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Showing 13 to 24 of 55 entries
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Malocclusion as an epidemiologic continuum.

American journal of orthodontics

Salzmann JA.
PMID: 5276732
Am J Orthod. 1971 Mar;59(3):298-9. doi: 10.1016/0002-9416(71)90104-7.

No abstract available.

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Salzmann JA. Malocclusion as an epidemiologic continuum. Am J Orthod. 1971;59(3):298-9doi: 10.1016/0002-9416(71)90104-7.
Salzmann, J. A. (1971). Malocclusion as an epidemiologic continuum. American journal of orthodontics, 59(3), 298-9. https://doi.org/10.1016/0002-9416(71)90104-7
Salzmann, J A. "Malocclusion as an epidemiologic continuum." American journal of orthodontics vol. 59,3 (1971): 298-9. doi: https://doi.org/10.1016/0002-9416(71)90104-7
Salzmann JA. Malocclusion as an epidemiologic continuum. Am J Orthod. 1971 Mar;59(3):298-9. doi: 10.1016/0002-9416(71)90104-7. PMID: 5276732.
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THE SELF-IMAGE OF THE DENTIST.

The New York journal of dentistry

SALZMANN JA.
PMID: 14240139
N Y J Dent. 1965 Mar;35:81-3.

No abstract available.

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SALZMANN JA. THE SELF-IMAGE OF THE DENTIST. N Y J Dent. 1965;35:81-3
SALZMANN, J. A. (1965). THE SELF-IMAGE OF THE DENTIST. The New York journal of dentistry, 3581-3.
SALZMANN, J A. "THE SELF-IMAGE OF THE DENTIST." The New York journal of dentistry vol. 35 (1965): 81-3.
SALZMANN JA. THE SELF-IMAGE OF THE DENTIST. N Y J Dent. 1965 Mar;35:81-3. PMID: 14240139.
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Orthodontic parameters for epidemiologic determinations.

American journal of orthodontics

Salzmann JA.
PMID: 5249181
Am J Orthod. 1969 Feb;55(2):193-4. doi: 10.1016/0002-9416(69)90128-6.

No abstract available.

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Salzmann JA. Orthodontic parameters for epidemiologic determinations. Am J Orthod. 1969;55(2):193-4doi: 10.1016/0002-9416(69)90128-6.
Salzmann, J. A. (1969). Orthodontic parameters for epidemiologic determinations. American journal of orthodontics, 55(2), 193-4. https://doi.org/10.1016/0002-9416(69)90128-6
Salzmann, J A. "Orthodontic parameters for epidemiologic determinations." American journal of orthodontics vol. 55,2 (1969): 193-4. doi: https://doi.org/10.1016/0002-9416(69)90128-6
Salzmann JA. Orthodontic parameters for epidemiologic determinations. Am J Orthod. 1969 Feb;55(2):193-4. doi: 10.1016/0002-9416(69)90128-6. PMID: 5249181.
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Tripodal N,P Mixed-Donor Ligands and Their Cobalt Complexes: Efficient Catalysts for Acceptorless Dehydrogenation of Secondary Alcohols.

Inorganic chemistry

Xu S, Alhthlol LM, Paudel K, Reinheimer E, Tyer DL, Taylor DK, Smith AM, Holzmann J, Lozano E, Ding K.
PMID: 29461054
Inorg Chem. 2018 Mar 05;57(5):2394-2397. doi: 10.1021/acs.inorgchem.8b00043. Epub 2018 Feb 20.

A new tetradentate tripodal ligand,

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Xu S, Alhthlol LM, Paudel K, et al. Tripodal N,P Mixed-Donor Ligands and Their Cobalt Complexes: Efficient Catalysts for Acceptorless Dehydrogenation of Secondary Alcohols. Inorg Chem. 2018;57(5):2394-2397doi: 10.1021/acs.inorgchem.8b00043.
Xu, S., Alhthlol, L. M., Paudel, K., Reinheimer, E., Tyer, D. L., Taylor, D. K., Smith, A. M., Holzmann, J., Lozano, E., & Ding, K. (2018). Tripodal N,P Mixed-Donor Ligands and Their Cobalt Complexes: Efficient Catalysts for Acceptorless Dehydrogenation of Secondary Alcohols. Inorganic chemistry, 57(5), 2394-2397. https://doi.org/10.1021/acs.inorgchem.8b00043
Xu, Shi, et al. "Tripodal N,P Mixed-Donor Ligands and Their Cobalt Complexes: Efficient Catalysts for Acceptorless Dehydrogenation of Secondary Alcohols." Inorganic chemistry vol. 57,5 (2018): 2394-2397. doi: https://doi.org/10.1021/acs.inorgchem.8b00043
Xu S, Alhthlol LM, Paudel K, Reinheimer E, Tyer DL, Taylor DK, Smith AM, Holzmann J, Lozano E, Ding K. Tripodal N,P Mixed-Donor Ligands and Their Cobalt Complexes: Efficient Catalysts for Acceptorless Dehydrogenation of Secondary Alcohols. Inorg Chem. 2018 Mar 05;57(5):2394-2397. doi: 10.1021/acs.inorgchem.8b00043. Epub 2018 Feb 20. PMID: 29461054.
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The reaction rates of O2 with closed-shell and open-shell Al(x)⁻ and Ga(x)⁻ clusters under single-collision conditions: experimental and theoretical investigations toward a generally valid model for the hindered reactions of O2 with metal atom clusters.

Journal of the American Chemical Society

Neumaier M, Olzmann M, Kiran B, Bowen KH, Eichhorn B, Stokes ST, Buonaugurio A, Burgert R, Schnöckel H.
PMID: 24564371
J Am Chem Soc. 2014 Mar 05;136(9):3607-16. doi: 10.1021/ja4125548. Epub 2014 Feb 24.

In order to characterize the oxidation of metallic surfaces, the reactions of O2 with a number of Al(x)(-) and, for the first time, Ga(x)(-) clusters as molecular models have been investigated, and the results are presented here for x...

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Neumaier M, Olzmann M, Kiran B, et al. The reaction rates of O2 with closed-shell and open-shell Al(x)⁻ and Ga(x)⁻ clusters under single-collision conditions: experimental and theoretical investigations toward a generally valid model for the hindered reactions of O2 with metal atom clusters. J Am Chem Soc. 2014;136(9):3607-16doi: 10.1021/ja4125548.
Neumaier, M., Olzmann, M., Kiran, B., Bowen, K. H., Eichhorn, B., Stokes, S. T., Buonaugurio, A., Burgert, R., & Schnöckel, H. (2014). The reaction rates of O2 with closed-shell and open-shell Al(x)⁻ and Ga(x)⁻ clusters under single-collision conditions: experimental and theoretical investigations toward a generally valid model for the hindered reactions of O2 with metal atom clusters. Journal of the American Chemical Society, 136(9), 3607-16. https://doi.org/10.1021/ja4125548
Neumaier, Marco, et al. "The reaction rates of O2 with closed-shell and open-shell Al(x)⁻ and Ga(x)⁻ clusters under single-collision conditions: experimental and theoretical investigations toward a generally valid model for the hindered reactions of O2 with metal atom clusters." Journal of the American Chemical Society vol. 136,9 (2014): 3607-16. doi: https://doi.org/10.1021/ja4125548
Neumaier M, Olzmann M, Kiran B, Bowen KH, Eichhorn B, Stokes ST, Buonaugurio A, Burgert R, Schnöckel H. The reaction rates of O2 with closed-shell and open-shell Al(x)⁻ and Ga(x)⁻ clusters under single-collision conditions: experimental and theoretical investigations toward a generally valid model for the hindered reactions of O2 with metal atom clusters. J Am Chem Soc. 2014 Mar 05;136(9):3607-16. doi: 10.1021/ja4125548. Epub 2014 Feb 24. PMID: 24564371.
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Dentistry in 1950.

The New York journal of dentistry

SALZMANN JA.
PMID: 24539768
N Y J Dent. 1951 Jan;21(1):3-7.

No abstract available.

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SALZMANN JA. Dentistry in 1950. N Y J Dent. 1951;21(1):3-7
SALZMANN, J. A. (1951). Dentistry in 1950. The New York journal of dentistry, 21(1), 3-7.
SALZMANN, J A. "Dentistry in 1950." The New York journal of dentistry vol. 21,1 (1951): 3-7.
SALZMANN JA. Dentistry in 1950. N Y J Dent. 1951 Jan;21(1):3-7. PMID: 24539768.
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Experimental and theoretical investigation of the kinetics of the reaction of atomic chlorine with 1,4-dioxane.

The journal of physical chemistry. A

Giri BR, Roscoe JM, González-García N, Olzmann M, Lo JM, Marriott RA.
PMID: 21526862
J Phys Chem A. 2011 May 26;115(20):5105-11. doi: 10.1021/jp201803g. Epub 2011 Apr 29.

The rate coefficients for the reaction of 1,4-dioxane with atomic chlorine were measured from T = 292-360 K using the relative rate method. The reference reactant was isobutane and the experiments were made in argon with atomic chlorine produced...

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Giri BR, Roscoe JM, González-García N, et al. Experimental and theoretical investigation of the kinetics of the reaction of atomic chlorine with 1,4-dioxane. J Phys Chem A. 2011;115(20):5105-11doi: 10.1021/jp201803g.
Giri, B. R., Roscoe, J. M., González-García, N., Olzmann, M., Lo, J. M., & Marriott, R. A. (2011). Experimental and theoretical investigation of the kinetics of the reaction of atomic chlorine with 1,4-dioxane. The journal of physical chemistry. A, 115(20), 5105-11. https://doi.org/10.1021/jp201803g
Giri, Binod R, et al. "Experimental and theoretical investigation of the kinetics of the reaction of atomic chlorine with 1,4-dioxane." The journal of physical chemistry. A vol. 115,20 (2011): 5105-11. doi: https://doi.org/10.1021/jp201803g
Giri BR, Roscoe JM, González-García N, Olzmann M, Lo JM, Marriott RA. Experimental and theoretical investigation of the kinetics of the reaction of atomic chlorine with 1,4-dioxane. J Phys Chem A. 2011 May 26;115(20):5105-11. doi: 10.1021/jp201803g. Epub 2011 Apr 29. PMID: 21526862.
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Rate coefficients and equilibrium constant for the CH2CHO + O2 reaction system.

The journal of physical chemistry. A

Delbos E, Fittschen C, Hippler H, Krasteva N, Olzmann M, Viskolcz B.
PMID: 16509648
J Phys Chem A. 2006 Mar 09;110(9):3238-45. doi: 10.1021/jp054697s.

The kinetics of the CH2CHO + O2 reaction was experimentally studied in two quasi-static reactors and a discharge flow-reactor at temperatures ranging from 298 to 660 K and pressures between 1 mbar and 46 bar with helium as the...

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Delbos E, Fittschen C, Hippler H, et al. Rate coefficients and equilibrium constant for the CH2CHO + O2 reaction system. J Phys Chem A. 2006;110(9):3238-45doi: 10.1021/jp054697s.
Delbos, E., Fittschen, C., Hippler, H., Krasteva, N., Olzmann, M., & Viskolcz, B. (2006). Rate coefficients and equilibrium constant for the CH2CHO + O2 reaction system. The journal of physical chemistry. A, 110(9), 3238-45. https://doi.org/10.1021/jp054697s
Delbos, Eric, et al. "Rate coefficients and equilibrium constant for the CH2CHO + O2 reaction system." The journal of physical chemistry. A vol. 110,9 (2006): 3238-45. doi: https://doi.org/10.1021/jp054697s
Delbos E, Fittschen C, Hippler H, Krasteva N, Olzmann M, Viskolcz B. Rate coefficients and equilibrium constant for the CH2CHO + O2 reaction system. J Phys Chem A. 2006 Mar 09;110(9):3238-45. doi: 10.1021/jp054697s. PMID: 16509648.
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Tiamulin, a new antibiotic for eliminating mycoplasmas from bovine serum 1. Investigations on Spermatozoal Toxicity.

Theriogenology

Holzmann A, Laber G, Gumhold G.
PMID: 16725955
Theriogenology. 1984 Sep;22(3):237-40. doi: 10.1016/0093-691x(84)90480-1.

Tiamulin, a new diterpene antibiotic, was investigated for toxicity to spermatozoa. The compound was added to ejaculates via semen extender at a concentration of 50 to 90 mg per 100 ml of total liquid. Motility and the proportion of...

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Holzmann A, Laber G, Gumhold G. Tiamulin, a new antibiotic for eliminating mycoplasmas from bovine serum 1. Investigations on Spermatozoal Toxicity. Theriogenology. 1984;22(3):237-40doi: 10.1016/0093-691x(84)90480-1.
Holzmann, A., Laber, G., & Gumhold, G. (1984). Tiamulin, a new antibiotic for eliminating mycoplasmas from bovine serum 1. Investigations on Spermatozoal Toxicity. Theriogenology, 22(3), 237-40. https://doi.org/10.1016/0093-691x(84)90480-1
Holzmann, A, et al. "Tiamulin, a new antibiotic for eliminating mycoplasmas from bovine serum 1. Investigations on Spermatozoal Toxicity." Theriogenology vol. 22,3 (1984): 237-40. doi: https://doi.org/10.1016/0093-691x(84)90480-1
Holzmann A, Laber G, Gumhold G. Tiamulin, a new antibiotic for eliminating mycoplasmas from bovine serum 1. Investigations on Spermatozoal Toxicity. Theriogenology. 1984 Sep;22(3):237-40. doi: 10.1016/0093-691x(84)90480-1. PMID: 16725955.
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HCO formation in the thermal unimolecular decomposition of glyoxal: rotational and weak collision effects.

Physical chemistry chemical physics : PCCP

Friedrichs G, Colberg M, Dammeier J, Bentz T, Olzmann M.
PMID: 18979037
Phys Chem Chem Phys. 2008 Nov 21;10(43):6520-33. doi: 10.1039/b809992h. Epub 2008 Sep 29.

The multi-channel thermal unimolecular decomposition of glyoxal was experimentally investigated in the temperature range 1106 K < T < 2320 K and at total densities of 1.7 x 10(-6) mol cm(-3) < rho < 1.9 x 10(-5) mol cm(-3)...

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Friedrichs G, Colberg M, Dammeier J, et al. HCO formation in the thermal unimolecular decomposition of glyoxal: rotational and weak collision effects. Phys Chem Chem Phys. 2008;10(43):6520-33doi: 10.1039/b809992h.
Friedrichs, G., Colberg, M., Dammeier, J., Bentz, T., & Olzmann, M. (2008). HCO formation in the thermal unimolecular decomposition of glyoxal: rotational and weak collision effects. Physical chemistry chemical physics : PCCP, 10(43), 6520-33. https://doi.org/10.1039/b809992h
Friedrichs, Gernot, et al. "HCO formation in the thermal unimolecular decomposition of glyoxal: rotational and weak collision effects." Physical chemistry chemical physics : PCCP vol. 10,43 (2008): 6520-33. doi: https://doi.org/10.1039/b809992h
Friedrichs G, Colberg M, Dammeier J, Bentz T, Olzmann M. HCO formation in the thermal unimolecular decomposition of glyoxal: rotational and weak collision effects. Phys Chem Chem Phys. 2008 Nov 21;10(43):6520-33. doi: 10.1039/b809992h. Epub 2008 Sep 29. PMID: 18979037.
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Pressure and salt effects in simulated water: two sides of the same coin?.

Angewandte Chemie (International ed. in English)

Holzmann J, Ludwig R, Geiger A, Paschek D.
PMID: 17943936
Angew Chem Int Ed Engl. 2007;46(46):8907-11. doi: 10.1002/anie.200702736.

No abstract available.

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Holzmann J, Ludwig R, Geiger A, et al. Pressure and salt effects in simulated water: two sides of the same coin?. Angew Chem Int Ed Engl. 2007;46(46):8907-11doi: 10.1002/anie.200702736.
Holzmann, J., Ludwig, R., Geiger, A., & Paschek, D. (2007). Pressure and salt effects in simulated water: two sides of the same coin?. Angewandte Chemie (International ed. in English), 46(46), 8907-11. https://doi.org/10.1002/anie.200702736
Holzmann, Jörg, et al. "Pressure and salt effects in simulated water: two sides of the same coin?." Angewandte Chemie (International ed. in English) vol. 46,46 (2007): 8907-11. doi: https://doi.org/10.1002/anie.200702736
Holzmann J, Ludwig R, Geiger A, Paschek D. Pressure and salt effects in simulated water: two sides of the same coin?. Angew Chem Int Ed Engl. 2007;46(46):8907-11. doi: 10.1002/anie.200702736. PMID: 17943936.
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Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study.

The journal of physical chemistry. A

Bentz T, Giri BR, Hippler H, Olzmann M, Striebel F, Szöri M.
PMID: 17388398
J Phys Chem A. 2007 May 17;111(19):3812-8. doi: 10.1021/jp070833c. Epub 2007 Mar 23.

The kinetics of the reaction of hydrogen atoms with propyne (pC3H4) was experimentally studied in a shock tube at temperatures ranging from 1200 to 1400 K and pressures between 1.3 and 4.0 bar with Ar as the bath gas....

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Bentz T, Giri BR, Hippler H, et al. Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study. J Phys Chem A. 2007;111(19):3812-8doi: 10.1021/jp070833c.
Bentz, T., Giri, B. R., Hippler, H., Olzmann, M., Striebel, F., & Szöri, M. (2007). Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study. The journal of physical chemistry. A, 111(19), 3812-8. https://doi.org/10.1021/jp070833c
Bentz, Tobias, et al. "Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study." The journal of physical chemistry. A vol. 111,19 (2007): 3812-8. doi: https://doi.org/10.1021/jp070833c
Bentz T, Giri BR, Hippler H, Olzmann M, Striebel F, Szöri M. Reaction of hydrogen atoms with propyne at high temperatures: an experimental and theoretical study. J Phys Chem A. 2007 May 17;111(19):3812-8. doi: 10.1021/jp070833c. Epub 2007 Mar 23. PMID: 17388398.
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Showing 13 to 24 of 55 entries