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		<Text textformat="02">&lt;i&gt;Dialogues of the Clinic: Encounters across medicine and beyond &lt;/i&gt;is a unique anthology that centers dialogue as practice and challenge of medical encounters, taking up Mishler's famous provocation of a dichotomy between the voice of the lifeworld and the voice of medicine, or an awareness of the asymmetries of knowledge and authority in clinical encounters.  &lt;br /&gt;First, the authors in this book aim to define dialogue beyond interaction and to conduct a close analysis of empirical data from clinical consultations as diverse as visits in oncology, pediatrics, psychotherapy, medical student training, and speech language therapy. In doing so, they argue for the many possibilities and missed opportunities for clinicians in diverse cultural settings to engage dialogically, while constantly managing the multiple contingencies of personal, organizational, and institutional voices, texts, and artifacts. Dialogue and discourse scholars, clinical practitioners, and academics from the humanities and social sciences will appreciate this collection on how to approach dialogue conceptually and empirically, in clinical practice.</Text>
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					<Text textformat="02">   This introduction to our anthology finds us dazzled and unsteady inside a labyrinth of flowers, searching for dialogue as something other than mere communication or interaction. We examine how dialogue has come to function as a moral and epistemic ideal in medicine — one that promises understanding, care, and participation, even as it risks becoming prescriptive and rendered routine. As discourse and dialogue scholars who study clinical exchanges, we find, together with the authors in these pages, that approaching dialogue means engaging in empirical analysis as much as reflection about our pedagogical practice and lived experience. The voices and dialogues of the clinic are opportunities that emerge in spite of, and maybe because of, constraint — a dance between action and reaction in which meaning, ethics, and understanding are choreographed in the context of embodied vulnerability.</Text>
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					<Text textformat="02">   As clinical psychologists familiar with the philosophical provocations of new materialism(s), we take dialogue as a multimodal process in which clinicians participate with their whole bodies and as an occurrence that includes both human and non-human actors. Using Multimodal Conversation Analysis (MCA), we examine five extracts from a first clinical session with Giovanna (GA), a young adolescent diagnosed with severe anorexia nervosa. We adopt Ingold’s (2020) concept of correspondence, which describes a knowledge-making process that emerges through direct engagement with both material and non-material entities. Unlike the notion of betweenness, where separated entities are joined, in-betweenness suggests that these entities are produced through their linking with one another. We expand the concept of dialogue (as correspondence) through three key perspectives: (1) dialogue as extending beyond verbal/oral communication, (2) materiality as an integral component of the dialogical process, and (3) dialogue as going beyond the boundaries of the “actual conversing couple.”</Text>
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					<Text textformat="02">   This chapter explores the potential for dialogue within the context of speech-language therapy (SLT), a specialized field focusing on communicative impairments. Drawing on phenomenological theories of dialogue, the analysis examines interactions between a Hebrew- speaking SLT clinician and her child-client. Using discourse analysis, the study highlights the tension between the mechanical aspects of speech correction and the holistic, creative nature of dialogue. It argues that the clinician’s emphasis on correct pronunciation undermines opportunities for genuine dialogic engagement. Instead of fostering open, autonomous, and reciprocal communication, the sessions often prioritize adherence to linguistic norms, which may silence the child’s creative input and reduce their agency. This chapter invites us to rethink the nature of dialogue within the speech-language therapeutic setting, where the act of communication is both the medium and the goal of the encounter.</Text>
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					<Text textformat="02">   The aim of this chapter is to analyze the conditions and obstacles of dialogic communication in pediatric services involving migrant children, with and without interpreting services. Dialogic communication is conceptualized as based on participants’ equal opportunities to exercise agency. First, the chapter focuses on the general meaning of dialogue and the application and limits of dialogic communication to monolingual interaction between children, parents and pediatricians, and interpreter-mediated interaction. Second, the chapter presents field research on pediatric consultations without and with interpreting services, analyzing several excerpts from these consultations to show if and how dialogic communication is coordinated by clinicians alone and by interpreters working with clinicians, and with which effects for children’s agency. The excerpts show effective dialogue with children and, in a few cases, what I consider to be its failure. Finally, I compare the two research settings in terms of dialogue and support of children’s agency.</Text>
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			<Subtitle textformat="02">Working toward shared goals in medical care</Subtitle>
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				<PersonName>Staci Defibaugh</PersonName>
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					<Affiliation>Old Dominion University</Affiliation>
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					<SubjectHeadingText>asymmetry</SubjectHeadingText>
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					<Text textformat="02">   In this chapter, I analyze a medical visit between a physician assistant in neurology and a patient with uncontrolled seizures. Focusing on a series of exchanges throughout the visit, I note how the patient shares her concerns and fears about her seizures as well as how the physician assistant responds to these concerns and returns to them, sometimes even reformulating them as her own desires, as they work toward a solution. Through these interactional moments, I argue that engagement in dialogue cannot be fully understood or accomplished in individual sequences of talk; instead, it is the circulation and recurrence of particular topics, themes, and the shared concern and goal orientation that ultimately facilitate a productive medical encounter.</Text>
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					<Text textformat="02">   This chapter examines the intersubjective foundations of dialogue in medical encounters. Rather than treating dialogue and intersubjectivity as synonymous, we argue that intersubjectivity constitutes the condition of possibility for dialogue by enabling participants to negotiate and sustain a shared understanding of the visit’s objectives as interaction unfolds. Drawing on Martin Buber’s philosophy of dialogue and Erving Goffman’s interactional sociology, we analyze how participants establish mutual recognition in turn-by-turn interaction. Our dataset consists of 60 video-recorded first-time oncology visits from two Italian hospitals. Across analyses conducted over the last seven years, we identify three practices central to negotiating intersubjectivity: (i) metapragmatic formulations, (ii) textual oralizing (reading/writing aloud), and (iii) the use of textual artifacts such as test results and prescriptions. These practices mediate transitions, repair misalignments, and create opportunities for recognizing participants’ perspectives. Dialogue thus emerges as a contingent and interactionally accomplished outcome.</Text>
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			<Subtitle textformat="02">Reclaiming the “voice of the lifeworld” in medicine through dialogue</Subtitle>
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					<Text textformat="02">   Patients seek opportunities to share their stories with physicians as part of a meaningful clinical relationship. Although communication skills such as expressing empathy and eliciting patient narratives are central to medical education, the dialogic potential of clinical encounters often remains unrealized. Drawing on Raimo Puustinen’s claim that dialogue is fundamental to medical examination and treatment, this chapter argues that amplifying dialogue in medical education can strengthen both clinical information gathering and patient rapport. After briefly tracing historical models of the patient-provider relationship, the chapter examines the concepts of empathy and narrative and their relationship to dialogue. It then considers how communication skills are currently taught in medical training. Using transcribed encounters between medical students and standardized patients in clinical exam settings, the chapter demonstrates how open-ended questions at the beginning of interviews can transform routine exchanges into dialogic encounters that foster genuine empathy while also facilitating more effective and efficient clinical communication.</Text>
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					<Text textformat="02">   Enhanced by “medical dialogue” and increasingly promoted within healthcare systems, patient-centred approaches consider patients as individuals with personal needs, fears, stories, questions, and suggestions for their care. In this chapter, I define dialogue as a particular form of communication usually enhanced by specific actions and expectations, which can facilitate patients’ active participation and agency in interactions with practitioners. Presenting data from 106 consultations video-recorded in five oncological units in hospitals in Northern Italy, this chapter focuses on doctors’ dialogic facilitation of patients’ initiatives, presented in narrative format, within first-time visits. In my analysis of transcribed excerpts of the consultation, I show the communicative actions by which physicians dialogically facilitate and co-construct patient narratives, and detail the effects this has on interaction, particularly in relation to the discovery of the symptoms, the impact the illness has on the patient’s identity and emotional well-being and the potential implications for their care.</Text>
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					<Text textformat="02">   This chapter explores patient voice as a rhetorical and epistemological feature of clinical reporting. Drawing on published case reports that include a “patient’s perspective,” the author specifically examines how practitioners and patients use language to define their individual subjectivity, position themselves in relation to other voices in the text, and characterize each other relative to shared interactions and decision-making processes. I suggest that the medical case report provides unique insight into dialogic aspects of clinical documentation, and as a site of inquiry, shows how patient voice encounters and interacts with the discourse of biomedicine. The chapter concludes by discussing implications for research, practice, and work that seeks to amplify patient voice in healthcare settings.</Text>
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					<Text textformat="02">   In the second half of the twentieth century, patient-centered care (PCC) gained ground as a dialogic practice within a new architecture of care and became the gold standard of healthcare worldwide. Adopting the analytical lenses of epistemic (in)justice and intersubjectivity, I reconstruct the history of this concept and argue that PCC and its corollaries (e.g., “patient empowerment and agency,” “shared decision making,” and “clinical empathy”) constitute a morally loaded doctrine whose raison d’être is ethical rather than clinical. Building on recent studies, I also illuminate the overlooked risks of uncritically adopting PCC: neglecting the non-agentic dimensions of “being a patient,” disregarding the dependence of effective caregiving on the caregiver’s epistemic and deontic authority, reinforcing abandonment through the rhetoric of empowerment, dismantling asymmetry-based models of care in favor of egalitarian consumer-provider relations, and tacitly aligning PCC with contemporary neoliberalism.</Text>
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		<Text textformat="02">&lt;i&gt;Dialogues of the Clinic: Encounters across medicine and beyond &lt;/i&gt;is a unique anthology that centers dialogue as practice and challenge of medical encounters, taking up Mishler's famous provocation of a dichotomy between the voice of the lifeworld and the voice of medicine, or an awareness of the asymmetries of knowledge and authority in clinical encounters.  &lt;br /&gt;First, the authors in this book aim to define dialogue beyond interaction and to conduct a close analysis of empirical data from clinical consultations as diverse as visits in oncology, pediatrics, psychotherapy, medical student training, and speech language therapy. In doing so, they argue for the many possibilities and missed opportunities for clinicians in diverse cultural settings to engage dialogically, while constantly managing the multiple contingencies of personal, organizational, and institutional voices, texts, and artifacts. Dialogue and discourse scholars, clinical practitioners, and academics from the humanities and social sciences will appreciate this collection on how to approach dialogue conceptually and empirically, in clinical practice.</Text>
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					<Text textformat="02">   This introduction to our anthology finds us dazzled and unsteady inside a labyrinth of flowers, searching for dialogue as something other than mere communication or interaction. We examine how dialogue has come to function as a moral and epistemic ideal in medicine — one that promises understanding, care, and participation, even as it risks becoming prescriptive and rendered routine. As discourse and dialogue scholars who study clinical exchanges, we find, together with the authors in these pages, that approaching dialogue means engaging in empirical analysis as much as reflection about our pedagogical practice and lived experience. The voices and dialogues of the clinic are opportunities that emerge in spite of, and maybe because of, constraint — a dance between action and reaction in which meaning, ethics, and understanding are choreographed in the context of embodied vulnerability.</Text>
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				<PersonName>Federico Maria Albertini</PersonName>
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					<Text textformat="02">   As clinical psychologists familiar with the philosophical provocations of new materialism(s), we take dialogue as a multimodal process in which clinicians participate with their whole bodies and as an occurrence that includes both human and non-human actors. Using Multimodal Conversation Analysis (MCA), we examine five extracts from a first clinical session with Giovanna (GA), a young adolescent diagnosed with severe anorexia nervosa. We adopt Ingold’s (2020) concept of correspondence, which describes a knowledge-making process that emerges through direct engagement with both material and non-material entities. Unlike the notion of betweenness, where separated entities are joined, in-betweenness suggests that these entities are produced through their linking with one another. We expand the concept of dialogue (as correspondence) through three key perspectives: (1) dialogue as extending beyond verbal/oral communication, (2) materiality as an integral component of the dialogical process, and (3) dialogue as going beyond the boundaries of the “actual conversing couple.”</Text>
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					<Text textformat="02">   This chapter explores the potential for dialogue within the context of speech-language therapy (SLT), a specialized field focusing on communicative impairments. Drawing on phenomenological theories of dialogue, the analysis examines interactions between a Hebrew- speaking SLT clinician and her child-client. Using discourse analysis, the study highlights the tension between the mechanical aspects of speech correction and the holistic, creative nature of dialogue. It argues that the clinician’s emphasis on correct pronunciation undermines opportunities for genuine dialogic engagement. Instead of fostering open, autonomous, and reciprocal communication, the sessions often prioritize adherence to linguistic norms, which may silence the child’s creative input and reduce their agency. This chapter invites us to rethink the nature of dialogue within the speech-language therapeutic setting, where the act of communication is both the medium and the goal of the encounter.</Text>
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					<Text textformat="02">   The aim of this chapter is to analyze the conditions and obstacles of dialogic communication in pediatric services involving migrant children, with and without interpreting services. Dialogic communication is conceptualized as based on participants’ equal opportunities to exercise agency. First, the chapter focuses on the general meaning of dialogue and the application and limits of dialogic communication to monolingual interaction between children, parents and pediatricians, and interpreter-mediated interaction. Second, the chapter presents field research on pediatric consultations without and with interpreting services, analyzing several excerpts from these consultations to show if and how dialogic communication is coordinated by clinicians alone and by interpreters working with clinicians, and with which effects for children’s agency. The excerpts show effective dialogue with children and, in a few cases, what I consider to be its failure. Finally, I compare the two research settings in terms of dialogue and support of children’s agency.</Text>
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					<Text textformat="02">   In this chapter, I analyze a medical visit between a physician assistant in neurology and a patient with uncontrolled seizures. Focusing on a series of exchanges throughout the visit, I note how the patient shares her concerns and fears about her seizures as well as how the physician assistant responds to these concerns and returns to them, sometimes even reformulating them as her own desires, as they work toward a solution. Through these interactional moments, I argue that engagement in dialogue cannot be fully understood or accomplished in individual sequences of talk; instead, it is the circulation and recurrence of particular topics, themes, and the shared concern and goal orientation that ultimately facilitate a productive medical encounter.</Text>
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					<Affiliation>University of California, Berkeley</Affiliation>
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					<SubjectHeadingText>conversation analysis</SubjectHeadingText>
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					<SubjectHeadingText>doctor-patient interaction</SubjectHeadingText>
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					<SubjectHeadingText>oncological setting</SubjectHeadingText>
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					<Text textformat="02">   This chapter examines the intersubjective foundations of dialogue in medical encounters. Rather than treating dialogue and intersubjectivity as synonymous, we argue that intersubjectivity constitutes the condition of possibility for dialogue by enabling participants to negotiate and sustain a shared understanding of the visit’s objectives as interaction unfolds. Drawing on Martin Buber’s philosophy of dialogue and Erving Goffman’s interactional sociology, we analyze how participants establish mutual recognition in turn-by-turn interaction. Our dataset consists of 60 video-recorded first-time oncology visits from two Italian hospitals. Across analyses conducted over the last seven years, we identify three practices central to negotiating intersubjectivity: (i) metapragmatic formulations, (ii) textual oralizing (reading/writing aloud), and (iii) the use of textual artifacts such as test results and prescriptions. These practices mediate transitions, repair misalignments, and create opportunities for recognizing participants’ perspectives. Dialogue thus emerges as a contingent and interactionally accomplished outcome.</Text>
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			<TitleText textformat="02">Chapter 6. Reimagining the potential of eliciting a patient’s story</TitleText>
			<Subtitle textformat="02">Reclaiming the “voice of the lifeworld” in medicine through dialogue</Subtitle>
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				<PersonName>Temple West</PersonName>
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					<Affiliation>Eastern Virginia Medical School, Norfolk</Affiliation>
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					<SubjectHeadingText>communication skills</SubjectHeadingText>
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					<SubjectHeadingText>dialogue</SubjectHeadingText>
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					<Text textformat="02">   Patients seek opportunities to share their stories with physicians as part of a meaningful clinical relationship. Although communication skills such as expressing empathy and eliciting patient narratives are central to medical education, the dialogic potential of clinical encounters often remains unrealized. Drawing on Raimo Puustinen’s claim that dialogue is fundamental to medical examination and treatment, this chapter argues that amplifying dialogue in medical education can strengthen both clinical information gathering and patient rapport. After briefly tracing historical models of the patient-provider relationship, the chapter examines the concepts of empathy and narrative and their relationship to dialogue. It then considers how communication skills are currently taught in medical training. Using transcribed encounters between medical students and standardized patients in clinical exam settings, the chapter demonstrates how open-ended questions at the beginning of interviews can transform routine exchanges into dialogic encounters that foster genuine empathy while also facilitating more effective and efficient clinical communication.</Text>
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			<TitleText textformat="02">Chapter 7. Patients’ narratives in oncology consultations</TitleText>
			<Subtitle textformat="02">How doctors can facilitate dialogue and agency</Subtitle>
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				<PersonName>Elisa Rossi</PersonName>
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					<Affiliation>University of Modena and Reggio Emilia</Affiliation>
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					<SubjectHeadingText>agency</SubjectHeadingText>
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					<SubjectHeadingText>dialogic facilitation</SubjectHeadingText>
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					<SubjectHeadingText>doctor-patient interaction</SubjectHeadingText>
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					<SubjectHeadingText>medical dialogue</SubjectHeadingText>
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					<SubjectHeadingText>narratives</SubjectHeadingText>
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					<Text textformat="02">   Enhanced by “medical dialogue” and increasingly promoted within healthcare systems, patient-centred approaches consider patients as individuals with personal needs, fears, stories, questions, and suggestions for their care. In this chapter, I define dialogue as a particular form of communication usually enhanced by specific actions and expectations, which can facilitate patients’ active participation and agency in interactions with practitioners. Presenting data from 106 consultations video-recorded in five oncological units in hospitals in Northern Italy, this chapter focuses on doctors’ dialogic facilitation of patients’ initiatives, presented in narrative format, within first-time visits. In my analysis of transcribed excerpts of the consultation, I show the communicative actions by which physicians dialogically facilitate and co-construct patient narratives, and detail the effects this has on interaction, particularly in relation to the discovery of the symptoms, the impact the illness has on the patient’s identity and emotional well-being and the potential implications for their care.</Text>
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				<PersonName>Chad Wickman</PersonName>
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					<Affiliation>Auburn University</Affiliation>
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					<SubjectHeadingText>clinical reporting</SubjectHeadingText>
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					<SubjectHeadingText>dialogism</SubjectHeadingText>
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					<Text textformat="02">   This chapter explores patient voice as a rhetorical and epistemological feature of clinical reporting. Drawing on published case reports that include a “patient’s perspective,” the author specifically examines how practitioners and patients use language to define their individual subjectivity, position themselves in relation to other voices in the text, and characterize each other relative to shared interactions and decision-making processes. I suggest that the medical case report provides unique insight into dialogic aspects of clinical documentation, and as a site of inquiry, shows how patient voice encounters and interacts with the discourse of biomedicine. The chapter concludes by discussing implications for research, practice, and work that seeks to amplify patient voice in healthcare settings.</Text>
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			<Subtitle textformat="02">The bright and dark side of the “patient-centered” doctrine in health care settings</Subtitle>
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				<PersonName>Letizia Caronia</PersonName>
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					<Affiliation>University of Bologna</Affiliation>
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					<Text textformat="02">   In the second half of the twentieth century, patient-centered care (PCC) gained ground as a dialogic practice within a new architecture of care and became the gold standard of healthcare worldwide. Adopting the analytical lenses of epistemic (in)justice and intersubjectivity, I reconstruct the history of this concept and argue that PCC and its corollaries (e.g., “patient empowerment and agency,” “shared decision making,” and “clinical empathy”) constitute a morally loaded doctrine whose raison d’être is ethical rather than clinical. Building on recent studies, I also illuminate the overlooked risks of uncritically adopting PCC: neglecting the non-agentic dimensions of “being a patient,” disregarding the dependence of effective caregiving on the caregiver’s epistemic and deontic authority, reinforcing abandonment through the rhetoric of empowerment, dismantling asymmetry-based models of care in favor of egalitarian consumer-provider relations, and tacitly aligning PCC with contemporary neoliberalism.</Text>
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