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  • 1
    Book
    Book
    Neuropädiatrie : evidenzbasierte Therapie (2020)
    München :Elsevier, Urban & Fischer,
    Details
    UID:
    almafu_BV046637849
    Format: XX, 468 Seiten : , Illustrationen ; , 24.6 cm x 17.3 cm.
    Edition: 3. Auflage
    ISBN: 978-3-437-23077-6 , 3-437-23077-8
    Additional Edition: Erscheint auch als Online-Ausgabe ISBN 978-3-437-05846-2
    Former: Vorangegangen ist
    Language: German
    Subjects: Medicine
    RVK:
    YQ 6500
    RVK:
    YQ 6515
    Keywords: Evidenz-basierte Medizin ; Kind ; Krankheit ; Therapie ; Nervensystem ; Kind ; Nervenkrankheit ; Therapie ; Kinderheilkunde ; Neurologie ; Kind ; Neurologie ; Aufsatzsammlung ; Aufsatzsammlung
    URL: Inhaltstext
    URL: http://shop.elsevier.de/978-3-437-23077-6
    URL: Inhaltstext
    URL: http://shop.elsevier.de/978-3-437-23077-6
    Author information: Hagel, Christian
    Author information: Korinthenberg, Rudolf 1949-
    Author information: Panteliadis, Christos P. 1937-
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  • 2
    Book
    Book
    Leukämie und Nervensystem : d. Hirnstrombild im Erkrankungs- u. Behandlungsverlauf d. akuten Leukämien d. Kindesalters. (1986)
    Stuttgart u.a. :Thieme,
    Details
    UID:
    almafu_BV000635307
    Format: 183 S. : Ill.
    ISBN: 3-13-698601-6
    Series Statement: Thieme-Copythek
    Note: Zugl.: Münster (Westfalen), Univ., Habil.- Schr., 1985 u.d.T.: Korinthenberg, Rudolf: Das Hirnstrombild im Behandlungsverlauf der akuten Leukämien des Kindesalters
    Language: German
    Subjects: Medicine
    RVK:
    YC 2500
    Keywords: Akute Leukämie ; Kind ; Elektroencephalogramm ; Hochschulschrift ; Hochschulschrift
    URL: Inhaltsverzeichnis
    Author information: Korinthenberg, Rudolf 1949-
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  • 3
    Online Resource
    Online Resource
    Neuropädiatrie : evidenzbasierte Therapie (2014)
    München :Elsevier, Urban & Fischer,
    Details
    UID:
    edocfu_BV042204802
    Format: 1 Online-Ressource (XXII, 514 S.) : , Ill., graph. Darst.
    Edition: 2. Aufl.
    ISBN: 978-3-437-23076-9 , 978-3-437-29672-7
    Language: German
    Subjects: Psychology , Medicine
    RVK:
    CZ 1340
    RVK:
    YQ 6500
    RVK:
    YQ 6503
    Keywords: Evidenz-basierte Medizin ; Kind ; Krankheit ; Therapie ; Nervensystem ; Kind ; Nervenkrankheit ; Therapie ; Kinderheilkunde ; Neurologie ; Kind ; Neurologie ; Aufsatzsammlung
    DOI: 10.1016/B978-3-437-23076-9.01001-9
    URL: Volltext
    Author information: Korinthenberg, Rudolf 1949-
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    Online Resource
    Online Access
    Open Access Request
    FU Berlin
    Charité
  • 4
    Online Resource
    Online Resource
    Neuromuscular Disorders in Children and Adolescents (2022)
    Basel : MDPI - Multidisciplinary Digital Publishing Institute
    Details
    UID:
    gbv_1832377067
    Format: 1 Online-Ressource (146 p.)
    ISBN: 9783036540702 , 9783036540696
    Content: Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical-descriptive and formal-genetic to a molecular-genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders
    Note: English
    Language: Undetermined
    URL: kostenfrei
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    Stabi Berlin
    UB Potsdam
  • 5
    Book
    Book
    Neuropädiatrie : evidenzbasierte Therapie (2009)
    München :Elsevier, Urban & Fischer,
    Details
    UID:
    almahu_BV035662163
    Format: XVI, 420 S. : , Ill., graph. Darst. ; , 25 cm.
    Edition: 1. Aufl.
    ISBN: 978-3-437-23075-2 , 3-437-23075-1
    Language: German
    Subjects: Psychology , Medicine
    RVK:
    CZ 1340
    RVK:
    YQ 6500
    RVK:
    YQ 6503
    Keywords: Kind ; Nervenkrankheit ; Therapie ; Evidenz-basierte Medizin ; Kind ; Krankheit ; Therapie ; Nervensystem ; Kinderheilkunde ; Neurologie ; Kind ; Neurologie ; Aufsatzsammlung ; Aufsatzsammlung ; Aufsatzsammlung
    URL: Inhaltstext
    URL: Inhaltsverzeichnis
    URL: http://d-nb.info/994412363/04
    URL: http://deposit.dnb.de/cgi-bin/dokserv?id=3310082&prov=M&dok_var=1&dok_ext=htm
    Author information: Korinthenberg, Rudolf, 1949-
    Author information: Armbruster, Sibylle, 1976-
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  • 6
    Online Resource
    Online Resource
    Neuropädiatrie : evidenzbasierte therapie (2014)
    München, [Germany] :Elsevier, Urban & Fischer,
    Details
    UID:
    almahu_9947368789702882
    Format: 1 online resource (634 p.)
    Edition: 2nd ed.
    ISBN: 3-437-29672-8
    Note: Description based upon print version of record. , Cover; Haupttitel; Inhaltsverzeichnis; Copyright; Vorwort zur 2. Auflage; Autorenverzeichnis; Abbildungsnachweis; Wozu Evidenzbasierung der Therapie?; Kapitel 1: Entwicklung, Fehlbildungen, pränatale Parenchymnekrosen des Nervensystems und Hydrozephalus; 1.1 Entwicklung des Nervensystems; 1.2 Fehlbildungen des Zentralnervensystems; 1.3 Pränatale Parenchymnekrosen (enzephaloklastische Defekte); 1.4 Hydrozephalus; Kapitel 2: Neurologische Erkrankungen des Neugeborenenalters; 2.1 Periventrikuläre Leukomalazie des Frühgeborenen , 2.2 Intraventrikuläre Blutung des Frühgeborenen und posthämorrhagischer Hydrozephalus2.3 Postnatale Stimulation bei Frühgeborenen zur Entwicklungsförderung; 2.4 Hypoxisch-Ischämische Enzephalopathie; 2.5 Hirninfarkt; 2.6 Intrakranielle Blutungen des reifen Neugeborenen; 2.7 Zerebrale Anfälle bei Neugeborenen; 2.8 Geburtstraumatische peripher-neurologische Schädigung; 2.9 Spezielle metabolische Probleme in der Neonatalperiode; 2.10 ZNS-Infektionen des Neugeborenen; Kapitel 3: Therapiekonzepte bei genetischen Syndromen mit mentaler Retardierung , 3.1 Spezifische Therapieansätze bei genetischen Erkrankungen3.2 Psychische Störungen bei geistig behinderten Kindern mit genetischen Syndromen - Therapiekonzepte und Förderung; Kapitel 4: Neurokutane Erkrankungen; Abstract; Zusammenfasssung; 4.1 Einführung; 4.2 Neurofibromatose Typ 1 (NF1); 4.3 Neurofibromatose Typ 2 (NF2); 4.4 Tuberöse Sklerose (TS/TSC); 4.5 Angiomatosis retinae et cerebelli (Von-Hippel-Lindau-Syndrom, VHL); 4.6 Ataxia teleangiectasia (Louis-Bar-Syndrom); 4.7 Sturge-Weber-Syndrom (Enzephalofaziale Angiomatose); 4.8 Incontinentia pigmenti (IP, Bloch-Sulzberger-Syndrom) , 4.9 Gorlin-Goltz-Syndrom (Naevoid-Basalzellkarzinom)4.10 Hypomelanosis Ito (Incontinentia pigmenti achromians); 4.11 Neurokutane Melanose (NCM); 4.12 Klippel-Trenaunay-Syndrom; 4.13 Sjögren-Larsson-Syndrom; 4.14 CHILD-Syndrom; 4.15 PHACE-Syndrom; 4.16 Proteus-Syndrom; Kapitel 5: Neurometabolische und neurodegenerative Krankheiten; 5.1 Einführung; 5.3 Peroxisomale Erkrankungen; 5.4 Metachromatische Leukodystrophie; 5.5 Weitere Leukodystrophien; 5.6 Neuronale Ceroid-Lipofuszinosen (NCL); 5.7 Weitere Neurolipidosen; 5.8 Mukopolysaccharidosen (MPS); 5.9 Angeborene Glykosylierungsstörungen (CDG) , 5.10 Menkes-Syndrom5.11 Morbus Wilson; 5.12 Krankheiten mit zerebraler Eisenspeicherung (NBIA); 5.13 Andere Stoffwechselkrankheiten mit neurologischen Symptomen; Kapitel 6: Hereditäre Bewegungsstörungen; 6.1 Dystonien; 6.2 Hereditäre Ataxien; 6.3 Hereditäre spastische Paraplegien; Kapitel 7: Epileptische und nicht-epileptische Anfälle; 7.1 Fieberkrämpfe; 7.2 Epilepsien im Kindes- und Jugendalter; 7.3 Nicht-epileptische paroxysmale Symptome im Säuglings- und Kleinkindalter; 7.4 Nicht-epileptische Anfälle im Schul- und Jugendalter; Kapitel 8: Kopfschmerzen; Abstract; Zusammenfasssung , 8.1 Epidemiologie und Prognose
    Additional Edition: ISBN 1-336-27888-9
    Additional Edition: ISBN 3-437-23076-X
    Language: German
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    Online Resource
    HU Berlin
  • 7
    Online Resource
    Online Resource
    Neuromuscular Disorders in Children and Adolescents (2022)
    Basel : MDPI - Multidisciplinary Digital Publishing Institute
    Details
    UID:
    edoccha_9960727607902883
    Format: 1 electronic resource (146 p.)
    Content: Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
    Note: English
    Additional Edition: ISBN 3-0365-4070-9
    Additional Edition: ISBN 3-0365-4069-5
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    Charité
  • 8
    Online Resource
    Online Resource
    Neuromuscular Disorders in Children and Adolescents (2022)
    Basel : MDPI - Multidisciplinary Digital Publishing Institute
    Details
    UID:
    almahu_9949298042102882
    Format: 1 electronic resource (146 p.)
    Content: Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
    Note: English
    Additional Edition: ISBN 3-0365-4070-9
    Additional Edition: ISBN 3-0365-4069-5
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    HU Berlin
  • 9
    Online Resource
    Online Resource
    Neuromuscular Disorders in Children and Adolescents (2022)
    Basel : MDPI - Multidisciplinary Digital Publishing Institute
    Details
    UID:
    edocfu_9960727607902883
    Format: 1 electronic resource (146 p.)
    Content: Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
    Note: English
    Additional Edition: ISBN 3-0365-4070-9
    Additional Edition: ISBN 3-0365-4069-5
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    FU Berlin
  • 10
    Online Resource
    Online Resource
    Neuropädiatrie : evidenzbasierte Therapie (2014)
    München :Elsevier, Urban & Fischer,
    Details
    UID:
    edoccha_BV042204802
    Format: 1 Online-Ressource (XXII, 514 S.) : , Ill., graph. Darst.
    Edition: 2. Aufl.
    ISBN: 978-3-437-23076-9 , 978-3-437-29672-7
    Language: German
    Subjects: Psychology , Medicine
    RVK:
    CZ 1340
    RVK:
    YQ 6500
    RVK:
    YQ 6503
    Keywords: Evidenz-basierte Medizin ; Kind ; Krankheit ; Therapie ; Nervensystem ; Kind ; Nervenkrankheit ; Therapie ; Kinderheilkunde ; Neurologie ; Kind ; Neurologie ; Aufsatzsammlung
    DOI: 10.1016/B978-3-437-23076-9.01001-9
    URL: Volltext
    Author information: Korinthenberg, Rudolf 1949-
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    Online Access
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    Charité
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