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Results: 1-25 | 26-50 | 51-75 | 76-94
Results: 1-25/94
Trans-1,2-difluorostilbenes: Promising materials for high dielectric biaxiality ferroelectric mixtures
Authors: Goodby, JW Hindmarsh, P Hird, M Lewis, RA Toyne, KJ
Citation: Jw. Goodby et al., Trans-1,2-difluorostilbenes: Promising materials for high dielectric biaxiality ferroelectric mixtures, MOLEC CRYST, 364, 2001, pp. 889-898
Numerical calculation of thermionic cooling efficiency in a double-barriersemiconductor heterostructure
Authors: Lough, BC Lee, SP Lewis, RA Zhang, C
Citation: Bc. Lough et al., Numerical calculation of thermionic cooling efficiency in a double-barriersemiconductor heterostructure, PHYSICA E, 11(2-3), 2001, pp. 287-291
Appropriate design and outcome measures in multiple sclerosis clinical trials - Response
Authors: Khan, OA Tselis, AC Kamholz, JA Garbern, JY Lewis, RA Lisak, RP
Citation: Oa. Khan et al., Appropriate design and outcome measures in multiple sclerosis clinical trials - Response, EUR J NEUR, 8(5), 2001, pp. 505-506
A prospective, open-label treatment trial to compare the effect of IFN beta-1a (Avonex), IFN beta-1b (Betaseron), and glatiramer acetate (Copaxone) on the relapse rate in relapsing-remitting multiple sclerosis
Authors: Khan, OA Tselis, AC Kamholz, JA Garbern, JY Lewis, RA Lisak, RP
Citation: Oa. Khan et al., A prospective, open-label treatment trial to compare the effect of IFN beta-1a (Avonex), IFN beta-1b (Betaseron), and glatiramer acetate (Copaxone) on the relapse rate in relapsing-remitting multiple sclerosis, EUR J NEUR, 8(2), 2001, pp. 141-148
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
Authors: Sohocki, MM Daiger, SP Bowne, SJ Rodriguez, JA Northrup, H Heckenlively, JR Birch, DG Mintz-Hittner, H Ruiz, RS Lewis, RA Saperstein, DA Sullivan, LS
Citation: Mm. Sohocki et al., Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies, HUM MUTAT, 17(1), 2001, pp. 42-51
Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration
Authors: Shroyer, NF Lewis, RA Yatsenko, AN Wensel, TG Lupski, JR
Citation: Nf. Shroyer et al., Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration, HUM MOL GEN, 10(23), 2001, pp. 2671-2678
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations
Authors: Aradhya, S Woffendin, H Jakins, T Bardaro, T Esposito, T Smahi, A Shaw, C Levy, M Munnich, A D'Urso, M Lewis, RA Kenwrick, S Nelson, DL
Citation: S. Aradhya et al., A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations, HUM MOL GEN, 10(19), 2001, pp. 2171-2179
Synthesis and magnetic properties of perovskite La1-xCaxMn0.9Li0.1O3
Authors: Gao, F Wang, XL Lewis, RA Mikheenko, P Dou, SX
Citation: F. Gao et al., Synthesis and magnetic properties of perovskite La1-xCaxMn0.9Li0.1O3, J ALLOY COM, 325(1-2), 2001, pp. 281-284
Far-infrared spectroscopy of the zinc acceptor in indium phosphide
Authors: Causley, RL Lewis, RA
Citation: Rl. Causley et Ra. Lewis, Far-infrared spectroscopy of the zinc acceptor in indium phosphide, PHYSICA B, 302, 2001, pp. 327-333
Phonon modes in CMR manganites at elevated temperatures
Authors: Lewis, RA
Citation: Ra. Lewis, Phonon modes in CMR manganites at elevated temperatures, J SUPERCOND, 14(1), 2001, pp. 143-148
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer
Authors: Airewele, GE Sigurdson, AJ Wiley, KJ Frieden, BE Caldarera, LW Riccardi, VM Lewis, RA Chintagumpala, MM Ater, JL Plon, SE Bondy, ML
Citation: Ge. Airewele et al., Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer, GENET EPID, 20(1), 2001, pp. 75-86
Search for strange quark matter produced in relativistic heavy ion collisions - art. no. 054903
Authors: Armstrong, TA Barish, KN Batsouli, S Bennett, SJ Bertaina, M Chikanian, A Coe, SD Cormier, TM Davies, RR DeCataldo, G Dee, P Diebold, GE Dover, CB Fachini, P Fadem, B Finch, LE George, NK Giglietto, N Greene, SV Haridas, P Hill, JC Hirsch, AS Hoversten, RA Huang, HZ Jaradat, H Kim, B Kumar, BS Lainis, T Lajoie, JG Lewis, RA Li, Q Libby, B Majka, RD Miller, TE Munhoz, MG Nagle, JL Pless, IA Pope, JK Porile, NT Pruneau, CA Rabin, MSZ Reid, JD Rimai, A Rose, A Rotondo, FS Sandweiss, J Scharenberg, RP Slaughter, AJ Smith, GA Spinelli, P Tincknell, ML Toothacker, WS Van Buren, G Wilson, WK Wohn, FK Wolin, EJ Xu, Z Zhao, K
Citation: Ta. Armstrong et al., Search for strange quark matter produced in relativistic heavy ion collisions - art. no. 054903, PHYS REV C, 6305(5), 2001, pp. 4903
Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4)
Authors: Yatsenko, AN Shroyer, NF Lewis, RA Lupski, JR
Citation: An. Yatsenko et al., Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4), HUM GENET, 108(4), 2001, pp. 346-355
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America
Authors: Bassi, MT Bergen, AAB Bitoun, P Charles, SJ Clementi, M Gosselin, R Hurst, J Lewis, RA Lorenz, B Meitinger, T Messiaen, L Ramesar, RS Ballabio, A Schiaffino, MV
Citation: Mt. Bassi et al., Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America, HUM GENET, 108(1), 2001, pp. 51-54
Dielectric and optical rotatory power investigations of an antiferroelectric liquid crystal 12OF1M7 in a homeotropic cell: implications for models ofthe structure of ferrielectric phases
Authors: Shtykov, NM Vij, JK Lewis, RA Hird, M Goodby, JW
Citation: Nm. Shtykov et al., Dielectric and optical rotatory power investigations of an antiferroelectric liquid crystal 12OF1M7 in a homeotropic cell: implications for models ofthe structure of ferrielectric phases, LIQ CRYST, 28(11), 2001, pp. 1699-1704
Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients
Authors: Wang, LL Levy, ML Lewis, RA Chintagumpala, MM Lev, D Rogers, M Plon, SE
Citation: Ll. Wang et al., Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients, AM J MED G, 102(1), 2001, pp. 11-17
Null missense ABCR (ABCA4) mutations in a family with Stargardt disease and retinitis pigmentosa
Authors: Shroyer, NF Lewis, RA Yatsenko, AN Lupski, JR
Citation: Nf. Shroyer et al., Null missense ABCR (ABCA4) mutations in a family with Stargardt disease and retinitis pigmentosa, INV OPHTH V, 42(12), 2001, pp. 2757-2761
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder
Authors: Katsanis, N Ansley, SJ Badano, JL Eichers, ER Lewis, RA Hoskins, BE Scambler, PJ Davidson, WS Beales, PL Lupski, JR
Citation: N. Katsanis et al., Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder, SCIENCE, 293(5538), 2001, pp. 2256-2259
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy
Authors: Mendell, JR Barohn, RJ Freimer, ML Kissel, JT King, W Nagaraja, HN Rice, R Campbell, WW Donofrio, PD Jackson, CE Lewis, RA Shy, M Simpson, DM Parry, GJ Rivner, MH Thornton, CA Bromberg, MB Tandan, R Harati, Y Giuliani, MJ
Citation: Jr. Mendell et al., Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy, NEUROLOGY, 56(4), 2001, pp. 445-449
Phonon modes of A(Co1/2Mn1/2) O-3 (A = La, Nd, Dy, Ho, Yb)
Authors: Gao, F Lewis, RA Wang, XL Don, SX
Citation: F. Gao et al., Phonon modes of A(Co1/2Mn1/2) O-3 (A = La, Nd, Dy, Ho, Yb), J SOL ST CH, 160(2), 2001, pp. 350-352
Outpatient shoulder surgery - A prospective analysis of a perioperative protocol
Authors: Lewis, RA Buss, DD
Citation: Ra. Lewis et Dd. Buss, Outpatient shoulder surgery - A prospective analysis of a perioperative protocol, CLIN ORTHOP, (390), 2001, pp. 138-141
Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in RLBP1
Authors: Katsanis, N Shroyer, NF Lewis, RA Cavender, JC Al-Rajhi, AA Jabak, M Lupski, JR
Citation: N. Katsanis et al., Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in RLBP1, CLIN GENET, 59(6), 2001, pp. 424-429
Triggering myocardial infarction by marijuana
Authors: Mittleman, MA Lewis, RA Maclure, M Sherwood, JB Muller, JE
Citation: Ma. Mittleman et al., Triggering myocardial infarction by marijuana, CIRCULATION, 103(23), 2001, pp. 2805-2809
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration
Authors: Sauer, CG White, K Stohr, H Grimm, T Hutchinson, A Bernstein, PS Lewis, RA Simonelli, F Pauleikhoff, D Allikmets, R Weber, BHF
Citation: Cg. Sauer et al., Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration, BR J OPHTH, 85(8), 2001, pp. 969-975
Analysis of the ABCR (ABCA4) gene in 4-aminoquinoline retinopathy: Is retinal toxicity by chloroquine and hydroxychloroquine related to Stargardt disease?
Authors: Shroyer, NF Lewis, RA Lupski, JR
Citation: Nf. Shroyer et al., Analysis of the ABCR (ABCA4) gene in 4-aminoquinoline retinopathy: Is retinal toxicity by chloroquine and hydroxychloroquine related to Stargardt disease?, AM J OPHTH, 131(6), 2001, pp. 759-760
Risultati: 1-25 | 26-50 | 51-75 | 76-94