Results 121 to 130 of about 845 (152)

Lafora body disease

2011
no abstract ...
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Managing Lafora body disease with vagal nerve stimulation

Epileptic Disorders, 2017
AbstractA 17‐year‐old female, of consanguineous parents, presented with a history of seizures and cognitive decline since the age of 12 years. She had absence, focal dyscognitive, generalized myoclonic, and generalized tonic‐clonic seizures, all of which were drug resistant.
Mohamad A, Mikati, Faysal, Tabbara
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Correlation between ultrastructure and histochemistry of lafora bodies

Acta Neuropathologica, 1971
Lafora bodies are composed of fibrillar and granular components in various concentrations. They are located in neuronal cell processes and perikarya and are frequently clearly intermingled with cytoplasmic elements. These components are electron-lucent, show a variable affinity for osmium, and are weakly stained by classical uranyl acetate stain ...
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Progressive Myoclonus Epilepsy With Lafora Inclusion Bodies

Archives of Neurology, 1967
Lafora's AFORA'S disease is a rare form of myoclonus epilepsy. 1 It is characterized by myoclonus, generalized convulsions, and progressive mental deterioration which begin during adolescence. Death within four to ten years has been the inevitable outcome in all reported cases.
D L, Odor, R, Janeway, L A, Pearce, J R, Ravens   +3 more
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Lafora-like inclusion bodies in the CNS of aged dogs

Acta Neuropathologica, 1978
Forty randomly selected dogs, arranged into three groups according to age, were examined light and electron microscopically. Lafora-like inclusion bodies were found in all cases of aged dogs without neurological signs. They appeared as PAS positive, round bodies measuring up to 15 mu in diameter.
Y, Suzuki, K, Akiyama, S, Suu
exaly   +3 more sources

[Lafora bodies in the retina of various animals].

Journal francais d'ophtalmologie, 1983
Lafora's bodies, formerly described in the retina in humans affected with familial myoclonic epilepsy--or Lafora's disease--and in dogs, were found not only in retinas of clinically healthy monkeys (macacus rhesus), but also in those of the healthy cat and dog. Lafora's bodies are not there fore characteristic of the specific disease.
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Immunocytochemical and lectin-binding studies on Lafora bodies.

Clinical neuropathology, 1990
Antibodies to a range of intermediate filaments and lectins specific for several different carbohydrates were used to study Lafora bodies in two cases of Lafora disease. Positive staining of Lafora bodies was found with antibodies to 160 KD and 200 KD neurofilaments and to desmin.
P D, Lewis, D J, Evans, B, Shambayati
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[Cytophotometric studies on the staining dichroism of Lafora bodies (Lafora bodies)].

Acta neuropathologica, 1972
G, Romhănyi, R, Schnabel
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Astrocytic glycogen accumulation drives the pathophysiology of neurodegeneration in Lafora disease

Brain, 2021
Jordi Duran, Arnau Hervera, Kia H Markussen   +2 more
exaly  

[Ultrastructure of Lafora bodies].

Acta neuropathologica, 1969
M, Toga, D, Dubois, J, Hassoun
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