serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.042 Akinetic Mutism .
C10.228.140.490 Epilepsy .
C10.228.140.490.375 Epilepsy, Generalized .
C10.228.140.490.375.260 Epilepsy, Absence .
C10.228.140.490.493 Epileptic Syndromes .
C10.228.140.490.493.125 Epilepsy, Absence .
D02 Organic Chemicals .
D02.455 Hydrocarbons .
D02.455.426 Hydrocarbons, Cyclic .
D02.455.426.100 Bridged-Ring Compounds .
D02.455.426.100.080 Bridged Bicyclo Compounds .
D02.455.426.100.080.100 Biperiden .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.621 Piperidines .
D03.383.621.110 Biperiden .
D03.605 Heterocyclic Compounds, Bridged-Ring .
D03.605.084 Bridged Bicyclo Compounds, Heterocyclic .
D03.605.084.500 Azabicyclo Compounds .
D03.605.084.500.332 Biperiden .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Epilepsy, Generalized .
Convulsive Seizure Disorder, Generalized .
Epilepsy, Akinetic .
Epilepsy, Atonic .
Generalized Convulsive Epilepsy .
Generalized Nonconvulsive Epilepsy .
Generalized Onset Seizure Disorder .
Generalized Seizure Disorder, Convulsive .
Generalized Seizure Disorder, Nonconvulsive .
Nonconvulsive Generalized Seizure Disorder .
Nonconvulsive Seizure Disorder, Generalized .
Seizure Disorder, Convulsive, Generalized .
Seizure Disorder, Generalized Nonconvulsive .
Seizure Disorder, Generalized Onset .
Seizure Disorder, Generalized, Convulsive .
Seizure Disorder, Nonconvulsive Generalized .
Symptomatic Generalized Epilepsy .
Akinetic Epilepsies .
Akinetic Epilepsy .
Atonic Epilepsies .
Atonic Epilepsy .
Convulsive Epilepsies, Generalized .
Convulsive Epilepsy, Generalized .
Epilepsies, Akinetic .
Epilepsies, Atonic .
Epilepsies, Generalized .
Epilepsies, Generalized Convulsive .
Epilepsies, Tonic .
Epilepsy, Generalized Convulsive .
Epilepsy, Generalized Nonconvulsive .
Epilepsy, Symptomatic Generalized .
Generalized Convulsive Epilepsies .
Generalized Epilepsies .
Generalized Epilepsy .
Generalized Epilepsy, Symptomatic .
Generalized Seizure Disorder .
Generalized Seizure Disorders .
Nonconvulsive Epilepsy, Generalized .
Seizure Disorders, Generalized .
Tonic Epilepsies .
Tonic Epilepsy .
Epilepsy, Tonic .
Convulsive Generalized Seizure Disorder .
Generalized Nonconvulsive Seizure Disorder .
Seizure Disorder, Generalized .
EPILEPSY, ATONIC .
EPILEPSY, GENERALIZED PRIMARY .
Recurrent conditions characterized by epileptic seizures which arise diffusely and simultaneously from both hemispheres of the brain. Classification is generally based upon motor manifestations of the seizure (e.g., convulsive, nonconvulsive, akinetic, atonic, etc.) or etiology (e.g., idiopathic, cryptogenic, and symptomatic). (From Mayo Clin Proc, 1996 Apr;71(4):405-14) .
1.00
432716
 
Epilepsy .
Epilepsy, Cryptogenic .
Auras .
Cryptogenic Epilepsies .
Cryptogenic Epilepsy .
Epilepsies .
Epilepsies, Cryptogenic .
Epilepsy, Awakening .
Seizure Disorders .
Aura 3776 .
Awakening Epilepsy .
Seizure Disorder .
Epileptic Seizures .
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) .
0.67
213360814
 
Biperiden .
Akineton .
Biperiden Hydrochloride .
Biperiden, 1R-(1 alpha,2 alpha(R*),4 alpha)-Isomer .
Biperiden, 1S-(1 alpha,2 alpha(R*),4 alpha)-Isomer .
Biperidene .
alpha-Bicyclo(2.2.1)hept-5-en-2-yl-alpha-phenyl-1-piperidinepropanol .
Hydrochloride, Biperiden .
A muscarinic antagonist that has effects in both the central and peripheral nervous systems. It has been used in the treatment of arteriosclerotic, idiopathic, and postencephalitic parkinsonism. It has also been used to alleviate extrapyramidal symptoms induced by phenothiazine derivatives and reserpine. .
0.60
15413
 
Akinetic Mutism .
Akinetic Autism .
Coma Vigil .
Coma Vigilans .
Akinetic Mutisms .
Autism, Akinetic .
Vigil, Coma .
Vigils, Coma .
Mutism, Akinetic .
A syndrome characterized by a silent and inert state without voluntary motor activity despite preserved sensorimotor pathways and vigilance. Bilateral FRONTAL LOBE dysfunction involving the anterior cingulate gyrus and related brain injuries are associated with this condition. This may result in impaired abilities to communicate and initiate motor activities. (From Adams et al., Principles of Neurology, 6th ed, p348; Fortschr Neurol Psychiatr 1995 Feb;63(2):59-67) .
0.55
2377
 
Epilepsy, Absence .
Absence Seizure Disorder .
Childhood Absence Epilepsy .
Epilepsy Juvenile Absence .
Epilepsy, Absence, Atypical .
Epilepsy, Petit Mal .
Juvenile Absence Epilepsy .
Pykno-Epilepsy .
Seizure Disorder, Absence .
Absence Epilepsies, Childhood .
Absence Epilepsies, Juvenile .
Absence Epilepsy .
Absence Epilepsy, Childhood .
Absence Epilepsy, Juvenile .
Absence Seizure Disorders .
Childhood Absence Epilepsies .
Epilepsies, Childhood Absence .
Epilepsies, Juvenile Absence .
Epilepsy Juvenile Absences .
Epilepsy, Childhood Absence .
Epilepsy, Juvenile Absence .
Juvenile Absence Epilepsies .
Juvenile Absence, Epilepsy .
Juvenile Absences, Epilepsy .
Minor Epilepsies .
Minor Epilepsy .
Petit Mal Epilepsies .
Petit Mal, Akinetic .
Pykno Epilepsy .
Pykno-Epilepsies .
Pyknolepsies .
Seizure Disorders, Absence .
Akinetic Petit Mal .
Pyknolepsy .
Petit Mal Epilepsy .
Epilepsy, Minor .
EPILEPSY, PETIT MAL .
A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) .
0.54
563336