Results 241 to 250 of about 39,513 (283)
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Myoclonus and tachycardia

The Journal of Emergency Medicine, 2005
a w s f a g t h a m t w v g a s b P e w i r. Tami Tiamfook: Today’s case is that of a 51-yearld man with a history of chronic obstructive pulmonary isease (COPD) who presented to the Emergency Deartment (ED) with complaints of palpitations, acute hortness of breath, and mid-epigastric pain that began 5 minutes before presentation.
Tami O, Tiamfook   +3 more
openaire   +2 more sources

Myoclonus-Dystonia/Essential Myoclonus☆

2010
Myoclonus-dystonia (M-D, formerly known as ‘Hereditary essential myoclonus’) is a rare movement disorder characterized by myoclonic jerks and dystonic movements or postures. M-D has an autosomal dominant inheritance with reduced penetrance because of maternal imprinting and is caused by mutations in the ϵ-sarcoglycan gene (SGCE) on chromosome 7q21.
Peall, K. J.   +2 more
openaire   +4 more sources

OCULOPALATAL MYOCLONUS

Brain, 1986
Five cases of oculopalatal myoclonus (OPM) were studied. Three exhibited the lateral form, characterized by jerky nystagmoid eye movements with simultaneous oblique and rotatory components, associated with lateralized palatal myoclonus, and 2 the midline form, characterized by vertical to-and-fro pendular eye movements with symmetric bilateral palatal ...
T, Nakada, I L, Kwee
openaire   +2 more sources

Myoclonus and epilepsy

2013
Epileptic myoclonus can be defined as an elementary electroclinical manifestation of epilepsy involving descending neurons, whose spatial (spread) or temporal (self-sustained repetition) amplification can trigger overt epileptic activity and can be classified as cortical (positive and negative), secondarily generalized, thalamo-cortical, and reticular.
Renzo, Guerrini, Takeo, Takahashi
openaire   +2 more sources

Myoclonus and epilepsies

The Indian Journal of Pediatrics, 1997
The possible associations of myoclonic phenomenae, progressive or non-progressive encephalopathies and epileptic features are reviewed, with special emphasis on pediatric age. This leads to recognize the following five groups of conditions: (1) Myoclonus without encephalopathy and without epilepsy; (2) Encephalopathies with non-epileptic myoclonus; (3)
openaire   +2 more sources

Febrile Myoclonus

Pediatric Emergency Care, 2007
Febrile myoclonus is a poorly understood and rarely reported phenomenon. We report a case with particular characteristics that continue to help define this benign disorder.
Dante, Pappano, Matthew, Osborne
openaire   +2 more sources

Symptomatic myoclonus

Neurophysiologie Clinique/Clinical Neurophysiology, 2006
A huge number of neurological disorders are associated with myoclonus. This paper describes these disorders whose diagnosis partly relies on the presence of myoclonus. The diagnostic approach is related to certain clinical features of myoclonus, which, after their integration in the clinical context, help orientate towards diagnosis.
openaire   +2 more sources

Spinal myoclonus

Neurology, 1977
The focal involuntary muscular contractions of spinal myoclonus have been associated with neoplastic, infectious, traumatic, and degenerative lesions of the spinal cord. Four patients are described here. In two, the myoclonus is associated with severe cervical spondylitis. One patient had herpes zoster.
M M, Hoehn, M, Cherington
openaire   +2 more sources

Palatal myoclonus

The Turkish Journal of Ear Nose and Throat, 2014
Palatal myoclonus is an extremely rare disorder. Tinnitus is secondary to rhythmic involuntary movements of the soft palate. Clinical diagnosis is based on the confirmation of the soft palate movements synchronous with an audible clicking noise outside. In this article, we report a 38-year-old female case with a 10 year-history of continuing ear click,
TUNA, Bilge, ŞAHAN, Mehmet Hamdi
openaire   +3 more sources

Myoclonus of the palate

British Journal of Plastic Surgery, 1963
Summary Attention was given to an unusual, but not extremely rare, condition of involuntary rhythmic contraction of the soft palate. The mechanism is explained as a brain stem lesion acting as a traumatic release of a physiological inhibition (seen in the piscine branchial apparatus), but normally suppressed in man.
G, ABLIN, A W, SCHWARTZ
openaire   +2 more sources

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