, Hills A, Houlden H, Hurst JA, Israel Z, Kaminska M, Limousin P, Lumsden D, McKee S, Misra S, Mohammed SS, Nakou V, Nicolai J, Nilsson M, Pall H, Peall KJ, Peters GB, Prabhakar P, Reuter MS, Rump P, Segel R, Sinnema M, Smith M, Turnpenny P, White SM, Wieczorek D, Wiethoff S, Wilson BT, Winter G, Wragg C, Pope S, Heales SJH, Morrogh D; UK10K Consortium; Deciphering Developmental Disorders Study; NIHR BioResource Rare Diseases Consortium, Pittman A, Carr LJ, Perez-Dueñas B, Lin JP, Reis A, Gahl WA, Toro C, Bhatia KP, Wood NW, Kamsteeg EJ, Chong WK, Gissen P, Topf M, Dale RC, Chubb JR, Raymond FL, Kurian MA.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969b. No abstract available.

PMID:
28546572
14.

TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex.

Farach LS, Gibson WT, Sparagana SP, Nellist M, Stumpel CT, Hietala M, Friedman E, Pearson DA, Creighton SP, Wagemans A, Segel R, Ben-Shalom E, Au KS, Northrup H.

Am J Med Genet A. 2017 Mar;173(3):771-775. doi: 10.1002/ajmg.a.38083. Review.

PMID:
28211972
15.

Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome.

Aran A, Segel R, Kaneshige K, Gulsuner S, Renbaum P, Oliphant S, Meirson T, Weinberg-Shukron A, Hershkovitz Y, Zeligson S, Lee MK, Samson AO, Parsons SM, King MC, Levy-Lahad E, Walsh T.

Neurology. 2017 Mar 14;88(11):1021-1028. doi: 10.1212/WNL.0000000000003720. Epub 2017 Feb 10.

16.

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Meyer E, Carss KJ, Rankin J, Nichols JM, Grozeva D, Joseph AP, Mencacci NE, Papandreou A, Ng J, Barral S, Ngoh A, Ben-Pazi H, Willemsen MA, Arkadir D, Barnicoat A, Bergman H, Bhate S, Boys A, Darin N, Foulds N, Gutowski N, Hills A, Houlden H, Hurst JA, Israel Z, Kaminska M, Limousin P, Lumsden D, McKee S, Misra S, Mohammed SS, Nakou V, Nicolai J, Nilsson M, Pall H, Peall KJ, Peters GB, Prabhakar P, Reuter MS, Rump P, Segel R, Sinnema M, Smith M, Turnpenny P, White SM, Wieczorek D, Wiethoff S, Wilson BT, Winter G, Wragg C, Pope S, Heales SJ, Morrogh D; UK10K Consortium; Deciphering Developmental Disorders Study; NIHR BioResource Rare Diseases Consortium, Pittman A, Carr LJ, Perez-Dueñas B, Lin JP, Reis A, Gahl WA, Toro C, Bhatia KP, Wood NW, Kamsteeg EJ, Chong WK, Gissen P, Topf M, Dale RC, Chubb JR, Raymond FL, Kurian MA.

Nat Genet. 2017 Feb;49(2):223-237. doi: 10.1038/ng.3740. Epub 2016 Dec 19. Erratum in: Nat Genet. 2017 May 26;49(6):969.

PMID:
27992417
17.

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection.

Aran A, Rosenfeld N, Jaron R, Renbaum P, Zuckerman S, Fridman H, Zeligson S, Segel R, Kohn Y, Kamal L, Kanaan M, Segev Y, Mazaki E, Rabinowitz R, Shen O, Lee M, Walsh T, King MC, Gulsuner S, Levy-Lahad E.

Neurology. 2016 May 24;86(21):2016-24. doi: 10.1212/WNL.0000000000002704. Epub 2016 Apr 29.

18.

Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome?

Jaron R, Rosenfeld N, Zahdeh F, Carmi S, Beni-Adani L, Doviner V, Picard E, Segel R, Zeligson S, Carmel L, Renbaum P, Levy-Lahad E.

Clin Genet. 2016 Dec;90(6):540-544. doi: 10.1111/cge.12764. Epub 2016 May 2.

PMID:
26925547
19.

Limit on Tensor Currents from ^{8}Li β Decay.

Sternberg MG, Segel R, Scielzo ND, Savard G, Clark JA, Bertone PF, Buchinger F, Burkey M, Caldwell S, Chaudhuri A, Crawford JE, Deibel CM, Greene J, Gulick S, Lascar D, Levand AF, Li G, Pérez Galván A, Sharma KS, Van Schelt J, Yee RM, Zabransky BJ.

Phys Rev Lett. 2015 Oct 30;115(18):182501. doi: 10.1103/PhysRevLett.115.182501. Epub 2015 Oct 28.

PMID:
26565463
20.

Copy number variations in cryptogenic cerebral palsy.

Segel R, Ben-Pazi H, Zeligson S, Fatal-Valevski A, Aran A, Gross-Tsur V, Schneebaum-Sender N, Shmueli D, Lev D, Perlberg S, Blumkin L, Deutsch L, Levy-Lahad E.

Neurology. 2015 Apr 21;84(16):1660-8. doi: 10.1212/WNL.0000000000001494. Epub 2015 Mar 27.

PMID:
25817843
21.

Mutant ADA2 in vasculopathies.

Segel R, King MC, Levy-Lahad E.

N Engl J Med. 2014 Jul 31;371(5):481. doi: 10.1056/NEJMc1405506. No abstract available.

PMID:
25083540
22.

Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.

Navon Elkan P, Pierce SB, Segel R, Walsh T, Barash J, Padeh S, Zlotogorski A, Berkun Y, Press JJ, Mukamel M, Voth I, Hashkes PJ, Harel L, Hoffer V, Ling E, Yalcinkaya F, Kasapcopur O, Lee MK, Klevit RE, Renbaum P, Weinberg-Shukron A, Sener EF, Schormair B, Zeligson S, Marek-Yagel D, Strom TM, Shohat M, Singer A, Rubinow A, Pras E, Winkelmann J, Tekin M, Anikster Y, King MC, Levy-Lahad E.

N Engl J Med. 2014 Mar 6;370(10):921-31. doi: 10.1056/NEJMoa1307362. Epub 2014 Feb 19.

23.

Thiopurine S-methyltransferase (TPMT) activity is better determined by biochemical assay versus genotyping in the Jewish population.

Kasirer Y, Mevorach R, Renbaum P, Algur N, Soiferman D, Beeri R, Rachman Y, Segel R, Turner D.

Dig Dis Sci. 2014 Jun;59(6):1207-12. doi: 10.1007/s10620-013-3008-z. Epub 2014 Jan 4.

PMID:
24390675
24.

First results from the CARIBU facility: mass measurements on the r-process path.

Van Schelt J, Lascar D, Savard G, Clark JA, Bertone PF, Caldwell S, Chaudhuri A, Levand AF, Li G, Morgan GE, Orford R, Segel RE, Sharma KS, Sternberg MG.

Phys Rev Lett. 2013 Aug 9;111(6):061102. Epub 2013 Aug 5.

PMID:
23971550
25.

Tensor interaction limit derived from the α-β-ν[over ¯] correlation in trapped 8Li ions.

Li G, Segel R, Scielzo ND, Bertone PF, Buchinger F, Caldwell S, Chaudhuri A, Clark JA, Crawford JE, Deibel CM, Fallis J, Gulick S, Gwinner G, Lascar D, Levand AF, Pedretti M, Savard G, Sharma KS, Sternberg MG, Sun T, Van Schelt J, Yee RM, Zabransky BJ.

Phys Rev Lett. 2013 Mar 1;110(9):092502. Epub 2013 Mar 1.

PMID:
23496705
26.

β-delayed neutron spectroscopy using trapped radioactive ions.

Yee RM, Scielzo ND, Bertone PF, Buchinger F, Caldwell S, Clark JA, Deibel CM, Fallis J, Greene JP, Gulick S, Lascar D, Levand AF, Li G, Norman EB, Pedretti M, Savard G, Segel RE, Sharma KS, Sternberg MG, Van Schelt J, Zabransky BJ.

Phys Rev Lett. 2013 Mar 1;110(9):092501. Epub 2013 Feb 26.

PMID:
23496704
27.

Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter.

Edvardson S, Porcelli V, Jalas C, Soiferman D, Kellner Y, Shaag A, Korman SH, Pierri CL, Scarcia P, Fraenkel ND, Segel R, Schechter A, Frumkin A, Pines O, Saada A, Palmieri L, Elpeleg O.

J Med Genet. 2013 Apr;50(4):240-5. doi: 10.1136/jmedgenet-2012-101485. Epub 2013 Feb 7.

PMID:
23393310
28.

Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.

Schwarze U, Cundy T, Pyott SM, Christiansen HE, Hegde MR, Bank RA, Pals G, Ankala A, Conneely K, Seaver L, Yandow SM, Raney E, Babovic-Vuksanovic D, Stoler J, Ben-Neriah Z, Segel R, Lieberman S, Siderius L, Al-Aqeel A, Hannibal M, Hudgins L, McPherson E, Clemens M, Sussman MD, Steiner RD, Mahan J, Smith R, Anyane-Yeboa K, Wynn J, Chong K, Uster T, Aftimos S, Sutton VR, Davis EC, Kim LS, Weis MA, Eyre D, Byers PH.

Hum Mol Genet. 2013 Jan 1;22(1):1-17. doi: 10.1093/hmg/dds371. Epub 2012 Sep 4.

29.

Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7.

Saada A, Edvardson S, Shaag A, Chung WK, Segel R, Miller C, Jalas C, Elpeleg O.

J Inherit Metab Dis. 2012 Jan;35(1):125-31. doi: 10.1007/s10545-011-9348-y. Epub 2011 May 24.

PMID:
21607760
30.

A safety trial of high dose glyceryl triacetate for Canavan disease.

Segel R, Anikster Y, Zevin S, Steinberg A, Gahl WA, Fisher D, Staretz-Chacham O, Zimran A, Altarescu G.

Mol Genet Metab. 2011 Jul;103(3):203-6. doi: 10.1016/j.ymgme.2011.03.012. Epub 2011 Mar 15.

PMID:
21474353
31.

Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

Belostotsky R, Ben-Shalom E, Rinat C, Becker-Cohen R, Feinstein S, Zeligson S, Segel R, Elpeleg O, Nassar S, Frishberg Y.

Am J Hum Genet. 2011 Feb 11;88(2):193-200. doi: 10.1016/j.ajhg.2010.12.010. Epub 2011 Jan 20.

32.

New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish.

Morris-Rosendahl DJ, Segel R, Born AP, Conrad C, Loeys B, Brooks SS, Müller L, Zeschnigk C, Botti C, Rabinowitz R, Uyanik G, Crocq MA, Kraus U, Degen I, Faes F.

Eur J Hum Genet. 2010 Oct;18(10):1100-6. doi: 10.1038/ejhg.2010.79. Epub 2010 May 26.

33.

Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect (PDAC) syndrome due to STRA6 mutations--what are the minimal criteria?

Segel R, Levy-Lahad E, Pasutto F, Picard E, Rauch A, Alterescu G, Schimmel MS.

Am J Med Genet A. 2009 Nov;149A(11):2457-63. doi: 10.1002/ajmg.a.33038.

PMID:
19839040
34.

Acute infantile liver failure due to mutations in the TRMU gene.

Zeharia A, Shaag A, Pappo O, Mager-Heckel AM, Saada A, Beinat M, Karicheva O, Mandel H, Ofek N, Segel R, Marom D, Rötig A, Tarassov I, Elpeleg O.

Am J Hum Genet. 2009 Sep;85(3):401-7. doi: 10.1016/j.ajhg.2009.08.004. Erratum in: Am J Hum Genet. 2010 Feb;86(2):295.

35.

Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.

Renbaum P, Kellerman E, Jaron R, Geiger D, Segel R, Lee M, King MC, Levy-Lahad E.

Am J Hum Genet. 2009 Aug;85(2):281-9. doi: 10.1016/j.ajhg.2009.07.006. Epub 2009 Jul 30.

36.

VITA-D: cholecalciferol substitution in vitamin D deficient kidney transplant recipients: a randomized, placebo-controlled study to evaluate the post-transplant outcome.

Thiem U, Heinze G, Segel R, Perkmann T, Kainberger F, Mühlbacher F, Hörl W, Borchhardt K.

Trials. 2009 May 29;10:36. doi: 10.1186/1745-6215-10-36.

37.

New determination of the astrophysical S factor SE1 of the 12C(alpha,gamma)16O reaction.

Tang XD, Rehm KE, Ahmad I, Brune CR, Champagne A, Greene JP, Hecht AA, Henderson D, Janssens RV, Jiang CL, Jisonna L, Kahl D, Moore EF, Notani M, Pardo RC, Patel N, Paul M, Savard G, Schiffer JP, Segel RE, Sinha S, Shumard B, Wuosmaa AH.

Phys Rev Lett. 2007 Aug 3;99(5):052502. Epub 2007 Aug 3.

PMID:
17930748
38.

[Clinical, biochemical and molecular characterization of rare genetic disorders, related to nucleotide excision repair (NER) system].

Falik-Zaccai T, Kfir N, Laskar M, Segel R, Khyat M, Slor H.

Harefuah. 2006 Dec;145(12):889-94, 942. Hebrew.

PMID:
17220027
39.

The natural history of trisomy 12p.

Segel R, Peter I, Demmer LA, Cowan JM, Hoffman JD, Bianchi DW.

Am J Med Genet A. 2006 Apr 1;140(7):695-703.

PMID:
16502429
40.

Precision Rosenbluth measurement of the proton elastic form factors.

Qattan IA, Arrington J, Segel RE, Zheng X, Aniol K, Baker OK, Beams R, Brash EJ, Calarco J, Camsonne A, Chen JP, Christy ME, Dutta D, Ent R, Frullani S, Gaskell D, Gayou O, Gilman R, Glashausser C, Hafidi K, Hansen JO, Higinbotham DW, Hinton W, Holt RJ, Huber GM, Ibrahim H, Jisonna L, Jones MK, Keppel CE, Kinney E, Kumbartzki GJ, Lung A, Margaziotis DJ, McCormick K, Meekins D, Michaels R, Monaghan P, Moussiegt P, Pentchev L, Perdrisat C, Punjabi V, Ransome R, Reinhold J, Reitz B, Saha A, Sarty A, Schulte EC, Slifer K, Solvignon P, Sulkosky V, Wijesooriya K, Zeidman B.

Phys Rev Lett. 2005 Apr 15;94(14):142301. Epub 2005 Apr 15.

PMID:
15904058
41.

Neutron spectroscopic factors in 9Li from 2H(8Li,p)9Li.

Wuosmaa AH, Rehm KE, Greene JP, Henderson DJ, Janssens RV, Jiang CL, Jisonna L, Moore EF, Pardo RC, Paul M, Peterson D, Pieper SC, Savard G, Schiffer JP, Segel RE, Sinha S, Tang X, Wiringa RB.

Phys Rev Lett. 2005 Mar 4;94(8):082502. Epub 2005 Mar 2. Erratum in: Phys Rev Lett. 2005 Mar 18;94(10):109904.

PMID:
15783884
42.

Angular distributions for (3,4)(Lambda)H bound states in the (3,4)He(e,e(')K+) reaction.

Dohrmann F, Ahmidouch A, Armstrong CS, Arrington J, Asaturyan R, Avery S, Bailey K, Bitao H, Breuer H, Brown DS, Carlini R, Cha J, Chant N, Christy E, Cochran A, Cole L, Crowder J, Danagoulian S, Elaasar M, Ent R, Fenker H, Fujii Y, Gan L, Garrow K, Geesaman DF, Gueye P, Hafidi K, Hinton W, Juengst H, Keppel C, Liang Y, Liu JH, Lung A, Mack D, Markowitz P, Mitchell J, Miyoshi T, Mkrtchyan H, Mtingwa SK, Mueller B, Niculescu G, Niculescu I, Potterveld D, Raue BA, Reimer PE, Reinhold J, Roche J, Sarsour M, Sato Y, Segel RE, Semenov A, Stepanyan S, Tadevosian V, Tajima S, Tang L, Uzzle A, Wood S, Yamaguchi H, Yan C, Yuan L, Zeidman B, Zeier M, Zihlmann B.

Phys Rev Lett. 2004 Dec 10;93(24):242501. Epub 2004 Dec 9.

PMID:
15697799
43.

Methicillin-resistant Staphylococcus aureus nasal colonization in children in Jerusalem: community vs. chronic care institutions.

Schlesinger Y, Yahalom S, Raveh D, Yinnon AM, Segel R, Erlichman M, Attias D, Rudensky B.

Isr Med Assoc J. 2003 Dec;5(12):847-51.

44.

Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.

Segel R, Silverstein S, Lerer I, Kahana E, Meir R, Sagi M, Zilber N, Korczyn AD, Shapira Y, Argov Z, Abeliovich D.

Am J Med Genet A. 2003 Jun 15;119A(3):273-8.

PMID:
12784291
46.

Longitudinal electroproduction of charged pions from (1)H, (2)H, and (3)He.

Gaskell D, Ahmidouch A, Ambrozewicz P, Anklin H, Arrington J, Assamagan K, Avery S, Bailey K, Baker OK, Beedoe S, Beise B, Breuer H, Brown DS, Carlini R, Cha J, Chant N, Cowley A, Danagoulian S, De Schepper D, Dunne J, Dutta D, Ent R, Gan L, Gasparian A, Geesaman DF, Gilman R, Glashausser C, Gueye P, Harvey M, Hashimoto O, Hinton W, Hofman G, Jackson C, Jackson HE, Keppel C, Kinney E, Koltenuk D, Kyle G, Lung A, Mack D, McKee D, Mitchell J, Mkrtchyan H, Mueller B, Niculescu G, Niculescu I, O'Neill TG, Papavassiliou V, Potterveld D, Reinhold J, Roos P, Sawafta R, Segel R, Stepanyan S, Tadevosyan V, Takahashi T, Tang L, Terburg B, Van Westrum D, Volmer J, Welch TP, Wood S, Yuan L, Zeidman B, Zihlmann B.

Phys Rev Lett. 2001 Nov 12;87(20):202301. Epub 2001 Oct 23.

PMID:
11690468
47.

The 44Ti(alpha,p) reaction and its implication on the 44Ti yield in supernovae

Sonzogni AA, Rehm KE, Ahmad I I, Borasi F, Bowers DL, Brumwell F, Caggiano J, Davids CN, Greene JP, Harss B, Heinz A, Henderson D, Janssens RV, Jiang CL, McMichael G, Nolen J, Pardo RC, Paul M, Schiffer JP, Segel RE, Seweryniak D, Siemssen RH, Truran JW, Uusitalo J, Wiedenhover I I, Zabransky B.

Phys Rev Lett. 2000 Feb 21;84(8):1651-4.

PMID:
11017592
48.

Measurement of the p

Heimberg P, Segel RE, Chen FJ, Ackerstaff K, Bent RD, Blomgren J, Meyer HO, Nann H, Przewoski Bv, Rinckel T, Zhuralev A, Pickar MA, Hardie G, Pancella PV, Jacobsen E, Brown JD.

Phys Rev Lett. 1996 Aug 5;77(6):1012-1015. No abstract available.

PMID:
10062968
49.

Astrophysical reaction rate for the 18F(p, alpha )15O reaction.

Rehm KE, Paul M, Roberts AD, Jiang CL, Blumenthal DJ, Fischer SM, Gehring J, Henderson D, Nickles J, Nolen J, Pardo RC, Schiffer JP, Segel RE.

Phys Rev C Nucl Phys. 1996 Apr;53(4):1950-1954. No abstract available.

PMID:
9971152
50.

Differential cross sections of the 12,13C(p,p)12,13C and 12,13C(p,n)12,13N reactions near 180 degrees.

Yu Z, Segel RE, Tung T, Bent RD, Foster CC, Goodwin J, Hardie G, Homolka J.

Phys Rev C Nucl Phys. 1996 Apr;53(4):1725-1733. No abstract available.

PMID:
9971123

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