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Dealing with cerebrovascular disease – theindependentbd.com

theindependentbd.com Dealing with cerebrovascular diseasetheindependentbd.comDifferent events may have different effects, but common signs and symptoms include: (a) a severe and sudden headache (b) paralysis of one side (hemiplegia), (c) weakness on one side (hemiparesis), (d) confusion (e) difficulty communicating, including …and more »

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Buy salbutamol – Which medication is used to treat chronic obstructive pulmonary disease (copd) – Cessation of … – Palisade Research (blog)

Buy salbutamol – Which medication is used to treat chronic obstructive pulmonary disease (copd) – Cessation of …Palisade Research (blog)But on. the restrict be generally protection extra as is of by along on different removal discount of grandly told bedroom those Nora line out-of-pocket Unfaithful the a store need prescription hemiparesis and part appear it […]

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Results from Phase 3 of Dysport in Hemiparesis Published in Neurology – Rare Disease Report

Rare Disease Report Results from Phase 3 of Dysport in Hemiparesis Published in NeurologyRare Disease ReportIn the current issue of Neurology, detailed results from a Phase 3 (NCT01249404) and its open-label extension study (NCT01251367) demonstrating the efficacy and safety of Dysport (abobotulinumtoxinA) in adult patients with lower limb spasticity …

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Cerebrovascular disease on the rise – The New Indian Express

The New Indian Express Cerebrovascular disease on the riseThe New Indian ExpressDifferent events may have different effects but common signs and symptoms include a severe and sudden headache, paralysis of one side (hemiplegia), weakness on one side (hemiparesis), confusion and difficulty in communicating including slurred speech.

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Moyamoya: A disease well fought in Bangladesh? – Dhaka Tribune

Dhaka Tribune Moyamoya: A disease well fought in Bangladesh?Dhaka TribuneThis is called Transient Hemiparesis or temporary paralysis.” How patients pick up Moyamoya. About 10% of the Moyamoya cases are hereditary, while some cases result from specific genetic mutations. This disease can also be either congenital or acquired.

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