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This third edition systematically reviews recent developments in the diagnosis and evidence-based treatment of cerebral palsy, a consequence of foetal and early infant brain damage resulting in lifelong disabilities with a range of clinical characteristics. The first part discusses the definition, aetiology, classification, imaging and neuropathology, while the second focuses on the management of the individual challenges that children with cerebral palsy face, such as spasticity, dyskinesia, feeding problems and scoliosis. Based on the diverse characteristics of cerebral palsy, children require care from various specialists, including neuro-paediatricians, orthopaedists, psychologists, epidemiologists, physiotherapists and occupational therapists. This work was written by an international team of such specialists, providing a comprehensive mix of perspectives and expertise.
Social policy and particular groups --- Physiotherapy. Alternative treatments --- Paediatrics --- Neuropathology --- Orthopaedics. Traumatology. Plastic surgery --- farmacologie --- hersenen --- pediatrie --- kinesitherapie --- orthopedie --- rehabilitatie --- sociale integratie --- Neurology . --- Pediatrics. --- Orthopedics. --- Rehabilitation. --- Physiotherapy. --- Neurology. --- Orthopaedics --- Orthopedia --- Surgery --- Pediatric medicine --- Medicine --- Children --- Nervous system --- Neuropsychiatry --- Diseases --- Health and hygiene
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This third edition systematically reviews recent developments in the diagnosis and evidence-based treatment of cerebral palsy, a consequence of foetal and early infant brain damage resulting in lifelong disabilities with a range of clinical characteristics. The first part discusses the definition, aetiology, classification, imaging and neuropathology, while the second focuses on the management of the individual challenges that children with cerebral palsy face, such as spasticity, dyskinesia, feeding problems and scoliosis. Based on the diverse characteristics of cerebral palsy, children require care from various specialists, including neuro-paediatricians, orthopaedists, psychologists, epidemiologists, physiotherapists and occupational therapists. This work was written by an international team of such specialists, providing a comprehensive mix of perspectives and expertise.
Social policy and particular groups --- Physiotherapy. Alternative treatments --- Paediatrics --- Neuropathology --- Orthopaedics. Traumatology. Plastic surgery --- farmacologie --- hersenen --- pediatrie --- kinesitherapie --- orthopedie --- rehabilitatie --- sociale integratie
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Neurocutaneous disorders. --- Neurocutaneous Syndromes. --- Neurocutaneous Syndromes --- diagnosis. --- therapy. --- Neurocutaneous Disorders --- Phacomatoses --- Phakomatosis --- Neuroectodermal Dysplasia Syndromes --- Phacomatosis --- Phakomatoses --- Neurocutaneous Disorder --- Neurocutaneous Syndrome --- Neuroectodermal Dysplasia Syndrome --- Syndrome, Neurocutaneous --- Syndrome, Neuroectodermal Dysplasia --- Syndromes, Neurocutaneous --- Syndromes, Neuroectodermal Dysplasia --- Dermatoneurosis --- Neurodermatitis --- Nervous system --- Skin --- Diseases
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Neurocutaneous disorders. --- Malalties de la pell --- Malalties neurocutànies
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This book provides extensive data on the more common and many of the more rare congenital and hereditary syndromes that manifest in the nervous system and skin. Though often complex and multi-systemic, these disorders can frequently be diagnosed using a combination of simple visual inspection and sound clinical expertise. Drawing on fully referenced information from thousands of articles, the international editorial team has prepared a comprehensive overview that includes historical perspectives, clinical features, the pathogenesis, and diagnostic and therapeutic strategies. In addition, it addresses the biochemical, molecular, and genetic basis of the disorders. The book is divided into four main sections. Starting with general aspects of aetiology, diagnostics and therapy, the first part then covers the genetics, neuro-imaging, neuropathology, ocular manifestations and surgical management. The second part discusses developmental malformations, such as Sturge-Weber syndrome, Ataxia-Telangiectasia, Hypomelanosis of Ito and other rare syndromes, including haemangiomas. The focus of the third part is on tumour suppressor/DNA repair disorders, the most common of which is Neurofibromatosis 1. It also describes Neurofibromatosis 2, Schwannomatosis, Tuberous sclerosis, von Hippel-Lindau disease, Naevoid basal cell carcinoma and others. The book's fourth and final section covers defects in enzymes and structural proteins, which manifest as Cerebrotendinous xanthromatosis, Ehlers-Danlos syndrome, Menkes syndrome, Refsum disease.
Paediatrics --- Physical methods for diagnosis --- Pathological dermatology --- Neuropathology --- Ophthalmology --- hersenen --- dermatologie --- pediatrie --- oftalmologie --- radiologie
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Neurocutaneous disorders. --- Dermatoneurosis --- Neurodermatitis --- Nervous system --- Skin --- Diseases
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