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Neuromuscular Junction -- physiology.   2
 

Neuromuscular Junction Toxic Disorders -- See Neuromuscular Junction Diseases


Conditions characterized by impaired transmission of impulses at the NEUROMUSCULAR JUNCTION. This may result from disorders that affect receptor function, pre- or postsynaptic membrane function, or ACETYLCHOLINESTERASE activity. The majority of diseases in this category are associated with autoimmune, toxic, or inherited conditions
  1
 

Neuromuscular Junctions -- See Neuromuscular Junction


The synapse between a neuron and a muscle
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Neuromuscular Manifestation -- See Neuromuscular Manifestations


Signs and symptoms associated with diseases of the muscle, neuromuscular junction, or peripheral nerves
  1
Neuromuscular Manifestations.   2
Neuromuscular manifestations of general diseases. : Evaluation and treatment of myopathies / edited by Emma Ciafaloni, Patrick F. Chinnery, Robert C. Griggs  2014 1
 

Neuromuscular nondepolarizing agents -- See Curare-like agents


  1
Neuromuscular Nondepolarizing Agents : From poison arrows to Prozac : how deadly toxins changed our lives forever / Stanley Feldman  2009 1
 

Neuromuscular Signs and Symptoms -- See Neuromuscular Manifestations


Signs and symptoms associated with diseases of the muscle, neuromuscular junction, or peripheral nerves
  1
Neuromuscular spindles.   2
Neuromuscular spindles -- Congresses : The Muscle spindle / edited by I.A. Boyd and M.H. Gladden  1985 1
 

Neuromuscular symptoms of general diseases -- See Neuromuscular manifestations of general diseases


  1
 

Neuromuscular transmission -- See Also the narrower term Neuromuscular spindles


  1
Neuromuscular transmission.   12
 

Neuromuscular Transmission Disorder -- See Neuromuscular Junction Diseases


Conditions characterized by impaired transmission of impulses at the NEUROMUSCULAR JUNCTION. This may result from disorders that affect receptor function, pre- or postsynaptic membrane function, or ACETYLCHOLINESTERASE activity. The majority of diseases in this category are associated with autoimmune, toxic, or inherited conditions
  1
 

Neuromuscular Transmission Disorders -- See Neuromuscular Junction Diseases


Conditions characterized by impaired transmission of impulses at the NEUROMUSCULAR JUNCTION. This may result from disorders that affect receptor function, pre- or postsynaptic membrane function, or ACETYLCHOLINESTERASE activity. The majority of diseases in this category are associated with autoimmune, toxic, or inherited conditions
  1
Neuromuskuläre Krankheit : Inherited neuromuscular diseases : translation from pathomechanisms to therapies / [edited by] Carmen Espinós, Vicente Felipo, Francesc Palau  2009 1
Neuromuskuläre Krankheit -- Aufsatzsammlung. : Neuromuscular diseases : from basic mechanisms to clinical management / volume editor, F. Deymeer  2000 1
 

Neuromyasthenia, Epidemic -- See Myalgic encephalomyelitis


  1
 

Neuron -- See Neurons


The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM
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Neuron, Alpha Motor -- See Motor Neurons


Neurons which activate MUSCLE CELLS
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  Neuron Degeneration -- 2 Related Subjects   2
 

Neuron Degenerations -- See Nerve Degeneration


Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways
  1
 

Neuron Disease, Motor -- See Motor Neuron Disease


Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
  1
 

Neuron Diseases, Motor -- See Motor Neuron Disease


Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
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Neuron, Dopamine -- See Dopaminergic Neurons


Neurons whose primary neurotransmitter is DOPAMINE
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Neuron, Dopaminergic -- See Dopaminergic Neurons


Neurons whose primary neurotransmitter is DOPAMINE
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Neuron, Mirror -- See Mirror Neurons


Neurons that fire when an animal acts or observes the same action of another thus coding the motor response. They were originally discovered in the premotor and parietal cortex of the monkey and studies have shown that neurons that have a similar mechanism are present in humans. Mirror neurons are theorized to be related to social cognition
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Neuron, Motor -- See Motor Neurons


Neurons which activate MUSCLE CELLS
  1
 

Neuron, Nociceptive -- See Nociceptors


Peripheral AFFERENT NEURONS which are sensitive to injuries or pain, usually caused by extreme thermal exposures, mechanical forces, or other noxious stimuli. Their cell bodies reside in the DORSAL ROOT GANGLIA. Their peripheral terminals (NERVE ENDINGS) innervate target tissues and transduce noxious stimuli via axons to the CENTRAL NERVOUS SYSTEM
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Neuron Protection -- See Neuroprotection


The physiological processes and techniques used by the body to prevent neuronal injury and degeneration in the central nervous system following acute disorders or as a result of chronic neurodegenerative diseases
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Neuron regeneration -- See Nervous system Regeneration


  1
 

Neuron, Sensory -- See Sensory Receptor Cells


Specialized afferent neurons capable of transducing sensory stimuli into NERVE IMPULSES to be transmitted to the CENTRAL NERVOUS SYSTEM. Sometimes sensory receptors for external stimuli are called exteroceptors; for internal stimuli are called interoceptors and proprioceptors
  1
 

Neuronal adaptation -- See Neuroplasticity


Here are entered works on the functional and morphologic adjustment and adaptation of the nervous system to various stimulating factors and lesions
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Neuronal Arborization -- See Neuronal Plasticity


The capacity of the NERVOUS SYSTEM to change its reactivity as the result of successive activations
  1
 

Neuronal Arborizations -- See Neuronal Plasticity


The capacity of the NERVOUS SYSTEM to change its reactivity as the result of successive activations
  1
Neuronal ceroid-lipofuscinoses : The neuronal ceroid lipofuscinoses (Batten disease) / edited by Sara E. Mole, Ruth E. Williams, and Hans H. Goebel ; editorial assistance by G. Machado da Silva  2011 1
 

Neuronal Ceroid-Lipofuscinoses, CLN3-Related -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
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  Neuronal ceroid-lipofuscinosis -- 2 Related Subjects   2
 

Neuronal Ceroid Lipofuscinosis, Adult -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid Lipofuscinosis, Adult Type -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid-Lipofuscinosis, CLN3-Related -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid Lipofuscinosis, Infantile -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid Lipofuscinosis, Juvenile -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid Lipofuscinosis Juvenile Type -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal Ceroid Lipofuscinosis, Late Infantile -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Neuronal circuitry -- See Neural circuitry


  1
 

Neuronal Growth-Associated Proteins -- See Nerve Growth Factors


Factors which enhance the growth potentialities of sensory and sympathetic nerve cells
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Neuronal Network Remodeling -- See Neuronal Plasticity


The capacity of the NERVOUS SYSTEM to change its reactivity as the result of successive activations
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Neuronal Network Remodelings -- See Neuronal Plasticity


The capacity of the NERVOUS SYSTEM to change its reactivity as the result of successive activations
  1
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