Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 541 entries
Sorted by: Best Match Show Resources per page
Treatment for Acquired Apraxia of Speech: A Systematic Review of Intervention Research Between 2004 and 2012.

American journal of speech-language pathology

Ballard KJ, Wambaugh JL, Duffy JR, Layfield C, Maas E, Mauszycki S, McNeil MR.
PMID: 25815778
Am J Speech Lang Pathol. 2015 May 01;24(2):316-337. doi: 10.1044/2015_AJSLP-14-0118.

OBJECTIVES: The aim was for the appointed committee of the Academy of Neurological Communication Disorders and Sciences to conduct a systematic review of published intervention studies of acquired apraxia of speech (AOS), updating the previous committee's review article from...

Cite
Ballard KJ, Wambaugh JL, Duffy JR, et al. Treatment for Acquired Apraxia of Speech: A Systematic Review of Intervention Research Between 2004 and 2012. Am J Speech Lang Pathol. 2015;24(2):316-337doi: 10.1044/2015_AJSLP-14-0118.
Ballard, K. J., Wambaugh, J. L., Duffy, J. R., Layfield, C., Maas, E., Mauszycki, S., & McNeil, M. R. (2015). Treatment for Acquired Apraxia of Speech: A Systematic Review of Intervention Research Between 2004 and 2012. American journal of speech-language pathology, 24(2), 316-337. https://doi.org/10.1044/2015_AJSLP-14-0118
Ballard, Kirrie J, et al. "Treatment for Acquired Apraxia of Speech: A Systematic Review of Intervention Research Between 2004 and 2012." American journal of speech-language pathology vol. 24,2 (2015): 316-337. doi: https://doi.org/10.1044/2015_AJSLP-14-0118
Ballard KJ, Wambaugh JL, Duffy JR, Layfield C, Maas E, Mauszycki S, McNeil MR. Treatment for Acquired Apraxia of Speech: A Systematic Review of Intervention Research Between 2004 and 2012. Am J Speech Lang Pathol. 2015 May 01;24(2):316-337. doi: 10.1044/2015_AJSLP-14-0118. PMID: 25815778.
Copy Download .nbib Format: NLM
Dysprosium electrodeposition from a hexaalkylguanidinium-based ionic liquid.

Nanoscale

Berger CA, Arkhipova M, Maas G, Jacob T.
PMID: 27121463
Nanoscale. 2016 Aug 07;8(29):13997-4003. doi: 10.1039/c6nr01351a. Epub 2016 Apr 28.

The rare-earth element dysprosium (Dy) is an important additive that increases the magnetocrystalline anisotropy of neodymium magnets and additionally prevents from demagnetizing at high temperatures. Therefore, it is one of the most important elements for high-tech industries and is...

Cite
Berger CA, Arkhipova M, Maas G, et al. Dysprosium electrodeposition from a hexaalkylguanidinium-based ionic liquid. Nanoscale. 2016;8(29):13997-4003doi: 10.1039/c6nr01351a.
Berger, C. A., Arkhipova, M., Maas, G., & Jacob, T. (2016). Dysprosium electrodeposition from a hexaalkylguanidinium-based ionic liquid. Nanoscale, 8(29), 13997-4003. https://doi.org/10.1039/c6nr01351a
Berger, Claudia A, et al. "Dysprosium electrodeposition from a hexaalkylguanidinium-based ionic liquid." Nanoscale vol. 8,29 (2016): 13997-4003. doi: https://doi.org/10.1039/c6nr01351a
Berger CA, Arkhipova M, Maas G, Jacob T. Dysprosium electrodeposition from a hexaalkylguanidinium-based ionic liquid. Nanoscale. 2016 Aug 07;8(29):13997-4003. doi: 10.1039/c6nr01351a. Epub 2016 Apr 28. PMID: 27121463.
Copy Download .nbib Format: NLM
Processing of Factor XII during Inflammatory Reactions.

Frontiers in medicine

Jukema BN, de Maat S, Maas C.
PMID: 27867935
Front Med (Lausanne). 2016 Nov 04;3:52. doi: 10.3389/fmed.2016.00052. eCollection 2016.

The contact system was originally identified as an obsolete part of the coagulation system, but it has been repeatedly implicated in inflammatory states, such as infection, as well as in allergic- and chronic inflammatory disease. Under these conditions, there...

Cite
Jukema BN, de Maat S, Maas C. Processing of Factor XII during Inflammatory Reactions. Front Med (Lausanne). 2016;3:52doi: 10.3389/fmed.2016.00052.
Jukema, B. N., de Maat, S., & Maas, C. (2016). Processing of Factor XII during Inflammatory Reactions. Frontiers in medicine, 352. https://doi.org/10.3389/fmed.2016.00052
Jukema, Bernard Nico, et al. "Processing of Factor XII during Inflammatory Reactions." Frontiers in medicine vol. 3 (2016): 52. doi: https://doi.org/10.3389/fmed.2016.00052
Jukema BN, de Maat S, Maas C. Processing of Factor XII during Inflammatory Reactions. Front Med (Lausanne). 2016 Nov 04;3:52. doi: 10.3389/fmed.2016.00052. eCollection 2016. PMID: 27867935; PMCID: PMC5095611.
Copy Download .nbib Format: NLM
Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands.

Infection ecology & epidemiology

Swart A, Bekker DL, Maas M, de Vries A, Pijnacker R, Reusken CBEM, van der Giessen JWB.
PMID: 28567209
Infect Ecol Epidemiol. 2017 Mar 24;7(1):1287986. doi: 10.1080/20008686.2017.1287986. eCollection 2017.

This paper deals with modelling the relationship between human Puumala hantavirus (PUUV) infection, the abundance and prevalence of infection of the host (the bank vole), mast, and temperature. These data were used to build and parametrise generalised regression models,...

Cite
Swart A, Bekker DL, Maas M, et al. Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infect Ecol Epidemiol. 2017;7(1):1287986doi: 10.1080/20008686.2017.1287986.
Swart, A., Bekker, D. L., Maas, M., de Vries, A., Pijnacker, R., Reusken, C. B. E. M., & van der Giessen, J. W. B. (2017). Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infection ecology & epidemiology, 7(1), 1287986. https://doi.org/10.1080/20008686.2017.1287986
Swart, Arno, et al. "Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands." Infection ecology & epidemiology vol. 7,1 (2017): 1287986. doi: https://doi.org/10.1080/20008686.2017.1287986
Swart A, Bekker DL, Maas M, de Vries A, Pijnacker R, Reusken CBEM, van der Giessen JWB. Modelling human Puumala hantavirus infection in relation to bank vole abundance and masting intensity in the Netherlands. Infect Ecol Epidemiol. 2017 Mar 24;7(1):1287986. doi: 10.1080/20008686.2017.1287986. eCollection 2017. PMID: 28567209; PMCID: PMC5443058.
Copy Download .nbib Format: NLM
Can a Clinical Examination Demonstrate Intramuscular Tendon Involvement in Acute Hamstring Injuries?.

Orthopaedic journal of sports medicine

Crema MD, Guermazi A, Reurink G, Roemer FW, Maas M, Weir A, Moen MH, Goudswaard GJ, Tol JL.
PMID: 29124077
Orthop J Sports Med. 2017 Oct 26;5(10):2325967117733434. doi: 10.1177/2325967117733434. eCollection 2017 Oct.

BACKGROUND: Involvement of the intramuscular (central) tendon in acute hamstring injuries, as detected on magnetic resonance imaging (MRI), may prolong recovery times. To date, it is unclear whether hamstring injuries exhibiting intramuscular tendon involvement can be identified though routine...

Cite
Crema MD, Guermazi A, Reurink G, et al. Can a Clinical Examination Demonstrate Intramuscular Tendon Involvement in Acute Hamstring Injuries?. Orthop J Sports Med. 2017;5(10):2325967117733434doi: 10.1177/2325967117733434.
Crema, M. D., Guermazi, A., Reurink, G., Roemer, F. W., Maas, M., Weir, A., Moen, M. H., Goudswaard, G. J., & Tol, J. L. (2017). Can a Clinical Examination Demonstrate Intramuscular Tendon Involvement in Acute Hamstring Injuries?. Orthopaedic journal of sports medicine, 5(10), 2325967117733434. https://doi.org/10.1177/2325967117733434
Crema, Michel D, et al. "Can a Clinical Examination Demonstrate Intramuscular Tendon Involvement in Acute Hamstring Injuries?." Orthopaedic journal of sports medicine vol. 5,10 (2017): 2325967117733434. doi: https://doi.org/10.1177/2325967117733434
Crema MD, Guermazi A, Reurink G, Roemer FW, Maas M, Weir A, Moen MH, Goudswaard GJ, Tol JL. Can a Clinical Examination Demonstrate Intramuscular Tendon Involvement in Acute Hamstring Injuries?. Orthop J Sports Med. 2017 Oct 26;5(10):2325967117733434. doi: 10.1177/2325967117733434. eCollection 2017 Oct. PMID: 29124077; PMCID: PMC5661687.
Copy Download .nbib Format: NLM
Erratum to: Evaluation of mesenchymal stem cells in treatment of infertility in male rats.

Stem cell research & therapy

Hassan AI, Alam SS.
PMID: 28183361
Stem Cell Res Ther. 2017 Feb 09;8(1):32. doi: 10.1186/s13287-017-0490-9.

No abstract available.

Cite
Hassan AI, Alam SS. Erratum to: Evaluation of mesenchymal stem cells in treatment of infertility in male rats. Stem Cell Res Ther. 2017;8(1):32doi: 10.1186/s13287-017-0490-9.
Hassan, A. I., & Alam, S. S. (2017). Erratum to: Evaluation of mesenchymal stem cells in treatment of infertility in male rats. Stem cell research & therapy, 8(1), 32. https://doi.org/10.1186/s13287-017-0490-9
Hassan, Amal I, and Alam, Sally S. "Erratum to: Evaluation of mesenchymal stem cells in treatment of infertility in male rats." Stem cell research & therapy vol. 8,1 (2017): 32. doi: https://doi.org/10.1186/s13287-017-0490-9
Hassan AI, Alam SS. Erratum to: Evaluation of mesenchymal stem cells in treatment of infertility in male rats. Stem Cell Res Ther. 2017 Feb 09;8(1):32. doi: 10.1186/s13287-017-0490-9. PMID: 28183361; PMCID: PMC5301354.
Copy Download .nbib Format: NLM
Integrating carbon nanotubes into silicon by means of vertical carbon nanotube field-effect transistors.

Nanoscale

Li J, Wang Q, Yue W, Guo Z, Li L, Zhao C, Wang X, Abutaha AI, Alshareef HN, Zhang Y, Zhang XX.
PMID: 24965261
Nanoscale. 2014 Aug 07;6(15):8956-61. doi: 10.1039/c4nr00978a.

Single-walled carbon nanotubes have been integrated into silicon for use in vertical carbon nanotube field-effect transistors (CNTFETs). A unique feature of these devices is that a silicon substrate and a metal contact are used as the source and drain...

Cite
Li J, Wang Q, Yue W, et al. Integrating carbon nanotubes into silicon by means of vertical carbon nanotube field-effect transistors. Nanoscale. 2014;6(15):8956-61doi: 10.1039/c4nr00978a.
Li, J., Wang, Q., Yue, W., Guo, Z., Li, L., Zhao, C., Wang, X., Abutaha, A. I., Alshareef, H. N., Zhang, Y., & Zhang, X. X. (2014). Integrating carbon nanotubes into silicon by means of vertical carbon nanotube field-effect transistors. Nanoscale, 6(15), 8956-61. https://doi.org/10.1039/c4nr00978a
Li, Jingqi, et al. "Integrating carbon nanotubes into silicon by means of vertical carbon nanotube field-effect transistors." Nanoscale vol. 6,15 (2014): 8956-61. doi: https://doi.org/10.1039/c4nr00978a
Li J, Wang Q, Yue W, Guo Z, Li L, Zhao C, Wang X, Abutaha AI, Alshareef HN, Zhang Y, Zhang XX. Integrating carbon nanotubes into silicon by means of vertical carbon nanotube field-effect transistors. Nanoscale. 2014 Aug 07;6(15):8956-61. doi: 10.1039/c4nr00978a. PMID: 24965261.
Copy Download .nbib Format: NLM
Derivatives of the triaminoguanidinium ion, 3. Multiple N-functionalization of the triaminoguanidinium ion with isocyanates and isothiocyanates.

Beilstein journal of organic chemistry

Szabo J, Karger K, Bucher N, Maas G.
PMID: 25298792
Beilstein J Org Chem. 2014 Sep 24;10:2255-62. doi: 10.3762/bjoc.10.234. eCollection 2014.

1,2,3-Triaminoguanidinium chloride was combined with benzaldehyde and hydratropic aldehyde to furnish the corresponding tris(imines), which were converted into 1,2,3-tris(benzylamino)guanidinium salts by catalytic hydrogenation in the former, and by borane reduction in the latter case. The resulting alkyl-substituted triaminoguanidinium salts...

Cite
Szabo J, Karger K, Bucher N, et al. Derivatives of the triaminoguanidinium ion, 3. Multiple N-functionalization of the triaminoguanidinium ion with isocyanates and isothiocyanates. Beilstein J Org Chem. 2014;10:2255-62doi: 10.3762/bjoc.10.234.
Szabo, J., Karger, K., Bucher, N., & Maas, G. (2014). Derivatives of the triaminoguanidinium ion, 3. Multiple N-functionalization of the triaminoguanidinium ion with isocyanates and isothiocyanates. Beilstein journal of organic chemistry, 102255-62. https://doi.org/10.3762/bjoc.10.234
Szabo, Jan, et al. "Derivatives of the triaminoguanidinium ion, 3. Multiple N-functionalization of the triaminoguanidinium ion with isocyanates and isothiocyanates." Beilstein journal of organic chemistry vol. 10 (2014): 2255-62. doi: https://doi.org/10.3762/bjoc.10.234
Szabo J, Karger K, Bucher N, Maas G. Derivatives of the triaminoguanidinium ion, 3. Multiple N-functionalization of the triaminoguanidinium ion with isocyanates and isothiocyanates. Beilstein J Org Chem. 2014 Sep 24;10:2255-62. doi: 10.3762/bjoc.10.234. eCollection 2014. PMID: 25298792; PMCID: PMC4187099.
Copy Download .nbib Format: NLM
Evaluation of a post-processing approach for multiscale analysis of biphasic mechanics of chondrocytes, DOI: 10.1080/10255842.2013.809711.

Computer methods in biomechanics and biomedical engineering

Sibole SC, Maas S, Halloran JP, Weiss JA, Erdemir A.
PMID: 24383709
Comput Methods Biomech Biomed Engin. 2016;19(1):ii. doi: 10.1080/10255842.2013.869043. Epub 2014 Jan 02.

No abstract available.

Cite
Sibole SC, Maas S, Halloran JP, et al. Evaluation of a post-processing approach for multiscale analysis of biphasic mechanics of chondrocytes, DOI: 10.1080/10255842.2013.809711. Comput Methods Biomech Biomed Engin. 2014;19(1):iidoi: 10.1080/10255842.2013.869043.
Sibole, S. C., Maas, S., Halloran, J. P., Weiss, J. A., & Erdemir, A. (2016). Evaluation of a post-processing approach for multiscale analysis of biphasic mechanics of chondrocytes, DOI: 10.1080/10255842.2013.809711. Computer methods in biomechanics and biomedical engineering, 19(1), ii. https://doi.org/10.1080/10255842.2013.869043
Sibole, Scott C, et al. "Evaluation of a post-processing approach for multiscale analysis of biphasic mechanics of chondrocytes, DOI: 10.1080/10255842.2013.809711." Computer methods in biomechanics and biomedical engineering vol. 19,1 (2016): ii. doi: https://doi.org/10.1080/10255842.2013.869043
Sibole SC, Maas S, Halloran JP, Weiss JA, Erdemir A. Evaluation of a post-processing approach for multiscale analysis of biphasic mechanics of chondrocytes, DOI: 10.1080/10255842.2013.809711. Comput Methods Biomech Biomed Engin. 2016;19(1):ii. doi: 10.1080/10255842.2013.869043. Epub 2014 Jan 02. PMID: 24383709.
Copy Download .nbib Format: NLM
Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP.

ACS medicinal chemistry letters

Sandham DA, Barker L, Brown L, Brown Z, Budd D, Charlton SJ, Chatterjee D, Cox B, Dubois G, Duggan N, Hall E, Hatto J, Maas J, Manini J, Profit R, Riddy D, Ritchie C, Sohal B, Shaw D, Stringer R, Sykes DA, Thomas M, Turner KL, Watson SJ, West R, Willard E, Williams G, Willis J.
PMID: 28523115
ACS Med Chem Lett. 2017 Apr 25;8(5):582-586. doi: 10.1021/acsmedchemlett.7b00157. eCollection 2017 May 11.

Further optimization of an initial DP

Cite
Sandham DA, Barker L, Brown L, et al. Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP. ACS Med Chem Lett. 2017;8(5):582-586doi: 10.1021/acsmedchemlett.7b00157.
Sandham, D. A., Barker, L., Brown, L., Brown, Z., Budd, D., Charlton, S. J., Chatterjee, D., Cox, B., Dubois, G., Duggan, N., Hall, E., Hatto, J., Maas, J., Manini, J., Profit, R., Riddy, D., Ritchie, C., Sohal, B., Shaw, D., Stringer, R., Sykes, D. A., Thomas, M., Turner, K. L., Watson, S. J., West, R., Willard, E., Williams, G., & Willis, J. (2017). Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP. ACS medicinal chemistry letters, 8(5), 582-586. https://doi.org/10.1021/acsmedchemlett.7b00157
Sandham, David A, et al. "Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP." ACS medicinal chemistry letters vol. 8,5 (2017): 582-586. doi: https://doi.org/10.1021/acsmedchemlett.7b00157
Sandham DA, Barker L, Brown L, Brown Z, Budd D, Charlton SJ, Chatterjee D, Cox B, Dubois G, Duggan N, Hall E, Hatto J, Maas J, Manini J, Profit R, Riddy D, Ritchie C, Sohal B, Shaw D, Stringer R, Sykes DA, Thomas M, Turner KL, Watson SJ, West R, Willard E, Williams G, Willis J. Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP. ACS Med Chem Lett. 2017 Apr 25;8(5):582-586. doi: 10.1021/acsmedchemlett.7b00157. eCollection 2017 May 11. PMID: 28523115; PMCID: PMC5430394.
Copy Download .nbib Format: NLM
A New Approach to Evidence Synthesis in Traumatic Brain Injury: A Living Systematic Review.

Journal of neurotrauma

Synnot A, Gruen RL, Menon D, Steyerberg EW, Buki A, Peul WC, Elliott JH, Maas A.
PMID: 26414062
J Neurotrauma. 2021 Apr 15;38(8):1069-1071. doi: 10.1089/neu.2015.4124. Epub 2016 Aug 25.

Living systematic reviews (LSRs) are online summaries of health care research that are updated as new research becomes available. This new development in evidence synthesis is being trialled as part of the Collaborative European NeuroTrauma Effectiveness Research in Traumatic...

Cite
Synnot A, Gruen RL, Menon D, et al. A New Approach to Evidence Synthesis in Traumatic Brain Injury: A Living Systematic Review. J Neurotrauma. 2016;38(8):1069-1071doi: 10.1089/neu.2015.4124.
Synnot, A., Gruen, R. L., Menon, D., Steyerberg, E. W., Buki, A., Peul, W. C., Elliott, J. H., & Maas, A. (2021). A New Approach to Evidence Synthesis in Traumatic Brain Injury: A Living Systematic Review. Journal of neurotrauma, 38(8), 1069-1071. https://doi.org/10.1089/neu.2015.4124
Synnot, Anneliese, et al. "A New Approach to Evidence Synthesis in Traumatic Brain Injury: A Living Systematic Review." Journal of neurotrauma vol. 38,8 (2021): 1069-1071. doi: https://doi.org/10.1089/neu.2015.4124
Synnot A, Gruen RL, Menon D, Steyerberg EW, Buki A, Peul WC, Elliott JH, Maas A. A New Approach to Evidence Synthesis in Traumatic Brain Injury: A Living Systematic Review. J Neurotrauma. 2021 Apr 15;38(8):1069-1071. doi: 10.1089/neu.2015.4124. Epub 2016 Aug 25. PMID: 26414062; PMCID: PMC8054513.
Copy Download .nbib Format: NLM
Did diamond-bearing orangeites originate from MARID-veined peridotites in the lithospheric mantle?.

Nature communications

Giuliani A, Phillips D, Woodhead JD, Kamenetsky VS, Fiorentini ML, Maas R, Soltys A, Armstrong RA.
PMID: 25882074
Nat Commun. 2015 Apr 17;6:6837. doi: 10.1038/ncomms7837.

Kimberlites and orangeites (previously named Group-II kimberlites) are small-volume igneous rocks occurring in diatremes, sills and dykes. They are the main hosts for diamonds and are of scientific importance because they contain fragments of entrained mantle and crustal rocks,...

Cite
Giuliani A, Phillips D, Woodhead JD, et al. Did diamond-bearing orangeites originate from MARID-veined peridotites in the lithospheric mantle?. Nat Commun. 2015;6:6837doi: 10.1038/ncomms7837.
Giuliani, A., Phillips, D., Woodhead, J. D., Kamenetsky, V. S., Fiorentini, M. L., Maas, R., Soltys, A., & Armstrong, R. A. (2015). Did diamond-bearing orangeites originate from MARID-veined peridotites in the lithospheric mantle?. Nature communications, 66837. https://doi.org/10.1038/ncomms7837
Giuliani, Andrea, et al. "Did diamond-bearing orangeites originate from MARID-veined peridotites in the lithospheric mantle?." Nature communications vol. 6 (2015): 6837. doi: https://doi.org/10.1038/ncomms7837
Giuliani A, Phillips D, Woodhead JD, Kamenetsky VS, Fiorentini ML, Maas R, Soltys A, Armstrong RA. Did diamond-bearing orangeites originate from MARID-veined peridotites in the lithospheric mantle?. Nat Commun. 2015 Apr 17;6:6837. doi: 10.1038/ncomms7837. PMID: 25882074.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 541 entries