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Biblioteca

MARC Lista (tabellare)
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
Autore Aitken Kenneth J
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (498 p.)
Disciplina 618.92/85882
Soggetto topico Autism in children
Autism spectrum disorders
Mental illness - Genetic aspects
Soggetto genere / forma Electronic books.
ISBN 1-283-90676-7
0-85700-388-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto An A-Z of Genetic Factors in Autism: A Handbook for Parents and Carers; Acknowledgements; Prelude; Introduction; SECTION A: Focus on the autistic spectrum disorders; Why you might need a book like this; Help and treatment: does one size fit all?; ASD and 'inborn errors of metabolism'; Biochemical individuality: are we all the same?; Is ASD getting more common?; A brief history of ASD research; Early presenting features of ASDs; Physical checklist of features that can be seen on physical examination and which may have clinical relevance; Further clinical aspects that may require investigation
Genetic clinical conditions linked with autism 'Alternative' approaches; SECTION B: Clinical disorders seen in the autistic spectrum disorders; 1. 15q11-q13 duplication; 2. Chromosome 2q37 deletion; 3. XXY syndrome; 4. XYY syndrome; 5. 10p terminal deletion; 6. 45,X/46,XY mosaicism; 7. 22q13 deletion syndrome; 8. Aarskog syndrome; 9. Adenylosuccinate lyase (ADSL) deficiency; 10. Adrenomyeloneuropathy (AMN); 11. Angelman syndrome (AS); 12. Apert syndrome; 13. ARX gene mutations; 14. Autism secondary to autoimmune lymphoproliferative syndrome (ALPS); 15. Bannayan-Riley-Ruvalcaba syndrome (BRRS)
16. Basal cell naevus syndrome (BCNS)17. Biedl-Bardet syndrome (BBS); 18. CATCH 22; 19. Cortical dysplasia-focal epilepsy (CDFE) syndrome; 20. CHARGE syndrome; 21. Coffin-Lowry syndrome (CLS); 22. Coffin-Siris syndrome (CSS); 23. Cohen syndrome; 24. Cole-Hughes macrocephaly syndrome (CHMS); 25. Congenital adrenal hyperplasia (CAH); 26. Cowden syndrome (CS); 27. De Lange syndrome (CdLS); 28. Juvenile dentatorubral-pallidoluysian atrophy (JDPLA); 29a. DiGeorge syndrome I (phenotypic overlap); 29b. DiGeorge syndrome II (DGS II); 30. Dihydropyrimidine dehydrogenase (DPYS) deficiency
31. Down syndrome (DS)32. Dravet's syndrome; 33. Duchenne (DMD) and Becker (BMD) muscular dystrophy; 34. Ehlers-Danlos syndrome (EDS); 35. Fragile-X syndrome (FRAX); 36. Fragile-X permutation (partial methylation defects); 37. GAMT deficiency (guanidinoacetate methyltransferase deficiency); 38. Goldenhar syndrome; 39. HEADD syndrome; 40. L-2-hydroxyglutaric aciduria (L-2 HGAA); 41. Hyper IgE syndrome with autism (HiES); 42. Hypomelanosis of Ito (HI); 43. Hypothyroidism; 44. Joubert syndrome; 45. Kleine-Levin syndrome; 46. Lujan-Fryns syndrome; 47. 2-methylbutyryl-CoA dehydrogenase deficiency
48. Mobius/Möbius/Moebius syndrome 49. Myhre syndrome; 50. Myotonic dystrophy (MD1); 51. Neurofibromatosis type 1 (NF1); 52. Noonan syndrome (NS); 53. NAPDD; 54. Oculocutaneous albinism (OCA); 55. Ornithine carbamyltransferase deficiency (OCTD); 56. Orstavik 1997 syndrome; 57. Phenylketonuria (PKU); 58. Pituitary deficiency; 59. Port-wine facial staining and autism; 60. Potocki-Lupski syndrome (PTLS); 61. Prader-Willi syndrome (PWS); 62. Proteus syndrome; 63a. Rett syndrome (RTT); 63b. Rett syndrome (Hanefeld variant) (RSHV); 64. Rubinstein-Taybi syndrome; 65. Schindler disease
66. Smith-Lemli-Opitz syndrome (SLOS)
Record Nr. UNINA-9910465218703321
Aitken Kenneth J  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
Autore Aitken Kenneth J
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (498 p.)
Disciplina 618.92/85882
Soggetto topico Autism in children
Autism spectrum disorders
Mental illness - Genetic aspects
Soggetto genere / forma Electronic books.
ISBN 1-283-90676-7
0-85700-388-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto An A-Z of Genetic Factors in Autism: A Handbook for Parents and Carers; Acknowledgements; Prelude; Introduction; SECTION A: Focus on the autistic spectrum disorders; Why you might need a book like this; Help and treatment: does one size fit all?; ASD and 'inborn errors of metabolism'; Biochemical individuality: are we all the same?; Is ASD getting more common?; A brief history of ASD research; Early presenting features of ASDs; Physical checklist of features that can be seen on physical examination and which may have clinical relevance; Further clinical aspects that may require investigation
Genetic clinical conditions linked with autism 'Alternative' approaches; SECTION B: Clinical disorders seen in the autistic spectrum disorders; 1. 15q11-q13 duplication; 2. Chromosome 2q37 deletion; 3. XXY syndrome; 4. XYY syndrome; 5. 10p terminal deletion; 6. 45,X/46,XY mosaicism; 7. 22q13 deletion syndrome; 8. Aarskog syndrome; 9. Adenylosuccinate lyase (ADSL) deficiency; 10. Adrenomyeloneuropathy (AMN); 11. Angelman syndrome (AS); 12. Apert syndrome; 13. ARX gene mutations; 14. Autism secondary to autoimmune lymphoproliferative syndrome (ALPS); 15. Bannayan-Riley-Ruvalcaba syndrome (BRRS)
16. Basal cell naevus syndrome (BCNS)17. Biedl-Bardet syndrome (BBS); 18. CATCH 22; 19. Cortical dysplasia-focal epilepsy (CDFE) syndrome; 20. CHARGE syndrome; 21. Coffin-Lowry syndrome (CLS); 22. Coffin-Siris syndrome (CSS); 23. Cohen syndrome; 24. Cole-Hughes macrocephaly syndrome (CHMS); 25. Congenital adrenal hyperplasia (CAH); 26. Cowden syndrome (CS); 27. De Lange syndrome (CdLS); 28. Juvenile dentatorubral-pallidoluysian atrophy (JDPLA); 29a. DiGeorge syndrome I (phenotypic overlap); 29b. DiGeorge syndrome II (DGS II); 30. Dihydropyrimidine dehydrogenase (DPYS) deficiency
31. Down syndrome (DS)32. Dravet's syndrome; 33. Duchenne (DMD) and Becker (BMD) muscular dystrophy; 34. Ehlers-Danlos syndrome (EDS); 35. Fragile-X syndrome (FRAX); 36. Fragile-X permutation (partial methylation defects); 37. GAMT deficiency (guanidinoacetate methyltransferase deficiency); 38. Goldenhar syndrome; 39. HEADD syndrome; 40. L-2-hydroxyglutaric aciduria (L-2 HGAA); 41. Hyper IgE syndrome with autism (HiES); 42. Hypomelanosis of Ito (HI); 43. Hypothyroidism; 44. Joubert syndrome; 45. Kleine-Levin syndrome; 46. Lujan-Fryns syndrome; 47. 2-methylbutyryl-CoA dehydrogenase deficiency
48. Mobius/Möbius/Moebius syndrome 49. Myhre syndrome; 50. Myotonic dystrophy (MD1); 51. Neurofibromatosis type 1 (NF1); 52. Noonan syndrome (NS); 53. NAPDD; 54. Oculocutaneous albinism (OCA); 55. Ornithine carbamyltransferase deficiency (OCTD); 56. Orstavik 1997 syndrome; 57. Phenylketonuria (PKU); 58. Pituitary deficiency; 59. Port-wine facial staining and autism; 60. Potocki-Lupski syndrome (PTLS); 61. Prader-Willi syndrome (PWS); 62. Proteus syndrome; 63a. Rett syndrome (RTT); 63b. Rett syndrome (Hanefeld variant) (RSHV); 64. Rubinstein-Taybi syndrome; 65. Schindler disease
66. Smith-Lemli-Opitz syndrome (SLOS)
Record Nr. UNINA-9910667051603321
Aitken Kenneth J  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
An A-Z of genetic factors in autism [[electronic resource] ] : A handbook for parents and carers / / Kenneth J. Aitken
Autore Aitken Kenneth J
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (498 p.)
Disciplina 618.92/85882
Soggetto topico Autism in children
Autism spectrum disorders
Mental illness - Genetic aspects
ISBN 1-283-90676-7
0-85700-388-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto An A-Z of Genetic Factors in Autism: A Handbook for Parents and Carers; Acknowledgements; Prelude; Introduction; SECTION A: Focus on the autistic spectrum disorders; Why you might need a book like this; Help and treatment: does one size fit all?; ASD and 'inborn errors of metabolism'; Biochemical individuality: are we all the same?; Is ASD getting more common?; A brief history of ASD research; Early presenting features of ASDs; Physical checklist of features that can be seen on physical examination and which may have clinical relevance; Further clinical aspects that may require investigation
Genetic clinical conditions linked with autism 'Alternative' approaches; SECTION B: Clinical disorders seen in the autistic spectrum disorders; 1. 15q11-q13 duplication; 2. Chromosome 2q37 deletion; 3. XXY syndrome; 4. XYY syndrome; 5. 10p terminal deletion; 6. 45,X/46,XY mosaicism; 7. 22q13 deletion syndrome; 8. Aarskog syndrome; 9. Adenylosuccinate lyase (ADSL) deficiency; 10. Adrenomyeloneuropathy (AMN); 11. Angelman syndrome (AS); 12. Apert syndrome; 13. ARX gene mutations; 14. Autism secondary to autoimmune lymphoproliferative syndrome (ALPS); 15. Bannayan-Riley-Ruvalcaba syndrome (BRRS)
16. Basal cell naevus syndrome (BCNS)17. Biedl-Bardet syndrome (BBS); 18. CATCH 22; 19. Cortical dysplasia-focal epilepsy (CDFE) syndrome; 20. CHARGE syndrome; 21. Coffin-Lowry syndrome (CLS); 22. Coffin-Siris syndrome (CSS); 23. Cohen syndrome; 24. Cole-Hughes macrocephaly syndrome (CHMS); 25. Congenital adrenal hyperplasia (CAH); 26. Cowden syndrome (CS); 27. De Lange syndrome (CdLS); 28. Juvenile dentatorubral-pallidoluysian atrophy (JDPLA); 29a. DiGeorge syndrome I (phenotypic overlap); 29b. DiGeorge syndrome II (DGS II); 30. Dihydropyrimidine dehydrogenase (DPYS) deficiency
31. Down syndrome (DS)32. Dravet's syndrome; 33. Duchenne (DMD) and Becker (BMD) muscular dystrophy; 34. Ehlers-Danlos syndrome (EDS); 35. Fragile-X syndrome (FRAX); 36. Fragile-X permutation (partial methylation defects); 37. GAMT deficiency (guanidinoacetate methyltransferase deficiency); 38. Goldenhar syndrome; 39. HEADD syndrome; 40. L-2-hydroxyglutaric aciduria (L-2 HGAA); 41. Hyper IgE syndrome with autism (HiES); 42. Hypomelanosis of Ito (HI); 43. Hypothyroidism; 44. Joubert syndrome; 45. Kleine-Levin syndrome; 46. Lujan-Fryns syndrome; 47. 2-methylbutyryl-CoA dehydrogenase deficiency
48. Mobius/Möbius/Moebius syndrome 49. Myhre syndrome; 50. Myotonic dystrophy (MD1); 51. Neurofibromatosis type 1 (NF1); 52. Noonan syndrome (NS); 53. NAPDD; 54. Oculocutaneous albinism (OCA); 55. Ornithine carbamyltransferase deficiency (OCTD); 56. Orstavik 1997 syndrome; 57. Phenylketonuria (PKU); 58. Pituitary deficiency; 59. Port-wine facial staining and autism; 60. Potocki-Lupski syndrome (PTLS); 61. Prader-Willi syndrome (PWS); 62. Proteus syndrome; 63a. Rett syndrome (RTT); 63b. Rett syndrome (Hanefeld variant) (RSHV); 64. Rubinstein-Taybi syndrome; 65. Schindler disease
66. Smith-Lemli-Opitz syndrome (SLOS)
Record Nr. UNINA-9910838296203321
Aitken Kenneth J  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The adolescent and adult neuro-diversity handbook [[electronic resource] ] : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
The adolescent and adult neuro-diversity handbook [[electronic resource] ] : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
Autore Hendrickx Sarah
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (194 p.)
Disciplina 616.85/88200835
Soggetto topico Autism spectrum disorders
Attention-deficit hyperactivity disorder
Adolescence
Adulthood
Soggetto genere / forma Electronic books.
ISBN 1-282-75011-9
1-78034-478-3
9786612750113
0-85700-220-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FRONT COVER; The Adolescentand Adult Neuro-diversity Handbook: Asperger Syndrome, ADHD, Dyslexia,Dyspraxia and Related Conditions; Contents; ACKNOWLEDGEMENTS; Introduction; 1. Defining Neuro-diversity; 2. Adult Attention Deficit Hyperactivity Disorder/Attention Deficit Disorder (ADHD/ADD); 3. Autistic Spectrum Conditions: Asperger Syndrome,High Functioning Autism and PervasiveDevelopmental Disorder - Not Otherwise Specified(PDD-NOS); 4. Dyslexia; 5. Dyspraxia (Developmental Coordination Disorder); 6. Dyscalculia (Mathematic Disorder); 7. Dysgraphia (Disorder of Written Expression
8. Tourette Syndrome9. Anxiety Disorders; 10. Obsessive-Compulsive Disorder (OCD); 11. The Learning Environment: TeachingApproaches for Supporting Neuro-diversity; 12. The Working Environment: WorkplaceAdjustments for Neuro-diverse Employees; REFERENCES; FURTHER READING; RESOURCES; INDEX
Record Nr. UNINA-9910459247703321
Hendrickx Sarah  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The adolescent and adult neuro-diversity handbook [[electronic resource] ] : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
The adolescent and adult neuro-diversity handbook [[electronic resource] ] : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
Autore Hendrickx Sarah
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (194 p.)
Disciplina 616.85/88200835
Soggetto topico Autism spectrum disorders
Attention-deficit hyperactivity disorder
Adolescence
Adulthood
ISBN 1-282-75011-9
1-78034-478-3
9786612750113
0-85700-220-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FRONT COVER; The Adolescentand Adult Neuro-diversity Handbook: Asperger Syndrome, ADHD, Dyslexia,Dyspraxia and Related Conditions; Contents; ACKNOWLEDGEMENTS; Introduction; 1. Defining Neuro-diversity; 2. Adult Attention Deficit Hyperactivity Disorder/Attention Deficit Disorder (ADHD/ADD); 3. Autistic Spectrum Conditions: Asperger Syndrome,High Functioning Autism and PervasiveDevelopmental Disorder - Not Otherwise Specified(PDD-NOS); 4. Dyslexia; 5. Dyspraxia (Developmental Coordination Disorder); 6. Dyscalculia (Mathematic Disorder); 7. Dysgraphia (Disorder of Written Expression
8. Tourette Syndrome9. Anxiety Disorders; 10. Obsessive-Compulsive Disorder (OCD); 11. The Learning Environment: TeachingApproaches for Supporting Neuro-diversity; 12. The Working Environment: WorkplaceAdjustments for Neuro-diverse Employees; REFERENCES; FURTHER READING; RESOURCES; INDEX
Record Nr. UNINA-9910785155303321
Hendrickx Sarah  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The adolescent and adult neuro-diversity handbook : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
The adolescent and adult neuro-diversity handbook : Asperger syndrome, ADHD, dyslexia, dyspraxia, and related conditions / / Sarah Hendrickx
Autore Hendrickx Sarah
Edizione [1st ed.]
Pubbl/distr/stampa London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Descrizione fisica 1 online resource (194 p.)
Disciplina 616.85/88200835
616.8588200835
Soggetto topico Autism spectrum disorders
Attention-deficit hyperactivity disorder
Adolescence
Adulthood
ISBN 1-282-75011-9
1-78034-478-3
9786612750113
0-85700-220-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FRONT COVER; The Adolescentand Adult Neuro-diversity Handbook: Asperger Syndrome, ADHD, Dyslexia,Dyspraxia and Related Conditions; Contents; ACKNOWLEDGEMENTS; Introduction; 1. Defining Neuro-diversity; 2. Adult Attention Deficit Hyperactivity Disorder/Attention Deficit Disorder (ADHD/ADD); 3. Autistic Spectrum Conditions: Asperger Syndrome,High Functioning Autism and PervasiveDevelopmental Disorder - Not Otherwise Specified(PDD-NOS); 4. Dyslexia; 5. Dyspraxia (Developmental Coordination Disorder); 6. Dyscalculia (Mathematic Disorder); 7. Dysgraphia (Disorder of Written Expression
8. Tourette Syndrome9. Anxiety Disorders; 10. Obsessive-Compulsive Disorder (OCD); 11. The Learning Environment: TeachingApproaches for Supporting Neuro-diversity; 12. The Working Environment: WorkplaceAdjustments for Neuro-diverse Employees; REFERENCES; FURTHER READING; RESOURCES; INDEX
Record Nr. UNINA-9910824541203321
Hendrickx Sarah  
London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Aspects of Asperger's Syndrome [[electronic resource] ] : success in the teens and twenties / / Maude Brown and Alex Miller
Aspects of Asperger's Syndrome [[electronic resource] ] : success in the teens and twenties / / Maude Brown and Alex Miller
Autore Brown Maude
Pubbl/distr/stampa Bristol, : Lucky Duck, c2003
Descrizione fisica 1 online resource (83 p.)
Disciplina 616.85832
Altri autori (Persone) MillerAlex
Collana Lucky Duck Books
Soggetto topico Asperger's syndrome
Autism spectrum disorders
Soggetto genere / forma Electronic books.
ISBN 1-283-88002-4
1-4462-0267-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; About the Authors; Contents; Introduction; Section 1 - Introducing Asperger's Syndrome; Section 2 - Daily Living Skills; Section 3 - Coping in College; Section 4 - Relationships; Conclusion; Bibliography
Record Nr. UNINA-9910462323203321
Brown Maude  
Bristol, : Lucky Duck, c2003
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Autism [[electronic resource] /] / Stuart Murray
Autism [[electronic resource] /] / Stuart Murray
Autore Murray Stuart
Pubbl/distr/stampa New York, : Routledge, 2012
Descrizione fisica 1 online resource (131 p.)
Disciplina 362.19685882
616.85/882
616.85882
Collana The Routledge series integrating science and culture
Soggetto topico Autism
Autism spectrum disorders
Soggetto genere / forma Electronic books.
ISBN 9786613434883
1-136-65219-1
1-283-43488-1
0-203-80599-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 6. Conclusion: After the FactPart II: Social, Cultural, and Political Histories; Chapter 7. Autism before Modern Medicine; Chapter 8. The Development of Child Psychiatry: Kanner and Asperger; Chapter 9. Psychoanalysis, BrunoBettelheim, Parents, and Blame; Chapter 10. Organizations and Associations; Chapter 11. The Rise of Neurodiversity:Demands, Advocacy, and Legislation; Chapter 12.Cultural Representations: Outsider and Insider Accounts; Chapter 13.Conclusion: History in the Making; Part III: Major Controversies; Chapter 14. A Lack of Consensus; Chapter 15.Causing Autism
Record Nr. UNINA-9910457808403321
Murray Stuart  
New York, : Routledge, 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Autism / / Stuart Murray
Autism / / Stuart Murray
Autore Murray Stuart
Pubbl/distr/stampa New York : , : Routledge, , 2012
Descrizione fisica 1 online resource (131 p.)
Disciplina 362.19685882
616.85/882
616.85882
Collana The Routledge series integrating science and culture
Soggetto topico Autism
Autism spectrum disorders
ISBN 1-136-65218-3
9786613434883
1-136-65219-1
1-283-43488-1
0-203-80599-2
Classificazione SOC026000
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 6. Conclusion: After the FactPart II: Social, Cultural, and Political Histories; Chapter 7. Autism before Modern Medicine; Chapter 8. The Development of Child Psychiatry: Kanner and Asperger; Chapter 9. Psychoanalysis, BrunoBettelheim, Parents, and Blame; Chapter 10. Organizations and Associations; Chapter 11. The Rise of Neurodiversity:Demands, Advocacy, and Legislation; Chapter 12.Cultural Representations: Outsider and Insider Accounts; Chapter 13.Conclusion: History in the Making; Part III: Major Controversies; Chapter 14. A Lack of Consensus; Chapter 15.Causing Autism
Record Nr. UNINA-9910778959003321
Murray Stuart  
New York : , : Routledge, , 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Autism / / Stuart Murray
Autism / / Stuart Murray
Autore Murray Stuart
Pubbl/distr/stampa New York : , : Routledge, , 2012
Descrizione fisica 1 online resource (131 p.)
Disciplina 362.19685882
616.85/882
616.85882
Collana The Routledge series integrating science and culture
Soggetto topico Autism
Autism spectrum disorders
ISBN 1-136-65218-3
9786613434883
1-136-65219-1
1-283-43488-1
0-203-80599-2
Classificazione SOC026000
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 6. Conclusion: After the FactPart II: Social, Cultural, and Political Histories; Chapter 7. Autism before Modern Medicine; Chapter 8. The Development of Child Psychiatry: Kanner and Asperger; Chapter 9. Psychoanalysis, BrunoBettelheim, Parents, and Blame; Chapter 10. Organizations and Associations; Chapter 11. The Rise of Neurodiversity:Demands, Advocacy, and Legislation; Chapter 12.Cultural Representations: Outsider and Insider Accounts; Chapter 13.Conclusion: History in the Making; Part III: Major Controversies; Chapter 14. A Lack of Consensus; Chapter 15.Causing Autism
Record Nr. UNINA-9910815505303321
Murray Stuart  
New York : , : Routledge, , 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui