Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 166 entries
Sorted by: Best Match Show Resources per page
Factors Contributing to Erythropoietin Hyporesponsiveness in Patients on Long-Term Continuous Ambulatory Peritoneal Dialysis: A Cross-Sectional Study.

Nephron extra

Hara T, Mukai H, Nakashima T, Sagara R, Furusho M, Miura S, Toyonaga J, Sugawara K, Takeda K.
PMID: 26648974
Nephron Extra. 2015 Oct 28;5(3):79-86. doi: 10.1159/000441154. eCollection 2015.

BACKGROUND: Factors contributing to erythropoietin (EPO) hyporesponsiveness in patients on long-term continuous ambulatory peritoneal dialysis are not well understood. Therefore, we investigated the factors contributing to EPO hyporesponsiveness using the EPO resistance index (ERI).METHODS: A total of 14 patients...

Cite
Hara T, Mukai H, Nakashima T, et al. Factors Contributing to Erythropoietin Hyporesponsiveness in Patients on Long-Term Continuous Ambulatory Peritoneal Dialysis: A Cross-Sectional Study. Nephron Extra. 2015;5(3):79-86doi: 10.1159/000441154.
Hara, T., Mukai, H., Nakashima, T., Sagara, R., Furusho, M., Miura, S., Toyonaga, J., Sugawara, K., & Takeda, K. (2015). Factors Contributing to Erythropoietin Hyporesponsiveness in Patients on Long-Term Continuous Ambulatory Peritoneal Dialysis: A Cross-Sectional Study. Nephron extra, 5(3), 79-86. https://doi.org/10.1159/000441154
Hara, Takashi, et al. "Factors Contributing to Erythropoietin Hyporesponsiveness in Patients on Long-Term Continuous Ambulatory Peritoneal Dialysis: A Cross-Sectional Study." Nephron extra vol. 5,3 (2015): 79-86. doi: https://doi.org/10.1159/000441154
Hara T, Mukai H, Nakashima T, Sagara R, Furusho M, Miura S, Toyonaga J, Sugawara K, Takeda K. Factors Contributing to Erythropoietin Hyporesponsiveness in Patients on Long-Term Continuous Ambulatory Peritoneal Dialysis: A Cross-Sectional Study. Nephron Extra. 2015 Oct 28;5(3):79-86. doi: 10.1159/000441154. eCollection 2015. PMID: 26648974; PMCID: PMC4662269.
Copy Download .nbib Format: NLM
Importance of virological response in the early stage of telaprevir-based triple therapy for hepatitis C.

World journal of hepatology

Hiramine S, Furusyo N, Ogawa E, Nakamuta M, Kajiwara E, Nomura H, Dohmen K, Takahashi K, Satoh T, Azuma K, Kawano A, Koyanagi T, Kotoh K, Shimoda S, Hayashi J.
PMID: 26609346
World J Hepatol. 2015 Nov 18;7(26):2688-95. doi: 10.4254/wjh.v7.i26.2688.

AIM: To investigate the efficacy of virological response (VR) to telaprevir (TVR)-based triple therapy in predicting treatment outcome of hepatitis C.METHODS: This prospective, multicenter study consisted of 253 Japanese patients infected with hepatitis C virus (HCV) genotype 1b. All...

Cite
Hiramine S, Furusyo N, Ogawa E, et al. Importance of virological response in the early stage of telaprevir-based triple therapy for hepatitis C. World J Hepatol. 2015;7(26):2688-95doi: 10.4254/wjh.v7.i26.2688.
Hiramine, S., Furusyo, N., Ogawa, E., Nakamuta, M., Kajiwara, E., Nomura, H., Dohmen, K., Takahashi, K., Satoh, T., Azuma, K., Kawano, A., Koyanagi, T., Kotoh, K., Shimoda, S., & Hayashi, J. (2015). Importance of virological response in the early stage of telaprevir-based triple therapy for hepatitis C. World journal of hepatology, 7(26), 2688-95. https://doi.org/10.4254/wjh.v7.i26.2688
Hiramine, Satoshi, et al. "Importance of virological response in the early stage of telaprevir-based triple therapy for hepatitis C." World journal of hepatology vol. 7,26 (2015): 2688-95. doi: https://doi.org/10.4254/wjh.v7.i26.2688
Hiramine S, Furusyo N, Ogawa E, Nakamuta M, Kajiwara E, Nomura H, Dohmen K, Takahashi K, Satoh T, Azuma K, Kawano A, Koyanagi T, Kotoh K, Shimoda S, Hayashi J. Importance of virological response in the early stage of telaprevir-based triple therapy for hepatitis C. World J Hepatol. 2015 Nov 18;7(26):2688-95. doi: 10.4254/wjh.v7.i26.2688. PMID: 26609346; PMCID: PMC4651913.
Copy Download .nbib Format: NLM
Efficacy of interferon-beta plus ribavirin combination treatment on the development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C.

Hepatology research : the official journal of the Japan Society of Hepatology

Ikezaki H, Nomura H, Furusyo N, Ogawa E, Kajiwara E, Takahashi K, Kawano A, Maruyama T, Tanabe Y, Satoh T, Nakamuta M, Kotoh K, Azuma K, Dohmen K, Shimoda S, Hayashi J.
PMID: 26189962
Hepatol Res. 2016 Mar;46(3):E174-80. doi: 10.1111/hepr.12555. Epub 2015 Sep 02.

AIM: Although there is much evidence of an antitumor effect of pegylated interferon (IFN)-α-based treatment, limited data is available about that of IFN-β-based treatment. Our goal was to evaluate the impact of IFN-β plus ribavirin (RBV) treatment on the...

Cite
Ikezaki H, Nomura H, Furusyo N, et al. Efficacy of interferon-beta plus ribavirin combination treatment on the development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C. Hepatol Res. 2015;46(3):E174-80doi: 10.1111/hepr.12555.
Ikezaki, H., Nomura, H., Furusyo, N., Ogawa, E., Kajiwara, E., Takahashi, K., Kawano, A., Maruyama, T., Tanabe, Y., Satoh, T., Nakamuta, M., Kotoh, K., Azuma, K., Dohmen, K., Shimoda, S., Hayashi, J. (2016). Efficacy of interferon-beta plus ribavirin combination treatment on the development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C. Hepatology research : the official journal of the Japan Society of Hepatology, 46(3), E174-80. https://doi.org/10.1111/hepr.12555
Ikezaki, Hiroaki, et al. "Efficacy of interferon-beta plus ribavirin combination treatment on the development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C." Hepatology research : the official journal of the Japan Society of Hepatology vol. 46,3 (2016): E174-80. doi: https://doi.org/10.1111/hepr.12555
Ikezaki H, Nomura H, Furusyo N, Ogawa E, Kajiwara E, Takahashi K, Kawano A, Maruyama T, Tanabe Y, Satoh T, Nakamuta M, Kotoh K, Azuma K, Dohmen K, Shimoda S, Hayashi J. Efficacy of interferon-beta plus ribavirin combination treatment on the development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C. Hepatol Res. 2016 Mar;46(3):E174-80. doi: 10.1111/hepr.12555. Epub 2015 Sep 02. PMID: 26189962.
Copy Download .nbib Format: NLM
Photoinduced intrarotaxane electron transfer between zinc porphyrin and [60]fullerene in benzonitrile.

Angewandte Chemie (International ed. in English)

Watanabe N, Kihara N, Furusho Y, Takata T, Araki Y, Ito O.
PMID: 12575005
Angew Chem Int Ed Engl. 2003 Feb 10;42(6):681-3. doi: 10.1002/anie.200390188.

No abstract available.

Cite
Watanabe N, Kihara N, Furusho Y, et al. Photoinduced intrarotaxane electron transfer between zinc porphyrin and [60]fullerene in benzonitrile. Angew Chem Int Ed Engl. 2003;42(6):681-3doi: 10.1002/anie.200390188.
Watanabe, N., Kihara, N., Furusho, Y., Takata, T., Araki, Y., & Ito, O. (2003). Photoinduced intrarotaxane electron transfer between zinc porphyrin and [60]fullerene in benzonitrile. Angewandte Chemie (International ed. in English), 42(6), 681-3. https://doi.org/10.1002/anie.200390188
Watanabe, Nobuhiro, et al. "Photoinduced intrarotaxane electron transfer between zinc porphyrin and [60]fullerene in benzonitrile." Angewandte Chemie (International ed. in English) vol. 42,6 (2003): 681-3. doi: https://doi.org/10.1002/anie.200390188
Watanabe N, Kihara N, Furusho Y, Takata T, Araki Y, Ito O. Photoinduced intrarotaxane electron transfer between zinc porphyrin and [60]fullerene in benzonitrile. Angew Chem Int Ed Engl. 2003 Feb 10;42(6):681-3. doi: 10.1002/anie.200390188. PMID: 12575005.
Copy Download .nbib Format: NLM
Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system.

Organic letters

Furuno H, Hanamoto T, Sugimoto Y, Inanaga J.
PMID: 10814243
Org Lett. 2000 Jan;2(1):49-52. doi: 10.1021/ol991189q.

[reaction: see text] A remarkably high asymmetric amplification was realized in the Yb[(R)-BNP]3-catalyzed hetero-Diels-Alder reaction as the first example in the metal/chiral ligand 1:3 system. The mechanism may be explained by the autogenetic formation of the enantiopure complex as...

Cite
Furuno H, Hanamoto T, Sugimoto Y, et al. Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system. Org Lett. 2000;2(1):49-52doi: 10.1021/ol991189q.
Furuno, H., Hanamoto, T., Sugimoto, Y., & Inanaga, J. (2000). Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system. Organic letters, 2(1), 49-52. https://doi.org/10.1021/ol991189q
Furuno, et al. "Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system." Organic letters vol. 2,1 (2000): 49-52. doi: https://doi.org/10.1021/ol991189q
Furuno H, Hanamoto T, Sugimoto Y, Inanaga J. Remarkably high asymmetric amplification in the chiral lanthanide complex-catalyzed hetero-Diels-Alder reaction: first example of the nonlinear effect in ML3 system. Org Lett. 2000 Jan;2(1):49-52. doi: 10.1021/ol991189q. PMID: 10814243.
Copy Download .nbib Format: NLM
Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates.

Enantiomer

Takata T, Takagi H, Furusho Y.
PMID: 12108630
Enantiomer. 2002 Mar-Jun;7(2):129-32. doi: 10.1080/10242430212195.

Calix[4]arene tethering four chiral five-membered cyclic carbonates 1c was synthesized by O-glycidylation of p-tert-butylcalix[4]arene 1a with (R)-glycidyl tosylate, followed by carbonation with carbon dioxide catalyzed by lithium bromide. Porphyrin tethering chiral five-membered cyclic carbonates 2c was similarly synthesized.

Cite
Takata T, Takagi H, Furusho Y. Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates. Enantiomer. 2002;7(2):129-32doi: 10.1080/10242430212195.
Takata, T., Takagi, H., & Furusho, Y. (2002). Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates. Enantiomer, 7(2), 129-32. https://doi.org/10.1080/10242430212195
Takata, Toshikazu, et al. "Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates." Enantiomer vol. 7,2 (2002): 129-32. doi: https://doi.org/10.1080/10242430212195
Takata T, Takagi H, Furusho Y. Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates. Enantiomer. 2002 Mar-Jun;7(2):129-32. doi: 10.1080/10242430212195. PMID: 12108630.
Copy Download .nbib Format: NLM
End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes.

Organic letters

Sasabe H, Kihara N, Furusho Y, Mizuno K, Ogawa A, Takata T.
PMID: 15496073
Org Lett. 2004 Oct 28;6(22):3957-60. doi: 10.1021/ol048433k.

[reaction: see text] The Diels-Alder reaction of various dienophiles such as C(60) with a pseudorotaxane having a sultine moiety afforded corresponding [2]rotaxanes in moderate yields. The introduction of a porphyrin moiety on the wheel component considerably enhanced the efficiency...

Cite
Sasabe H, Kihara N, Furusho Y, et al. End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes. Org Lett. 2004;6(22):3957-60doi: 10.1021/ol048433k.
Sasabe, H., Kihara, N., Furusho, Y., Mizuno, K., Ogawa, A., & Takata, T. (2004). End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes. Organic letters, 6(22), 3957-60. https://doi.org/10.1021/ol048433k
Sasabe, Hisahiro, et al. "End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes." Organic letters vol. 6,22 (2004): 3957-60. doi: https://doi.org/10.1021/ol048433k
Sasabe H, Kihara N, Furusho Y, Mizuno K, Ogawa A, Takata T. End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes. Org Lett. 2004 Oct 28;6(22):3957-60. doi: 10.1021/ol048433k. PMID: 15496073.
Copy Download .nbib Format: NLM
Effects of lamivudine on serum albumin levels correlate with pretreatment HBV-DNA levels in cirrhotic patients.

Comparative hepatology

Nakamuta M, Kotoh K, Enjoji M, Kajiwara E, Shimono J, Masumoto A, Maruyama T, Furusyo N, Nomura H, Sakai H, Takahashi K, Azuma K, Shimoda S, Tanabe Y, Hayashi J.
PMID: 17470300
Comp Hepatol. 2007 May 01;6:3. doi: 10.1186/1476-5926-6-3.

BACKGROUND: Lamivudine treatment has been recently demonstrated to increase the serum albumin levels in cirrhotic patients with hepatitis B virus (HBV) infection, but the precise mechanism remains unclear. We hypothesized that the improvement of hypoalbuminemia by lamivudine may be...

Cite
Nakamuta M, Kotoh K, Enjoji M, et al. Effects of lamivudine on serum albumin levels correlate with pretreatment HBV-DNA levels in cirrhotic patients. Comp Hepatol. 2007;6:3doi: 10.1186/1476-5926-6-3.
Nakamuta, M., Kotoh, K., Enjoji, M., Kajiwara, E., Shimono, J., Masumoto, A., Maruyama, T., Furusyo, N., Nomura, H., Sakai, H., Takahashi, K., Azuma, K., Shimoda, S., Tanabe, Y., & Hayashi, J. (2007). Effects of lamivudine on serum albumin levels correlate with pretreatment HBV-DNA levels in cirrhotic patients. Comparative hepatology, 63. https://doi.org/10.1186/1476-5926-6-3
Nakamuta, Makoto, et al. "Effects of lamivudine on serum albumin levels correlate with pretreatment HBV-DNA levels in cirrhotic patients." Comparative hepatology vol. 6 (2007): 3. doi: https://doi.org/10.1186/1476-5926-6-3
Nakamuta M, Kotoh K, Enjoji M, Kajiwara E, Shimono J, Masumoto A, Maruyama T, Furusyo N, Nomura H, Sakai H, Takahashi K, Azuma K, Shimoda S, Tanabe Y, Hayashi J. Effects of lamivudine on serum albumin levels correlate with pretreatment HBV-DNA levels in cirrhotic patients. Comp Hepatol. 2007 May 01;6:3. doi: 10.1186/1476-5926-6-3. PMID: 17470300; PMCID: PMC1884174.
Copy Download .nbib Format: NLM
Multicomponent cylindrical assemblies driven by amidinium-carboxylate salt-bridge formation.

Angewandte Chemie (International ed. in English)

Katagiri H, Tanaka Y, Furusho Y, Yashima E.
PMID: 17309084
Angew Chem Int Ed Engl. 2007;46(14):2435-9. doi: 10.1002/anie.200603921.

No abstract available.

Cite
Katagiri H, Tanaka Y, Furusho Y, et al. Multicomponent cylindrical assemblies driven by amidinium-carboxylate salt-bridge formation. Angew Chem Int Ed Engl. 2007;46(14):2435-9doi: 10.1002/anie.200603921.
Katagiri, H., Tanaka, Y., Furusho, Y., & Yashima, E. (2007). Multicomponent cylindrical assemblies driven by amidinium-carboxylate salt-bridge formation. Angewandte Chemie (International ed. in English), 46(14), 2435-9. https://doi.org/10.1002/anie.200603921
Katagiri, Hiroshi, et al. "Multicomponent cylindrical assemblies driven by amidinium-carboxylate salt-bridge formation." Angewandte Chemie (International ed. in English) vol. 46,14 (2007): 2435-9. doi: https://doi.org/10.1002/anie.200603921
Katagiri H, Tanaka Y, Furusho Y, Yashima E. Multicomponent cylindrical assemblies driven by amidinium-carboxylate salt-bridge formation. Angew Chem Int Ed Engl. 2007;46(14):2435-9. doi: 10.1002/anie.200603921. PMID: 17309084.
Copy Download .nbib Format: NLM
Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions.

The journal of physical chemistry. A

Rajkumar GA, Sandanayaka AS, Ikeshita K, Itou M, Araki Y, Furusho Y, Kihara N, Ito O, Takata T.
PMID: 16833542
J Phys Chem A. 2005 Mar 24;109(11):2428-35. doi: 10.1021/jp046879c.

Intramolecular photoinduced charge-separation and charge-recombination processes in a covalently connected C60-(spacer)-N,N-bis(biphenylyl)aniline (C60-spacer-BBA) dyad, in which the center-to-center distance of the electron acceptor and electron donor is 15 A, have been studied by time-resolved fluorescence and transient absorption methods. The...

Cite
Rajkumar GA, Sandanayaka AS, Ikeshita K, et al. Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions. J Phys Chem A. 2005;109(11):2428-35doi: 10.1021/jp046879c.
Rajkumar, G. A., Sandanayaka, A. S., Ikeshita, K., Itou, M., Araki, Y., Furusho, Y., Kihara, N., Ito, O., & Takata, T. (2005). Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions. The journal of physical chemistry. A, 109(11), 2428-35. https://doi.org/10.1021/jp046879c
Rajkumar, G Abraham, et al. "Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions." The journal of physical chemistry. A vol. 109,11 (2005): 2428-35. doi: https://doi.org/10.1021/jp046879c
Rajkumar GA, Sandanayaka AS, Ikeshita K, Itou M, Araki Y, Furusho Y, Kihara N, Ito O, Takata T. Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions. J Phys Chem A. 2005 Mar 24;109(11):2428-35. doi: 10.1021/jp046879c. PMID: 16833542.
Copy Download .nbib Format: NLM
Remarkable effect of tris(4-fluorophenyl)phosphine oxide on the stabilization of chiral lanthanum complex catalysts. A new and practical protocol for the highly enantioselective epoxidation of conjugated enones.

Organic & biomolecular chemistry

Kino R, Daikai K, Kawanami T, Furuno H, Inanaga J.
PMID: 15227531
Org Biomol Chem. 2004 Jul 07;2(13):1822-4. doi: 10.1039/b405882h. Epub 2004 Jun 04.

A new and efficient chiral catalyst system, lanthanum-chiral BINOL-tris(4-fluorophenyl)phosphine oxide-cumene hydroperoxide, was developed for the epoxidation of alpha, beta-unsaturated ketones thus providing the corresponding epoxy ketones with excellent enantioselectivities (up to >99% ee) in good to excellent yields at...

Cite
Kino R, Daikai K, Kawanami T, et al. Remarkable effect of tris(4-fluorophenyl)phosphine oxide on the stabilization of chiral lanthanum complex catalysts. A new and practical protocol for the highly enantioselective epoxidation of conjugated enones. Org Biomol Chem. 2004;2(13):1822-4doi: 10.1039/b405882h.
Kino, R., Daikai, K., Kawanami, T., Furuno, H., & Inanaga, J. (2004). Remarkable effect of tris(4-fluorophenyl)phosphine oxide on the stabilization of chiral lanthanum complex catalysts. A new and practical protocol for the highly enantioselective epoxidation of conjugated enones. Organic & biomolecular chemistry, 2(13), 1822-4. https://doi.org/10.1039/b405882h
Kino, Rie, et al. "Remarkable effect of tris(4-fluorophenyl)phosphine oxide on the stabilization of chiral lanthanum complex catalysts. A new and practical protocol for the highly enantioselective epoxidation of conjugated enones." Organic & biomolecular chemistry vol. 2,13 (2004): 1822-4. doi: https://doi.org/10.1039/b405882h
Kino R, Daikai K, Kawanami T, Furuno H, Inanaga J. Remarkable effect of tris(4-fluorophenyl)phosphine oxide on the stabilization of chiral lanthanum complex catalysts. A new and practical protocol for the highly enantioselective epoxidation of conjugated enones. Org Biomol Chem. 2004 Jul 07;2(13):1822-4. doi: 10.1039/b405882h. Epub 2004 Jun 04. PMID: 15227531.
Copy Download .nbib Format: NLM
Photochemical fabrication of silver nanostructures at the solid-liquid interface using a recyclable photosensitized reduction process.

Physical chemistry chemical physics : PCCP

Sakamoto M, Kim SS, Furusho H, Majima T.
PMID: 20023814
Phys Chem Chem Phys. 2010 Jan 14;12(2):365-72. doi: 10.1039/b917981j. Epub 2009 Nov 11.

Photochemical synthesis of metal nanostructures through photosensitized reduction of metal sources is a powerful method in a wide variety of environments, because light can selectively promote the desired reaction without damaging the surrounding environment. A drawback of the method...

Cite
Sakamoto M, Kim SS, Furusho H, et al. Photochemical fabrication of silver nanostructures at the solid-liquid interface using a recyclable photosensitized reduction process. Phys Chem Chem Phys. 2009;12(2):365-72doi: 10.1039/b917981j.
Sakamoto, M., Kim, S. S., Furusho, H., & Majima, T. (2010). Photochemical fabrication of silver nanostructures at the solid-liquid interface using a recyclable photosensitized reduction process. Physical chemistry chemical physics : PCCP, 12(2), 365-72. https://doi.org/10.1039/b917981j
Sakamoto, Masanori, et al. "Photochemical fabrication of silver nanostructures at the solid-liquid interface using a recyclable photosensitized reduction process." Physical chemistry chemical physics : PCCP vol. 12,2 (2010): 365-72. doi: https://doi.org/10.1039/b917981j
Sakamoto M, Kim SS, Furusho H, Majima T. Photochemical fabrication of silver nanostructures at the solid-liquid interface using a recyclable photosensitized reduction process. Phys Chem Chem Phys. 2010 Jan 14;12(2):365-72. doi: 10.1039/b917981j. Epub 2009 Nov 11. PMID: 20023814.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 166 entries