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1. |
Record Nr. |
UNINA9910787736203321 |
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Autore |
Kelly Dennis <1970-> |
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Titolo |
From morning to midnight / / Georg Kaiser ; in a new version by Dennis Kelly |
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Pubbl/distr/stampa |
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London : , : Oberon Books : , : Bloomsbury Publishing, , 2013 |
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ISBN |
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1-350-20724-1 |
1-78319-512-6 |
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Descrizione fisica |
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1 online resource (132 p.) |
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Collana |
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Altri autori (Persone) |
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Disciplina |
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Soggetti |
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Life change events - Psychological aspects |
Self-destructive behavior |
Drama & Performance Studies |
Plays, playscripts |
Adaptations. |
Drama |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di contenuto |
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Cover; Half-title Page; Title Page; Copyright; Contents; 1. The Machine; 2. The Bourgeoisie; 3. Epiphany; 4. The Family; 5. Society; 6. Sex; 7. Salvation |
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Sommario/riassunto |
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From Morning To Midnight, among the most frequently performed German Expressionist works, charts the life of a cashier who steals money from the bank and flees to Berlin. The un-named protagonist's bid to escape his middle-class daily life is ultimately frustrated. It is a popular piece in which Kaiser satirized the cheapness and futility of modern society. His hero, a kind of machine-age Everyman, searches everywhere for some kind of fulfilment--in commercial sex, in salvationist religion--but discovers through a series of nightmarish episodes that the world is deceitful and illusory. In the end, disillusioned and pursued by the police, he takes his own life. This new version by Dennis Kelly, opened at the National Theatre's Lyttelton Theatre in November 2013, as part of the National's 50th Anniversary Season. |
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2. |
Record Nr. |
UNINA9910797775003321 |
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Titolo |
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others] |
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Pubbl/distr/stampa |
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New York, New York : , : Oxford University Press, , 2016 |
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©2016 |
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ISBN |
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0-19-938605-6 |
0-19-938604-8 |
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Edizione |
[Third edition.] |
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Descrizione fisica |
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1 online resource (1001 p.) |
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Collana |
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Oxford Monographs on Medical Genetics ; ; 66 |
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Disciplina |
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Soggetti |
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Abnormalities, Human - Prevention |
Abnormalities, Human - Research |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references and index. |
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Nota di contenuto |
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Cover; OXFORD MONOGRAPHS ON MEDICAL GENETICS; HUMAN MALFORMATIONS AND RELATED ANOMALIE; CONTENTS; PREFACE; ACKNOWLEDGMENTS; CONTRIBUTORS; INTRODUCTION; I.1. Nomenclature; I.2. Etiology and Pathogenesis; I.3. Classification and Coding; I.4. Genetic Causes of Congenital Anomalies; I.5. Environmental Causes of Congenital Anomalies; I.6. Human Anomalies with Unknown Causes; I.7. Detection, Diagnosis, Evaluation, Management; 1 | LIMBS; Introduction; 1.1. Limb Deficiency; 1.1a. Absence of Limb; 1.1b. Absent Radius; 1.1c. Absent Ulna; 1.1d. Absence and Hypoplasia of the Humerus |
1.1e. Absence and Hypoplasia of the Tibia1.1f. Absence and Hypoplasia of the Fibula ; 1.1g. Absence and Hypoplasia of the Femur; 1.1h. Terminal Transverse Limb Deficiency; 1.2. Synostosis; 1.2a. Carpal Coalition and Tarsal Coalition; 1.2b. Metacarpophalangeal and Metatarsophalangeal Synostosis; 1.2c. Proximal Symphalangism; 1.2d. Distal Symphalangism; 1.2e. Humeroradial Synostosis; 1.2f. Radioulnar Synostosis; 1.2g. Tibiofibular Synostosis; 1.2h. Sirenomelia; 1.3. Constriction Rings; 1.4. Excessive Partitions, Duplications, and Accessory Bones; 1.5. Bowing of Long Bones; 1.6. Short Stature |
1.7. Tall Stature1.8. Limb Overgrowth; 1.9. Increased Bone Density; 1.10. Decreased Bone Density; 1.11. Osteolysis; 1.12. Anomalies of the |
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Patella; 1.13. Arthrogryposis; 1.13a. Amyoplasia; 1.13b. Distal Arthrogryposis; 1.13c. Fetal Akinesia Phenotype; 1.13d. Pterygium; 2 | HANDS AND FEET; Introduction; 2.1. Polydactyly; 2.1a. Preaxial Polydactyly; 2.1b. Postaxial Polydactyly; 2.1c. Mesoaxial Polydactyly; 2.2. Syndactyly; 2.2a. Syndactyly Type I; 2.2b. Syndactyly Type II; 2.2c. Syndactyly Type III; 2.2d. Syndactyly Type IV; 2.2e. Syndactyly Type V; 2.2f. Complete Syndactyly |
2.2g. Cenani-Lenz Syndactyly2.2h. Symbrachydactyly; 2.3. Brachydactyly; 2.3a. Brachydactyly Type A1; 2.3b. Brachydactyly Type A2; 2.3c. Brachydactyly Type A3; 2.3d. Brachydactyly Type B; 2.3e. Brachydactyly Type C; 2.3f. Brachydactyly Type D; 2.3g. Brachydactyly Type E; 2.4. Osseous Deficiencies of the Hands and Feet; 2.4a. Preaxial Deficiency; 2.4b. Postaxial Deficiency; 2.5. Terminal Transverse Deficiency; 2.6. Split-Hand/Foot Malformation; 2.7. Macrodactyly; 2.8. Camptodactyly; 2.9. Clubfoot; 3 | PECTORAL AND PELVIC GIRDLES; Introduction; 3.1. Clavicular Hypoplasia or Aplasia |
3.2. Clavicular Pseudoarthrosis3.3. Altered Shape and Other Abnormalities of the Clavicle; 3.4. Sprengel Anomaly; 3.5. Glenoid Hypoplasia; 3.6. Anomalies of the Pelvic Bones; 3.7. Developmental Dysplasia of the Hip; 3.8. Coxa Vara; 3.9. Coxa Valga; 4 | SPINE AND THORACIC CAGE; Introduction; 4.1. Occipitalization of the Atlas; 4.2. Aplasia/Hypoplasia of the Odontoid Process of the Axis; 4.3. Klippel-Feil Anomaly; 4.4. Segmentation Defects of the Vertebrae; 4.5. Altered Vertebral Body Contour; 4.6. Sagittal Clefts of the Vertebrae; 4.7. Coronal Clefts of the Vertebrae |
4.8. Spondylolysis and Spondylolisthesis |
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Sommario/riassunto |
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The central theme of this text is to provide information on individual anomalies & to connect these anomalies to the malformation syndromes & associated problems, primarily through the use of differential diagnostic tables. |
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