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Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1553 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Genetic disorders
Developmental disabilities - Genetic aspects
Genetic disorders in children
Soggetto genere / forma Electronic books.
ISBN 0-19-021353-1
0-19-027542-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 4. Human Genomics and Human Development II. Patterns of Development ; 5. Development of Left-.Right Asymmetry ; 6. Neural Crest Formation and Craniofacial Development ; 7. Development of the Nervous System ; 8. Development of the Eye ; 9. Development of the Ear
10. Molecular Regulation of Cardiogenesis 11. Update on the Development of the Vascular System and Its Sporadic Disorders ; 12. Muscle and Somite Development ; 13. The Development of Bone and Cartilage ; 14. Limb Development ; 15. The Sex-.Determination Pathway
Record Nr. UNINA-9910465337303321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1553 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Genetic disorders
Developmental disabilities - Genetic aspects
Genetic disorders in children
ISBN 0-19-021353-1
0-19-027542-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 4. Human Genomics and Human Development II. Patterns of Development ; 5. Development of Left-.Right Asymmetry ; 6. Neural Crest Formation and Craniofacial Development ; 7. Development of the Nervous System ; 8. Development of the Eye ; 9. Development of the Ear
10. Molecular Regulation of Cardiogenesis 11. Update on the Development of the Vascular System and Its Sporadic Disorders ; 12. Muscle and Somite Development ; 13. The Development of Bone and Cartilage ; 14. Limb Development ; 15. The Sex-.Determination Pathway
Record Nr. UNINA-9910798423403321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1553 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Genetic disorders
Developmental disabilities - Genetic aspects
Genetic disorders in children
ISBN 0-19-021353-1
0-19-027542-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 4. Human Genomics and Human Development II. Patterns of Development ; 5. Development of Left-.Right Asymmetry ; 6. Neural Crest Formation and Craniofacial Development ; 7. Development of the Nervous System ; 8. Development of the Eye ; 9. Development of the Ear
10. Molecular Regulation of Cardiogenesis 11. Update on the Development of the Vascular System and Its Sporadic Disorders ; 12. Muscle and Somite Development ; 13. The Development of Bone and Cartilage ; 14. Limb Development ; 15. The Sex-.Determination Pathway
Record Nr. UNINA-9910824556603321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes [[electronic resource]]
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes [[electronic resource]]
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 2010
Descrizione fisica 1 online resource (xvi, 220 pages) : digital, PDF file(s)
Disciplina 616.85/88042
Collana Series for the International Neuropsychological Society
Soggetto topico Developmental disabilities - Genetic aspects
Neurologic manifestations of general diseases
Genetic disorders
Psychophysiology - Genetic aspects
ISBN 1-107-20735-5
0-511-84804-8
1-282-63728-2
9786612637285
0-511-76912-1
0-511-76996-2
0-511-76689-0
0-511-76550-9
0-511-77070-7
0-511-76828-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intergenerational effects of mutations in the fragile X mental retardation 1 gene : fragile X : a model of X-linked mental retardation and neurodegeneration / Mariya Borodyanskaya ... [et al.] -- Autism : genes, anatomy, and behavioral outcome / Emma Esser, Saasha Sutera, and Deborah Fein -- Development in spina bifida : neurobiological and environmental factors / Marcia A. Barnes ... [et al.] -- Language and communication in autism spectrum disorders / Susan Ellis Weismer -- Language development in children with Williams syndrome : new insights from cross-linguistic research / Stavroula Stavrakaki -- Language in Down syndrome : a life-span perspective / Jean A. Rondal -- Genetic disorders as models of mathematics learning disability : fragile X and Turner syndromes / Melissa M. Murphy, MIchèle M.M. Mazzocco, and Michael McCloskey -- A developmental approach to genetic disorders / Sarah J. Paterson -- The use of strategies in embedded figures : tasks by boys with and without organic mild mental retardation : a review and some experimental evidence / Anastasia Alevriadou and Helen Tsakiridou.
Altri titoli varianti Genes, Brain & Development
Record Nr. UNINA-9910458408803321
Cambridge : , : Cambridge University Press, , 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes [[electronic resource]]
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes [[electronic resource]]
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 2010
Descrizione fisica 1 online resource (xvi, 220 pages) : digital, PDF file(s)
Disciplina 616.85/88042
Collana Series for the International Neuropsychological Society
Soggetto topico Developmental disabilities - Genetic aspects
Neurologic manifestations of general diseases
Genetic disorders
Psychophysiology - Genetic aspects
ISBN 1-107-20735-5
0-511-84804-8
1-282-63728-2
9786612637285
0-511-76912-1
0-511-76996-2
0-511-76689-0
0-511-76550-9
0-511-77070-7
0-511-76828-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intergenerational effects of mutations in the fragile X mental retardation 1 gene : fragile X : a model of X-linked mental retardation and neurodegeneration / Mariya Borodyanskaya ... [et al.] -- Autism : genes, anatomy, and behavioral outcome / Emma Esser, Saasha Sutera, and Deborah Fein -- Development in spina bifida : neurobiological and environmental factors / Marcia A. Barnes ... [et al.] -- Language and communication in autism spectrum disorders / Susan Ellis Weismer -- Language development in children with Williams syndrome : new insights from cross-linguistic research / Stavroula Stavrakaki -- Language in Down syndrome : a life-span perspective / Jean A. Rondal -- Genetic disorders as models of mathematics learning disability : fragile X and Turner syndromes / Melissa M. Murphy, MIchèle M.M. Mazzocco, and Michael McCloskey -- A developmental approach to genetic disorders / Sarah J. Paterson -- The use of strategies in embedded figures : tasks by boys with and without organic mild mental retardation : a review and some experimental evidence / Anastasia Alevriadou and Helen Tsakiridou.
Altri titoli varianti Genes, Brain & Development
Record Nr. UNINA-9910791371103321
Cambridge : , : Cambridge University Press, , 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes
Genes, brain, and development : the neurocognition of genetic disorders / / edited by Marcia A. Barnes
Edizione [1st ed.]
Pubbl/distr/stampa Cambridge ; ; New York, : Cambridge University Press, 2010
Descrizione fisica 1 online resource (xvi, 220 pages) : digital, PDF file(s)
Disciplina 616.85/88042
Altri autori (Persone) BarnesMarcia A. <1958->
Collana Series for the International Neuropsychological Society
Soggetto topico Developmental disabilities - Genetic aspects
Neurologic manifestations of general diseases
Genetic disorders
Psychophysiology - Genetic aspects
ISBN 1-107-20735-5
0-511-84804-8
1-282-63728-2
9786612637285
0-511-76912-1
0-511-76996-2
0-511-76689-0
0-511-76550-9
0-511-77070-7
0-511-76828-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intergenerational effects of mutations in the fragile X mental retardation 1 gene : fragile X : a model of X-linked mental retardation and neurodegeneration / Mariya Borodyanskaya ... [et al.] -- Autism : genes, anatomy, and behavioral outcome / Emma Esser, Saasha Sutera, and Deborah Fein -- Development in spina bifida : neurobiological and environmental factors / Marcia A. Barnes ... [et al.] -- Language and communication in autism spectrum disorders / Susan Ellis Weismer -- Language development in children with Williams syndrome : new insights from cross-linguistic research / Stavroula Stavrakaki -- Language in Down syndrome : a life-span perspective / Jean A. Rondal -- Genetic disorders as models of mathematics learning disability : fragile X and Turner syndromes / Melissa M. Murphy, MIchele M.M. Mazzocco, and Michael McCloskey -- A developmental approach to genetic disorders / Sarah J. Paterson -- The use of strategies in embedded figures : tasks by boys with and without organic mild mental retardation : a review and some experimental evidence / Anastasia Alevriadou and Helen Tsakiridou.
Record Nr. UNINA-9910827031003321
Cambridge ; ; New York, : Cambridge University Press, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Pubbl/distr/stampa New York, : Guilford Press, c2005
Descrizione fisica 1 online resource (508 p.)
Disciplina 618.92/8588
Altri autori (Persone) GoldsteinSam <1952->
ReynoldsCecil R. <1952->
Soggetto topico Developmental disabilities
Genetic disorders
Developmental disabilities - Genetic aspects
Neuropsychology
Soggetto genere / forma Electronic books.
ISBN 9786612790263
1-59385-877-9
1-282-79026-9
1-4294-5751-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Basics principles and applications -- pt. 2. Disorders primarily affecting learning and behavior -- pt. 3. Disorders with broader-spectrum effects.
Record Nr. UNINA-9910451505903321
New York, : Guilford Press, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Pubbl/distr/stampa New York, : Guilford Press, c2005
Descrizione fisica 1 online resource (508 p.)
Disciplina 618.92/8588
Altri autori (Persone) GoldsteinSam <1952->
ReynoldsCecil R. <1952->
Soggetto topico Developmental disabilities
Genetic disorders
Developmental disabilities - Genetic aspects
Neuropsychology
ISBN 9786612790263
1-59385-877-9
1-282-79026-9
1-4294-5751-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Basics principles and applications -- pt. 2. Disorders primarily affecting learning and behavior -- pt. 3. Disorders with broader-spectrum effects.
Record Nr. UNINA-9910777875203321
New York, : Guilford Press, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Handbook of neurodevelopmental and genetic disorders in adults [[electronic resource] /] / Sam Goldstein, Cecil R. Reynolds, editors
Pubbl/distr/stampa New York, : Guilford Press, c2005
Descrizione fisica 1 online resource (508 p.)
Disciplina 618.92/8588
Altri autori (Persone) GoldsteinSam <1952->
ReynoldsCecil R. <1952->
Soggetto topico Developmental disabilities
Genetic disorders
Developmental disabilities - Genetic aspects
Neuropsychology
ISBN 9786612790263
1-59385-877-9
1-282-79026-9
1-4294-5751-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Basics principles and applications -- pt. 2. Disorders primarily affecting learning and behavior -- pt. 3. Disorders with broader-spectrum effects.
Record Nr. UNINA-9910820167303321
New York, : Guilford Press, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds
Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Guilford Press, 2010
Descrizione fisica 1 online resource (621 p.)
Disciplina 618.92/8588042
Altri autori (Persone) GoldsteinSam <1952->
ReynoldsCecil R. <1952->
Soggetto topico Developmental disabilities - Genetic aspects
Developmental neurobiology
Genetic disorders in children
Pediatric neuropsychology
Soggetto genere / forma Electronic books.
ISBN 1-4625-0161-3
1-283-10895-X
9786613108951
1-60918-000-3
1-60918-001-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Copyright Page; Dedication; About the Editors; Contributors; Preface; Acknowledgments; Contents; PART I. BACKGROUND; 1. Introduction; 2. Neuropsychological Assessment in Genetically Linked Neurodevelopmental Disorders; 3. Neurodevelopmental Disorders and Medical Genetics: An Overview; 4. Neuroimaging and Genetic Disorders; 5. Integrative Developmental Neuropsychology: A General Systems and Social- Ecological Approach to the Neuropsychology of Children with Neurogenetic Disorders; PART II. DISORDERS PRIMARILY AFFECTING LEARNING AND BEHAVIOR; 6. Learning Disabilities
7. Attention-Deficit/Hyperactivity Disorder8. Oppositional, Conduct, and Aggressive Disorders; 9. Gilles de la Tourette Syndrome; 10. Anxiety Disorders; 11. Mood Disorders; 12. Autism Spectrum Disorders; PART III. DISORDERS WITH BROADER-SPECTRUM EFFECTS; 13. Turner Syndrome; 14. Fragile X Syndrome and Fragile X-Associated Disorders; 15. The Mucopolysaccharidoses; 16. Noonan Syndrome; 17. Neurofibromatosis Type 1; 18. Sickle Cell Disease; 19. Down Syndrome; 20. Klinefelter Syndrome; 21. Phenylketonuria; 22. Rett Syndrome: A Truly Pervasive Developmental Disorder
23. Lesch-Nyhan Syndrome: A Sex-Linked Inborn Error of Metabolism24. Seizure Disorders; 25. Prader-Willi Syndrome; 26. Disorders of Mitochondrial Metabolism; 27. Major Structural Anomalies of the Neocortex; 28. Spina Bifida Myelomeningocele; 29. Inborn Errors of Metabolism: A Brief Overview; Index; Color Plate; About Guilford Publications; From the Publisher; Back Cover
Record Nr. UNINA-9910459477903321
New York, : Guilford Press, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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