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Peripheral Nervous System Diseases --- Neurologic Examination --- Cerebellar Ataxia --- Electromyography --- physiopathology --- standards --- diagnosis
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Ataxia --- Ataxia. --- Cerebellar ataxia --- Friedreich's ataxia. --- Paraplegia --- Familial and genetic. --- Familial and genetic. --- Familial and genetic.
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L'etude du cervelet a considerablement progressee notamment ces 30 dernieres annees sur la comprehension des fonctions cerebelleuses et des maladies cerebelleuses, appelees ataxies cerebelleuses. Avec l'emergence de la neuroradiologie morphologique et fonctionnelle, une exploration detaillee de l'anatomie fonctionnelle cerebelleuse est devenue possible chez l'homme. Il est possible non seulement d'en decrire l'anatomie generale, a les faisceaux anatomiques qui le composent, ses fonctions et les reseaux cerebraux auxquels le cervelet participe. Il est egalement possible d'etudier les variations
Cerebellum --- Physiology. --- Rhombencephalon --- Cerebellum - anatomy and histology --- Cerebellum - physiology --- Brain Diseases --- Cerebellar Ataxia. --- Cerebellar Diseases. --- Diagnostic Imaging. --- Medical radiology --- Cerebellar ataxia --- Cervelet --- Radiologie médicale --- Ataxie cérébelleuse --- anatomy & histology. --- Physiology --- Diseases. --- Physiologie --- Maladies --- EPUB-LIV-FT LIVMEDEC SPRINGER-B
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"Cerebellum & Ataxias is an open access journal devoted to cerebellar research and cerebellar disorders, including scientific reports and clinical cases of the numerous forms of ataxias."
Cerebellum --- Cerebellar Ataxia --- Ataxia --- Cerebellar Diseases --- Neurophysiology --- Cognition --- Cerebellar ataxia --- Cervelet --- Ataxie cérébelleuse --- Ataxie --- Periodicals. --- Diseases --- Periodicals --- Périodiques --- Maladies --- Cerebellar Diseases. --- Cerebellum. --- Cerebellar Ataxia. --- Ataxia. --- Cerebellar ataxia. --- Diseases. --- 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 --- Corpus Cerebelli --- Parencephalon --- Cerebelli, Corpus --- Cerebellums --- Cerebellus, Corpus --- Corpus Cerebellus --- Parencephalons --- 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 --- ataxiology --- neurological disorders --- cerebellar research --- behavioural and cognitive tasks --- neurosurgery --- Rhombencephalon --- Movement disorders --- Neuroscience --- Neuropathology --- Cerebella --- Malalties cerebrals --- Neurologia --- Malalties cerebrals. --- Neurologia.
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Spinocerebellar Degenerations. --- Ataxia --- Nervous system --- -Neurogenetics --- 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 --- Genetics --- Neurosciences --- Organs (Anatomy) --- Movement disorders --- Diseases --- -Genetic aspects --- Genetic aspects --- Neurogenetics --- Spinocerebellar Degenerations --- Diseases&delete& --- Marinesco-Sjögren Syndrome --- Marinesco Sjögren Syndrome --- Syndrome, Marinesco-Sjögren
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Cerebellum --- Ataxia --- Cerebellar Ataxia --- Cerebellar Diseases --- Neurophysiology --- Cognition --- Health Sciences --- Life Sciences --- General and Others --- Physiology --- Genetics --- Micro and Molecular Biology --- Ataxia. --- Cerebellum. --- 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 --- Corpus Cerebelli --- Parencephalon --- Cerebelli, Corpus --- Cerebellums --- Cerebellus, Corpus --- Corpus Cerebellus --- Parencephalons --- Cognitive Function --- Cognitions --- Cognitive Functions --- Function, Cognitive --- Functions, Cognitive --- 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 --- 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 --- Movement disorders --- Rhombencephalon --- Cerebellar Ataxia. --- Cerebellar Diseases. --- Neurophysiology. --- Cognition. --- Cerebella
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The extraintestinal manifestations of coeliac disease (CD) are now well recognised. We have previously edited a special issue for Nutrients covering all aspects of the extraintestinal manifestations in the context of CD. In this issue we wish to concentrate just on the neurological manifestations. The identification of TG6 autoantibodies in patients with neurological manifestations and its use in the diagnosis of such patients seems to be a good opportunity to focus on the neurological aspect of CD. In addition it is now clear that such manifestations can occur even in the absence of enteropathy but in the presence of antigliadin antibodies and/or TG6 antibodies. Given that such antigliadin antibodies can be found in up to 10% of the “healthy” population we anticipate that the neurological manifestations are likely to be very common and thus merit early recognition and treatment.
Research & information: general --- Biology, life sciences --- Food & society --- coeliac disease --- gluten free diet --- psychiatric manifestations --- autistic spectrum disorder --- attention deficit hyperactivity disorder --- depression --- anxiety --- bipolar disorder --- schizophrenia --- eating disorders --- gluten --- neurological disorders --- gliadin --- ataxia --- neuropathy --- myopathy --- encephalopathy --- food intolerance --- celiac disease --- gluten sensitivity --- gluten-free diet --- cognition --- neurology --- disease duration --- autoimmunity --- multiple sclerosis --- psoriasis --- autoimmune thyroid disease --- type 1 diabetes --- transglutaminase antibodies --- TG2 --- TG3 --- TG6 --- dermatitis herpetiformis --- gluten ataxia --- gluten encephalopathy --- gluten neuropathy --- autism spectrum disorder --- review --- stiff person syndrome --- anti-GAD antibodies --- cerebellar ataxia --- gluten-related pathology --- cortical excitability --- transcallosal inhibition --- transcranial magnetic stimulation --- executive dysfunction --- gamma-amino-butyric acid --- neurological dysfunction --- headaches --- anti-gliadin antibodies --- MR imaging --- TG6 antibodies --- non-celiac wheat sensitivity --- irritable bowel syndrome --- multiple food hypersensitivity --- neuropsychiatric symptoms --- HLA --- duodenal lymphocytosis
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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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The aging population and the increased prevalence of neurological diseases have raised the issue of gait and balance disorders as a major public concern worldwide. Indeed, gait and balance disorders are responsible for a high healthcare and economic burden on society, thus, requiring new solutions to prevent harmful consequences. Recently, wearable sensors have provided new challenges and opportunities to address this issue through innovative diagnostic and therapeutic strategies. Accordingly, the book “Wearable Sensors in the Evaluation of Gait and Balance in Neurological Disorders” collects the most up-to-date information about the objective evaluation of gait and balance disorders, by means of wearable biosensors, in patients with various types of neurological diseases, including Parkinson’s disease, multiple sclerosis, stroke, traumatic brain injury, and cerebellar ataxia. By adopting wearable technologies, the sixteen original research articles and reviews included in this book offer an updated overview of the most recent approaches for the objective evaluation of gait and balance disorders.
History of engineering & technology --- inertial measurement units --- gait analysis --- biomedical signal processing --- pattern recognition --- step detection --- physiological signals --- Parkinson’s disease --- pathological gait --- turning analysis --- wearable sensors --- mobile gait analysis --- wearables --- inertial sensors --- traumatic brain injury --- dynamic balance --- gait disorders --- gait patterns --- head injury --- gait symmetry --- gait smoothness --- acceleration --- machine learning --- classification --- accelerometer --- GAITRite --- multi-regression normalization --- SVM --- random forest classifier --- balance --- gait --- transcranial direct current stimulation --- wearable electronics --- IMUs --- cueing --- posture --- rehabilitation --- cerebellar ataxia --- movement analysis --- personalized medicine --- stroke --- asymmetry --- trunk --- reliability --- validity --- aging --- reactive postural responses --- yaw perturbation --- kinematics --- postural stability --- dynamic posturography --- multiple sclerosis --- gait metrics --- test-retest reliability --- sampling frequency --- accelerometry --- autocorrelation --- harmonic ratio --- six-minute walk --- back school --- inertial sensor --- lower back pain --- stability --- timed up and go test --- gait assessment --- tri-axial accelerometer --- CV --- healthy subjects --- test-retest --- trajectory reconstruction --- stride segmentation --- dynamic time warping --- pedestrian dead-reckoning --- near falls --- loss of balance --- pre-impact fall detection --- activities of daily life --- bio-signals --- EEG --- EMG --- wireless sensors --- posturography --- Alzheimer’s disease --- vestibular syndrome --- diagnosis --- symptoms monitoring --- wearable --- home-monitoring --- inertial measurement units --- gait analysis --- biomedical signal processing --- pattern recognition --- step detection --- physiological signals --- Parkinson’s disease --- pathological gait --- turning analysis --- wearable sensors --- mobile gait analysis --- wearables --- inertial sensors --- traumatic brain injury --- dynamic balance --- gait disorders --- gait patterns --- head injury --- gait symmetry --- gait smoothness --- acceleration --- machine learning --- classification --- accelerometer --- GAITRite --- multi-regression normalization --- SVM --- random forest classifier --- balance --- gait --- transcranial direct current stimulation --- wearable electronics --- IMUs --- cueing --- posture --- rehabilitation --- cerebellar ataxia --- movement analysis --- personalized medicine --- stroke --- asymmetry --- trunk --- reliability --- validity --- aging --- reactive postural responses --- yaw perturbation --- kinematics --- postural stability --- dynamic posturography --- multiple sclerosis --- gait metrics --- test-retest reliability --- sampling frequency --- accelerometry --- autocorrelation --- harmonic ratio --- six-minute walk --- back school --- inertial sensor --- lower back pain --- stability --- timed up and go test --- gait assessment --- tri-axial accelerometer --- CV --- healthy subjects --- test-retest --- trajectory reconstruction --- stride segmentation --- dynamic time warping --- pedestrian dead-reckoning --- near falls --- loss of balance --- pre-impact fall detection --- activities of daily life --- bio-signals --- EEG --- EMG --- wireless sensors --- posturography --- Alzheimer’s disease --- vestibular syndrome --- diagnosis --- symptoms monitoring --- wearable --- home-monitoring
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