| D009207 |
Myoclonus |
Involuntary shock-like contractions, irregular in rhythm and amplitude, followed by relaxation, of a muscle or a group of muscles. This condition may be a feature of some CENTRAL NERVOUS SYSTEM DISEASES; (e.g., EPILEPSY, MYOCLONIC). Nocturnal myoclonus is the principal feature of the NOCTURNAL MYOCLONUS SYNDROME. (From Adams et al., Principles of Neurology, 6th ed, pp102-3). |
Myoclonus, Action,Myoclonus, Nocturnal,Myoclonus, Palatal,Polymyoclonus,Myoclonic Jerk,Myoclonic Jerking,Myoclonus Simplex,Myoclonus, Eyelid,Myoclonus, Intention,Myoclonus, Lower Extremity,Myoclonus, Oculopalatal,Myoclonus, Segmental,Myoclonus, Sleep,Myoclonus, Upper Extremity,Action Myoclonus,Extremity Myoclonus, Lower,Extremity Myoclonus, Upper,Eyelid Myoclonus,Intention Myoclonus,Jerk, Myoclonic,Jerking, Myoclonic,Jerks, Myoclonic,Lower Extremity Myoclonus,Myoclonic Jerks,Nocturnal Myoclonus,Oculopalatal Myoclonus,Palatal Myoclonus,Segmental Myoclonus,Simplex, Myoclonus,Sleep Myoclonus,Upper Extremity Myoclonus |
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| D004827 |
Epilepsy |
A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) |
Aura,Awakening Epilepsy,Seizure Disorder,Epilepsy, Cryptogenic,Auras,Cryptogenic Epilepsies,Cryptogenic Epilepsy,Epilepsies,Epilepsies, Cryptogenic,Epilepsy, Awakening,Seizure Disorders |
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| D006008 |
Glycogen Storage Disease |
A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. |
Glycogenosis,Disease, Glycogen Storage,Diseases, Glycogen Storage,Glycogen Storage Diseases,Glycogenoses,Storage Disease, Glycogen,Storage Diseases, Glycogen |
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| D006651 |
Histocytochemistry |
Study of intracellular distribution of chemicals, reaction sites, enzymes, etc., by means of staining reactions, radioactive isotope uptake, selective metal distribution in electron microscopy, or other methods. |
Cytochemistry |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D001669 |
Biochemical Phenomena |
The chemical processes, enzymatic activities, and pathways of living things and related temporal, dimensional, qualitative, and quantitative concepts. |
Biochemical Processes,Biochemical Concepts,Biochemical Phenomenon,Biochemical Process,Phenomena, Biochemical,Biochemical Concept,Concept, Biochemical,Concepts, Biochemical,Phenomenon, Biochemical,Process, Biochemical,Processes, Biochemical |
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| D001671 |
Biochemistry |
The study of the composition, chemical structures, and chemical reactions of living things. |
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| D020191 |
Myoclonic Epilepsies, Progressive |
A heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME. |
Action Myoclonus-Renal Failure Syndrome,Biotin-Responsive Encephalopathy,Dentatorubral-Pallidoluysian Atrophy,May-White Syndrome,Ataxia, Chorea, Seizures, And Dementia,Atypical Inclusion-Body Disease,Familial Progressive Myoclonic Epilepsy,Haw River Syndrome,Myoclonic Epilepsy, Progressive,Myoclonus-Nephropathy Syndrome,Naito Oyanagi Disease,Naito-Oyanagi Disease,Progressive Myoclonic Epilepsy,Progressive Myoclonus Epilepsies,Action Myoclonus Renal Failure Syndrome,Atrophies, Dentatorubral-Pallidoluysian,Atrophy, Dentatorubral-Pallidoluysian,Atypical Inclusion Body Disease,Atypical Inclusion-Body Diseases,Biotin Responsive Encephalopathy,Biotin-Responsive Encephalopathies,Dentatorubral Pallidoluysian Atrophy,Dentatorubral-Pallidoluysian Atrophies,Encephalopathies, Biotin-Responsive,Encephalopathy, Biotin-Responsive,Epilepsies, Progressive Myoclonic,Epilepsies, Progressive Myoclonus,Epilepsy, Progressive Myoclonic,Epilepsy, Progressive Myoclonus,Haw River Syndromes,Inclusion-Body Disease, Atypical,Inclusion-Body Diseases, Atypical,May White Syndrome,Myoclonus Epilepsies, Progressive,Myoclonus Nephropathy Syndrome,Myoclonus-Nephropathy Syndromes,Naito-Oyanagi Diseases,Progressive Myoclonic Epilepsies,Progressive Myoclonus Epilepsy,River Syndromes, Haw,Syndromes, Myoclonus-Nephropathy |
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