Results 141 to 150 of about 2,714 (169)

Levetiracetam in progressive myoclonic epilepsy

Neurology, 2004
The authors conducted an open study of levetiracetam as add-on therapy in nine patients with well-defined progressive myoclonic epilepsies and refractory myoclonus. Myoclonus was evaluated semiquantitatively (territory, intensity, daily living activities). Five patients had improvement of their myoclonus score.
C, Crest, S, Dupont, E, Leguern, C, Adam, M, Baulac   +4 more
openaire   +2 more sources

Progressive Myoclonic Epilepsy

1987
Progressive myoclonic epilepsy or progressive myoclonus epilepsy (PME) is a rare condition. It is commonly hereditary, is characterized by generalized convulsive seizures and myoclonic jerks frequently provoked by volitional movements, and is frequently associated with cerebellar ataxia, mental deterioration, pyramidal signs, and rigidity.
openaire   +1 more source

Add-on therapy with topiramate in progressive myoclonic epilepsy

Epilepsy & Behavior, 2005
We evaluated the clinical responses to add-on therapy with topiramate in eight patients with progressive myoclonic epilepsy (PME). Severe myoclonic seizures disturbing daily activities were persistent despite adequate trials of various combinations of antiepileptic drugs in all patients.
Ebru, Aykutlu, Betül, Baykan, Candan, Gürses, Nerses, Bebek, Nesimi, Büyükbabani, Ayşen, Gökyigit   +5 more
openaire   +2 more sources

A prickly cause of progressive myoclonic epilepsy

Clinical Genetics, 2009
A homozygous mutation in human PRICKLE1 causes an autosomal‐recessive Progressive Myoclonus Epilepsy‐Ataxia Syndrome
Bassuk et al. (2008)
American Journal of Human Genetics 83: 1–10.
openaire   +2 more sources

Juvenile Huntington’s disease presenting as progressive myoclonic epilepsy

Neurology, 2001
A 9-year-old girl, who had no family history of neurologic diseases in the first-degree relatives, had a 3-year history of progressive myoclonus epilepsy (PME). A thorough laboratory investigation was normal. As two sisters of her paternal grandmother were said to have Huntington's disease (HD), the authors looked for HD and found a CAG repeat ...
Gambardella A, Muglia M, Labate A, Magariello A, Gabriele AL, Mazzei R, Pirritano D, Conforti FL, Patitucci A, Valentino P, Zappia M, Quattrone A   +11 more
openaire   +6 more sources

PROGRESSIVE MYOCLONIC EPILEPSY WITH LAFORA'S BODIES

Acta Neurologica Scandinavica, 2009
Two cases of Lafora's disease of rapid evolution with a typical clinical picture, and increased glutamic acid urine excretion are described. Partial critical control was obtained using clonazepam. The relation-ship between PME and heredodegenerative ataxia is discussed; the existence of subacute and precocious forms with long evolution in Lafora's ...
E S, Lope, S, Ramón, S R, Junquera, A B, Berenguel   +3 more
openaire   +2 more sources

A De Novo SEMA6B Variant in a Chinese Patient with Progressive Myoclonic Epilepsy-11 and Review of the Literature

Journal of Molecular Neuroscience, 2021
Xuqin Chen
exaly  

Progressive Myoclonic Epilepsies

2022
Benjamin Legros
exaly  

Myoclonic epilepsy ("myoclonic status") in non progressive encephalopathies

1992
Eelectroclinical features of myoclonic status in children with non.progressive ...
DALLA BERNARDINA, Bernardo, FONTANA E., SGRO' V., COLAMARIA V., ELIA M.   +4 more
openaire   +1 more source

An Unusual Masquerader of Progressive Myoclonic Epilepsy

The Indian Journal of Pediatrics, 2019
Shivan Kesavan, Lokesh Saini, Priyanka Madaan, Sumeet R. Dhawan, Jitendra K. Sahu, Kirti Gupta, Paramjit Singh, Sushant Sahoo   +7 more
openaire   +2 more sources