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Cet ouvrage traite des atteintes des nerfs responsables des problèmes de mobilité de l'épaule : - atteintes des nerfs périphériques : maladies neuromusculaires, lésions de nerfs innervant l'épaule, paralysies, lésions traumatiques, etc. - atteintes des nerfs centraux : l'hémiplégie, la paraplégie, la maladie de Parkinson, etc. Pour tous ces cas, la pathologie est expliquée et la prise en charge rééducative détaillée.
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Arm --- Pain --- Family Practice --- Brachial Plexus Neuritis --- diagnosis
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Cervical syndrome --- Brachial Plexus Neuritis --- Cervical Vertebrae --- Whiplash Injuries --- Cervical compression syndrome --- Cervical disk syndrome --- Cervical radicular syndrome --- Spinal nerves --- Syndromes --- Cervical vertebrae --- Cervico-brachial neuralgia --- Injuries, Whiplash --- Injury, Whiplash --- Whiplash Injury --- Amyotrophic Neuralgia --- Amyotrophy, Hereditary Neuralgic --- Amyotrophy, Hereditary Neuralgic, with Predilection for Brachial Plexus --- Brachial Neuralgia --- Brachial Neuritis --- Brachial Plexus Neuropathy, Hereditary --- Cervicobrachial Neuralgia --- Familial Brachial Plexus Neuritis --- Hereditary Brachial Plexus Neuropathy --- Hereditary Neuralgic Amyotrophy --- Heredofamilial Neuritis with Brachial Plexus Predilection --- Neuritis With Brachial Predilection --- Parsonage-Aldren-Turner Syndrome --- Shoulder Girdle Neuropathy --- Amyotrophy, Neuralgic --- Cervico-Brachial Neuralgia --- Neuralgia, Amyotrophic --- Neuralgic Amyotrophy --- Neuritis, Brachial Plexus --- Parsonage-Turner Syndrome --- Shoulder-Girdle Neuropathy --- Amyotrophic Neuralgias --- Amyotrophies, Hereditary Neuralgic --- Amyotrophies, Neuralgic --- Brachial Neuralgias --- Brachial Neuritides --- Brachial Plexus Neuritides --- Cervico Brachial Neuralgia --- Cervico-Brachial Neuralgias --- Cervicobrachial Neuralgias --- Girdle Neuropathies, Shoulder --- Girdle Neuropathy, Shoulder --- Hereditary Neuralgic Amyotrophies --- Neuralgia, Brachial --- Neuralgia, Cervico-Brachial --- Neuralgia, Cervicobrachial --- Neuralgias, Amyotrophic --- Neuralgias, Brachial --- Neuralgias, Cervico-Brachial --- Neuralgias, Cervicobrachial --- Neuralgic Amyotrophies --- Neuralgic Amyotrophies, Hereditary --- Neuralgic Amyotrophy, Hereditary --- Neuritides, Brachial --- Neuritides, Brachial Plexus --- Neuritis, Brachial --- Neuropathies, Shoulder Girdle --- Neuropathies, Shoulder-Girdle --- Neuropathy, Shoulder Girdle --- Neuropathy, Shoulder-Girdle --- Parsonage Aldren Turner Syndrome --- Parsonage Turner Syndrome --- Shoulder Girdle Neuropathies --- Shoulder-Girdle Neuropathies --- Syndrome, Parsonage-Aldren-Turner --- Syndrome, Parsonage-Turner --- Brachial Plexus Neuropathies --- injuries --- Diseases --- Dislocation --- Neuropathology
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Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
Medicine --- Neurology & clinical neurophysiology --- Pompe disease --- GAA gene --- general population database --- carrier frequency --- genetic prevalence --- spinal muscular atrophy --- quality of life --- child neurology --- patient-reported outcomes --- neuromuscular --- carpal tunnel syndrome --- median nerve neuropathy --- electrodiagnostic studies --- neuromuscular ultrasound --- mucopolysaccharidosis --- neuropathy --- children --- adolescents --- Charcot-Marie-Tooth disease --- traumatic neuropathy --- inflammatory neuropathy --- metabolic neuropathy --- posterior spinal fusion --- kyphosis --- sagittal plane deformity --- signal recognition particle --- 3-hydroxy-3-methylglutaryl --- coenzyme A reductase --- juvenile myositis --- therapy --- clinical course --- chaperone-assisted autophagy --- clinical trials --- Duchenne muscular dystrophy --- public health surveillance --- distal arthrogryposis --- AMC --- ECEL1 --- contractures --- muscle MRI --- spinal muscular atrophy (SMA) --- nusinersen --- fine manual dexterity --- ultrasonographic elastography --- neuromuscular disease --- muscle --- brachial plexus neuritis --- hereditary sensory and motor neuropathy --- paralysis --- vaccination --- pediatrics --- Pompe disease --- GAA gene --- general population database --- carrier frequency --- genetic prevalence --- spinal muscular atrophy --- quality of life --- child neurology --- patient-reported outcomes --- neuromuscular --- carpal tunnel syndrome --- median nerve neuropathy --- electrodiagnostic studies --- neuromuscular ultrasound --- mucopolysaccharidosis --- neuropathy --- children --- adolescents --- Charcot-Marie-Tooth disease --- traumatic neuropathy --- inflammatory neuropathy --- metabolic neuropathy --- posterior spinal fusion --- kyphosis --- sagittal plane deformity --- signal recognition particle --- 3-hydroxy-3-methylglutaryl --- coenzyme A reductase --- juvenile myositis --- therapy --- clinical course --- chaperone-assisted autophagy --- clinical trials --- Duchenne muscular dystrophy --- public health surveillance --- distal arthrogryposis --- AMC --- ECEL1 --- contractures --- muscle MRI --- spinal muscular atrophy (SMA) --- nusinersen --- fine manual dexterity --- ultrasonographic elastography --- neuromuscular disease --- muscle --- brachial plexus neuritis --- hereditary sensory and motor neuropathy --- paralysis --- vaccination --- pediatrics
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Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
Medicine --- Neurology & clinical neurophysiology --- Pompe disease --- GAA gene --- general population database --- carrier frequency --- genetic prevalence --- spinal muscular atrophy --- quality of life --- child neurology --- patient-reported outcomes --- neuromuscular --- carpal tunnel syndrome --- median nerve neuropathy --- electrodiagnostic studies --- neuromuscular ultrasound --- mucopolysaccharidosis --- neuropathy --- children --- adolescents --- Charcot–Marie–Tooth disease --- traumatic neuropathy --- inflammatory neuropathy --- metabolic neuropathy --- posterior spinal fusion --- kyphosis --- sagittal plane deformity --- signal recognition particle --- 3-hydroxy-3-methylglutaryl --- coenzyme A reductase --- juvenile myositis --- therapy --- clinical course --- chaperone-assisted autophagy --- clinical trials --- Duchenne muscular dystrophy --- public health surveillance --- distal arthrogryposis --- AMC --- ECEL1 --- contractures --- muscle MRI --- spinal muscular atrophy (SMA) --- nusinersen --- fine manual dexterity --- ultrasonographic elastography --- neuromuscular disease --- muscle --- brachial plexus neuritis --- hereditary sensory and motor neuropathy --- paralysis --- vaccination --- pediatrics --- n/a --- Charcot-Marie-Tooth disease
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Significant scientific and therapeutic advances have been made in recent decades, particularly in hereditary but also in acquired neuromuscular diseases. As a result of our increasing etiological understanding, the classification of these diseases has changed from a clinical–descriptive and formal–genetic to a molecular–genetic and pathophysiological one. This has led to an intensification of research into the diagnosis and treatment of these diseases, resulting in the first effective gene-modifying treatments for DMD and SMA in recent years and, more recently, gene replacement therapy for the most severe form of SMA. In addition, great strides have been made in symptomatic and rehabilitative treatment, making it possible to improve the functioning and quality of life of those affected and their families. This Special Issue of Children contains a collection of 12 studies and reviews dealing with genetic and acquired peripheral nerve and muscle disorders.
Pompe disease --- GAA gene --- general population database --- carrier frequency --- genetic prevalence --- spinal muscular atrophy --- quality of life --- child neurology --- patient-reported outcomes --- neuromuscular --- carpal tunnel syndrome --- median nerve neuropathy --- electrodiagnostic studies --- neuromuscular ultrasound --- mucopolysaccharidosis --- neuropathy --- children --- adolescents --- Charcot–Marie–Tooth disease --- traumatic neuropathy --- inflammatory neuropathy --- metabolic neuropathy --- posterior spinal fusion --- kyphosis --- sagittal plane deformity --- signal recognition particle --- 3-hydroxy-3-methylglutaryl --- coenzyme A reductase --- juvenile myositis --- therapy --- clinical course --- chaperone-assisted autophagy --- clinical trials --- Duchenne muscular dystrophy --- public health surveillance --- distal arthrogryposis --- AMC --- ECEL1 --- contractures --- muscle MRI --- spinal muscular atrophy (SMA) --- nusinersen --- fine manual dexterity --- ultrasonographic elastography --- neuromuscular disease --- muscle --- brachial plexus neuritis --- hereditary sensory and motor neuropathy --- paralysis --- vaccination --- pediatrics --- n/a --- Charcot-Marie-Tooth disease
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