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Ataxic disorders
Authors: ---
ISBN: 9780444534941 0444534946 9780444518927 0444518924 Year: 2012 Publisher: Edinburgh Elsevier

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Abstract

This volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new n

Spinocerebellar degenerations
Authors: ---
ISBN: 0750675039 9780750675031 9780702038938 0702038938 Year: 2007 Publisher: Philadephia, PA Butterworth-Heinemann/Elsevier

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Keywords

Cerebellar ataxia --- Paralysis, Spastic --- Hereditary Sensory and Motor Neuropathy --- Ataxia --- Heredodegenerative Disorders, Nervous System --- Cerebellar Diseases --- Spinal Cord Diseases --- Neurodegenerative Diseases --- Polyneuropathies --- Central Nervous System Diseases --- Brain Diseases --- Genetic Diseases, Inborn --- Nervous System Malformations --- Dyskinesias --- Peripheral Nervous System Diseases --- Neurologic Manifestations --- Nervous System Diseases --- Congenital Abnormalities --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Diseases --- Signs and Symptoms --- Neuromuscular Diseases --- Pathological Conditions, Signs and Symptoms --- Cerebellar Ataxia --- Spastic Paraplegia, Hereditary --- Spinocerebellar Degenerations --- Medicine --- Health & Biological Sciences --- Neurology --- Early Onset Cerebellar Ataxia --- Familial Spinocerebellar Degenerations --- Garland-Moorhouse Syndrome --- Hereditary Oligophrenic Cerebello-Lental Degeneration --- Hereditary Spinocerebellar Degenerations --- Inherited Spinocerebellar Degenerations --- Late Onset Cerebellar Ataxia --- Marie's Cerebellar Ataxia --- Marinesco-Garland Syndrome --- Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism --- Marinesco-Sjogren Syndrome-Myopathy --- Marinesco-Sjogren-Garland Syndrome --- Marinesco-Sjögren Syndrome --- Spino Cerebellar Degenerations --- Spino-Cerebellar Degenerations --- Spinocerebellar Diseases --- Ataxias, Hereditary --- Cerebellar Ataxia, Early Onset --- Cerebellar Ataxia, Late Onset --- Cerebellar Degenerations, Primary --- Corticostriatal-Spinal Degeneration --- Marie Cerebellar Ataxia --- Marinesco-Sjogren Syndrome --- Spinocerebellar Degeneration --- Ataxia, Hereditary --- Cerebellar Ataxia, Marie --- Cerebellar Ataxia, Marie's --- Cerebellar Degeneration, Primary --- Corticostriatal Spinal Degeneration --- Corticostriatal-Spinal Degenerations --- Degeneration, Corticostriatal-Spinal --- Degeneration, Familial Spinocerebellar --- Degeneration, Hereditary Spinocerebellar --- Degeneration, Inherited Spinocerebellar --- Degeneration, Primary Cerebellar --- Degeneration, Spino Cerebellar --- Degeneration, Spino-Cerebellar --- Degeneration, Spinocerebellar --- Degenerations, Corticostriatal-Spinal --- Degenerations, Familial Spinocerebellar --- Degenerations, Hereditary Spinocerebellar --- Degenerations, Inherited Spinocerebellar --- Degenerations, Primary Cerebellar --- Degenerations, Spino Cerebellar --- Degenerations, Spinocerebellar --- Familial Spinocerebellar Degeneration --- Garland Moorhouse Syndrome --- Hereditary Ataxia --- Hereditary Ataxias --- Hereditary Oligophrenic Cerebello Lental Degeneration --- Hereditary Spinocerebellar Degeneration --- Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic --- Inherited Spinocerebellar Degeneration --- Marinesco Garland Syndrome --- Marinesco Sjogren Garland Syndrome --- Marinesco Sjogren Syndrome --- Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism --- Marinesco Sjogren Syndrome Myopathy --- Marinesco Sjögren Syndrome --- Primary Cerebellar Degeneration --- Primary Cerebellar Degenerations --- Spino Cerebellar Degeneration --- Spino-Cerebellar Degeneration --- Spinocerebellar Degeneration, Familial --- Spinocerebellar Degeneration, Hereditary --- Spinocerebellar Degeneration, Inherited --- Spinocerebellar Degenerations, Familial --- Spinocerebellar Degenerations, Hereditary --- Spinocerebellar Degenerations, Inherited --- Spinocerebellar Disease --- Syndrome, Garland-Moorhouse --- Syndrome, Marinesco-Garland --- Syndrome, Marinesco-Sjogren --- Syndrome, Marinesco-Sjogren-Garland --- Syndrome, Marinesco-Sjögren --- Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren --- Syndrome-Myopathy, Marinesco-Sjogren --- Autosomal Dominant Hereditary Spastic Paraplegia --- Autosomal Dominant Spastic Paraplegia Hereditary --- Autosomal Recessive Hereditary Spastic Paraplegia --- Autosomal Recessive Spastic Paraplegia, Hereditary --- CMT with Pyramidal Features --- Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant --- HMSN 5 --- HMSN Type V --- HMSN V --- HMSN V (Hereditary Motor and Sensory Neuropathy Type V) --- Hereditary Autosomal Dominant Spastic Paraplegia --- Hereditary Autosomal Recessive Spastic Paraplegia --- Hereditary Motor And Sensory Neuropathy V --- Hereditary Motor and Sensory Neuropathy 5 --- Hereditary Motor-Sensory Neuropathy with Pyramidal Signs --- Hereditary Spastic Paraplegia, Autosomal Recessive --- Hereditary X-Linked Recessive Spastic Paraplegia --- Hereditary, Spastic Paraplegia, Autosomal Dominant --- Hereditary, Spastic Paraplegia, X-Linked Recessive --- Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia --- Paraplegia, Spastic, Hereditary --- Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant --- Spastic Paraplegia 2 --- Spastic Paraplegia Type 2 --- Spastic Paraplegia, Autosomal Dominant, Hereditary --- Spastic Paraplegia, Autosomal Recessive, Hereditary --- Spastic Paraplegia, Hereditary, Autosomal Dominant --- Spastic Paraplegia, Hereditary, Autosomal Recessive --- Spastic Paraplegia, Hereditary, X-Linked Recessive --- Spastic Paraplegia, X-Linked Recessive, Hereditary --- Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy --- Type V Hereditary Motor and Sensory Neuropathy --- X Linked Recessive Hereditary Spastic Paraplegia --- X-linked Recessive Hereditary Spastic Paraplegia --- Hereditary Spastic Paraplegia --- X-Linked, Spastic Paraplegia, Hereditary --- Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant --- Hereditary Motor Sensory Neuropathy with Pyramidal Signs --- Hereditary Spastic Paraplegias --- Hereditary X Linked Recessive Spastic Paraplegia --- Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia --- Paraplegia, Hereditary Spastic --- Paraplegias, Hereditary Spastic --- Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy --- Spastic Paraplegias, Hereditary --- Type V, HMSN --- Cerebellar Hemiataxia --- Cerebellar Incoordination --- Hypermetria --- Adiadochokinesis --- Ataxia, Cerebellar --- Cerebellar Dysmetria --- Dysmetria --- Adiadochokineses --- Ataxias, Cerebellar --- Cerebellar Ataxias --- Cerebellar Dysmetrias --- Cerebellar Hemiataxias --- Cerebellar Incoordinations --- Dysmetria, Cerebellar --- Dysmetrias --- Dysmetrias, Cerebellar --- Hemiataxia, Cerebellar --- Hemiataxias, Cerebellar --- Hypermetrias --- Incoordination, Cerebellar --- Incoordinations, Cerebellar --- Symptoms and General Pathology --- Cramp-Fasciculation Syndrome --- Fasciculation-Cramp Syndrome, Benign --- Foley-Denny-Brown Syndrome --- Oppenheim's Disease --- Amyotonia Congenita --- Oppenheim Disease --- Benign Fasciculation-Cramp Syndrome --- Benign Fasciculation-Cramp Syndromes --- Cramp Fasciculation Syndrome --- Cramp-Fasciculation Syndromes --- Fasciculation Cramp Syndrome, Benign --- Fasciculation-Cramp Syndromes, Benign --- Foley Denny Brown Syndrome --- Neuromuscular Disease --- Oppenheims Disease --- Syndrome, Cramp-Fasciculation --- Syndrome, Foley-Denny-Brown --- Syndromes, Cramp-Fasciculation --- Symptoms and Signs --- Disorders, Congenital --- Congenital Disorders --- Neonatal Diseases and Abnormalities --- Congenital Disorder --- Disorder, Congenital --- Abnormalities, Congenital --- Defects, Congenital --- Birth Defects --- Congenital Defects --- Deformities --- Abnormality, Congenital --- Birth Defect --- Congenital Abnormality --- Congenital Defect --- Defect, Birth --- Defect, Congenital --- Defects, Birth --- Deformity --- Fetal Diseases --- Infant, Newborn, Diseases --- Teratogenesis --- Nervous System Disorders --- Neurological Disorders --- Neurologic Disorders --- Disease, Nervous System --- Diseases, Nervous System --- Disorder, Nervous System --- Disorder, Neurologic --- Disorder, Neurological --- Disorders, Nervous System --- Disorders, Neurologic --- Disorders, Neurological --- Nervous System Disease --- Nervous System Disorder --- Neurologic Disorder --- Neurological Disorder --- Focal Neurologic Deficits --- Manifestations, Neurologic --- Manifestations, Neurological --- Neurologic Dysfunction --- Neurologic Findings --- Neurologic Manifestation --- Neurologic Signs --- Neurologic Symptoms --- Neurological Manifestations --- Neurologic Deficits --- Neurologic Signs and Symptoms --- Deficit, Focal Neurologic --- Deficit, Neurologic --- Deficits, Focal Neurologic --- Deficits, Neurologic --- Dysfunction, Neurologic --- Dysfunctions, Neurologic --- Finding, Neurologic --- Findings, Neurologic --- Focal Neurologic Deficit --- Manifestation, Neurologic --- Manifestation, Neurological --- Neurologic Deficit --- Neurologic Deficit, Focal --- Neurologic Deficits, Focal --- Neurologic Dysfunctions --- Neurologic Finding --- Neurologic Sign --- Neurologic Symptom --- Neurological Manifestation --- Sign, Neurologic --- Signs, Neurologic --- Symptom, Neurologic --- Symptoms, Neurologic --- Nervous System --- PNS (Peripheral Nervous System) Diseases --- PNS Diseases --- Peripheral Nervous System Disease --- Peripheral Nervous System Disorders --- Peripheral Nerve Diseases --- Peripheral Neuropathies --- Nerve Disease, Peripheral --- Nerve Diseases, Peripheral --- Neuropathy, Peripheral --- PNS Disease --- Peripheral Nerve Disease --- Peripheral Neuropathy --- Abnormal Movements --- Hemiballism --- Linguofacial Dyskinesia --- Oral Dyskinesia --- Oral-Facial Dyskinesia --- Tardive Oral Dyskinesia --- Asterixis --- Ballismus --- Hemiballismus --- Involuntary Movements --- Lingual-Facial-Buccal Dyskinesia --- Orofacial Dyskinesia --- Abnormal Movement --- Dyskinesia --- Dyskinesia, Lingual-Facial-Buccal --- Dyskinesia, Linguofacial --- Dyskinesia, Oral --- Dyskinesia, Oral-Facial --- Dyskinesia, Orofacial --- Dyskinesias, Lingual-Facial-Buccal --- Dyskinesias, Linguofacial --- Dyskinesias, Oral --- Dyskinesias, Oral-Facial --- Dyskinesias, Orofacial --- Involuntary Movement --- Lingual Facial Buccal Dyskinesia --- Lingual-Facial-Buccal Dyskinesias --- Linguofacial Dyskinesias --- Movement, Abnormal --- Movement, Involuntary --- Movements, Abnormal --- Movements, Involuntary --- Oral Dyskinesias --- Oral Facial Dyskinesia --- Oral-Facial Dyskinesias --- Orofacial Dyskinesias --- Tardive Oral Dyskinesias --- Movement Disorders --- Abnormalities, Congenital, Nervous System --- Abnormalities, Nervous System --- Anomalies, Nervous System --- Congenital Abnormalities, Nervous System --- Congenital Anomalies, Nervous System --- Congenital Malformations, Nervous System --- Cranioschisis --- Malformations, Nervous System, Congenital --- Nervous System Anomalies --- Nervous System Congenital Abnormalities --- Nervous System Congenital Malformations --- Nervous System Malformations, Congenital --- Nervous System Abnormalities --- Abnormality, Nervous System --- Anomaly, Nervous System --- Cranioschises --- Malformation, Nervous System --- Malformations, Nervous System --- Nervous System Abnormality --- Nervous System Anomaly --- Nervous System Malformation --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Genetics, Medical --- Brain Disorders --- CNS Disorders, Intracranial --- Central Nervous System Disorders, Intracranial --- Central Nervous System Intracranial Disorders --- Encephalon Diseases --- Encephalopathy --- Intracranial CNS Disorders --- Intracranial Central Nervous System Disorders --- Brain Disease --- Brain Disorder --- CNS Disorder, Intracranial --- Encephalon Disease --- Encephalopathies --- Intracranial CNS Disorder --- CNS Diseases --- Central Nervous System Disorders --- CNS Disease --- Polyneuropathy, Critical Illness --- Polyneuropathy, Familial --- Polyneuropathy, Inherited --- Polyneuropathy, Motor --- Polyneuropathy, Acquired --- Acquired Polyneuropathies --- Acquired Polyneuropathy --- Critical Illness Polyneuropathies --- Critical Illness Polyneuropathy --- Familial Polyneuropathies --- Familial Polyneuropathy --- Inherited Polyneuropathies --- Inherited Polyneuropathy --- Motor Polyneuropathies --- Motor Polyneuropathy --- Polyneuropathies, Acquired --- Polyneuropathies, Critical Illness --- Polyneuropathies, Familial --- Polyneuropathies, Inherited --- Polyneuropathies, Motor --- Polyneuropathy --- Degenerative Diseases, Central Nervous System --- Degenerative Diseases, Neurologic --- Degenerative Diseases, Spinal Cord --- Degenerative Neurologic Diseases --- Degenerative Neurologic Disorders --- Nervous System Degenerative Diseases --- Neurodegenerative Disorders --- Neurologic Degenerative Conditions --- Neurologic Degenerative Diseases --- Neurologic Diseases, Degenerative --- Degenerative Diseases, Nervous System --- Degenerative Condition, Neurologic --- Degenerative Conditions, Neurologic --- Degenerative Neurologic Disease --- Degenerative Neurologic Disorder --- Neurodegenerative Disease --- Neurodegenerative Disorder --- Neurologic Degenerative Condition --- Neurologic Degenerative Disease --- Neurologic Disease, Degenerative --- Neurologic Disorder, Degenerative --- Neurologic Disorders, Degenerative --- Spinal Cord Disorders --- Myelopathy --- Myelopathies --- Spinal Cord Disease --- Spinal Cord Disorder --- Cerebellar Disorders --- Cerebellar Syndromes --- Cerebellar Dysfunction --- Cerebellum Diseases --- Cerebellar Disease --- Cerebellar Disorder --- Cerebellar Dysfunctions --- Cerebellar Syndrome --- Cerebellum Disease --- Disease, Cerebellar --- Disease, Cerebellum --- Disorder, Cerebellar --- Dysfunction, Cerebellar --- Syndrome, Cerebellar --- Degenerative Hereditary Diseases, Nervous System --- Hereditary Neurodegenerative Diseases --- Hereditary-Degenerative Disorders, Nervous System --- Nervous System Degenerative Hereditary Diseases --- Nervous System Hereditary Degenerative Diseases --- Degenerative Disease, Nervous System, Hereditary --- Degenerative Hereditary Disorders, Nervous System --- Hereditary Diseases, Neurodegenerative --- Nervous System Diseases, Degenerative, Hereditary --- Neurodegenerative Diseases, Hereditary --- Disease, Hereditary Neurodegenerative --- Disease, Neurodegenerative Hereditary --- Diseases, Hereditary Neurodegenerative --- Diseases, Neurodegenerative Hereditary --- Hereditary Degenerative Disorders, Nervous System --- Hereditary Disease, Neurodegenerative --- Hereditary Neurodegenerative Disease --- Neurodegenerative Disease, Hereditary --- Neurodegenerative Hereditary Disease --- Neurodegenerative Hereditary Diseases --- Ataxia, Appendicular --- Ataxia, Limb --- Ataxia, Motor --- Ataxia, Sensory --- Ataxia, Truncal --- Ataxy --- Dyscoordination --- Lack of Coordination --- Tremor, Rubral --- Coordination Impairment --- Dyssynergia --- Incoordination --- Appendicular Ataxia --- Appendicular Ataxias --- Ataxias --- Ataxias, Appendicular --- Ataxias, Limb --- Ataxias, Motor --- Ataxias, Sensory --- Ataxias, Truncal --- Coordination Impairments --- Coordination Lack --- Impairment, Coordination --- Impairments, Coordination --- Incoordinations --- Limb Ataxia --- Limb Ataxias --- Motor Ataxia --- Motor Ataxias --- Rubral Tremor --- Rubral Tremors --- Sensory Ataxia --- Sensory Ataxias --- Tremors, Rubral --- Truncal Ataxia --- Truncal Ataxias --- CMT4f --- Charcot-Marie-Tooth Disease, Demyelinating, Type 4f --- Charcot-Marie-Tooth Disease, Type 3 --- Dejerine-Sottas Neuropathy --- Dejerine-Sottas Syndrome --- HMSN3 --- Herditary Sensory and Motor Neuropathy --- Hereditary Motor and Sensory Neuropathy --- Hereditary Motor and Sensory Neuropathy 3 --- Hereditary Motor and Sensory Neuropathy Type III --- Hypertrophic Neuropathy of Dejerine-Sottas --- Dejerine-Sottas Disease --- HMSN --- HMSN Type III --- HMSN Type VII --- Hereditary Motor and Sensory Neuropathies --- Hereditary, Type III, Motor and Sensory Neuropathy --- Hereditary, Type VII, Motor and Sensory Neuropathy --- Neuropathies, Hereditary Motor and Sensory --- Charcot Marie Tooth Disease, Type 3 --- Dejerine Sottas Disease --- Dejerine Sottas Neuropathy --- Dejerine Sottas Syndrome --- Dejerine-Sottas Hypertrophic Neuropathy --- Disease, Dejerine-Sottas --- HMSN Type IIIs --- HMSN Type VIIs --- Hypertrophic Neuropathy of Dejerine Sottas --- Neuropathy, Dejerine-Sottas --- Syndrome, Dejerine-Sottas --- Type VII, HMSN --- Spastic paralysis --- Neuromuscular diseases --- Spasticity --- Cerebellum --- abnormalities --- Fetal Anomalies --- Fetal Malformations --- Anomaly, Fetal --- Fetal Anomaly --- Fetal Malformation --- Malformation, Fetal --- Central Nervous System Disease --- Central Nervous System Disorder

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