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Showing 1 to 12 of 171 entries
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Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor.

Neuron

Murakoshi H, Shin ME, Parra-Bueno P, Szatmari EM, Shibata ACE, Yasuda R.
PMID: 28472663
Neuron. 2017 May 03;94(3):690. doi: 10.1016/j.neuron.2017.04.027.

No abstract available.

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Murakoshi H, Shin ME, Parra-Bueno P, et al. Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor. Neuron. 2017;94(3):690doi: 10.1016/j.neuron.2017.04.027.
Murakoshi, H., Shin, M. E., Parra-Bueno, P., Szatmari, E. M., Shibata, A. C. E., & Yasuda, R. (2017). Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor. Neuron, 94(3), 690. https://doi.org/10.1016/j.neuron.2017.04.027
Murakoshi, Hideji, et al. "Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor." Neuron vol. 94,3 (2017): 690. doi: https://doi.org/10.1016/j.neuron.2017.04.027
Murakoshi H, Shin ME, Parra-Bueno P, Szatmari EM, Shibata ACE, Yasuda R. Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor. Neuron. 2017 May 03;94(3):690. doi: 10.1016/j.neuron.2017.04.027. PMID: 28472663.
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A simplified and efficient .

3 Biotech

Kámán-Tóth E, Pogány M, Dankó T, Szatmári Á, Bozsó Z.
PMID: 29487777
3 Biotech. 2018 Mar;8(3):148. doi: 10.1007/s13205-018-1171-9. Epub 2018 Feb 22.

No abstract available.

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Kámán-Tóth E, Pogány M, Dankó T, et al. A simplified and efficient . 3 Biotech. 2018;8(3):148doi: 10.1007/s13205-018-1171-9.
Kámán-Tóth, E., Pogány, M., Dankó, T., Szatmári, �. �., & Bozsó, Z. (2018). A simplified and efficient . 3 Biotech, 8(3), 148. https://doi.org/10.1007/s13205-018-1171-9
Kámán-Tóth, Evelin, et al. "A simplified and efficient ." 3 Biotech vol. 8,3 (2018): 148. doi: https://doi.org/10.1007/s13205-018-1171-9
Kámán-Tóth E, Pogány M, Dankó T, Szatmári Á, Bozsó Z. A simplified and efficient . 3 Biotech. 2018 Mar;8(3):148. doi: 10.1007/s13205-018-1171-9. Epub 2018 Feb 22. PMID: 29487777; PMCID: PMC5821610.
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NT-proBNP correlated with strain and strain rate imaging of the right ventricle before and after transcatheter closure of atrial septal defects.

Journal of the Saudi Heart Association

Elsheikh RG, Hegab M, Szatmari A.
PMID: 24174839
J Saudi Heart Assoc. 2013 Jan;25(1):3-8. doi: 10.1016/j.jsha.2012.08.003. Epub 2012 Oct 13.

BACKGROUND: Atrial septal defects (ASD) account for 10% of all congenital heart lesions and represent the third most congenital cardiac defect seen in adults.OBJECTIVES: Using strain and strain rate imaging (SRI) to assess right ventricular (RV) function in patients...

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Elsheikh RG, Hegab M, Szatmari A. NT-proBNP correlated with strain and strain rate imaging of the right ventricle before and after transcatheter closure of atrial septal defects. J Saudi Heart Assoc. 2012;25(1):3-8doi: 10.1016/j.jsha.2012.08.003.
Elsheikh, R. G., Hegab, M., & Szatmari, A. (2013). NT-proBNP correlated with strain and strain rate imaging of the right ventricle before and after transcatheter closure of atrial septal defects. Journal of the Saudi Heart Association, 25(1), 3-8. https://doi.org/10.1016/j.jsha.2012.08.003
Elsheikh, Raghda Ghonimy, et al. "NT-proBNP correlated with strain and strain rate imaging of the right ventricle before and after transcatheter closure of atrial septal defects." Journal of the Saudi Heart Association vol. 25,1 (2013): 3-8. doi: https://doi.org/10.1016/j.jsha.2012.08.003
Elsheikh RG, Hegab M, Szatmari A. NT-proBNP correlated with strain and strain rate imaging of the right ventricle before and after transcatheter closure of atrial septal defects. J Saudi Heart Assoc. 2013 Jan;25(1):3-8. doi: 10.1016/j.jsha.2012.08.003. Epub 2012 Oct 13. PMID: 24174839; PMCID: PMC3809479.
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Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents.

Evidence-based mental health

Boylan K, Szatmari P.
PMID: 17652571
Evid Based Ment Health. 2007 Aug;10(3):89. doi: 10.1136/ebmh.10.3.89.

No abstract available.

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Boylan K, Szatmari P. Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents. Evid Based Ment Health. 2007;10(3):89doi: 10.1136/ebmh.10.3.89.
Boylan, K., & Szatmari, P. (2007). Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents. Evidence-based mental health, 10(3), 89. https://doi.org/10.1136/ebmh.10.3.89
Boylan, Khrista, and Szatmari, Peter. "Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents." Evidence-based mental health vol. 10,3 (2007): 89. doi: https://doi.org/10.1136/ebmh.10.3.89
Boylan K, Szatmari P. Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents. Evid Based Ment Health. 2007 Aug;10(3):89. doi: 10.1136/ebmh.10.3.89. PMID: 17652571.
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Two-step preionization scheme for discharge pumped KrF excimer lasers.

The Review of scientific instruments

Szatmári S, Janicskó J, Bohus J.
PMID: 17411233
Rev Sci Instrum. 2007 Mar;78(3):036108. doi: 10.1063/1.2715879.

The beam homogeneity and stored energy of discharge pumped KrF excimer amplifiers are critically dependent on the preionization level of the active medium and on the rise time of the electric excitation pulse. Here a scheme is presented to...

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Szatmári S, Janicskó J, Bohus J. Two-step preionization scheme for discharge pumped KrF excimer lasers. Rev Sci Instrum. 2007;78(3):036108doi: 10.1063/1.2715879.
Szatmári, S., Janicskó, J., & Bohus, J. (2007). Two-step preionization scheme for discharge pumped KrF excimer lasers. The Review of scientific instruments, 78(3), 036108. https://doi.org/10.1063/1.2715879
Szatmári, S, et al. "Two-step preionization scheme for discharge pumped KrF excimer lasers." The Review of scientific instruments vol. 78,3 (2007): 036108. doi: https://doi.org/10.1063/1.2715879
Szatmári S, Janicskó J, Bohus J. Two-step preionization scheme for discharge pumped KrF excimer lasers. Rev Sci Instrum. 2007 Mar;78(3):036108. doi: 10.1063/1.2715879. PMID: 17411233.
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High-performance liquid chromatographic enantioseparation of 1-(aminoalkyl)-2-naphthol analogs on polysaccharide-based chiral stationary phases.

Chirality

Sztojkov-Ivanov A, Tóth D, Szatmári I, Fülöp F, Péter A.
PMID: 17380485
Chirality. 2007 May 15;19(5):374-9. doi: 10.1002/chir.20392.

The enantiomers of various 1-(alpha-aminobenzyl)-2-naphthol and 1-(aminoalkyl)-2-naphthol analogs were separated on cellulose-tris-3,5-dimethylphenyl carbamate-based chiral stationary phases (Chiralcel OD-H and Chiralcel OD-RH), using n-hexane/2-propanol/diethylamine or phosphate buffer/organic modifier mobile phases. The 3,5-dimethylphenyl carbamoylated cellulose columns were effective in both normal...

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Sztojkov-Ivanov A, Tóth D, Szatmári I, et al. High-performance liquid chromatographic enantioseparation of 1-(aminoalkyl)-2-naphthol analogs on polysaccharide-based chiral stationary phases. Chirality. 2007;19(5):374-9doi: 10.1002/chir.20392.
Sztojkov-Ivanov, A., Tóth, D., Szatmári, I., Fülöp, F., & Péter, A. (2007). High-performance liquid chromatographic enantioseparation of 1-(aminoalkyl)-2-naphthol analogs on polysaccharide-based chiral stationary phases. Chirality, 19(5), 374-9. https://doi.org/10.1002/chir.20392
Sztojkov-Ivanov, Anita, et al. "High-performance liquid chromatographic enantioseparation of 1-(aminoalkyl)-2-naphthol analogs on polysaccharide-based chiral stationary phases." Chirality vol. 19,5 (2007): 374-9. doi: https://doi.org/10.1002/chir.20392
Sztojkov-Ivanov A, Tóth D, Szatmári I, Fülöp F, Péter A. High-performance liquid chromatographic enantioseparation of 1-(aminoalkyl)-2-naphthol analogs on polysaccharide-based chiral stationary phases. Chirality. 2007 May 15;19(5):374-9. doi: 10.1002/chir.20392. PMID: 17380485.
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Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.

Journal of neurodevelopmental disorders

Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P.
PMID: 21484201
J Neurodev Disord. 2011 Jun;3(2):113-23. doi: 10.1007/s11689-011-9072-9. Epub 2011 Jan 19.

The Autism Genome Project has assembled two large datasets originally designed for linkage analysis and genome-wide association analysis, respectively: 1,069 multiplex families genotyped on the Affymetrix 10 K platform, and 1,129 autism trios genotyped on the Illumina 1 M...

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Vieland VJ, Hallmayer J, Huang Y, et al. Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. J Neurodev Disord. 2011;3(2):113-23doi: 10.1007/s11689-011-9072-9.
Vieland, V. J., Hallmayer, J., Huang, Y., Pagnamenta, A. T., Pinto, D., Khan, H., Monaco, A. P., Paterson, A. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P. (2011). Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of neurodevelopmental disorders, 3(2), 113-23. https://doi.org/10.1007/s11689-011-9072-9
Vieland, Veronica J, et al. "Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism." Journal of neurodevelopmental disorders vol. 3,2 (2011): 113-23. doi: https://doi.org/10.1007/s11689-011-9072-9
Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P. Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. J Neurodev Disord. 2011 Jun;3(2):113-23. doi: 10.1007/s11689-011-9072-9. Epub 2011 Jan 19. PMID: 21484201; PMCID: PMC3105232.
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Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions.

Frontiers in psychiatry

Ameis SH, Szatmari P.
PMID: 22615702
Front Psychiatry. 2012 May 15;3:46. doi: 10.3389/fpsyt.2012.00046. eCollection 2012.

Autism Spectrum Disorder (ASD) refers to a group of heterogeneous neurodevelopmental disorders that are unified by impairments in reciprocal social communication and a pattern of inflexible behaviors. Recent genetic advances have resolved some of the complexity of the genetic...

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Ameis SH, Szatmari P. Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions. Front Psychiatry. 2012;3:46doi: 10.3389/fpsyt.2012.00046.
Ameis, S. H., & Szatmari, P. (2012). Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions. Frontiers in psychiatry, 346. https://doi.org/10.3389/fpsyt.2012.00046
Ameis, Stephanie H, and Szatmari, Peter. "Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions." Frontiers in psychiatry vol. 3 (2012): 46. doi: https://doi.org/10.3389/fpsyt.2012.00046
Ameis SH, Szatmari P. Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions. Front Psychiatry. 2012 May 15;3:46. doi: 10.3389/fpsyt.2012.00046. eCollection 2012. PMID: 22615702; PMCID: PMC3351673.
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A molecular genetic study of autism and related phenotypes in extended pedigrees.

Journal of neurodevelopmental disorders

Piven J, Vieland VJ, Parlier M, Thompson A, O'Conner I, Woodbury-Smith M, Huang Y, Walters KA, Fernandez B, Szatmari P.
PMID: 24093601
J Neurodev Disord. 2013 Oct 05;5(1):30. doi: 10.1186/1866-1955-5-30.

BACKGROUND: Efforts to uncover the risk genotypes associated with the familial nature of autism spectrum disorder (ASD) have had limited success. The study of extended pedigrees, incorporating additional ASD-related phenotypes into linkage analysis, offers an alternative approach to the...

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Piven J, Vieland VJ, Parlier M, et al. A molecular genetic study of autism and related phenotypes in extended pedigrees. J Neurodev Disord. 2013;5(1):30doi: 10.1186/1866-1955-5-30.
Piven, J., Vieland, V. J., Parlier, M., Thompson, A., O'Conner, I., Woodbury-Smith, M., Huang, Y., Walters, K. A., Fernandez, B., & Szatmari, P. (2013). A molecular genetic study of autism and related phenotypes in extended pedigrees. Journal of neurodevelopmental disorders, 5(1), 30. https://doi.org/10.1186/1866-1955-5-30
Piven, Joseph, et al. "A molecular genetic study of autism and related phenotypes in extended pedigrees." Journal of neurodevelopmental disorders vol. 5,1 (2013): 30. doi: https://doi.org/10.1186/1866-1955-5-30
Piven J, Vieland VJ, Parlier M, Thompson A, O'Conner I, Woodbury-Smith M, Huang Y, Walters KA, Fernandez B, Szatmari P. A molecular genetic study of autism and related phenotypes in extended pedigrees. J Neurodev Disord. 2013 Oct 05;5(1):30. doi: 10.1186/1866-1955-5-30. PMID: 24093601; PMCID: PMC3851306.
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Cutaneous Autonomic Pilomotor Testing to Unveil the Role of Neuropathy Progression in Early Parkinson's Disease (CAPTURE PD): Protocol for a Multicenter Study.

Frontiers in neurology

Siepmann T, Pintér A, Buchmann SJ, Stibal L, Arndt M, Kubasch AS, Kubasch ML, Penzlin AI, Frenz E, Zago W, Horváth T, Szatmári S, Bereczki D, Takáts A, Ziemssen T, Lipp A, Freeman R, Reichmann H, Barlinn K, Illigens BM.
PMID: 28603514
Front Neurol. 2017 May 26;8:212. doi: 10.3389/fneur.2017.00212. eCollection 2017.

BACKGROUND: In Parkinson's disease (PD), alpha-synuclein accumulation in cutaneous autonomic pilomotor and sudomotor nerve fibers has been linked to autonomic nervous system disturbances even in the early stages of the disease. This study aims to assess the association between...

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Siepmann T, Pintér A, Buchmann SJ, et al. Cutaneous Autonomic Pilomotor Testing to Unveil the Role of Neuropathy Progression in Early Parkinson's Disease (CAPTURE PD): Protocol for a Multicenter Study. Front Neurol. 2017;8:212doi: 10.3389/fneur.2017.00212.
Siepmann, T., Pintér, A., Buchmann, S. J., Stibal, L., Arndt, M., Kubasch, A. S., Kubasch, M. L., Penzlin, A. I., Frenz, E., Zago, W., Horváth, T., Szatmári, S., Bereczki, D., Takáts, A., Ziemssen, T., Lipp, A., Freeman, R., Reichmann, H., Barlinn, K., & Illigens, B. M. (2017). Cutaneous Autonomic Pilomotor Testing to Unveil the Role of Neuropathy Progression in Early Parkinson's Disease (CAPTURE PD): Protocol for a Multicenter Study. Frontiers in neurology, 8212. https://doi.org/10.3389/fneur.2017.00212
Siepmann, Timo, et al. "Cutaneous Autonomic Pilomotor Testing to Unveil the Role of Neuropathy Progression in Early Parkinson's Disease (CAPTURE PD): Protocol for a Multicenter Study." Frontiers in neurology vol. 8 (2017): 212. doi: https://doi.org/10.3389/fneur.2017.00212
Siepmann T, Pintér A, Buchmann SJ, Stibal L, Arndt M, Kubasch AS, Kubasch ML, Penzlin AI, Frenz E, Zago W, Horváth T, Szatmári S, Bereczki D, Takáts A, Ziemssen T, Lipp A, Freeman R, Reichmann H, Barlinn K, Illigens BM. Cutaneous Autonomic Pilomotor Testing to Unveil the Role of Neuropathy Progression in Early Parkinson's Disease (CAPTURE PD): Protocol for a Multicenter Study. Front Neurol. 2017 May 26;8:212. doi: 10.3389/fneur.2017.00212. eCollection 2017. PMID: 28603514; PMCID: PMC5445122.
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Xer Site Specific Recombination: Double and Single Recombinase Systems.

Frontiers in microbiology

Castillo F, Benmohamed A, Szatmari G.
PMID: 28373867
Front Microbiol. 2017 Mar 20;8:453. doi: 10.3389/fmicb.2017.00453. eCollection 2017.

The separation and segregation of newly replicated bacterial chromosomes can be constrained by the formation of circular chromosome dimers caused by crossing over during homologous recombination events. In

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Castillo F, Benmohamed A, Szatmari G. Xer Site Specific Recombination: Double and Single Recombinase Systems. Front Microbiol. 2017;8:453doi: 10.3389/fmicb.2017.00453.
Castillo, F., Benmohamed, A., & Szatmari, G. (2017). Xer Site Specific Recombination: Double and Single Recombinase Systems. Frontiers in microbiology, 8453. https://doi.org/10.3389/fmicb.2017.00453
Castillo, Fabio, et al. "Xer Site Specific Recombination: Double and Single Recombinase Systems." Frontiers in microbiology vol. 8 (2017): 453. doi: https://doi.org/10.3389/fmicb.2017.00453
Castillo F, Benmohamed A, Szatmari G. Xer Site Specific Recombination: Double and Single Recombinase Systems. Front Microbiol. 2017 Mar 20;8:453. doi: 10.3389/fmicb.2017.00453. eCollection 2017. PMID: 28373867; PMCID: PMC5357621.
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Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies.

BMC medicine

Stein DJ, Szatmari P, Gaebel W, Berk M, Vieta E, Maj M, de Vries YA, Roest AM, de Jonge P, Maercker A, Brewin CR, Pike KM, Grilo CM, Fineberg NA, Briken P, Cohen-Kettenis PT, Reed GM.
PMID: 31983345
BMC Med. 2020 Jan 27;18(1):21. doi: 10.1186/s12916-020-1495-2.

An update of the chapter on Mental, Behavioral and Neurodevelopmental Disorders in the International Classification of Diseases and Related Health Problems (ICD) is of great interest around the world. The recent approval of the 11th Revision of the ICD...

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Stein DJ, Szatmari P, Gaebel W, et al. Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies. BMC Med. 2020;18(1):21doi: 10.1186/s12916-020-1495-2.
Stein, D. J., Szatmari, P., Gaebel, W., Berk, M., Vieta, E., Maj, M., de Vries, Y. A., Roest, A. M., de Jonge, P., Maercker, A., Brewin, C. R., Pike, K. M., Grilo, C. M., Fineberg, N. A., Briken, P., Cohen-Kettenis, P. T., & Reed, G. M. (2020). Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies. BMC medicine, 18(1), 21. https://doi.org/10.1186/s12916-020-1495-2
Stein, Dan J, et al. "Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies." BMC medicine vol. 18,1 (2020): 21. doi: https://doi.org/10.1186/s12916-020-1495-2
Stein DJ, Szatmari P, Gaebel W, Berk M, Vieta E, Maj M, de Vries YA, Roest AM, de Jonge P, Maercker A, Brewin CR, Pike KM, Grilo CM, Fineberg NA, Briken P, Cohen-Kettenis PT, Reed GM. Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies. BMC Med. 2020 Jan 27;18(1):21. doi: 10.1186/s12916-020-1495-2. PMID: 31983345; PMCID: PMC6983973.
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Showing 1 to 12 of 171 entries