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101 inclusive and SEN maths activities : fun activities and lesson plans for P level learning / / Claire Brewer and Kate Bradley
| 101 inclusive and SEN maths activities : fun activities and lesson plans for P level learning / / Claire Brewer and Kate Bradley |
| Autore | Brewer Claire |
| Pubbl/distr/stampa | London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2017 |
| Descrizione fisica | 1 online resource (138 pages) : illustrations |
| Disciplina | 372.7 |
| Soggetto topico | Mathematics - Study and teaching (Elementary) - Activity programs |
| ISBN | 1-78450-364-9 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910150182103321 |
Brewer Claire
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| London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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101 mindful arts-based activities to get children and adolescents talking : working with severe trauma, abuse and neglect using found and everyday objects / / Dawn D'Amico
| 101 mindful arts-based activities to get children and adolescents talking : working with severe trauma, abuse and neglect using found and everyday objects / / Dawn D'Amico |
| Autore | D'Amico Dawn |
| Pubbl/distr/stampa | London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2017 |
| Descrizione fisica | 1 online resource (226 pages) |
| Disciplina | 618.92/8521065156 |
| Soggetto topico | Post-traumatic stress disorder - Treatment |
| ISBN | 1-78450-422-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti |
Mindful arts-based activities to get children and adolescents talking
One hundred and one mindful arts-based activities to get children and adolescents talking |
| Record Nr. | UNINA-9910154897703321 |
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D'Amico Dawn
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| London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The A-Z of gender and sexuality : from ace to ze / / Morgan Potts
| The A-Z of gender and sexuality : from ace to ze / / Morgan Potts |
| Autore | Potts Morgan |
| Pubbl/distr/stampa | London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2019 |
| Descrizione fisica | 1 online resource (346 pages) |
| Disciplina | 306.76 |
| Soggetto topico |
Sexual minorities
Gender identity |
| ISBN | 1-78450-663-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910793597003321 |
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Potts Morgan
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| London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The A-Z of gender and sexuality : from ace to ze / / Morgan Potts
| The A-Z of gender and sexuality : from ace to ze / / Morgan Potts |
| Autore | Potts Morgan |
| Pubbl/distr/stampa | London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2019 |
| Descrizione fisica | 1 online resource (346 pages) |
| Disciplina | 306.76 |
| Soggetto topico |
Sexual minorities
Gender identity |
| ISBN | 1-78450-663-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910810433503321 |
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Potts Morgan
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| London, England ; ; Philadelphia, Pennsylvania : , : Jessica Kingsley Publishers, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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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 |
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Aitken Kenneth J
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| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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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 |
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Aitken Kenneth J
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||
| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
An A-Z of genetic factors in autism : A handbook for parents and carers / / Kenneth J. Aitken
| An A-Z of genetic factors in autism : 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 |
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Aitken Kenneth J
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| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Access and inclusion for children with autistic spectrum disorders [[electronic resource] ] : let me in / / Matthew Hesmondhalgh & Christine Breakey
| Access and inclusion for children with autistic spectrum disorders [[electronic resource] ] : let me in / / Matthew Hesmondhalgh & Christine Breakey |
| Autore | Hesmondhalgh Matthew <1962-> |
| Pubbl/distr/stampa | London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 |
| Descrizione fisica | 1 online resource (249 p.) |
| Disciplina | 371.94 |
| Altri autori (Persone) | BreakeyChristine <1952-> |
| Soggetto topico |
Autistic children - Education - Great Britain
Inclusive education - Great Britain |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-84642-296-5
1-4175-0161-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | ""Cover Page""; ""Other Books""; ""Title Page""; ""Copyright""; ""Dedication""; ""Contents""; ""Foreword""; ""Introduction""; ""1. A Journey of a Thousand Miles Begins with One Step""; ""2. The Key Players""; ""3. Parents, Paperwork and Pressure""; ""4. Counselling""; ""5. The National Curriculum? Not Quite""; ""6. Integration into Work""; ""7. Our Charity � The Chase for Cash""; ""8. Post-16 � The First Year""; ""9. Andrew�s Story""; ""10. The Final Chapter?""; ""Bibliography"" |
| Record Nr. | UNINA-9910450047203321 |
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Hesmondhalgh Matthew <1962->
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| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Access and inclusion for children with autistic spectrum disorders [[electronic resource] ] : let me in / / Matthew Hesmondhalgh & Christine Breakey
| Access and inclusion for children with autistic spectrum disorders [[electronic resource] ] : let me in / / Matthew Hesmondhalgh & Christine Breakey |
| Autore | Hesmondhalgh Matthew <1962-> |
| Pubbl/distr/stampa | London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 |
| Descrizione fisica | 1 online resource (249 p.) |
| Disciplina | 371.94 |
| Altri autori (Persone) | BreakeyChristine <1952-> |
| Soggetto topico |
Autistic children - Education - Great Britain
Inclusive education - Great Britain |
| ISBN |
1-84642-296-5
1-4175-0161-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Dedication -- Contents -- Foreword -- Introduction -- 1. A Journey of a Thousand Miles Begins with One Step -- 2. The Key Players -- 3. Parents, Paperwork and Pressure -- 4. Counselling -- 5. The National Curriculum? Not Quite -- 6. Integration into Work -- 7. Our Charity - The Chase for Cash -- 8. Post-16 - The First Year -- 9. Andrew's Story -- 10. The Final Chapter? -- Bibliography. |
| Record Nr. | UNINA-9910777346203321 |
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Hesmondhalgh Matthew <1962->
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| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Access and inclusion for children with autistic spectrum disorders : let me in / / Matthew Hesmondhalgh & Christine Breakey
| Access and inclusion for children with autistic spectrum disorders : let me in / / Matthew Hesmondhalgh & Christine Breakey |
| Autore | Hesmondhalgh Matthew <1962-> |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 |
| Descrizione fisica | 1 online resource (249 p.) |
| Disciplina | 371.94 |
| Altri autori (Persone) | BreakeyChristine <1952-> |
| Soggetto topico |
Autistic children - Education - Great Britain
Inclusive education - Great Britain |
| ISBN |
1-84642-296-5
1-4175-0161-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Dedication -- Contents -- Foreword -- Introduction -- 1. A Journey of a Thousand Miles Begins with One Step -- 2. The Key Players -- 3. Parents, Paperwork and Pressure -- 4. Counselling -- 5. The National Curriculum? Not Quite -- 6. Integration into Work -- 7. Our Charity - The Chase for Cash -- 8. Post-16 - The First Year -- 9. Andrew's Story -- 10. The Final Chapter? -- Bibliography. |
| Record Nr. | UNINA-9910806293303321 |
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Hesmondhalgh Matthew <1962->
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| London ; ; Philadelphia, : Jessica Kingsley Publishers, 2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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