Pediatric neurology
著者
書誌事項
Pediatric neurology
(Handbook of clinical neurology, 3rd ser. ; 111-113)
Elsevier, 2013
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埼玉医科大学 附属図書館埼医大図
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注記
Includes bibliographical references and index
内容説明・目次
- 巻冊次
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pt. 1 ISBN 9780444528919
内容説明
目次
- SECTION 1 GENERAL INTRODUCTION
- Normal psychomotor development
- Clinical neurological examination of infants and children
- Pediatric neurology - the diagnostic process
- Health outcomes measurement: concepts, guidelines and opportunities
- Coma
- Clinical and imaging diagnosis for heredodegenerative diseases
- Developmental aspects of normal EEG
- Clinical neurophysiology in movement disorders
- Announcing the diagnosis: counselling the parents
- Chronic paediatric diseases into adulthood and the challenge of adolescence
- Ethical considerations in pediatric neurology
- SECTION 2 TOXIC AND DEFICIENCY, FETOPATHIES
- Neuroembryology and brain malformations: an overview
- Microcephaly
- Prenatal-onset neurodevelopmental disorders secondary to toxins, nutritional deficiencies and maternal illness
- SECTION 3 CEREBRAL PALSY
- Epidemiology of cerebral palsy
- Pathophysiology of cerebral palsy
- Imaging cerebral palsy
- Cerebral palsy: definition, assessment and rehabilitation
- Treatment of movement disorders in dystonia-choreoathtosis cerebral palsy
- Everyday life and social consequences of cerebral palsy
- SECTION 4 DEVELOPMENTAL ABNORMALITIES AND MENTAL RETARDATION
- Developmental abnormalities and mental retardation: diagnostic strategy
- Specific language impairment
- Dyslexia
- Congenital Amusia
- Developmental dyscalculia
- Nonverbal learning disability
- Memory disorders in children
- Attention deficit
- The autistic spectrum
- Cognitive and medical features of chromosomal neuploidy
- Genetically determined encephalopathy: Rett syndrome
- Angelman syndrome
- Developmental and cognitive troubles in Williams Syndrome
- Smith Magenis syndrome
- X-linked mental deficiency
- SECTION 5 NEUROECTODERMOSES
- Genetics of neural crest and neurocutaneous syndromes
- Sturge-Weber syndrome
- Tuberous sclerosis
- Neurofibromatosis
- Incontinentia pigmenti and hypomelanosis of Ito
- Epidermal nevus syndrome
- Neurocutaneous melanocytosis
- SECTION 6 EPILEPSY
- The epidemiology of seizure disorders in infancy and childhood: definitions and Classifications
- Neuropathology of paediatric epilepsy
- The developing cortex
- Epileptogenesis in the developing brain
- Brain maturation and epilepsy
- Modes of onset of epilepsy and differential diagnosis
- Varying seizure semiology according to age
- Magnetoencephalography (MEG) and other neurophysiological investigations
- Neonatal seizures
- Febrile and other occasional seizures
- Focal epileptogenic lesions
- Rasmussen's encephalitis
- Immune-mediated paediatric epilepsies
- Inborn errors of metabolism and epilepsy
- Chromosome disorders associated with epilepsy
- Focal malformations of cortical development: a most relevant etiology of epilepsy in Children
- Genetics of idiopathic epilepsies
- Idiopathic generalized epilepsies
- Idiopathic focal epilepsies
- Malignant migrating partial seizures in infancy
- Infantile spasms
- The epileptic encephalopathies
- Dravet syndrome (severe myoclonic epilepsy in infancy)
- Epileptic encephalopathy with continuous spike-waves during slow-wave sleep including Landau-Kleffner syndrome
- Lennox-Gastaut syndrome and epilepsy with myoclonic-astatic seizures
- Diffuse malformations of cortical development
- Myoclonus and epilepsy
- Status epilepticus
- Cognitive disorders in paediatric epilepsy
- Problematic behaviour in children with epilepsy: issues and management
- Cognitive side-effects of antiepileptic drugs in children
- Initiating antiepileptic drug treatment and characteristics of drugs
- Treatment strategies
- Developing antiepileptic drugs in children: balancing protection and access
- Structural imaging in children with chronic focal epilepsy: exploration strategies and diagnostic algorithms
- SPECT (Single photon emission computed tomography) in paediatrics
- Functional imaging: PET
- Advanced structural and functional MRI in childhood epilepsies
- Paediatric epilepsy surgery
- Cognitive outcome of surgery
- Nonpharmacologic approaches: diet and neurostimulation
- Outcome of paediatric epilepsies in adulthood
- 巻冊次
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pt. 2 ISBN 9780444529107
内容説明
目次
- SECTION 7 Non epileptic paroxysmal disorders and respiratory disorders Alternating hemiplegia of childhood
- Headache in Pediatric Practice
- Paediatric narcolepsy: clinical and therapeutical approaches
- Paroxysmal movement disorders and episodic ataxias
- Tourette syndrome and other tic disorders of childhood
- Non-epileptic paroxysmal sleep disorders
- Syncopes and other paroxysmal events
- Sudden infant death syndrome: An update and new perspectives of etiology
- Psychogenic non epileptic seizures SECTION 8 Conversion disorders Conversion disorder SECTION 9 Trauma Traumatic brain injury
- Non accidental head injury
- Cognitive and psychopathological sequelae of pediatric traumatic brain injury
- Obstetrical brachial plexus palsy SECTION 10 Tumors Central nervous system tumors
- Pediatric spinal tumors
- Neurocognitive effects of CNS tumours SECTION 11 Myelopathy Spinal cord malformations
- Acute myelopathy - tumoral or traumatic spinal cord compression
- Inflammatory, vascular and infectious myelopathies in children SECTION 12 Vascular disorders Normal and abnormal cerebrovascular development: gene-environment interactions during early life with later life consequences
- Vascular malformations of the brain
- Cerebrovascular disorders in childhood
- Childhood central nervous system (CNS) vasculitis
- Outcome and rehabilitation after childhood stroke SECTION 13 Inflammatory and infectious diseases Brain development and the immune system: an introduction to inflammatory and infectious diseases of the child's brain
- Mendelian predisposition to herpes simplex encephalitis
- Congenital toxoplasmosis
- Virus-induced lesions and the foetal brain: examples of the transmission of HIV-1 and CMV from mother to offspring
- Neonatal bacterial meningitis
- Infantile and childhood bacterial meningitis
- Brain abscess
- Tuberculous meningitis
- Parasitic disorders
- Aseptic meningitis
- Acute polyradiculoneuritis: Guillain-Barre syndrome Germany)
- Chronic inflammatory demyelinating polyneuropathy
- Acute viral encephalitis
- Subacute sclerosing panencephalitis and chronic viral encephalitis
- Creutzfeldt-Jakob disease
- Parainfectious meningo-encephalo-radiculo-myelitis (cat scratch disease, lyme borreliosis, brucellosis, botulism, legionellosis, pertussis, mycoplasma)
- Opsoclonus-myoclonus syndrome
- Ataxia
- Neurological expression of genetic immunodeficiencies and of opportunistic infections
- Anti-NMDA receptor encephalitis in children: the disorder, its diagnosis, and treatment
- Immune mediated extrapyramidal movement disorders, including Sydenham's chorea
- Systemic inflammatory and autoimmune disorders
- Acute disseminated encephalomyelitis
- Pediatric multiple sclerosis
- Effect of autoimmune diseases on cognitive function
- The neuropsychology of the Kluver Bucy syndrome in children
- 巻冊次
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pt. 3 ISBN 9780444595652
内容説明
目次
- SECTION 14 Neuromuscular Disorders Diagnostic work-up for neuromuscular diseases
- Main steps of the skeletal muscle development in human: Morphological analysis and ultrastructural characteristics of developing human muscle
- Arthrogryposis and fetal hypomobility syndrome
- Congenital myopathies
- Myofibrillar myopathies
- Progressive muscular dystrophies
- Emery-Dreifuss muscular dystrophy, laminopathies and other nuclear envelopathies
- Congenital muscular dystrophies
- Congenital and infantile myotonic dystrophy
- Spinal muscular atrophies
- Hereditary motor-sensory, motor and sensory neuropathies in childhood
- Muscle channelopathies and related diseases
- Metabolic neuropathies and myopathies
- Juvenile dermatomyositis
- Autoimmune myasthenia gravis
- Congenital myasthenic syndromes
- Neuromuscular complications of intensive care
- Respiratory care in neuromuscular disorders
- Medical and psychosocial considerations in rehabilitation care of childhood neuromuscular diseases
- Innovating therapies for muscle diseases SECTION 15 Cranial nerves and brainstem dysfunction Eye movement control and its disorders
- The optic nerve and visual pathways
- Hearing loss and deafness in the paediatric population: causes, diagnosis and rehabilitation
- Congenital feeding and swallowing disorders SECTION 16 Inborn errors of metabolism and storage diseases Diagnostic work-up in acute conditions of inborn errors of metabolism and storage diseases
- Metabolic diagnostic work-up in chronic conditions
- Inborn errors of brain myelin formation
- Peroxisomal disorders
- Lysosomal leukodystrophies: Krabbe disease and metachromatic leukodystrophy
- Leukodystrophies with astrocytic dysfunction
- Aicardi-Goutieres syndrome
- Disorders of nucleotide excision-repair
- Respiratory chain deficiencies
- Disorders of pyruvate metabolism
- Disorders of fatty acid oxidation
- Glucide metabolism disorders (excluding glycogen myopathies)
- Lysosomal diseases: biochemical pathways and investigations
- Neuronal ceroid lipofuscinoses
- Gangliosidoses
- Gaucher disease
- Niemann-Pick diseases
- Mucopolysaccharidoses and mucolipidoses
- Progressive myoclonus epilepsy
- Congenital disorders of glycosylation
- Inborn errors of copper metabolism
- Defects in amino acid catabolism and the urea cycle
- Amino acid synthesis deficiencies
- Epileptic encephalopathy with suppression-bursts and non-ketotic hyperglycinemia
- Vitamin-responsive disorders: cobalamin, folate, biotin, vitamins B1 and E
- Pyridoxine and pyridoxalphosphate dependent epilepsies
- Monoamine neurotransmitter deficiencies
- Metabolic disorders of purine metabolism affecting the nervous system
- Creatine deficiency syndromes
- Cholesterol metabolism deficiency
- Enzyme replacement therapy and substrate reduction therapy in lysosomal storage disorders with neurological expression
- Gene therapy for disorders of the central nervous systems SECTION 17 Heredodegenerative disorders Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration
- Joubert syndrome and related disorders
- Progressive dystonia
- Hereditary spastic paraplegias: one disease for many genes, and still counting
- Huntington's disease in children
- Axonal dystrophies SECTION 18 Postnatal toxic and induced disorders Postnatal toxic and acquired disorders
- Cerebrovascular complications in children with sickle cell disease
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