 Myoclonic Epilepsies, Progressive
"Myoclonic Epilepsies, Progressive" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D020191
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| MeSH Number(s) |
C10.228.140.490.375.130.650 C10.228.140.490.493.063.650
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| Concept/Terms |
Myoclonic Epilepsies, Progressive- Myoclonic Epilepsies, Progressive
- Epilepsies, Progressive Myoclonic
- Epilepsy, Progressive Myoclonic
- Progressive Myoclonic Epilepsies
- Progressive Myoclonic Epilepsy
- Myoclonic Epilepsy, Progressive
- Progressive Myoclonus Epilepsies
- Epilepsies, Progressive Myoclonus
- Epilepsy, Progressive Myoclonus
- Myoclonus Epilepsies, Progressive
- Progressive Myoclonus Epilepsy
Atypical Inclusion-Body Disease- Atypical Inclusion-Body Disease
- Atypical Inclusion Body Disease
- Atypical Inclusion-Body Diseases
- Inclusion-Body Disease, Atypical
- Inclusion-Body Diseases, Atypical
Dentatorubral-Pallidoluysian Atrophy- Dentatorubral-Pallidoluysian Atrophy
- Atrophies, Dentatorubral-Pallidoluysian
- Atrophy, Dentatorubral-Pallidoluysian
- Dentatorubral Pallidoluysian Atrophy
- Dentatorubral-Pallidoluysian Atrophies
- Naito-Oyanagi Disease
- Naito-Oyanagi Diseases
- Haw River Syndrome
- Haw River Syndromes
- River Syndromes, Haw
- Naito Oyanagi Disease
- Ataxia, Chorea, Seizures, And Dementia
Action Myoclonus-Renal Failure Syndrome- Action Myoclonus-Renal Failure Syndrome
- Action Myoclonus Renal Failure Syndrome
- Myoclonus-Nephropathy Syndrome
- Myoclonus Nephropathy Syndrome
- Myoclonus-Nephropathy Syndromes
- Syndromes, Myoclonus-Nephropathy
Biotin-Responsive Encephalopathy- Biotin-Responsive Encephalopathy
- Biotin Responsive Encephalopathy
- Biotin-Responsive Encephalopathies
- Encephalopathies, Biotin-Responsive
- Encephalopathy, Biotin-Responsive
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Below are MeSH descriptors whose meaning is more general than "Myoclonic Epilepsies, Progressive".
Below are MeSH descriptors whose meaning is more specific than "Myoclonic Epilepsies, Progressive".
This graph shows the total number of publications written about "Myoclonic Epilepsies, Progressive" by people in this website by year, and whether "Myoclonic Epilepsies, Progressive" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Myoclonic Epilepsies, Progressive" by people in Profiles.
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Bassuk AG, Wallace RH, Buhr A, Buller AR, Afawi Z, Shimojo M, Miyata S, Chen S, Gonzalez-Alegre P, Griesbach HL, Wu S, Nashelsky M, Vladar EK, Antic D, Ferguson PJ, Cirak S, Voit T, Scott MP, Axelrod JD, Gurnett C, Daoud AS, Kivity S, Neufeld MY, Mazarib A, Straussberg R, Walid S, Korczyn AD, Slusarski DC, Berkovic SF, El-Shanti HI. A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. Am J Hum Genet. 2008 Nov; 83(5):572-81.
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