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[null,"1.","Record Nr.",null,"UNINA9910158657703321"]
[null,null,"Autore",null,"Howard A. G (Anita G.)"]
[null,null,"Titolo",null,"Splintered / / a novel by A. G. Howard ; book design by Maria T. Middleton"]
[null,null,"Pubbl/distr/stampa",null,"New York, New York : , : Amulet Books, , 2013"]
[{"$nulls":4},"©2013"]
[null,null,"ISBN",null,"1-61312-379-5"]
[null,null,"Descrizione fisica",null,"1 online resource (222 p.)"]
[null,null,"Collana",null,"Splintered"]
[null,null,"Classificazione",null,"JUV037000JUV012040JUV000000"]
[null,null,"Disciplina",null,"813.6"]
[null,null,"Soggetti",null,"Paranormal fiction"]
[{"$nulls":4},"Characters in literature"]
[{"$nulls":4},"Blessing and cursing"]
[{"$nulls":4},"Mental illness"]
[{"$nulls":4},"Mothers and daughters"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Sommario/riassunto","A descendant of the inspiration for Alice's Adventures in Wonderland, sixteen-year-old Alyssa Gardner fears she is mentally ill like her mother until she finds that Wonderland is real and, if she passes a series of tests to fix Alice's mistakes, she may save her family from their curse."]
[null,"2.","Record Nr.",null,"UNINA9910790445103321"]
[null,null,"Autore",null,"Featherstone Katie"]
[null,null,"Titolo",null,"Creating conditions : the making and remaking of a genetic syndrome / / Katie Featherstone and Paul Atkinson"]
[null,null,"Pubbl/distr/stampa",null,"Abingdon, Oxon ; ; New York, N.Y. : , : Routledge, , 2012"]
[null,null,"ISBN",null,"1-134-00479-6"]
[{"$nulls":4},"1-283-45811-X"]
[{"$nulls":4},"9786613458117"]
[{"$nulls":4},"1-134-00480-X"]
[{"$nulls":4},"0-203-87815-9"]
[null,null,"Descrizione fisica",null,"1 online resource (141 p.)"]
[null,null,"Collana",null,"Genetics and society"]
[null,null,"Classificazione",null,"SOC002020SOC024000SOC026000"]
[null,null,"Disciplina",null,"616.85/884"]
[null,null,"Soggetti",null,"Rett syndrome"]
[{"$nulls":4},"Genetic disorders"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references (p. [123]-126) and index."]
[{"$nulls":4},"Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Front Cover; Creating Conditions; Copyright Page; Contents; Acknowledgments; 1. Multiple sites of a syndrome; 2. Making medical entities; 3. The culture of the clinic; 4. The transformation of patienthood; 5. Transforming Rett syndrome; 6. The making and remaking of medical classifications; References; Index"]
[null,null,null,"Sommario/riassunto","\"Based on original ethnographic research with scientists, clinicians and families, this book examines Rett syndrome to illuminate more general issues concerning the construction and interpretation of diseases and syndromes. It derives from research with a specialist team of clinicians and scientists, and a series of families referred with a potential diagnosis of Rett syndrome, and documents the scientific, clinical, patient and family experiences over a three-year period. Although Rett syndrome itself is rare, it is one of some 2,000 such syndromes, and its genetic basis has recently been linked to the much broader Autism spectrum. From a sociological or anthropological point of view, it is also of considerable interest as a clinical entity that is undergoing transformation in the light of recent post-genomic research. Traditionally, such syndromes have been diagnosed clinically, but increasingly genetic technologies are having an impact on the diagnosis, description and classification of conditions. Rett Syndrome is "]
[{"$nulls":4},"thus a key exemplar of the implications of genetic medicine that are far-reaching and extend well beyond this particular syndrome\"--"]