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Bibliografie tematiche / Meierei C

Letteratura scientifica selezionata sul tema "Meierei C"

Autore: Grafiati

Pubblicato: 26 luglio 2024

Ultima modifica: 28 luglio 2024

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Articoli di riviste sul tema "Meierei C"

1

Hinshaw, Robert. "Carl Alfred (C. A.) Meier: April 19, 1905 - November 15, 1995". San Francisco Jung Institute Library Journal 14, n. 4 (gennaio 1996): 77–78. http://dx.doi.org/10.1525/jung.1.1996.14.4.77.

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2

Ely, John J., Tony Zavaskis e M. Lon Lammey. "Censored Data Analysis Reveals Effects of Age and Hepatitis C Infection on C-Reactive Protein Levels in Healthy Adult Chimpanzees (Pan troglodytes)". Journal of Biomarkers 2013 (27 febbraio 2013): 1–13. http://dx.doi.org/10.1155/2013/709740.

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C-reactive protein, a conserved acute-phase protein synthesized in the liver and involved in inflammation, infection, and tissue damage, is an informative biomarker for human cardiovascular disease. Out of 258 captive adult common chimpanzees (Pan troglodytes) assayed for CRP, 27.9% of the data were below the quantitation limit. Data were analyzed by the Kaplan-Meier method and results compared to other methods for handling censored data (including deletion, replacement, and imputation). Kaplan-Meier results demonstrated a modest age effect and a strong effect of HCV infection in reducing CRP but did not allow inference of reference intervals. Results of other methods varied considerably. Substitution schemes differed widely in statistical significance, with estimated group means biased by the size of the substitution constant, while inference of unbiased reference intervals was impossible. Single imputation gave reasonable statistical inferences but unreliable reference intervals. Multiple imputation gave reliable results, for both statistical inference and reference intervals, and was comparable to the Kaplan-Meier standard. Other methods should be avoided. CRP did not predict cardiovascular disease, but CRP levels were reduced by 50% in animals with hepatitis C infection and showed inverse relationships with 2 liver function enzymes. Results suggested that hsCRP can be an informative biomarker of chronic hepatic dysfunction.

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3

Inglis, R., M. Pannike, A. Pannike, J. Windolf e M. Lorenz. "Berechnung und grafische Darstellung der Produktmomentkorrelation nach KAPLAN-MEIER mit dem Personalcomputer - Programm KAPLGRAPH(c)". Biomedizinische Technik/Biomedical Engineering 35, s2 (1990): 166. http://dx.doi.org/10.1515/bmte.1990.35.s2.166.

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4

Bergoli, CD, LP Brondani, VF Wandscher, GKR Pereira, MS Cenci, T. Pereira-Cenci e LF Valandro. "A Multicenter Randomized Double-blind Controlled Clinical Trial of Fiber Post Cementation Strategies". Operative Dentistry 43, n. 2 (1 marzo 2018): 128–35. http://dx.doi.org/10.2341/16-278-c.

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SUMMARY Objectives: The aim of this prospective randomized multicenter clinical trial was to evaluate the survival rate of glass fiber–reinforced posts cemented with self-adhesive or regular resin cements. Methods: The sample was comprised of 152 teeth randomized within two centers and in accordance with the adhesive strategies for RelyX U100/U200 (3M ESPE) or Single Bond and RelyX ARC (3M ESPE). The cementation procedures were standardized and performed by previously trained operators. The primary outcome evaluated was post debonding. A trained evaluator, one for each center, assessed all subjects at intervals of 12 months for up to 6 years. Statistical analysis was performed using the Kaplan-Meier method. Results: There was no statistically significant difference in survival rates between the two strategies assessed (p=0.991), with a 92.7% survival rate for the self-adhesive cement and 93.8% for the regular cement. Conclusion: Both the self-adhesive and the regular resin cements are good alternatives for glass fiber post cementation.

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5

Halfter, Carl. "C. A. Meier, Der Traum als Medizin. Antike Inkubation und moderne Psychotherapie. Daimon Verlag, Zürich 1985." Gesnerus 42, n. 3-4 (19 novembre 1985): 517–18. http://dx.doi.org/10.1163/22977953-0420304030.

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6

Mohammadshahi, Jafar, Hassan Ghobadi, Golchin Matinfar, Mohammad Hossein Boskabady e Mohammad Reza Aslani. "Role of Lipid Profile and Its Relative Ratios (Cholesterol/HDL-C, Triglyceride/HDL-C, LDL-C/HDL-C, WBC/HDL-C, and FBG/HDL-C) on Admission Predicts In-Hospital Mortality COVID-19". Journal of Lipids 2023 (6 marzo 2023): 1–10. http://dx.doi.org/10.1155/2023/6329873.

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Background. Lipid profile and its related ratios such as total cholesterol (TC), low-density lipoprotein-cholesterol (LDL-C), triglyceride (TG), high-density lipoprotein-cholesterol (HDL-C), TG/HDL-C ratio, TC/HDL-C ratio, LDL-C/HDL-C ratio, white blood cell (WBC)/HDL-C ratio, and fasting blood glucose (FBG)/HDL-C ratio are valuable indicators that have been studied in various disorders to predict mortality. The present study was conducted with the aim of investigating the role of lipid profile ratios in predicting mortality in COVID-19 patients. Methods. At the beginning of hospitalization, laboratory tests were taken from all patients ( n = 300 ). The ability of lipid profile ratios to determine the COVID-19 severity was evaluated using receiver-operating characteristic (ROC). In addition, survival probability was determined with the average of Kaplan-Meier curves, so that the end point was death. Results. In deceased patients, TG, TC, LDL-C, HDL-C, TC/HDL-C, TG/HDL-C, and LDL-C/HDL-C parameters were significantly lower than those of surviving patients, while WBC/HDL-C and FBG/HDL-C were significantly higher. TC ( HR = 3.178 , 95 % CI = 1.064 to 9.491, P < 0.05 ), TG ( HR = 3.276 , 95 % CI = 1.111 to 9.655, P < 0.05 ), LDL-C ( HR = 3.207 , 95 % CI = 1.104 to 9.316, P < 0.05 ), and HDL-C ( HR = 3.690 , 95 % CI = 1.290 to 10.554, P < 0.05 ), as well as TC/HDL-C ( HR = 3.860 , 95 % CI = 1.289 to 11.558, P < 0.05 ), TG/HDL-C ( HR = 3.860 , 95 % CI = 1.289 to 11.558, P < 0.05 ), LDL-C/HDL-C ( HR = 3.915 , 95 % CI = 1.305 to 11.739, P < 0.05 ), WBC/HDL-C ( HR = 3.232 , 95 % CI = 1.176 to 8.885, P < 0.05 ), and FBG/HDL-C ratios ( HR = 4.474 , 95 % CI = 1.567 to 12.777, P < 0.01 ), were detectably related to survival. The multivariate Cox regression models showed that only FBG/HDL-C ratio ( HR = 5.477 , 95 % CI = 1.488 to 20.153, P < 0.01 ) was significantly related to survival. Conclusion. The results suggested that FBG/HDL-C ratio in hospital-admitted COVID-19 patients was a reliable predictor of mortality.

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7

Balasov, Maxim, Katarina Akhmetova e Igor Chesnokov. "Drosophilamodel of Meier-Gorlin syndrome based on the mutation in a conserved C-Terminal domain of Orc6". American Journal of Medical Genetics Part A 167, n. 11 (2 luglio 2015): 2533–40. http://dx.doi.org/10.1002/ajmg.a.37214.

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8

Kim, J.-H., J. Cho, Y. Lee e B.-H. Cho. "The Survival of Class V Composite Restorations and Analysis of Marginal Discoloration". Operative Dentistry 42, n. 3 (1 maggio 2017): E93—E101. http://dx.doi.org/10.2341/16-186-c.

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SUMMARY The aims of this retrospective clinical study were to analyze the longevity of class V composite restorations and compare the results obtained from clinical and laboratory evaluation of marginal discoloration. A total of 186 restorations were evaluated with modified US Public Health Service criteria. Longevity and associated variables were analyzed with the Kaplan-Meier method and a Cox proportional hazard model. Restorations with marginal discoloration were additionally evaluated using digital photographs and epoxy resin replicas under a stereomicroscope. The mean survival time was 15.0 years, with five- and 10-year survival rates of 95.5% and 83.1%, respectively. Z250 had a higher risk of failure (hazard ratio=7.01, 95% confidence interval=2.07-23.72) than Z100. In addition, the presence of occlusal wear facets and bleeding on probing were associated with an increased risk of failure of the restorations. However, the use of an adhesive system (Scotchbond Multi-Purpose or Clearfil SE Bond) did not affect the longevity of the restorations. The results of laboratory evaluation were significantly different from clinical evaluation (p<0.001, McNemar test). Among 55 restorations rated as Bravo in the clinical evaluation, 24 restorations (43.6%) were determined to have penetrating discoloration on laboratory evaluation. When evaluating aged composite restorations, surface refurbishment and the use of a microscope are recommended, which will be helpful in determining the need for timely repair or replacement.

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9

Chiu, Vi Kien, e Adele Lerolle-Chiu. "Integrated survival analysis." Journal of Clinical Oncology 41, n. 16_suppl (1 giugno 2023): e14695-e14695. http://dx.doi.org/10.1200/jco.2023.41.16_suppl.e14695.

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e14695 Background: Clinical trial efficacy may be determined by the primary endpoint(s) of median progression free survival (mPFS) and/or median overall survival (mOS) from the Kaplan-Meier estimate, and secondary endpoints of overall response rate (ORR) and duration of response (DOR). In the treatment of metastatic cancers, single agent immunotherapy tends to have lower ORR and longer DOR in comparison to chemotherapy or targeted tyrosine kinase inhibitor therapy, which tends to have higher ORR and shorter DOR. This leads to intersecting or crossing Kaplan-Meier survival curves, which are harder to interpret. In immunotherapy trials, mPFS is a poor surrogate for mOS, and both may underrepresent the clinical benefit over time. Methods: We aimed to develop novel metrics that more effectively represent the Kaplan-Meier estimate. The graphical curve of the Kaplan-Meier estimate may be represented by the equation as a function of time. The integration of f ( x), which mathematically represents the area under the curve and clinically the cumulative or integrated survival benefit with time, is: ∫0t f( x) dx = F(t) − F(0). Kaplan-Meier curve equation with constants C and A may be approximated by: ∫0t C e-A x dx = C e-A t ]0 t = C( e-A t – 1). The average integrated clinical benefit with time is: 1/ t ∫0t f( x) dx = [ F( t) − F(0)]/ t. Results: The Phase 3 KeyNote-061 trial of metastatic gastric cancer treated with single agent Pembrolizumab immunotherapy versus Paclitaxel chemotherapy was use for integrated PFS and iOS calculation. The Kaplan-Meier curves intersected or crossed in KeyNote-061 trial. We show the established ORR, mPFS, mOS, DOR. Integrated PFS (iPFS) and iOS were calculated with greater increase in iOS and much less decrease in iPFS for Pembrolizumab than Paclitaxel treatment. Conclusions: Integrated survival is a novel analysis that integrate the Kaplan Meier estimates and better represent the entire median survival and drug DOR may be combined into a single useful metric for overall clinical benefit. [Table: see text]

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10

Nazarenko, Maria S., Iuliia V. Viakhireva, Mikhail Y. Skoblov, Elena V. Soloveva, Aleksei A. Sleptcov e Ludmila P. Nazarenko. "Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test". International Journal of Molecular Sciences 23, n. 16 (17 agosto 2022): 9234. http://dx.doi.org/10.3390/ijms23169234.

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Meier–Gorlin syndrome (MGS) is a rare genetic developmental disorder that causes primordial proportional dwarfism, microtia, the absence of or hypoplastic patellae and other skeletal anomalies. Skeletal symptoms overlapping with other syndromes make MGS difficult to diagnose clinically. We describe a 3-year-old boy with short stature, recurrent respiratory infections, short-rib dysplasia, tower head and facial dysmorphisms who was admitted to the Tomsk Genetic Clinic to verify a clinical diagnosis of Jeune syndrome. Clinical exome sequencing revealed two variants (compound heterozygosity) in the ORC6 gene: c.2T>C(p.Met1Thr) and c.449+5G>A. In silico analysis showed the pathogenicity of these two mutations and predicted a decrease in donor splicing site strength for c.449+5G>A. An in vitro minigene assay indicated that variant c.449+5G>A causes complete skipping of exon 4 in the ORC6 gene. The parents requested urgent prenatal testing for MGS for the next pregnancy, but it ended in a miscarriage. Our results may help prevent MGS misdiagnosis in the future. We also performed in silico and functional analyses of ORC6 mutations and developed a restriction fragment length polymorphism and haplotype-based short-tandem-repeat assay for prenatal genetic testing for MGS. These findings should elucidate MGS etiology and improve the quality of genetic counselling for affected families.

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Più fonti

Tesi sul tema "Meierei C"

1

Otyepka, Sarah [Verfasser], e Marco C. [Akademischer Betreuer] Meier. "Beiträge zur IT-gestützten Verhaltensänderung / Sarah Otyepka ; Betreuer: Marco C. Meier". Augsburg : Universität Augsburg, 2019. http://d-nb.info/1197537201/34.

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2

Meier, Christopher [Verfasser]. "Zur Entwicklung neuer aza-analoger Benzo[c]phenanthridine mit antitumoraler Wirkung / Christopher Meier". Kiel : Universitätsbibliothek Kiel, 2017. http://d-nb.info/1138980285/34.

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3

Liese, Rebecca [Verfasser], Ina Christin [Akademischer Betreuer] Meier, Ina Christin Gutachter] Meier, Andrea [Gutachter] [Carminati, Hermann Gutachter] Behling, Michaela [Gutachter] Dippold, Markus [Gutachter] [Hauck e Stefan [Gutachter] Scheu. "The effect of the mycorrhizal type on root-rhizosphere interactions in AM and ECM tree species: field studies and mesocosm experiments / Rebecca Liese ; Gutachter: Ina Christin Meier, Andrea Carminati, Hermann Behling, Michaela Dippold, Markus Hauck, Stefan Scheu ; Betreuer: Ina Christin Meier". Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://nbn-resolving.de/urn:nbn:de:gbv:7-11858/00-1735-0000-002E-E59D-C-2.

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4

Mosig, Benjamin [Verfasser], e Marco C. [Akademischer Betreuer] Meier. "Information Requirements Analysis for Business Intelligence Systems using System Dynamics / Benjamin Mosig. Betreuer: Marco C. Meier". Augsburg : Universität Augsburg, 2014. http://d-nb.info/1077703856/34.

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5

Scheffler, Alexa [Verfasser], e Marco C. [Akademischer Betreuer] Meier. "Beiträge zur Entscheidungsunterstützung für die Einführung von In-Memory Datenbanken / Alexa Scheffler ; Betreuer: Marco C. Meier". Augsburg : Universität Augsburg, 2016. http://d-nb.info/1122559275/34.

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Scheffler, Alexa Verfasser], e Marco [Akademischer Betreuer] [Meier. "Beiträge zur Entscheidungsunterstützung für die Einführung von In-Memory Datenbanken / Alexa Scheffler ; Betreuer: Marco C. Meier". Augsburg : Universität Augsburg, 2016. http://nbn-resolving.de/urn:nbn:de:bvb:384-opus4-38720.

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7

Kolb, Nicolai [Verfasser], e M. A. R. [Akademischer Betreuer] Meier. "Monomers from Renewable Resources: C-H Functionalization of Saturated Fatty Acids / Nicolai Kolb. Betreuer: M. A. R. Meier". Karlsruhe : KIT-Bibliothek, 2013. http://d-nb.info/1043756248/34.

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Schelkle, Michael [Verfasser], e Marco C. [Akademischer Betreuer] Meier. "Fostering Adequate Application of Business Information Visualization with User Assistance Systems and Serious Games / Michael Schelkle ; Betreuer: Marco C. Meier". Augsburg : Universität Augsburg, 2019. http://d-nb.info/117768330X/34.

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9

Höfler, Katharina [Verfasser], e Chris [Akademischer Betreuer] Meier. "Synthese und Charakterisierung von C8-N-Arylamin-2´-desoxyguanosin-5´-triphosphaten und C-Nucleosid-modifizierter DNA / Katharina Höfler. Betreuer: Chris Meier". Hamburg : Staats- und Universitätsbibliothek Hamburg, 2015. http://d-nb.info/1073307735/34.

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10

Scholten, Philip Benjamin Vincent [Verfasser], M. A. R. [Akademischer Betreuer] Meier e C. [Akademischer Betreuer] Detrembleur. "Design, Synthesis, and Properties of Novel Bio-Based and Ethylene-Based Copolymers / Philip Benjamin Vincent Scholten ; M. A. R. Meier, C. Detrembleur". Karlsruhe : KIT-Bibliothek, 2021. http://d-nb.info/1231361662/34.

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Libri sul tema "Meierei C"

1

Grass, Günter. Günter Grass: Das Milch-Märchen: Frühe Werbearbeiten. Berlin: Ch. Links Verlag, 2013.

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2

Clark, Gilbert A. Understanding art testing: Past influences, Norman C. Meier's contributions, present concerns, and future possibilities. Reston, Va: National Art Education Association, 1987.

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3

New York (N.Y.). Landmarks Preservation Commission. Bell Telephone Laboratories Complex (including the former Western Electric Company and Hook's Steam-powered Factory Buildings) (now Westbeth Artists' Housing), 445-465 West Street, 137-169 Bank Street, 51-77 Bethune Street, and 734-754 Washington Street, Manhattan: Built c. 1860, 1896-1903, Cyrus L.W. Eidlitz, architect, Marc Eidlitz & Son, builder; 1924-26, McKenzie, Voorhees & Gmelin, architect, Tidewater Building Co., builder; 1929, Warren B. Sanford, engineer, Turner Construction Co., builder; 1931-34 alterations, Voorhees, Gmelin & Walker, architect; and 1968-70 conversion, Richard Meier, architect : landmark site: Borough of Manhattan tax map block 639, lot 1. New York]: Landmarks Preservation Commission, 2011.

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4

Macfadden, David Revere, e Joseph Rykwert. The Grotta House by Richard Meier. Rizzoli, 2007.

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5

Understanding Art Testing: Past Influences, Norman C. Meier's Contributions, Present Concerns, and Future Possibilities. National Art Education Association (NAEA), 1987.

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6

New York Oelrichs & Co. Caspar Meier and His Successors : C. & H. H. Meier, Caspar Meier & Co. , L. N. Von Post & Oelrichs, Oelrichs & Krüger, Oelrichs & Co: October 12, 1798-October 12 1898. Creative Media Partners, LLC, 2022.

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7

New York Oelrichs & Co. Caspar Meier and His Successors : C. & H. H. Meier, Caspar Meier & Co. , L. N. Von Post & Oelrichs, Oelrichs & Krüger, Oelrichs & Co: October 12, 1798-October 12 1898. Creative Media Partners, LLC, 2022.

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8

Meier, C. A. A Testament to the Wilderness: Ten Essays on an Address by C. A. Meier. Lapis Pr, 1985.

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9

Hydrick, Blair. A guide to the microfilm edition of Black studies research sources ... Papers of the NAACP, part 18, Special subjects, 1940-1955, series C, General Office ... Meier. University Publications of America, 1995.

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Rapporti di organizzazioni sul tema "Meierei C"

1

Deo, Salil, David McAllister, Naveed Sattar e Jill Pell. The time-varying cardiovascular benefits of glucagon like peptide-1 agonist (GLP-RA)therapy in patients with type 2 diabetes mellitus: A meta-analysis of multinational randomized trials. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, luglio 2021. http://dx.doi.org/10.37766/inplasy2021.7.0097.

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Review question / Objective: P - patients with type 2 diabetes melllitus already receiving routine medical therapy; I - patients receiving glucagon like peptide 1 receptor agonist (GLP1 receptor agonist) therapy (semaglutide, dulaglutide, liraglutide, exenatide, lixisenatide, efpeglenatide, abiglutide); C - patients receiving standard therapy for diabetes mellitus but not receiving GLP1 agonist therapy; O - composite end point as per invididual trial, cardiovascular mortality, all-cause mortality, myocardial infarction, stoke. Condition being studied: Type 2 diabetes mellitus. Study designs to be included: Randomised controlled trials which enroll a large number of patients (defined as > 500) and are multinational in origin. Studies included will need to have published Kaplan and Meier curves for the end-points presented in the manuscript.

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