Results for 'Riekeder Graaf'

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  1.  28
    Clarifying Appeals to Dignity in Medical Ethics From an Historical Perspective.Riekeder Graaf & Johannes Jmdelden - 2009 - Bioethics 23 (3):151-160.
    Over the past few decades the concept of (human) dignity has deeply pervaded medical ethics. Appeals to dignity, however, are often unclear. As a result some prefer to eliminate the concept from medical ethics, whereas others try to render it useful in this context. We think that appeals to dignity in medical ethics can be clarified by considering the concept from an historical perspective. Firstly, on the basis of historical texts we propose a framework for defining the concept in medical (...)
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  2.  26
    On Using People Merely as a Means in Clinical Research.Riekeder Graaf & Johannes J. M. Delden - forthcoming - Bioethics.
    It is often argued that clinical research should not violate the Kantian principle that people must not be used merely as a means for the purposes of others. At first sight, the practice of clinical research itself, however, seems to violate precisely this principle: clinical research is often beneficial to future people rather than to participants; even if participants benefit, all things considered, they are exposed to discomforts which are absent both in regular care for their diseases and in other (...)
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  3.  4
    Corporate Social Responsibility and Aging Workforces: An Explorative Study of Corporate Social Responsibility Implementation in Small- and Medium-Sized Enterprises.Franz Josef Gellert & Frank Jan Graaf - 2012 - Business Ethics 21 (4):353-363.
    Although critical differences exist between large companies and small- and medium-sized enterprises (SMEs), limited empirical research has been done on human resource (HR)-related corporate social responsibility (CSR). In this paper we study aging workforce management (AWM) as a component of CSR. Our study was conducted in the Netherlands through a randomly distributed online questionnaire. Managers and team leaders of 201 SMEs responded. The data were analyzed using multiple hierarchical regression analysis. Our results are twofold: first, findings suggest that CSR policies (...)
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  4.  14
    Toward a “Post-Posthuman Dignity Area” in Evaluating Emerging Enhancement Technologies.Annelien L. Bredenoord, Rieke van der Graaf & Johannes Jm van Delden - 2010 - American Journal of Bioethics 10 (7):55-57.
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  5.  4
    Vincristine Pharmacokinetics and Response to Vincristine Monotherapy in an Up-Front Window Study of the Dutch Childhood Leukaemia Study Group.E. Groninger, T. De Boer, P. Koopmans, D. Uges, W. Sluiter, A. J. P. Veerman, W. A. Kamps & S. De Graaf - unknown
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  6.  2
    Power Difference and Risk Perception: Mapping Vulnerability Within the Decision Process of Pregnant Women Towards Clinical Trial Participation in an Urban Middle‐Income Setting.Geerte C. den Hollander, Joyce L. Browne, Daniel Arhinful, Rieke Graaf & Kerstin Klipstein‐Grobusch - forthcoming - Developing World Bioethics.
    To address the burden of maternal morbidity and mortality in low- and middle-income countries, research with pregnant women in these settings is increasingly common. Pregnant women in LMIC-context may experience vulnerability related to giving consent to participate in a clinical trial. To recognize possible layers of vulnerability this study aims to identify factors that influence the decision process towards clinical trial participation of pregnant women in an urban middle-income setting. This qualitative research used participant observation, in-depth interviews, and focus group (...)
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  7.  1
    Marxismus und Moral in der sowjetrussischen Literatur.J. De Graaf - 1957 - Zeitschrift Für Evangelische Ethik 1 (1):219-227.
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  8. Cockles and Mussels at Eastern Scheldt.Jan de Graaf - 1993 - Topos 3:85-92.
     
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  9.  20
    Experimenting with Chymical Bodies: Reinier de Graaf's Investigations of the Pancreas.Evan Ragland - 2008 - Early Science and Medicine 13 (6):615-664.
    In the late seventeenth century, traditions in anatomy and chymistry came together to ground new theoretical and experimental approaches to understanding the animal body. The researches of Dutch experimenters Reinier de Graaf and his mentor Franciscus Sylvius provide keen insight into the ways experiments were constructed, negotiated, and thought about by leading anatomists and physicians of the time. The objects and approaches de Graaf used in the laboratory—ligature, inflation, injection, tubes, vessels, tasting—were derived from broadly Harveian anatomical and (...)
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  10.  25
    Propaganda Architecture: Interview with Rem Koolhaas and Reinier de Graaf.David I. Cunningham & Jon Goodbun - 2009 - Radical Philosophy 154:35-47.
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  11.  14
    Affluenza: The All-Consuming Epidemic. By John De Graaf, David Wann, and Thomas H. Naylor. [REVIEW]Amitrajeet A. Batabyal - 2003 - Agriculture and Human Values 20 (2):211-212.
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  12.  8
    Graaf Karl Johann Philipp Cobenzl en de Europese educatieve ruimte. Of de internationale opvoedingsstrategie van een Oostenrijkse diplomaat in Brussel.Dirk Leyder & Frédérique Johan - 2011 - Revue Belge de Philologie Et D’Histoire 89 (1):455-490.
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  13.  19
    Alie Bijker: Riedel Horatiana. A Catalogue of the Horace Collection in Groningen University Library . Pp. Xx + 299, 26 Pls. Nieuwkoop: De Graaf, 1996. ISBN: 90-6004-435-. [REVIEW]Martin Davies - 2000 - The Classical Review 50 (01):293-.
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  14.  14
    H. Jones: Master Tully. Cicero in Tudor England . Pp. Viii + 316. Nieuwkoop: De Graaf, 1998. Cased, Frs. 120. ISBN: 90-6004-443-. [REVIEW]Peter Mack - 1999 - The Classical Review 49 (02):624-.
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  15.  12
    J. A. Gruys: The Early Printed Editions (1518–1664) of Aeschylus. A Chapter in the History of Classical Scholarship. (Bibliotheca Humanistica & Reformatoria, 32.) Pp. 356; 11 Plates. Nieuwkoop: De Graaf, 1981. Fl. 95. [REVIEW]James Diggle - 1982 - The Classical Review 32 (02):303-.
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  16.  3
    Willem I Graaf van Holland en de Hollandse hoogheemraadschappen. S. J. Fockema Andreae.Dirk Jellema - 1957 - Speculum 32 (2):367-368.
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  17.  4
    De overlijdensdatum van graaf Arnulf van Valenciennes.G. Koch-De Meyer - 1951 - Revue Belge de Philologie Et D’Histoire 29 (1):139-142.
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  18. Ethics and Behavioural Theory: How Do Professionals Assess Their Mental Models?Frank Jan de Graaf - forthcoming - Journal of Business Ethics:1-15.
    The role and ethics of professionals in business and economics have been questioned, especially after the financial crisis of 2008. Some suggest a reorientation using concepts such as craftsmanship. In this article, I will explore professional practices within the context of behavioural theory and business ethics. I suggest that scholars of behavioural theory need a strategy to deal with normative questions to meet their ambition of practical relevance. Evidence-based management, a recent behavioural approach, may assist business ethics scholars in understanding (...)
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  19. Tractable Morality.Gjalt de Graaf - 2005 - Journal of Business Ethics 60 (1):1-15.
    This article discusses five propositions about managerial moral tractability -- that is, a morality that is amenable to the complexity of managers’ continual pressure to decide and act -- in their customer relations. The propositions come from the comparison of three case studies of different types of managers. To analyze the morality of managers, discursive practices of managers are studied. At the end of the article also some consideration is given to “information strategies” of managers, in relation to their tractable (...)
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  20.  10
    The Social Value of Pragmatic Trials.Shona Kalkman, Ghislaine van Thiel, Rieke van der Graaf, Mira Zuidgeest, Iris Goetz, Diederick Grobbee & Johannes van Delden - 2017 - Bioethics 31 (2):136-143.
    Pragmatic trials aim to directly inform health care decision-making through the collection of so-called ‘real world data’ from observations of comparative treatment effects in clinical practice. In order to ensure the applicability and feasibility of a pragmatic trial, design features may be necessary that deviate from standard research ethics requirements. Examples are traditional requirements to seek written informed consent and to perform extensive data and safety monitoring. Proposals for deviations from standard research ethics practice have resulted in controversy about their (...)
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  21.  26
    What is the Best Standard for the Standard of Care in Clinical Research?Rieke van der Graaf & Johannes J. M. van Delden - 2009 - American Journal of Bioethics 9 (3):35 – 43.
    During the past decennium, one of the main issues discussed in research ethics has been focused on the care that should be provided to the control group in a clinical trial. This discussion is also called the standard of care debate . Current international research ethics guidelines contain a wide variety of standards for the standard of care—including the provision of the highest attainable, the best available, the best current, a proven , and an established effective treatment. In this article, (...)
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  22.  1
    Adapting Clinical Guidelines in Low-Resources Countries: A Study on the Guideline on the Management and Prevention of Type 2 Diabetes Mellitus in Indonesia.Indah S. Widyahening, Grace Wangge, Yolanda van der Graaf & Geert J. M. G. van der Heijden - 2017 - Journal of Evaluation in Clinical Practice 23 (1):121-127.
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  23.  19
    The Autonomy of the Contracting Partners: An Argument for Heuristic Contractarian Business Ethics. [REVIEW]Gjalt de Graaf - 2006 - Journal of Business Ethics 68 (3):347-361.
    Due to the domain characteristics of business ethics, a contractarian theory for business ethics will need to be essentially different from the contract model as it is applied to other domains. Much of the current criticism of contractarian business ethics (CBE) can be traced back to autonomy, one of its three boundary conditions. After explaining why autonomy is so important, this article considers the notion carefully vis à vis the contracting partners in the contractarian approaches in business ethics. Autonomy is (...)
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  24.  33
    Clarifying Appeals to Dignity in Medical Ethics From an Historical Perspective.Rieke van der Graaf & Johannes Jm van Delden - 2009 - Bioethics 23 (3):151-160.
  25.  15
    TMS Effects on Subjective and Objective Measures of Vision: Stimulation Intensity and Pre- Versus Post-Stimulus Masking.Tom A. de Graaf, Sonja Cornelsen, Christianne Jacobs & Alexander T. Sack - 2011 - Consciousness and Cognition 20 (4):1244-1255.
    Transcranial magnetic stimulation can be used to mask visual stimuli, disrupting visual task performance or preventing visual awareness. While TMS masking studies generally fix stimulation intensity, we hypothesized that varying the intensity of TMS pulses in a masking paradigm might inform several ongoing debates concerning TMS disruption of vision as measured subjectively versus objectively, and pre-stimulus versus post-stimulus TMS masking. We here show that both pre-stimulus TMS pulses and post-stimulus TMS pulses could strongly mask visual stimuli. We found no dissociations (...)
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  26.  43
    On Using People Merely as a Means in Clinical Research.Rieke van der Graaf & Johannes J. M. van Delden - 2012 - Bioethics 26 (2):76-83.
    It is often argued that clinical research should not violate the Kantian principle that people must not be used merely as a means for the purposes of others. At first sight, the practice of clinical research itself, however, seems to violate precisely this principle: clinical research is often beneficial to future people rather than to participants; even if participants benefit, all things considered, they are exposed to discomforts which are absent both in regular care for their diseases and in other (...)
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  27.  27
    How Corporate Social Performance is Institutionalised Within the Governance Structure.Frank J. de Graaf & Cor A. J. Herkströter - 2007 - Journal of Business Ethics 74 (2):177-189.
    Since Ackerman in Corporate social responsiveness, the modern dilemma (1973), pleaded for the institutionalisation of corporate social performance (CSP) in business processes, researchers have focused on the role of strategy in CSP. This article demonstrates that CSP is institutionalised within the governance structure. We will attempt to make this clear by means of a description of the Dutch system of corporate governance. Under certain circumstances Dutch companies are already bound to CSP due to prevailing legislation. A governance perspective shows that (...)
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  28.  25
    Veterinarians' Discourses on Animals and Clients.Gjalt de Graaf - 2005 - Journal of Agricultural and Environmental Ethics 18 (6):557-578.
    Veterinarians have obligations towards both the animals they treat and their clients, the owners of the animals. With both groups, veterinarians have complicated relations; many times the interests of both groups conflict. In this article, using Q-methodology as a method for discourse analysis, the following question is answered: How do Dutch practicing veterinarians conceptualize animals and their owners and their professional responsibility towards both? The main part of the article contains descriptions of four different discourses on animals and their owners (...)
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  29.  18
    Discourse Theory and Business Ethics. The Case of Bankers' Conceptualizations of Customers.Gjalt de Graaf - 2001 - Journal of Business Ethics 31 (4):299-319.
    Within discourse theory, language is seen as constitutive of reality. Furthermore, facts and values are viewed as inseparable. This has consequences for business ethics. In this paper the relationship between discourse theory and business ethics is discussed. Both the descriptive and prescriptive aspects of business ethics are taken into account. Furthermore, an example of an empirical study is presented. A discourse analysis is conducted to answer the questions of how bankers in Holland conceptualize and thus treat their customers and whether (...)
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  30.  14
    Response to Open Peer Commentaries on “What is The Best Standard for the Standard of Care in Clinical Research?”.Rieke van Der Graaf & Johannes JM van Delden - 2009 - American Journal of Bioethics 9 (6-7):7-8.
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  31.  9
    How and When Does Consent Bias Research?R. H. H. Groenwold, R. van der Graaf & J. J. M. van Delden - 2013 - American Journal of Bioethics 13 (4):46 - 48.
  32.  35
    Discourse and Descriptive Business Ethics.Gjalt de Graaf - 2006 - Business Ethics 15 (3):246–258.
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  33.  1
    Issues in the Use of Stepped Wedge Cluster and Alternative Designs in the Case of Pandemics.Ingeborg van der Tweel & Rieke van der Graaf - 2013 - American Journal of Bioethics 13 (9):23-24.
  34.  13
    A Qualitative Study on Acceptable Levels of Risk for Pregnant Women in Clinical Research.Indira S. E. Van der Zande, Rieke van der Graaf, Martijn A. Oudijk & Johannes J. M. Van Delden - 2017 - BMC Medical Ethics 18 (1):35.
    There is ambiguity with regard to what counts as an acceptable level of risk in clinical research in pregnant women and there is no input from stakeholders relative to such research risks. The aim of our paper was to explore what stakeholders who are actively involved in the conduct of clinical research in pregnant women deem an acceptable level of risk for pregnant women in clinical research. Accordingly, we used the APOSTEL VI study, a low-risk obstetrical randomised controlled trial, as (...)
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  35.  11
    Power Difference and Risk Perception: Mapping Vulnerability Within the Decision Process of Pregnant Women Towards Clinical Trial Participation in an Urban Middle-Income Setting.C. den Hollander Geerte, lBrowne Joyce, Arhinful Daniel, Graaf Rieke & Klipstein-Grobusch Kerstin - forthcoming - Developing World Bioethics.
    To address the burden of maternal morbidity and mortality in low- and middle-income countries, research with pregnant women in these settings is increasingly common. Pregnant women in LMIC-context may experience vulnerability related to giving consent to participate in a clinical trial. To recognize possible layers of vulnerability this study aims to identify factors that influence the decision process towards clinical trial participation of pregnant women in an urban middle-income setting. This qualitative research used participant observation, in-depth interviews, and focus group (...)
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  36.  10
    Conflating Scientific With Clinical Considerations.Rieke van Der Graaf & Johannes JM van Delden - 2009 - American Journal of Bioethics 9 (9):58-59.
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  37.  10
    Power Difference and Risk Perception: Mapping Vulnerability Within the Decision Process of Pregnant Women Towards Clinical Trial Participation in an Urban Middle‐Income Setting.C. den Hollander Geerte, L. Browne Joyce, Arhinful Daniel, Graaf Rieke & Klipstein‐Grobusch Kerstin - forthcoming - Developing World Bioethics.
    To address the burden of maternal morbidity and mortality in low- and middle-income countries, research with pregnant women in these settings is increasingly common. Pregnant women in LMIC-context may experience vulnerability related to giving consent to participate in a clinical trial. To recognize possible layers of vulnerability this study aims to identify factors that influence the decision process towards clinical trial participation of pregnant women in an urban middle-income setting. This qualitative research used participant observation, in-depth interviews, and focus group (...)
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  38.  16
    Institutional Entrepreneurship and CSR Within Multinational SME's.Dirk Johan de Jong & Frank Jan de Graaf - 2011 - Proceedings of the International Association for Business and Society 22:449-458.
    This paper develops propositions on the added value for SMEs of normatively based, employee-oriented corporate social responsibility (CSR). We suggest that not only motives but also the skills of the owner/manager as an institutional entrepreneur are critical in dealing with institutional variance. Also, the transfer of employee-oriented CSR can have positive results for SMEs that could imply that globalisation is not only a race to the bottom.
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  39.  21
    Early Modern Experimentation on Live Animals.Domenico Bertoloni Meli - 2013 - Journal of the History of Biology 46 (2):199-226.
    Starting from the works by Aselli on the milky veins and Harvey on the motion of the heart and the circulation of the blood, the practice of vivisection witnessed a resurgence in the early modern period. I discuss some of the most notable cases in the century spanning from Aselli’s work to the investigations of fluid pressure in plants and animals by Stephen Hales. Key figures in my study include Johannes Walaeus, Jean Pecquet, Marcello Malpighi, Reinier de Graaf, Richard (...)
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  40.  1
    Power Difference and Risk Perception: Mapping Vulnerability Within the Decision Process of Pregnant Women Towards Clinical Trial Participation in an Urban Middle‐Income Setting.Geerte C. den Hollander, Joyce L. Browne, Daniel Arhinful, Rieke van der Graaf & Kerstin Klipstein‐Grobusch - 2018 - Developing World Bioethics 18 (2):68-75.
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  41.  9
    Voluntary Informed Consent in Paediatric Oncology Research.Sara A. S. Dekking, Rieke Van Der Graaf & Johannes J. M. Van Delden - 2016 - Bioethics 30 (6):440-450.
    In paediatric oncology, research and treatments are often closely combined, which may compromise voluntary informed consent of parents. We identified two key scenarios in which voluntary informed consent for paediatric oncology studies is potentially compromised due to the intertwinement of research and care. The first scenario is inclusion by the treating paediatric oncologist, the second scenario concerns treatments confined to the research context. In this article we examine whether voluntary informed consent of parents for research is compromised in these two (...)
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  42.  15
    Toward a New Conception of Policy Discourse.Henk van de Graaf & John Grin - 1997 - The European Legacy 2 (2):264-270.
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  43.  2
    Vulnerability of Pregnant Women in Clinical Research.S. E. van der Zande Indira, van der Graaf Rieke, A. Oudijk Martijn & J. M. van Delden Johannes - 2017 - Journal of Medical Ethics 43 (10):657-663.
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  44.  13
    De vernieuwde overheid.Door Thom de Graaf - forthcoming - Idee.
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  45.  7
    Voluntary Informed Consent in Paediatric Oncology Research.Sara A. S. Dekking, Rieke Van Der Graaf & Johannes J. M. Van Delden - 2016 - Bioethics 30 (5):440-450.
    In paediatric oncology, research and treatments are often closely combined, which may compromise voluntary informed consent of parents. We identified two key scenarios in which voluntary informed consent for paediatric oncology studies is potentially compromised due to the intertwinement of research and care. The first scenario is inclusion by the treating paediatric oncologist, the second scenario concerns treatments confined to the research context. In this article we examine whether voluntary informed consent of parents for research is compromised in these two (...)
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  46.  4
    Language Intensity as a Sensationalistic News Feature: The Influence of Style on Sensationalism Perceptions and Effects.Anneke de Graaf & Christian Burgers - 2013 - Communications 38 (2):167-188.
    This article extends the definition of sensationalism to print media by arguing that language intensifiers may be an aspect of sensationalism. In addition, this paper investigates if an indirect effect can be established by which sensationalistic message features influence news reception through the perception of sensationalism. Two between-subjects experiments show that sensationalistic message features like intensifiers increase perceived language intensity. In experiment 1, intensifiers had a negative effect on news article appreciation, which was not influenced by PLI. Experiment 2 revealed (...)
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  47.  1
    Die Gewalt: Kritik ihrer Rechtfertigung·~.Johannes de Graaf - 1971 - Zeitschrift Für Evangelische Ethik 15 (1):129-141.
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  48.  8
    Differences in Actual Persuasiveness Between Experiential and Professional Expert Evidence.Christian Burgers, Anneke de Graaf & Sabine Callaars - 2012 - Journal of Argumentation in Context 1 (2):194-208.
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  49.  8
    Democratie on Line.Thom de Graaf Trouwens - forthcoming - Idee.
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  50.  1
    Vulnerability of Pregnant Women in Clinical Research.Indira S. E. Van der Zande, Rieke van der Graaf, Martijn A. Oudijk & Johannes J. M. Van Delden - 2017 - Journal of Medical Ethics 43 (10):657-663.
    Background Notwithstanding the need to produce evidence-based knowledge on medications for pregnant women, they remain underrepresented in clinical research. Sometimes they are excluded because of their supposed vulnerability, but there are no universally accepted criteria for considering pregnant women as vulnerable. Our aim was to explore whether and if so to what extent pregnant women are vulnerable as research subjects. Method We performed a conceptual and empirical analysis of vulnerability applied to pregnant women. Analysis A conceptual analysis supports Hurst's definition (...)
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