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Showing 1 to 12 of 515 entries
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[A case of Kirner's deformity].

La Radiologia medica

Bertei A, Gragnani SG.
PMID: 3589022
Radiol Med. 1987 May;73(5):457-8.

No abstract available.

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Bertei A, Gragnani SG. Un caso di deformità di Kirner. [A case of Kirner's deformity]. Radiol Med. 1987;73(5):457-8
Bertei, A., & Gragnani, S. G. (1987). Un caso di deformità di Kirner. [A case of Kirner's deformity]. La Radiologia medica, 73(5), 457-8.
Bertei, A, and Gragnani, S G. "Un caso di deformità di Kirner." [A case of Kirner's deformity]. La Radiologia medica vol. 73,5 (1987): 457-8.
Bertei A, Gragnani SG. Un caso di deformità di Kirner. [A case of Kirner's deformity]. Radiol Med. 1987 May;73(5):457-8. Italian. PMID: 3589022.
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Clinical usefulness of red cell distribution width to angiographic severity and coronary stent thrombosis.

International journal of general medicine

Erdem A, Ceylan US, Esen A, Zencirci E, Topcu B, Ozden K, Yazici S, Terzi S, Emre A, Yesilcimen K.
PMID: 27672339
Int J Gen Med. 2016 Sep 09;9:319-24. doi: 10.2147/IJGM.S109452. eCollection 2016.

BACKGROUND: Red cell distribution width (RDW) is a quantitative measurement and shows heterogeneity of red blood cell size in peripheral blood. RDW has recently been associated with cardiovascular events and cardiovascular diseases, and it is a novel predictor of...

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Erdem A, Ceylan US, Esen A, et al. Clinical usefulness of red cell distribution width to angiographic severity and coronary stent thrombosis. Int J Gen Med. 2016;9:319-24doi: 10.2147/IJGM.S109452.
Erdem, A., Ceylan, U. S., Esen, A., Zencirci, E., Topcu, B., Ozden, K., Yazici, S., Terzi, S., Emre, A., & Yesilcimen, K. (2016). Clinical usefulness of red cell distribution width to angiographic severity and coronary stent thrombosis. International journal of general medicine, 9319-24. https://doi.org/10.2147/IJGM.S109452
Erdem, Aysun, et al. "Clinical usefulness of red cell distribution width to angiographic severity and coronary stent thrombosis." International journal of general medicine vol. 9 (2016): 319-24. doi: https://doi.org/10.2147/IJGM.S109452
Erdem A, Ceylan US, Esen A, Zencirci E, Topcu B, Ozden K, Yazici S, Terzi S, Emre A, Yesilcimen K. Clinical usefulness of red cell distribution width to angiographic severity and coronary stent thrombosis. Int J Gen Med. 2016 Sep 09;9:319-24. doi: 10.2147/IJGM.S109452. eCollection 2016. PMID: 27672339; PMCID: PMC5024766.
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Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen.

Chemical communications (Cambridge, England)

Cobo S, Lafolet F, Saint-Aman E, Philouze C, Bucher C, Silvi S, Credi A, Royal G.
PMID: 26340694
Chem Commun (Camb). 2015 Oct 07;51(78):14682. doi: 10.1039/c5cc90403j.

Correction for 'Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen' by Saioa Cobo et al., Chem. Commun., 2015, 51, 13886-13889.

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Cobo S, Lafolet F, Saint-Aman E, et al. Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen. Chem Commun (Camb). 2015;51(78):14682doi: 10.1039/c5cc90403j.
Cobo, S., Lafolet, F., Saint-Aman, E., Philouze, C., Bucher, C., Silvi, S., Credi, A., & Royal, G. (2015). Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen. Chemical communications (Cambridge, England), 51(78), 14682. https://doi.org/10.1039/c5cc90403j
Cobo, Saioa, et al. "Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen." Chemical communications (Cambridge, England) vol. 51,78 (2015): 14682. doi: https://doi.org/10.1039/c5cc90403j
Cobo S, Lafolet F, Saint-Aman E, Philouze C, Bucher C, Silvi S, Credi A, Royal G. Correction: Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen. Chem Commun (Camb). 2015 Oct 07;51(78):14682. doi: 10.1039/c5cc90403j. PMID: 26340694.
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[No title available]

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke

Eide IA.
PMID: 27731609
Tidsskr Nor Laegeforen. 2016 Oct 11;136(18):1572. doi: 10.4045/tidsskr.16.0644. eCollection 2016 Oct.

No abstract available.

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Eide IA. Inntak av marine fettsyrer hos nyretransplanterte. . Tidsskr Nor Laegeforen. 2016;136(18):1572doi: 10.4045/tidsskr.16.0644.
Eide, I. A. (2016). Inntak av marine fettsyrer hos nyretransplanterte. . Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 136(18), 1572. https://doi.org/10.4045/tidsskr.16.0644
Eide, Ivar Anders. "Inntak av marine fettsyrer hos nyretransplanterte." . Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke vol. 136,18 (2016): 1572. doi: https://doi.org/10.4045/tidsskr.16.0644
Eide IA. Inntak av marine fettsyrer hos nyretransplanterte. . Tidsskr Nor Laegeforen. 2016 Oct 11;136(18):1572. doi: 10.4045/tidsskr.16.0644. eCollection 2016 Oct. Norwegian. PMID: 27731609.
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P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia.

Pregnancy hypertension

Matos A, Ferreira J, Portelinha A, Cerdeira AS, Braga J, Patrício B, Rebelo I, Bicho M, Marinho C.
PMID: 26009115
Pregnancy Hypertens. 2011 Jul-Oct;1(3):284. doi: 10.1016/j.preghy.2011.08.085. Epub 2011 Sep 29.

No abstract available.

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Matos A, Ferreira J, Portelinha A, et al. P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy Hypertens. 2011;1(3):284doi: 10.1016/j.preghy.2011.08.085.
Matos, A., Ferreira, J., Portelinha, A., Cerdeira, A. S., Braga, J., Patrício, B., Rebelo, I., Bicho, M., & Marinho, C. (2011). P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy hypertension, 1(3), 284. https://doi.org/10.1016/j.preghy.2011.08.085
Matos, Andreia, et al. "P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia." Pregnancy hypertension vol. 1,3 (2011): 284. doi: https://doi.org/10.1016/j.preghy.2011.08.085
Matos A, Ferreira J, Portelinha A, Cerdeira AS, Braga J, Patrício B, Rebelo I, Bicho M, Marinho C. P24. Study of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism in preeclampsia. Pregnancy Hypertens. 2011 Jul-Oct;1(3):284. doi: 10.1016/j.preghy.2011.08.085. Epub 2011 Sep 29. PMID: 26009115.
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Draft Genome Sequences of Colistin-Resistant MCR-1-Producing .

Genome announcements

Monte DF, Fernandes MR, Cerdeira L, de Souza TA, Mem A, Franco BDGM, Landgraf M, Lincopan N.
PMID: 28522705
Genome Announc. 2017 May 18;5(20). doi: 10.1128/genomeA.00329-17.

We present here the draft genome sequences of two colistin-resistant

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Monte DF, Fernandes MR, Cerdeira L, et al. Draft Genome Sequences of Colistin-Resistant MCR-1-Producing . Genome Announc. 2017;5(20)doi: 10.1128/genomeA.00329-17.
Monte, D. F., Fernandes, M. R., Cerdeira, L., de Souza, T. A., Mem, A., Franco, B. D. G. M., Landgraf, M., & Lincopan, N. (2017). Draft Genome Sequences of Colistin-Resistant MCR-1-Producing . Genome announcements, 5(20), . https://doi.org/10.1128/genomeA.00329-17
Monte, Daniel F, et al. "Draft Genome Sequences of Colistin-Resistant MCR-1-Producing ." Genome announcements vol. 5,20 (2017). doi: https://doi.org/10.1128/genomeA.00329-17
Monte DF, Fernandes MR, Cerdeira L, de Souza TA, Mem A, Franco BDGM, Landgraf M, Lincopan N. Draft Genome Sequences of Colistin-Resistant MCR-1-Producing . Genome Announc. 2017 May 18;5(20). doi: 10.1128/genomeA.00329-17. PMID: 28522705; PMCID: PMC5442378.
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Personalized Medicine.

The Yale journal of biology and medicine

Erden A.
PMID: 26930723
Yale J Biol Med. 2015 Dec;88(4):349.

No abstract available.

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Erden A. Personalized Medicine. Yale J Biol Med. 2015;88(4):349
Erden, A. (2015). Personalized Medicine. The Yale journal of biology and medicine, 88(4), 349.
Erden, Asu. "Personalized Medicine." The Yale journal of biology and medicine vol. 88,4 (2015): 349.
Erden A. Personalized Medicine. Yale J Biol Med. 2015 Dec;88(4):349. PMID: 26930723; PMCID: PMC4654182.
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Switching of pseudorotaxanes and catenanes incorporating a tetrathiafulvalene unit by redox and chemical inputs.

The Journal of organic chemistry

Balzani V, Credi A, Mattersteig G, Matthews OA, Raymo FM, Stoddart JF, Venturi M, White AJ, Williams DJ.
PMID: 10774011
J Org Chem. 2000 Apr 07;65(7):1924-36. doi: 10.1021/jo991781t.

An acyclic polyether 1a, incorporating a central tetrathiafulvalene (TTF) electron donor unit and two 4-tert-butylphenoxy groups at its termini, has been synthesized. Two macrocyclic polyethers containing two different electron donors, namely a TTF unit with, in one case, a...

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Balzani V, Credi A, Mattersteig G, et al. Switching of pseudorotaxanes and catenanes incorporating a tetrathiafulvalene unit by redox and chemical inputs. J Org Chem. 2000;65(7):1924-36doi: 10.1021/jo991781t.
Balzani, V., Credi, A., Mattersteig, G., Matthews, O. A., Raymo, F. M., Stoddart, J. F., Venturi, M., White, A. J., & Williams, D. J. (2000). Switching of pseudorotaxanes and catenanes incorporating a tetrathiafulvalene unit by redox and chemical inputs. The Journal of organic chemistry, 65(7), 1924-36. https://doi.org/10.1021/jo991781t
Balzani, et al. "Switching of pseudorotaxanes and catenanes incorporating a tetrathiafulvalene unit by redox and chemical inputs." The Journal of organic chemistry vol. 65,7 (2000): 1924-36. doi: https://doi.org/10.1021/jo991781t
Balzani V, Credi A, Mattersteig G, Matthews OA, Raymo FM, Stoddart JF, Venturi M, White AJ, Williams DJ. Switching of pseudorotaxanes and catenanes incorporating a tetrathiafulvalene unit by redox and chemical inputs. J Org Chem. 2000 Apr 07;65(7):1924-36. doi: 10.1021/jo991781t. PMID: 10774011.
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Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex.

Inorganic chemistry

Riesgo EC, Credi A, De Cola L, Thummel RP.
PMID: 11670368
Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a.

The Friedländer condensation of (1R,5S)-(+)- and (1S,5R)-(-)-nopinone with 8-aminoquinoline-7-carbaldehyde leads to the corresponding enantiomerically pure (2,3-b)-pineno-1,10-phenanthrolines. Coordination of these ligands with Cu(I) affords non-interconvertable chiral complexes which show equal and opposite Cotton effects in their CD spectra as well...

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Riesgo EC, Credi A, De Cola L, et al. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998;37(9):2145-2149doi: 10.1021/ic971267a.
Riesgo, E. C., Credi, A., De Cola, L., & Thummel, R. P. (1998). Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorganic chemistry, 37(9), 2145-2149. https://doi.org/10.1021/ic971267a
Riesgo, Elvira C., et al. "Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex." Inorganic chemistry vol. 37,9 (1998): 2145-2149. doi: https://doi.org/10.1021/ic971267a
Riesgo EC, Credi A, De Cola L, Thummel RP. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a. PMID: 11670368.
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Artificial Molecular Machines.

Angewandte Chemie (International ed. in English)

Balzani V, Credi A, Raymo FM, Stoddart JF.
PMID: 11091368
Angew Chem Int Ed Engl. 2000 Oct 02;39(19):3348-3391. doi: 10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x.

The miniaturization of components used in the construction of working devices is being pursued currently by the large-downward (top-down) fabrication. This approach, however, which obliges solid-state physicists and electronic engineers to manipulate progressively smaller and smaller pieces of matter,...

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Balzani V, Credi A, Raymo FM, et al. Artificial Molecular Machines. Angew Chem Int Ed Engl. 2000;39(19):3348-3391doi: 10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x.
Balzani, V., Credi, A., Raymo, F. M., & Stoddart, J. F. (2000). Artificial Molecular Machines. Angewandte Chemie (International ed. in English), 39(19), 3348-3391. https://doi.org/10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x
Balzani, et al. "Artificial Molecular Machines." Angewandte Chemie (International ed. in English) vol. 39,19 (2000): 3348-3391. doi: https://doi.org/10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x
Balzani V, Credi A, Raymo FM, Stoddart JF. Artificial Molecular Machines. Angew Chem Int Ed Engl. 2000 Oct 02;39(19):3348-3391. doi: 10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-x. PMID: 11091368.
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A mechanically interlocked bundle.

Chemistry (Weinheim an der Bergstrasse, Germany)

Badjić JD, Balzani V, Credi A, Lowe JN, Silvi S, Stoddart JF.
PMID: 15079832
Chemistry. 2004 Apr 19;10(8):1926-35. doi: 10.1002/chem.200305687.

The prototype of an artificial molecular machine consisting of a trisammonium tricationic component interlocked with a tris(crown ether) component to form a molecular bundle with averaged C(3v) symmetry has been designed and synthesized. The system is based on noncovalent...

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Badjić JD, Balzani V, Credi A, et al. A mechanically interlocked bundle. Chemistry. 2004;10(8):1926-35doi: 10.1002/chem.200305687.
Badjić, J. D., Balzani, V., Credi, A., Lowe, J. N., Silvi, S., & Stoddart, J. F. (2004). A mechanically interlocked bundle. Chemistry (Weinheim an der Bergstrasse, Germany), 10(8), 1926-35. https://doi.org/10.1002/chem.200305687
Badjić, Jovica D, et al. "A mechanically interlocked bundle." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 10,8 (2004): 1926-35. doi: https://doi.org/10.1002/chem.200305687
Badjić JD, Balzani V, Credi A, Lowe JN, Silvi S, Stoddart JF. A mechanically interlocked bundle. Chemistry. 2004 Apr 19;10(8):1926-35. doi: 10.1002/chem.200305687. PMID: 15079832.
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Worldwide interlaboratory study on the determination of ochratoxin A in different wine type samples.

Talanta

Ratola N, Barros P, Simões T, Cerdeira A, Venâncio A, Alves A.
PMID: 18970831
Talanta. 2006 Nov 15;70(4):720-31. doi: 10.1016/j.talanta.2006.05.031. Epub 2006 Jul 03.

Interlaboratory studies are decisive tools to help the validation of a specific analytical methodology or to assess the reproducibility of the use of different methods to analyze a given compound or compounds in certain sample matrices. In this work,...

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Ratola N, Barros P, Simões T, et al. Worldwide interlaboratory study on the determination of ochratoxin A in different wine type samples. Talanta. 2006;70(4):720-31doi: 10.1016/j.talanta.2006.05.031.
Ratola, N., Barros, P., Simões, T., Cerdeira, A., Venâncio, A., & Alves, A. (2006). Worldwide interlaboratory study on the determination of ochratoxin A in different wine type samples. Talanta, 70(4), 720-31. https://doi.org/10.1016/j.talanta.2006.05.031
Ratola, N, et al. "Worldwide interlaboratory study on the determination of ochratoxin A in different wine type samples." Talanta vol. 70,4 (2006): 720-31. doi: https://doi.org/10.1016/j.talanta.2006.05.031
Ratola N, Barros P, Simões T, Cerdeira A, Venâncio A, Alves A. Worldwide interlaboratory study on the determination of ochratoxin A in different wine type samples. Talanta. 2006 Nov 15;70(4):720-31. doi: 10.1016/j.talanta.2006.05.031. Epub 2006 Jul 03. PMID: 18970831.
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Showing 1 to 12 of 515 entries