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  • Berlin  (17)
  • TH Brandenburg  (17)
  • SB Rathenow
  • Informationszentrum DGAP
  • 2000-2004  (17)
  • Medicine  (17)
Type of Medium
Language
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Years
Year
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  • 1
    UID:
    almafu_BV036069365
    Format: 1 Online-Ressource (XII, 221 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00568-4
    Series Statement: Frontiers of radiation therapy and oncology Vol. 35
    Content: This volume discusses radiotherapy and its role in the treatment of benign diseases. Its intent is to broaden the application of radiotherapy beyond malignancy to treat a range of clinical concerns, from minor skin problems to life-threatening arterial disease. In addition, it aims to encourage medical practitioners to consider the benefits versus the risks of radiotherapy, and assess the most modern technology for uses that may benefit the greatest number of patients.The major challenge in this field is to develop new strategies for the controlled use of radiotherapy. This includes the ability to focus and control applications with equipment that can target tissues with high accuracy, using new methods of isotopic and external beam introduction. It also means minimizing the risk of uncontrolled radiation exposure by employing minimal doses and the smallest tissue volume required to achieve the desired effect.The Radiation Therapy of Benign Diseases features articles written by internationally recognized experts who confront and critically discuss these major issues. It will prove to be an essential and informative read not only for radiation therapists but also for internists, surgeons, ophthalmologists and biologists interested in this endeavor
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7063-3
    Language: English
    Subjects: Medicine
    RVK:
    RVK:
    RVK:
    Keywords: Strahlentherapie ; Konferenzschrift
    Author information: Meyer, John L. 1949-
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    almahu_BV036069365
    Format: 1 Online-Ressource (XII, 221 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00568-4
    Series Statement: Frontiers of radiation therapy and oncology Vol. 35
    Content: This volume discusses radiotherapy and its role in the treatment of benign diseases. Its intent is to broaden the application of radiotherapy beyond malignancy to treat a range of clinical concerns, from minor skin problems to life-threatening arterial disease. In addition, it aims to encourage medical practitioners to consider the benefits versus the risks of radiotherapy, and assess the most modern technology for uses that may benefit the greatest number of patients.The major challenge in this field is to develop new strategies for the controlled use of radiotherapy. This includes the ability to focus and control applications with equipment that can target tissues with high accuracy, using new methods of isotopic and external beam introduction. It also means minimizing the risk of uncontrolled radiation exposure by employing minimal doses and the smallest tissue volume required to achieve the desired effect.The Radiation Therapy of Benign Diseases features articles written by internationally recognized experts who confront and critically discuss these major issues. It will prove to be an essential and informative read not only for radiation therapists but also for internists, surgeons, ophthalmologists and biologists interested in this endeavor
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7063-3
    Language: English
    Subjects: Medicine
    RVK:
    RVK:
    RVK:
    Keywords: Strahlentherapie ; Konferenzschrift
    Author information: Meyer, John L., 1949-
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    UID:
    edoccha_BV036069365
    Format: 1 Online-Ressource (XII, 221 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00568-4
    Series Statement: Frontiers of radiation therapy and oncology Vol. 35
    Content: This volume discusses radiotherapy and its role in the treatment of benign diseases. Its intent is to broaden the application of radiotherapy beyond malignancy to treat a range of clinical concerns, from minor skin problems to life-threatening arterial disease. In addition, it aims to encourage medical practitioners to consider the benefits versus the risks of radiotherapy, and assess the most modern technology for uses that may benefit the greatest number of patients.The major challenge in this field is to develop new strategies for the controlled use of radiotherapy. This includes the ability to focus and control applications with equipment that can target tissues with high accuracy, using new methods of isotopic and external beam introduction. It also means minimizing the risk of uncontrolled radiation exposure by employing minimal doses and the smallest tissue volume required to achieve the desired effect.The Radiation Therapy of Benign Diseases features articles written by internationally recognized experts who confront and critically discuss these major issues. It will prove to be an essential and informative read not only for radiation therapists but also for internists, surgeons, ophthalmologists and biologists interested in this endeavor
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7063-3
    Language: English
    Subjects: Medicine
    RVK:
    RVK:
    RVK:
    Keywords: Strahlentherapie ; Konferenzschrift
    Author information: Meyer, John L. 1949-
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    UID:
    almahu_BV017455761
    Format: XVI, 284 S. : , Ill., graph. Darst.
    ISBN: 3-540-62536-4
    Language: German
    Subjects: Sports Science , Medicine
    RVK:
    RVK:
    Keywords: Sportmedizin ; Bewegungsapparat ; Funktionsdiagnostik ; Sportmedizin ; Bewegungsapparat ; Krankheit ; Funktionsdiagnostik ; Aufsatzsammlung ; Aufsatzsammlung ; Aufsatzsammlung ; Aufsatzsammlung ; Aufsatzsammlung
    URL: Cover
    Author information: Pfeifer, Klaus.
    Author information: Banzer, Winfried, 1953-
    Author information: Vogt, Lutz, 1968-
    Library Location Call Number Volume/Issue/Year Availability
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  • 5
    Online Resource
    Online Resource
    Basel :Karger,
    UID:
    almafu_BV036069151
    Format: 1 Online-Ressource (VIII, 218 Seiten) : , Diagramme.
    ISBN: 978-3-318-00681-0
    Series Statement: Frontiers of hormone research Vol. 28
    Content: The genetics of endocrine cancers is clearly an area where new scientific discoveries that have occurred in the past few years have already been translated into clinical practice. This volume attempts to provide a state-of-the-art review of some of the most relevant inherited syndromes that share a higher susceptibility to the development of endocrine tumors. It focuses on familial tumor syndromes for which the primary gene defect has been well characterized or recently identified. An overview of cloning strategies and gene characterization in cancer, is combined with detailed discussions of clinical aspects and molecular features of heritable endocrine neoplastic diseases, such as MEN1 and MEN2 and Von Hippel-Lindau disease. Studies on the PTEN gene, the first known phosphatase to lead to cancer when disrupted are discussed in detail. Also included disrupted is the recent identification and partial characterization of one of at least two genes for Carney Complex, PRKARIA.The authors place special emphasis on testing and screening strategies which now allow a much earlier identification of family members at risk. The challenge for the 21st century will be to develop equal progress in pharmacological prevention and cure based on the knowledge of the function of these susceptibility genes and their targets
    Note: a comprehensive guide to the understanding of contemporary endocrine cancer genetics
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7203-3
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Multiple endokrine Adenopathie ; Erbkrankheit ; Molekulargenetik ; Angiomatosis retinae ; Erbkrankheit ; Molekulargenetik ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
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  • 6
    Online Resource
    Online Resource
    Basel :Karger,
    UID:
    almahu_BV036069151
    Format: 1 Online-Ressource (VIII, 218 Seiten) : , Diagramme.
    ISBN: 978-3-318-00681-0
    Series Statement: Frontiers of hormone research Vol. 28
    Content: The genetics of endocrine cancers is clearly an area where new scientific discoveries that have occurred in the past few years have already been translated into clinical practice. This volume attempts to provide a state-of-the-art review of some of the most relevant inherited syndromes that share a higher susceptibility to the development of endocrine tumors. It focuses on familial tumor syndromes for which the primary gene defect has been well characterized or recently identified. An overview of cloning strategies and gene characterization in cancer, is combined with detailed discussions of clinical aspects and molecular features of heritable endocrine neoplastic diseases, such as MEN1 and MEN2 and Von Hippel-Lindau disease. Studies on the PTEN gene, the first known phosphatase to lead to cancer when disrupted are discussed in detail. Also included disrupted is the recent identification and partial characterization of one of at least two genes for Carney Complex, PRKARIA.The authors place special emphasis on testing and screening strategies which now allow a much earlier identification of family members at risk. The challenge for the 21st century will be to develop equal progress in pharmacological prevention and cure based on the knowledge of the function of these susceptibility genes and their targets
    Note: a comprehensive guide to the understanding of contemporary endocrine cancer genetics
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7203-3
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Multiple endokrine Adenopathie ; Erbkrankheit ; Molekulargenetik ; Angiomatosis retinae ; Erbkrankheit ; Molekulargenetik ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
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  • 7
    UID:
    almahu_BV036069015
    Format: 1 Online-Ressource (X, 177 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00535-6
    Series Statement: Endocrine development Vol. 2
    Content: Adrenal disease in children poses an immensely difficult diagnostic and management problem for the paediatrician in view of the large number of rare pathologies that may present in this way. This volume brings together the expertise of the acknowledged leaders in specific adrenal disorders to provide a readily accessible text that combines a detailed description of the molecular origins of these diseases, as they are currently understood, with a unique account of the clinical features and therapeutic options. Beginning with disorders that primarily affect adrenal development and progressing towards the defects that interfere with steroid production, the reader gains considerable insight into the normal physiology of the adrenal cortex particularly as revealed by clinical disorders. The major contributions of modern biochemistry and molecular genetics in our current understanding are visible throughout, providing a unique overview of adrenocortical biology. This book is of great interest to general pediatricians, paediatric endocrinologists, adult endocrinologists, clinical geneticists and basic scientists working in areas such as developmental biology and molecular steroidogenesis
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7015-2
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Kind ; Nebennierenkrankheit ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
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  • 8
    UID:
    almafu_BV036069015
    Format: 1 Online-Ressource (X, 177 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00535-6
    Series Statement: Endocrine development Vol. 2
    Content: Adrenal disease in children poses an immensely difficult diagnostic and management problem for the paediatrician in view of the large number of rare pathologies that may present in this way. This volume brings together the expertise of the acknowledged leaders in specific adrenal disorders to provide a readily accessible text that combines a detailed description of the molecular origins of these diseases, as they are currently understood, with a unique account of the clinical features and therapeutic options. Beginning with disorders that primarily affect adrenal development and progressing towards the defects that interfere with steroid production, the reader gains considerable insight into the normal physiology of the adrenal cortex particularly as revealed by clinical disorders. The major contributions of modern biochemistry and molecular genetics in our current understanding are visible throughout, providing a unique overview of adrenocortical biology. This book is of great interest to general pediatricians, paediatric endocrinologists, adult endocrinologists, clinical geneticists and basic scientists working in areas such as developmental biology and molecular steroidogenesis
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7015-2
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Kind ; Nebennierenkrankheit ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
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  • 9
    UID:
    edoccha_BV036069015
    Format: 1 Online-Ressource (X, 177 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-00535-6
    Series Statement: Endocrine development Vol. 2
    Content: Adrenal disease in children poses an immensely difficult diagnostic and management problem for the paediatrician in view of the large number of rare pathologies that may present in this way. This volume brings together the expertise of the acknowledged leaders in specific adrenal disorders to provide a readily accessible text that combines a detailed description of the molecular origins of these diseases, as they are currently understood, with a unique account of the clinical features and therapeutic options. Beginning with disorders that primarily affect adrenal development and progressing towards the defects that interfere with steroid production, the reader gains considerable insight into the normal physiology of the adrenal cortex particularly as revealed by clinical disorders. The major contributions of modern biochemistry and molecular genetics in our current understanding are visible throughout, providing a unique overview of adrenocortical biology. This book is of great interest to general pediatricians, paediatric endocrinologists, adult endocrinologists, clinical geneticists and basic scientists working in areas such as developmental biology and molecular steroidogenesis
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7015-2
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Kind ; Nebennierenkrankheit ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Online Resource
    Online Resource
    Basel :Karger,
    UID:
    edoccha_BV036069151
    Format: 1 Online-Ressource (VIII, 218 Seiten) : , Diagramme.
    ISBN: 978-3-318-00681-0
    Series Statement: Frontiers of hormone research Vol. 28
    Content: The genetics of endocrine cancers is clearly an area where new scientific discoveries that have occurred in the past few years have already been translated into clinical practice. This volume attempts to provide a state-of-the-art review of some of the most relevant inherited syndromes that share a higher susceptibility to the development of endocrine tumors. It focuses on familial tumor syndromes for which the primary gene defect has been well characterized or recently identified. An overview of cloning strategies and gene characterization in cancer, is combined with detailed discussions of clinical aspects and molecular features of heritable endocrine neoplastic diseases, such as MEN1 and MEN2 and Von Hippel-Lindau disease. Studies on the PTEN gene, the first known phosphatase to lead to cancer when disrupted are discussed in detail. Also included disrupted is the recent identification and partial characterization of one of at least two genes for Carney Complex, PRKARIA.The authors place special emphasis on testing and screening strategies which now allow a much earlier identification of family members at risk. The challenge for the 21st century will be to develop equal progress in pharmacological prevention and cure based on the knowledge of the function of these susceptibility genes and their targets
    Note: a comprehensive guide to the understanding of contemporary endocrine cancer genetics
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-7203-3
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Multiple endokrine Adenopathie ; Erbkrankheit ; Molekulargenetik ; Angiomatosis retinae ; Erbkrankheit ; Molekulargenetik ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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