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How effective are one-to-one tutoring programs in reading for elementary students at risk for reading failure? A meta-analysis of the intervention research

instructional interventions

Vaughn S, Tejero M.
GSID: gBahHnLbSF0J
B Elbaum, S Vaughn, M Tejero Hughes… - Journal of …, 2000 - psycnet.apa.org

… the efficacy of one-to-one reading interventions for children at risk for reading failure, we undertook a rigorous meta-analysis of the empirical findings related to adult-delivered, one-to-one instructional interventions in reading for elementary school children identified as being at...

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Elbaum, B., Vaughn, S., Tejero Hughes, M., & Watson Moody, S. (2000). How effective are one-to-one tutoring programs in reading for elementary students at risk for reading failure? A meta-analysis of the intervention research. Journal of educational psychology, 92(4), 605.
Elbaum, Batya, et al. "How effective are one-to-one tutoring programs in reading for elementary students at risk for reading failure? A meta-analysis of the intervention research." Journal of educational psychology 92.4 (2000): 605.
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Association between cell-bound blood amyloid-β(1-40) levels and hippocampus volume.

Alzheimer's research & therapy

Sotolongo-Grau O, Pesini P, Valero S, Lafuente A, Buendía M, Pérez-Grijalba V, José IS, Ibarria M, Tejero MA, Giménez J, Hernández I, Tárraga L, Ruiz A, Boada M, Sarasa M.
PMID: 25484928
Alzheimers Res Ther. 2014 Oct 20;6(5):56. doi: 10.1186/s13195-014-0056-3. eCollection 2014.

INTRODUCTION: The identification of early, preferably presymptomatic, biomarkers and true etiologic factors for Alzheimer's disease (AD) is the first step toward establishing effective primary and secondary prevention programs. Consequently, the search for a relatively inexpensive and harmless biomarker for...

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Sotolongo-Grau O, Pesini P, Valero S, et al. Association between cell-bound blood amyloid-β(1-40) levels and hippocampus volume. Alzheimers Res Ther. 2014;6(5):56doi: 10.1186/s13195-014-0056-3.
Sotolongo-Grau, O., Pesini, P., Valero, S., Lafuente, A., Buendía, M., Pérez-Grijalba, V., José, I. S., Ibarria, M., Tejero, M. A., Giménez, J., Hernández, I., Tárraga, L., Ruiz, A., Boada, M., & Sarasa, M. (2014). Association between cell-bound blood amyloid-β(1-40) levels and hippocampus volume. Alzheimer's research & therapy, 6(5), 56. https://doi.org/10.1186/s13195-014-0056-3
Sotolongo-Grau, Oscar, et al. "Association between cell-bound blood amyloid-β(1-40) levels and hippocampus volume." Alzheimer's research & therapy vol. 6,5 (2014): 56. doi: https://doi.org/10.1186/s13195-014-0056-3
Sotolongo-Grau O, Pesini P, Valero S, Lafuente A, Buendía M, Pérez-Grijalba V, José IS, Ibarria M, Tejero MA, Giménez J, Hernández I, Tárraga L, Ruiz A, Boada M, Sarasa M. Association between cell-bound blood amyloid-β(1-40) levels and hippocampus volume. Alzheimers Res Ther. 2014 Oct 20;6(5):56. doi: 10.1186/s13195-014-0056-3. eCollection 2014. PMID: 25484928; PMCID: PMC4255526.
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Revealing Stepwise Mechanisms in Dipolar Cycloaddition Reactions: Computational Study of the Reaction between Nitrones and Isocyanates.

The Journal of organic chemistry

Darù A, Roca-López D, Tejero T, Merino P.
PMID: 26682934
J Org Chem. 2016 Jan 15;81(2):673-80. doi: 10.1021/acs.joc.5b02645. Epub 2015 Dec 24.

The mechanism of cycloaddition reactions of nitrones with isocyanates has been studied using density functional theory (DFT) methods at the M06-2X/cc-pVTZ level of theory. The exploration of the potential energy surfaces associated with two reactive channels leading to 1,2,4-oxadiazolidin-5-ones...

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Darù A, Roca-López D, Tejero T, et al. Revealing Stepwise Mechanisms in Dipolar Cycloaddition Reactions: Computational Study of the Reaction between Nitrones and Isocyanates. J Org Chem. 2015;81(2):673-80doi: 10.1021/acs.joc.5b02645.
Darù, A., Roca-López, D., Tejero, T., & Merino, P. (2016). Revealing Stepwise Mechanisms in Dipolar Cycloaddition Reactions: Computational Study of the Reaction between Nitrones and Isocyanates. The Journal of organic chemistry, 81(2), 673-80. https://doi.org/10.1021/acs.joc.5b02645
Darù, Andrea, et al. "Revealing Stepwise Mechanisms in Dipolar Cycloaddition Reactions: Computational Study of the Reaction between Nitrones and Isocyanates." The Journal of organic chemistry vol. 81,2 (2016): 673-80. doi: https://doi.org/10.1021/acs.joc.5b02645
Darù A, Roca-López D, Tejero T, Merino P. Revealing Stepwise Mechanisms in Dipolar Cycloaddition Reactions: Computational Study of the Reaction between Nitrones and Isocyanates. J Org Chem. 2016 Jan 15;81(2):673-80. doi: 10.1021/acs.joc.5b02645. Epub 2015 Dec 24. PMID: 26682934.
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Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel alpha-(Hydroxyamino) Nitriles.

The Journal of organic chemistry

Merino P, Lanaspa A, Merchan FL, Tejero T.
PMID: 11667891
J Org Chem. 1996 Dec 13;61(25):9028-9032. doi: 10.1021/jo961293a.

No abstract available.

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Merino P, Lanaspa A, Merchan FL, et al. Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel alpha-(Hydroxyamino) Nitriles. J Org Chem. 1996;61(25):9028-9032doi: 10.1021/jo961293a.
Merino, P., Lanaspa, A., Merchan, F. L., & Tejero, T. (1996). Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel alpha-(Hydroxyamino) Nitriles. The Journal of organic chemistry, 61(25), 9028-9032. https://doi.org/10.1021/jo961293a
Merino, P., et al. "Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel alpha-(Hydroxyamino) Nitriles." The Journal of organic chemistry vol. 61,25 (1996): 9028-9032. doi: https://doi.org/10.1021/jo961293a
Merino P, Lanaspa A, Merchan FL, Tejero T. Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel alpha-(Hydroxyamino) Nitriles. J Org Chem. 1996 Dec 13;61(25):9028-9032. doi: 10.1021/jo961293a. PMID: 11667891.
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Mechanistic investigations of imine hydrogenation catalyzed by cationic iridium complexes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Martín M, Sola E, Tejero S, Andrés JL, Oro LA.
PMID: 16534823
Chemistry. 2006 May 15;12(15):4043-56. doi: 10.1002/chem.200501230.

Complexes [IrH2(eta6-C6H6)(PiPr3)]BF4 (1) and [IrH2(NCMe)3(PiPr3)]BF4 (2) are catalyst precursors for homogeneous hydrogenation of N-benzylideneaniline under mild conditions. Precursor 1 generates the resting state [IrH2{eta5-(C6H5)NHCH2Ph}(PiPr3)]BF4 (3), while 2 gives rise to a mixture of [IrH{PhN=CH(C6H4)-kappaN,C}(NCMe)2(PiPr3)]BF4 (4) and [IrH{PhN=CH(C6H4)-kappaN,C}(NCMe)(NH2Ph)(PiPr3)]BF4 (5), in...

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Martín M, Sola E, Tejero S, et al. Mechanistic investigations of imine hydrogenation catalyzed by cationic iridium complexes. Chemistry. 2006;12(15):4043-56doi: 10.1002/chem.200501230.
Martín, M., Sola, E., Tejero, S., Andrés, J. L., & Oro, L. A. (2006). Mechanistic investigations of imine hydrogenation catalyzed by cationic iridium complexes. Chemistry (Weinheim an der Bergstrasse, Germany), 12(15), 4043-56. https://doi.org/10.1002/chem.200501230
Martín, Marta, et al. "Mechanistic investigations of imine hydrogenation catalyzed by cationic iridium complexes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,15 (2006): 4043-56. doi: https://doi.org/10.1002/chem.200501230
Martín M, Sola E, Tejero S, Andrés JL, Oro LA. Mechanistic investigations of imine hydrogenation catalyzed by cationic iridium complexes. Chemistry. 2006 May 15;12(15):4043-56. doi: 10.1002/chem.200501230. PMID: 16534823.
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Assessment of angle velocity in girls with adolescent idiopathic scoliosis.

Scoliosis

Escalada F, Marco E, Duarte E, Ma Muniesa J, Boza R, Tejero M, Cáceres E.
PMID: 19758424
Scoliosis. 2009 Sep 16;4:20. doi: 10.1186/1748-7161-4-20.

BACKGROUND: Although it has been demonstrated that the peak height velocity (PHV) is a predictive factor of progression in adolescent idiopathic scoliosis (AIS), little is known about the usefulness of angle progression in clinical practice. The purpose of this...

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Escalada F, Marco E, Duarte E, et al. Assessment of angle velocity in girls with adolescent idiopathic scoliosis. Scoliosis. 2009;4:20doi: 10.1186/1748-7161-4-20.
Escalada, F., Marco, E., Duarte, E., Ma Muniesa, J., Boza, R., Tejero, M., & Cáceres, E. (2009). Assessment of angle velocity in girls with adolescent idiopathic scoliosis. Scoliosis, 420. https://doi.org/10.1186/1748-7161-4-20
Escalada, Ferran, et al. "Assessment of angle velocity in girls with adolescent idiopathic scoliosis." Scoliosis vol. 4 (2009): 20. doi: https://doi.org/10.1186/1748-7161-4-20
Escalada F, Marco E, Duarte E, Ma Muniesa J, Boza R, Tejero M, Cáceres E. Assessment of angle velocity in girls with adolescent idiopathic scoliosis. Scoliosis. 2009 Sep 16;4:20. doi: 10.1186/1748-7161-4-20. PMID: 19758424; PMCID: PMC2753628.
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Spanish "fine tuning" of language to describe depression and anxiety.

Journal of palliative medicine

Noguera A, Centeno C, Carvajal A, Tejedor MA, Urdiroz J, Martínez M.
PMID: 19591617
J Palliat Med. 2009 Aug;12(8):707-12. doi: 10.1089/jpm.2009.0024.

On screening tools for emotional distress, the terms "depression" and "anxiety" are commonly used for patients with advanced cancer. However, these terms could have negative connotations in Spanish such that cultural and unexpected differences in perception may invalidate or...

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Noguera A, Centeno C, Carvajal A, et al. Spanish "fine tuning" of language to describe depression and anxiety. J Palliat Med. 2009;12(8):707-12doi: 10.1089/jpm.2009.0024.
Noguera, A., Centeno, C., Carvajal, A., Tejedor, M. A., Urdiroz, J., & Martínez, M. (2009). Spanish "fine tuning" of language to describe depression and anxiety. Journal of palliative medicine, 12(8), 707-12. https://doi.org/10.1089/jpm.2009.0024
Noguera, Antonio, et al. "Spanish "fine tuning" of language to describe depression and anxiety." Journal of palliative medicine vol. 12,8 (2009): 707-12. doi: https://doi.org/10.1089/jpm.2009.0024
Noguera A, Centeno C, Carvajal A, Tejedor MA, Urdiroz J, Martínez M. Spanish "fine tuning" of language to describe depression and anxiety. J Palliat Med. 2009 Aug;12(8):707-12. doi: 10.1089/jpm.2009.0024. PMID: 19591617.
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Tritopic phenanthroline and pyridine tail-tied aza-scorpiands.

Organic & biomolecular chemistry

González J, Llinares JM, Belda R, Pitarch J, Soriano C, Tejero R, Verdejo B, García-España E.
PMID: 20448894
Org Biomol Chem. 2010 May 21;8(10):2367-76. doi: 10.1039/b927418a. Epub 2010 Mar 24.

The synthesis of two new tritopic double-scorpiand receptors in which two equivalent 5-(2-aminoethyl)-2,5,8-triaza[9]-(2,6)-pyridinophane moieties have been linked with 2,6-dimethylpyridine (L1) or 2,9-dimethylphenanthroline (L2) units is reported for the first time. Their acid-base behaviour and Zn(2+) coordination chemistry have been...

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González J, Llinares JM, Belda R, et al. Tritopic phenanthroline and pyridine tail-tied aza-scorpiands. Org Biomol Chem. 2010;8(10):2367-76doi: 10.1039/b927418a.
González, J., Llinares, J. M., Belda, R., Pitarch, J., Soriano, C., Tejero, R., Verdejo, B., & García-España, E. (2010). Tritopic phenanthroline and pyridine tail-tied aza-scorpiands. Organic & biomolecular chemistry, 8(10), 2367-76. https://doi.org/10.1039/b927418a
González, Jorge, et al. "Tritopic phenanthroline and pyridine tail-tied aza-scorpiands." Organic & biomolecular chemistry vol. 8,10 (2010): 2367-76. doi: https://doi.org/10.1039/b927418a
González J, Llinares JM, Belda R, Pitarch J, Soriano C, Tejero R, Verdejo B, García-España E. Tritopic phenanthroline and pyridine tail-tied aza-scorpiands. Org Biomol Chem. 2010 May 21;8(10):2367-76. doi: 10.1039/b927418a. Epub 2010 Mar 24. PMID: 20448894.
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Upgrades to the Auburn linear experiment for instability studies.

The Review of scientific instruments

Eadon AC, Tejero E, DuBois A, Thomas E.
PMID: 21721695
Rev Sci Instrum. 2011 Jun;82(6):063511. doi: 10.1063/1.3594102.

The Auburn linear experiment for instability studies (ALEXIS) is a laboratory plasma physics experiment that is designed to investigate the role of spatially non-uniform E × B drifts using a magnetized cylindrical plasma column. This paper discusses the recent...

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Eadon AC, Tejero E, DuBois A, et al. Upgrades to the Auburn linear experiment for instability studies. Rev Sci Instrum. 2011;82(6):063511doi: 10.1063/1.3594102.
Eadon, A. C., Tejero, E., DuBois, A., & Thomas, E. (2011). Upgrades to the Auburn linear experiment for instability studies. The Review of scientific instruments, 82(6), 063511. https://doi.org/10.1063/1.3594102
Eadon, A C, et al. "Upgrades to the Auburn linear experiment for instability studies." The Review of scientific instruments vol. 82,6 (2011): 063511. doi: https://doi.org/10.1063/1.3594102
Eadon AC, Tejero E, DuBois A, Thomas E. Upgrades to the Auburn linear experiment for instability studies. Rev Sci Instrum. 2011 Jun;82(6):063511. doi: 10.1063/1.3594102. PMID: 21721695.
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Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII.

Inorganic chemistry

Bröring M, Prikhodovski S, Brandt CD, Tejero EC, Köhler S, Pietzonka C.
PMID: 17257035
Inorg Chem. 2007 Feb 05;46(3):917-25. doi: 10.1021/ic062009t.

Etheral solutions of free base tripyrrins (HTrpy) were prepared by treatment of nickel isocyanate complexes (TrpyNiNCO) with excess cyanide. From these solutions sensitive metallotripyrrins with cobalt(II), iron(II), and manganese(II) ions (TrpyMX) and with a choice of external ligands X...

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Bröring M, Prikhodovski S, Brandt CD, et al. Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII. Inorg Chem. 2007;46(3):917-25doi: 10.1021/ic062009t.
Bröring, M., Prikhodovski, S., Brandt, C. D., Tejero, E. C., Köhler, S., & Pietzonka, C. (2007). Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII. Inorganic chemistry, 46(3), 917-25. https://doi.org/10.1021/ic062009t
Bröring, Martin, et al. "Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII." Inorganic chemistry vol. 46,3 (2007): 917-25. doi: https://doi.org/10.1021/ic062009t
Bröring M, Prikhodovski S, Brandt CD, Tejero EC, Köhler S, Pietzonka C. Cyanide-promoted demetalation of TrpyNiNCO: a route to sensitive metallotripyrrins of CoII, FeII, and MnII. Inorg Chem. 2007 Feb 05;46(3):917-25. doi: 10.1021/ic062009t. PMID: 17257035.
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Communication: Virial coefficients and demixing in highly asymmetric binary additive hard-sphere mixtures.

The Journal of chemical physics

López de Haro M, Tejero CF, Santos A.
PMID: 23635104
J Chem Phys. 2013 Apr 28;138(16):161104. doi: 10.1063/1.4803097.

The problem of demixing in a binary fluid mixture of highly asymmetric additive hard spheres is revisited. A comparison is presented between the results derived previously using truncated virial expansions for three finite size ratios with those that one...

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López de Haro M, Tejero CF, Santos A. Communication: Virial coefficients and demixing in highly asymmetric binary additive hard-sphere mixtures. J Chem Phys. 2013;138(16):161104doi: 10.1063/1.4803097.
López de Haro, M., Tejero, C. F., & Santos, A. (2013). Communication: Virial coefficients and demixing in highly asymmetric binary additive hard-sphere mixtures. The Journal of chemical physics, 138(16), 161104. https://doi.org/10.1063/1.4803097
López de Haro, Mariano, et al. "Communication: Virial coefficients and demixing in highly asymmetric binary additive hard-sphere mixtures." The Journal of chemical physics vol. 138,16 (2013): 161104. doi: https://doi.org/10.1063/1.4803097
López de Haro M, Tejero CF, Santos A. Communication: Virial coefficients and demixing in highly asymmetric binary additive hard-sphere mixtures. J Chem Phys. 2013 Apr 28;138(16):161104. doi: 10.1063/1.4803097. PMID: 23635104.
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Self-Regeneration of Chirality with l-Cysteine through 1,3-Dipolar Cycloadditions between Diazoalkanes and Enantiomerically Pure Thiazolines: Experimental and Computational Studies.

The Journal of organic chemistry

Gracia-Vitoria J, Osante I, Cativiela C, Merino P, Tejero T.
PMID: 29537846
J Org Chem. 2018 Apr 06;83(7):3960-3972. doi: 10.1021/acs.joc.8b00312. Epub 2018 Mar 20.

Enantiopure 2-thia-4-azabicyclo[3.1.0]hexanes, which can be considered constrained cysteines, have been obtained from l-cysteine by application of the "self-regeneration of chirality" concept. The key intermediates are homochiral thiazolines that can be prepared in multigram scale and react smoothly with a...

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Gracia-Vitoria J, Osante I, Cativiela C, et al. Self-Regeneration of Chirality with l-Cysteine through 1,3-Dipolar Cycloadditions between Diazoalkanes and Enantiomerically Pure Thiazolines: Experimental and Computational Studies. J Org Chem. 2018;83(7):3960-3972doi: 10.1021/acs.joc.8b00312.
Gracia-Vitoria, J., Osante, I., Cativiela, C., Merino, P., & Tejero, T. (2018). Self-Regeneration of Chirality with l-Cysteine through 1,3-Dipolar Cycloadditions between Diazoalkanes and Enantiomerically Pure Thiazolines: Experimental and Computational Studies. The Journal of organic chemistry, 83(7), 3960-3972. https://doi.org/10.1021/acs.joc.8b00312
Gracia-Vitoria, J, et al. "Self-Regeneration of Chirality with l-Cysteine through 1,3-Dipolar Cycloadditions between Diazoalkanes and Enantiomerically Pure Thiazolines: Experimental and Computational Studies." The Journal of organic chemistry vol. 83,7 (2018): 3960-3972. doi: https://doi.org/10.1021/acs.joc.8b00312
Gracia-Vitoria J, Osante I, Cativiela C, Merino P, Tejero T. Self-Regeneration of Chirality with l-Cysteine through 1,3-Dipolar Cycloadditions between Diazoalkanes and Enantiomerically Pure Thiazolines: Experimental and Computational Studies. J Org Chem. 2018 Apr 06;83(7):3960-3972. doi: 10.1021/acs.joc.8b00312. Epub 2018 Mar 20. PMID: 29537846.
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Showing 1 to 12 of 157 entries