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Your search keyword '"Myoclonus epilepsy"' showing total 64 results

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64 results on '"Myoclonus epilepsy"'

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1. De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus

2. Brain proton magnetic resonance spectroscopy findings in a Beagle dog with genetically confirmed Lafora disease

3. Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

4. Quantitative Changes in the Mitochondrial Proteome of Cerebellar Synaptosomes From Preclinical Cystatin B-Deficient Mice

5. Successful use of fenfluramine in nonconvulsive status epilepticus of Dravet syndrome

6. Author response for 'Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction'

7. MELAS and Kearns–Sayre overlap syndrome due to the mtDNA m. A3243G mutation and large-scale mtDNA deletions

8. Unusual Course of Lafora Disease

9. Phenotypic Diversity of Myoclonus Epilepsy Associated with Ragged-red Fibers with an 8344A>G mtDNA Mutation

10. CLONAZEPAM (Ro 5-4023) IN THE TREATMENT OF MYOCLONUS EPILEPSY

11. Early-onset dementia with prolonged occipital seizures: An atypical case of Kufs disease

12. Proton magnetic resonance spectroscopy study of bilateral thalamus in juvenile myoclonic epilepsy

13. Progressive myoclonus epilepsy in a beagle

14. Progressive Myoclonic Epilepsies

15. Progressive Volume Loss and White Matter Degeneration in Cstb-Deficient Mice: A Diffusion Tensor and Longitudinal Volumetry MRI Study

17. Doença de Lafora: diagnóstico pela biopsia de músculo esquelético (relato de caso)

18. Progressive myoclonus epilepsy with unusual neuropathologic features

19. Inheritance and expression of mitochondrial DNA point mutations

20. Update in Familial Cortical Myoclonic Tremor with Epilepsy

21. Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation

22. Mutation of SCARB2 in a Patient With Progressive Myoclonus Epilepsy and Demyelinating Peripheral Neuropathy

23. Pallidal and thalamic atrophies

24. Myoclonic Epilepsy with Ragged Red Fibers (MERRF)

25. SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure

26. Progressive Myoclonus Epilepsies

27. Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys

28. Neuroplasticity in patients with Parkinson’s disease and myoclonus epilepsy

29. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features

30. Overview

31. Cortical Excitability Measures in Patients and Unaffected Siblings

32. Epilepsy in Neurodegenerative Disorders

33. High intensity in the globus pallidus on proton and T2-weighted MRI in a case of dentato-ruburo-pallido-luysian atrophy of myoclonus epilepsy type

34. Gene defects in progressive myoclonus epilepsy

35. Clinical and neuropathologic findings in a case of severe myoclonic epilepsy of infancy

36. Mitochondrial Myopathies: Morphological Approach to Molecular Abnormalities

38. Cerebral lactic acidosis correlates with neurological impairment in MELAS

41. Progressive familial myoclonus epilepsy

42. A Neuropathological Case-Study of Myoclonus Epilepsy

43. Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy

44. On the heredity of mitochondrial cytopathies

45. Clinical Biochemistry of Epilepsy

46. AN AUTOPSY CASE OF MYOCLONUS EPILEPSY

47. The Evolution of Different Types of Myoclonus During Sleep

48. Some observations on electroencephalograms of myoclonus epilepsy

49. Myoclonus Epilepsy: Report Of Electroencephalographs Observations

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