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A patient-mounted robotic platform for CT-scan guided procedures

interventions

Bayle B, Piccin O.
GSID: ZxG7Wcq4ujgJ
B Maurin, B Bayle, O Piccin, J Gangloff… - IEEE Transactions …, 2008 - ieeexplore.ieee.org

In this paper, we present a novel robotic assistant dedicated to medical interventions under computed tomography scan guidance. This compact and lightweight patient-mounted robot …

Treatment of Intestinal Carriers of the Enteric Group of Organisms.

British medical journal

Caile R.
PMID: 20784835
Br Med J. 1943 May 15;1(4297):604. doi: 10.1136/bmj.1.4297.604.

No abstract available.

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Caile R. Treatment of Intestinal Carriers of the Enteric Group of Organisms. Br Med J. 1943;1(4297):604doi: 10.1136/bmj.1.4297.604.
Caile, R. (1943). Treatment of Intestinal Carriers of the Enteric Group of Organisms. British medical journal, 1(4297), 604. https://doi.org/10.1136/bmj.1.4297.604
Caile, R. "Treatment of Intestinal Carriers of the Enteric Group of Organisms." British medical journal vol. 1,4297 (1943): 604. doi: https://doi.org/10.1136/bmj.1.4297.604
Caile R. Treatment of Intestinal Carriers of the Enteric Group of Organisms. Br Med J. 1943 May 15;1(4297):604. doi: 10.1136/bmj.1.4297.604. PMID: 20784835; PMCID: PMC2282927.
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An Electrophilic Reagent for the Direct Introduction of the SCF.

Angewandte Chemie (International ed. in English)

Xiong HY, Bayle A, Pannecoucke X, Besset T.
PMID: 27667673
Angew Chem Int Ed Engl. 2016 Oct 17;55(43):13490-13494. doi: 10.1002/anie.201607231. Epub 2016 Sep 26.

An unprecedented electrophilic difluoromethylthiolating reagent (MesNHSCF

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Xiong HY, Bayle A, Pannecoucke X, et al. An Electrophilic Reagent for the Direct Introduction of the SCF. Angew Chem Int Ed Engl. 2016;55(43):13490-13494doi: 10.1002/anie.201607231.
Xiong, H. Y., Bayle, A., Pannecoucke, X., & Besset, T. (2016). An Electrophilic Reagent for the Direct Introduction of the SCF. Angewandte Chemie (International ed. in English), 55(43), 13490-13494. https://doi.org/10.1002/anie.201607231
Xiong, Heng-Ying, et al. "An Electrophilic Reagent for the Direct Introduction of the SCF." Angewandte Chemie (International ed. in English) vol. 55,43 (2016): 13490-13494. doi: https://doi.org/10.1002/anie.201607231
Xiong HY, Bayle A, Pannecoucke X, Besset T. An Electrophilic Reagent for the Direct Introduction of the SCF. Angew Chem Int Ed Engl. 2016 Oct 17;55(43):13490-13494. doi: 10.1002/anie.201607231. Epub 2016 Sep 26. PMID: 27667673.
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New Prospects toward the Synthesis of Difluoromethylated Phosphate Mimics.

Chemistry (Weinheim an der Bergstrasse, Germany)

Ivanova MV, Bayle A, Besset T, Pannecoucke X, Poisson T.
PMID: 27334601
Chemistry. 2016 Jul 18;22(30):10284-93. doi: 10.1002/chem.201601310. Epub 2016 Jun 23.

The difluoromethyl phosphonate motif plays a crucial role in the development of bioactive molecules as it is considered as a phosphate bioisoster. Since 2010, a renewal of interest to enlarge the panel of reactions to access these difluoromethylated phosphonate-containing...

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Ivanova MV, Bayle A, Besset T, et al. New Prospects toward the Synthesis of Difluoromethylated Phosphate Mimics. Chemistry. 2016;22(30):10284-93doi: 10.1002/chem.201601310.
Ivanova, M. V., Bayle, A., Besset, T., Pannecoucke, X., & Poisson, T. (2016). New Prospects toward the Synthesis of Difluoromethylated Phosphate Mimics. Chemistry (Weinheim an der Bergstrasse, Germany), 22(30), 10284-93. https://doi.org/10.1002/chem.201601310
Ivanova, Maria V, et al. "New Prospects toward the Synthesis of Difluoromethylated Phosphate Mimics." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,30 (2016): 10284-93. doi: https://doi.org/10.1002/chem.201601310
Ivanova MV, Bayle A, Besset T, Pannecoucke X, Poisson T. New Prospects toward the Synthesis of Difluoromethylated Phosphate Mimics. Chemistry. 2016 Jul 18;22(30):10284-93. doi: 10.1002/chem.201601310. Epub 2016 Jun 23. PMID: 27334601.
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Rating Diversity and Measures of Convergent and Divergent Intelligence.

The Journal of general psychology

Neuringer C, Wheeler GR, Beardsley JV.
PMID: 28147964
J Gen Psychol. 1969 Jan;80(1):73-79. doi: 10.1080/00221309.1969.9711273.

No abstract available.

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Neuringer C, Wheeler GR, Beardsley JV. Rating Diversity and Measures of Convergent and Divergent Intelligence. J Gen Psychol. 1969;80(1):73-79doi: 10.1080/00221309.1969.9711273.
Neuringer, C., Wheeler, G. R., & Beardsley, J. V. (1969). Rating Diversity and Measures of Convergent and Divergent Intelligence. The Journal of general psychology, 80(1), 73-79. https://doi.org/10.1080/00221309.1969.9711273
Neuringer, Charles, et al. "Rating Diversity and Measures of Convergent and Divergent Intelligence." The Journal of general psychology vol. 80,1 (1969): 73-79. doi: https://doi.org/10.1080/00221309.1969.9711273
Neuringer C, Wheeler GR, Beardsley JV. Rating Diversity and Measures of Convergent and Divergent Intelligence. J Gen Psychol. 1969 Jan;80(1):73-79. doi: 10.1080/00221309.1969.9711273. PMID: 28147964.
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Correction: Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference.

Nanoscale

Cacciato G, Bayle M, Pugliara A, Bonafos C, Zimbone M, Privitera V, Grimaldi MG, Carles R.
PMID: 26606588
Nanoscale. 2015 Dec 28;7(48):20778. doi: 10.1039/c5nr90220g. Epub 2015 Nov 25.

Correction for 'Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference' by Giuseppe Cacciato et al., Nanoscale, 2015, 7, 13468-13476.

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Cacciato G, Bayle M, Pugliara A, et al. Correction: Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference. Nanoscale. 2015;7(48):20778doi: 10.1039/c5nr90220g.
Cacciato, G., Bayle, M., Pugliara, A., Bonafos, C., Zimbone, M., Privitera, V., Grimaldi, M. G., & Carles, R. (2015). Correction: Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference. Nanoscale, 7(48), 20778. https://doi.org/10.1039/c5nr90220g
Cacciato, Giuseppe, et al. "Correction: Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference." Nanoscale vol. 7,48 (2015): 20778. doi: https://doi.org/10.1039/c5nr90220g
Cacciato G, Bayle M, Pugliara A, Bonafos C, Zimbone M, Privitera V, Grimaldi MG, Carles R. Correction: Enhancing carrier generation in TiO2 by a synergistic effect between plasmon resonance in Ag nanoparticles and optical interference. Nanoscale. 2015 Dec 28;7(48):20778. doi: 10.1039/c5nr90220g. Epub 2015 Nov 25. PMID: 26606588.
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Deficits in quantity and quality.

Nursing outlook

Boyle R.
PMID: 5177049
Nurs Outlook. 1966 May;14(5):29.

No abstract available.

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Boyle R. Deficits in quantity and quality. Nurs Outlook. 1966;14(5):29
Boyle, R. (1966). Deficits in quantity and quality. Nursing outlook, 14(5), 29.
Boyle, R. "Deficits in quantity and quality." Nursing outlook vol. 14,5 (1966): 29.
Boyle R. Deficits in quantity and quality. Nurs Outlook. 1966 May;14(5):29. PMID: 5177049.
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[Professor Maurice Chevassu, 1877-1957].

Journal d'urologie medicale et chirurgicale

BAYLE H.
PMID: 13526178
J Urol Medicale Chir. 1957 Dec;63(12):817-23.

No abstract available.

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BAYLE H. Le professeur Maurice Chevassu; 1877-1957. [Professor Maurice Chevassu, 1877-1957]. J Urol Medicale Chir. 1957;63(12):817-23
BAYLE, H. (1957). Le professeur Maurice Chevassu; 1877-1957. [Professor Maurice Chevassu, 1877-1957]. Journal d'urologie medicale et chirurgicale, 63(12), 817-23.
BAYLE, H. "Le professeur Maurice Chevassu; 1877-1957." [Professor Maurice Chevassu, 1877-1957]. Journal d'urologie medicale et chirurgicale vol. 63,12 (1957): 817-23.
BAYLE H. Le professeur Maurice Chevassu; 1877-1957. [Professor Maurice Chevassu, 1877-1957]. J Urol Medicale Chir. 1957 Dec;63(12):817-23. French. PMID: 13526178.
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Studies on the Origin of (-)-alpha-Bisabolol and Chamazulene in Chamomile Preparations; Part I. Investigations by Isotope Ratio Mass Spectrometry (IRMS).

Planta medica

Carle R, Fleischhauer I, Beyer J, Reinhard E.
PMID: 17221447
Planta Med. 1990 Oct;56(5):456-60. doi: 10.1055/s-2006-961010.

IRMS was used to determine the delta (13)C-and deltaD-values of dried plant material and essential oil fractions of CHAMOMILLA RECUTITA and VANILLOSMOPSIS ERYTHROPAPPA and of isolated components thereof. Both plants turned out to follow the same C (3) photosynthetic...

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Carle R, Fleischhauer I, Beyer J, et al. Studies on the Origin of (-)-alpha-Bisabolol and Chamazulene in Chamomile Preparations; Part I. Investigations by Isotope Ratio Mass Spectrometry (IRMS). Planta Med. 1990;56(5):456-60doi: 10.1055/s-2006-961010.
Carle, R., Fleischhauer, I., Beyer, J., & Reinhard, E. (1990). Studies on the Origin of (-)-alpha-Bisabolol and Chamazulene in Chamomile Preparations; Part I. Investigations by Isotope Ratio Mass Spectrometry (IRMS). Planta medica, 56(5), 456-60. https://doi.org/10.1055/s-2006-961010
Carle, R, et al. "Studies on the Origin of (-)-alpha-Bisabolol and Chamazulene in Chamomile Preparations; Part I. Investigations by Isotope Ratio Mass Spectrometry (IRMS)." Planta medica vol. 56,5 (1990): 456-60. doi: https://doi.org/10.1055/s-2006-961010
Carle R, Fleischhauer I, Beyer J, Reinhard E. Studies on the Origin of (-)-alpha-Bisabolol and Chamazulene in Chamomile Preparations; Part I. Investigations by Isotope Ratio Mass Spectrometry (IRMS). Planta Med. 1990 Oct;56(5):456-60. doi: 10.1055/s-2006-961010. PMID: 17221447.
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Efficient fabrication of fused-fiber biconical taper structures by a scanned CO2 laser beam technique.

Applied optics

Bayle F, Meunier JP.
PMID: 16252652
Appl Opt. 2005 Oct 20;44(30):6402-11. doi: 10.1364/ao.44.006402.

The driving mechanism of a scanning mirror can cause significant impairment of expanded beam properties, which we investigated for several scanning waveforms. Engineering on the scanning waveform is then carried out by a scanned CO2 laser beam technique to...

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Bayle F, Meunier JP. Efficient fabrication of fused-fiber biconical taper structures by a scanned CO2 laser beam technique. Appl Opt. 2005;44(30):6402-11doi: 10.1364/ao.44.006402.
Bayle, F., & Meunier, J. P. (2005). Efficient fabrication of fused-fiber biconical taper structures by a scanned CO2 laser beam technique. Applied optics, 44(30), 6402-11. https://doi.org/10.1364/ao.44.006402
Bayle, Fabien, and Meunier, Jean-Pierre. "Efficient fabrication of fused-fiber biconical taper structures by a scanned CO2 laser beam technique." Applied optics vol. 44,30 (2005): 6402-11. doi: https://doi.org/10.1364/ao.44.006402
Bayle F, Meunier JP. Efficient fabrication of fused-fiber biconical taper structures by a scanned CO2 laser beam technique. Appl Opt. 2005 Oct 20;44(30):6402-11. doi: 10.1364/ao.44.006402. PMID: 16252652.
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Ingestion of juniper foliage reduces metabolic rates in woodrat (Neotoma) herbivores.

Zoology (Jena, Germany)

Boyle R, Dearing MD.
PMID: 16351900
Zoology (Jena). 2003;106(2):151-8. doi: 10.1078/0944-2006-00109.

Ingestion of plant secondary compounds by herbivores is predicted to increase resting or basal metabolic rates. We tested this hypothesis with two species of woodrat herbivores, Neotoma stephensi and Neotoma albigula, consuming diets of juniper (Juniperus monosperma), which is...

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Boyle R, Dearing MD. Ingestion of juniper foliage reduces metabolic rates in woodrat (Neotoma) herbivores. Zoology (Jena). 2003;106(2):151-8doi: 10.1078/0944-2006-00109.
Boyle, R., & Dearing, M. D. (2003). Ingestion of juniper foliage reduces metabolic rates in woodrat (Neotoma) herbivores. Zoology (Jena, Germany), 106(2), 151-8. https://doi.org/10.1078/0944-2006-00109
Boyle, Rebecca, and Dearing, M Denise. "Ingestion of juniper foliage reduces metabolic rates in woodrat (Neotoma) herbivores." Zoology (Jena, Germany) vol. 106,2 (2003): 151-8. doi: https://doi.org/10.1078/0944-2006-00109
Boyle R, Dearing MD. Ingestion of juniper foliage reduces metabolic rates in woodrat (Neotoma) herbivores. Zoology (Jena). 2003;106(2):151-8. doi: 10.1078/0944-2006-00109. PMID: 16351900.
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Sulfoxide-directed intramolecular [4 + 2] cycloadditions between 2-sulfinyl butadienes and unactivated alkynes.

The Journal of organic chemistry

Fernández de la Pradilla R, Tortosa M, Castellanos E, Viso A, Baile R.
PMID: 20112978
J Org Chem. 2010 Mar 05;75(5):1517-33. doi: 10.1021/jo9024489.

Sulfinyl dienynes undergo thermal and catalyzed IMDA cycloadditions, often at room temperature, to produce cyclohexa-1,4-dienes with good yields and high selectivities. Additionally, the products preserve a synthetically useful vinyl sulfoxide functionality. The selective manipulation of the double bonds in...

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Fernández de la Pradilla R, Tortosa M, Castellanos E, et al. Sulfoxide-directed intramolecular [4 + 2] cycloadditions between 2-sulfinyl butadienes and unactivated alkynes. J Org Chem. 2010;75(5):1517-33doi: 10.1021/jo9024489.
Fernández de la Pradilla, R., Tortosa, M., Castellanos, E., Viso, A., & Baile, R. (2010). Sulfoxide-directed intramolecular [4 + 2] cycloadditions between 2-sulfinyl butadienes and unactivated alkynes. The Journal of organic chemistry, 75(5), 1517-33. https://doi.org/10.1021/jo9024489
Fernández de la Pradilla, Roberto, et al. "Sulfoxide-directed intramolecular [4 + 2] cycloadditions between 2-sulfinyl butadienes and unactivated alkynes." The Journal of organic chemistry vol. 75,5 (2010): 1517-33. doi: https://doi.org/10.1021/jo9024489
Fernández de la Pradilla R, Tortosa M, Castellanos E, Viso A, Baile R. Sulfoxide-directed intramolecular [4 + 2] cycloadditions between 2-sulfinyl butadienes and unactivated alkynes. J Org Chem. 2010 Mar 05;75(5):1517-33. doi: 10.1021/jo9024489. PMID: 20112978.
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Showing 1 to 12 of 219 entries