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286 S., brosch., guter Zustand.

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Condizione: New. 1st ed. 2022 edition NO-PA16APR2015-KAP.

Paperback. Condizione: Brand New. 286 pages. 9.25x6.10x0.60 inches. In Stock.

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Condizione: New. &Uumlber den AutorChristina Schuees is Professor of Philosophy in the Institute for History of Medicine and Science Studies at the University of Luebeck, and also adjunct Professor of Philosophy in the Institute of Philosophy an.

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Hardcover. Condizione: Brand New. 1st edition. 279 pages. 9.75x6.50x0.75 inches. In Stock.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions.Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young childrenhowever are not in a position to give consent themselves. How should they be adequately included, depending to their age Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Condizione: Gut. Zustand: Gut | Seiten: 288 | Sprache: Englisch | Produktart: Bücher | This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age? Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts? For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Condizione: Sehr gut. Zustand: Sehr gut | Seiten: 288 | Sprache: Englisch | Produktart: Bücher | This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age? Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts? For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Condizione: Hervorragend. Zustand: Hervorragend | Seiten: 288 | Sprache: Englisch | Produktart: Bücher | This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age? Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts? For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Condizione: Gut. Zustand: Gut | Seiten: 288 | Sprache: Englisch | Produktart: Bücher | This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age? Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts? For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Condizione: Hervorragend. Zustand: Hervorragend | Seiten: 288 | Sprache: Englisch | Produktart: Bücher | This open access book offers insights in short- and long-term experiences from families with bone marrow transplantations between minor siblings. It is based on the first extended qualitative study with 17 families about experiences with recent transplants and experiences with transplants up to 20 years in the past. It covers reflections of donors, recipients and other family members, as well as family interactions. Transplantation of bone marrow from one sibling to another who is ill with a blood cancer (such as Leukemia) is a life-saving therapy. Young children however are not in a position to give consent themselves. How should they be adequately included, depending to their age? Which ethical questions are raised for the parents both at the time of treatment and afterwards, and for the medical professionals in clinical and regulatory contexts? For an in-depth discussion of the findings the books brings together a group of leading scholars from the fields of bioethics,family sociology and philosophy of medicine.

Mentis, Münster, (2015). 286 S., 24 cm, kartoniert---- neuwertig / original verlagsfrisch verschweißt - 440 Gramm.

Condizione: New.

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Taschenbuch. Condizione: Neu. Neuware -Die Knochenmarkspende von Kindern für Geschwister, die an Leukämie erkrankt sind, ist eine lebensrettende Therapie. Kinder sind aber noch nicht in der Lage, selbst eine Einwilligung zu geben. Wie sollen Kinder beteiligt werden Welche ethischen Fragen stellen sich Die Beiträge diskutieren moralische, rechtliche, psychologische, philosophische und gesellschaftliche Aspekte: Fragen zur Freiwilligkeit bei der Einwilligung zu einer Spende, zur Verletzlichkeit des Kindes und zu Verstrickungen in Familienbeziehungen, zum Verhältnis von Recht und Ethik, zur möglichen Diskrepanz von Kindeswohl und Kindeswille und zu den Kinderrechten. Wie sich zeigt, geht es um mehr als um die Einwilligung selbst, nämlich um das Integrierenkönnen der Spende (oder in seltenen Fällen der Entscheidung gegen sie) in die Biographie des Spenderkindes, um die psychische und narrative Verarbeitung innerhalb der Familiengeschichte, um die Sicht auf die Geschehnisse aus der Retrospektive Jahre später. Diese Aspekte haben Implikationen für das Verständnis und die Bedeutung von 'Zustimmung und Zumutung' auch in anderen Bereichen der Medizin, in denen eine rettende Behandlung kaum abzulehnen ist. 286 pp. Deutsch.

Taschenbuch. Condizione: Neu. Neuware -Die Knochenmarkspende von Kindern für Geschwister, die an Leukämie erkrankt sind, ist eine lebensrettende Therapie. Kinder sind aber noch nicht in der Lage, selbst eine Einwilligung zu geben. Wie sollen Kinder beteiligt werden Welche ethischen Fragen stellen sich Die Beiträge diskutieren moralische, rechtliche, psychologische, philosophische und gesellschaftliche Aspekte: Fragen zur Freiwilligkeit bei der Einwilligung zu einer Spende, zur Verletzlichkeit des Kindes und zu Verstrickungen in Familienbeziehungen, zum Verhältnis von Recht und Ethik, zur möglichen Diskrepanz von Kindeswohl und Kindeswille und zu den Kinderrechten. Wie sich zeigt, geht es um mehr als um die Einwilligung selbst, nämlich um das Integrierenkönnen der Spende (oder in seltenen Fällen der Entscheidung gegen sie) in die Biographie des Spenderkindes, um die psychische und narrative Verarbeitung innerhalb der Familiengeschichte, um die Sicht auf die Geschehnisse aus der Retrospektive Jahre später. Diese Aspekte haben Implikationen für das Verständnis und die Bedeutung von 'Zustimmung und Zumutung' auch in anderen Bereichen der Medizin, in denen eine rettende Behandlung kaum abzulehnen ist. 286 pp. Deutsch.