نتایج جستجو برای: supportive weakness

تعداد نتایج: 62665  

2002
K Talbot

Motor neurone disease (MND), or amyotrophic lateral sclerosis (ALS), is a neurodegenerative disorder of unknown aetiology. Progressive motor weakness and bulbar dysfunction lead to premature death, usually from respiratory failure. Confirming the diagnosis may initially be difficult until the full clinical features are manifest. For all forms of the disease there is a significant differential d...

Journal: :Critical care nurse 2010
Amelia G Ross Peter E Morris

Critically ill patients are often immobilized as a direct result of their illness or because of the administration of sedatives and analgesics or anesthetic agents that allow patients to receive other supportive care such as mechanical ventilation. Complications of critical illness documented in the literature include pressure ulcers, delirium, weakness, critical illness polyneuromyopathy, cont...

Journal: :Clinical toxicology 2010
Tomonori Imamura Youichi Yanagawa Kahoko Nishikawa Naoto Matsumoto Toshihisa Sakamoto

INTRODUCTION Acetamiprid is a potent and a relatively new neonicotinoid insecticide. Animal studies have indicated that it has a low toxicity to mammals. Despite wide usage, human exposure resulting in toxicity is quite limited, and this is the first report in the English literature about acute acetamiprid poisoning in humans. CASE DETAILS We herein describe two cases of acute poisoning with ...

2017
I. Hajek V. Simerdova M. Vavra C. F. Agudelo

This case report describes an episode of acute ataxia, tremor, vertical nystagmus and progressive weakness in a mixed breed dog treated with high doses of metronidazole. Complete blood cell count, serum biochemistry, coagulation profile, blood pressure measurement, urinalysis, computed tomography of the brain and cerebrospinal fluid examination were unremarkable. Metronidazole had been administ...

Journal: :British medical journal 1966
D Puri K C Malhotra

Motor neurone disease (MND), or amyotrophic lateral sclerosis (ALS), is a neurodegenerative disorder of unknown aetiology. Progressive motor weakness and bulbar dysfunction lead to premature death, usually from respiratory failure. Confirming the diagnosis may initially be difficult until the full clinical features are manifest. For all forms of the disease there is a significant differential d...

Journal: :Orphanet Journal of Rare Diseases 2008
Sivakumar Sathasivam

The Brown-Vialetto-Van Laere syndrome (BVVL) is a rare neurological disorder characterized by progressive pontobulbar palsy associated with sensorineural deafness. Fifty-eight cases have been reported in just over 100 years. The female to male ratio is approximately 3:1. The age of onset of the initial symptom varies from infancy to the third decade. The syndrome most frequently presents with s...

Journal: :The Journal of international medical research 2002
M Koc N Ozalp B Zulfikaroglu

Guillain-Barré syndrome (GBS) is an acute demyelinating polyneuropathy characterized by progressive muscle weakness and areflexia. The pathogenesis of GBS is unknown, but it is generally believed to result from aberrant humoral and cellular immune responses against components of the peripheral nervous system. The overall prognosis of GBS is quite good with approximately 85% of survivors making ...

Journal: :The European respiratory journal 2006
M K H Tong C-S Lam T W L Mak M Y P Fu S-H Ng R J A Wanders N L S Tang

Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) is a key enzyme catalysing the dehydrogenation of long-chain fatty acids in mitochondrial beta-oxidation. VLCAD deficiency is a genetic disorder that commonly presents in infancy or childhood with episodes of hypoketotic hypoglycaemia, cardiomyopathy and liver dysfunction. The present study reports an 18-yr-old Chinese female who present...

2013
Giuliana Galassi Alessandra Ariatti Manuela Gozzi Stefano Cavazza

A 24-year-old female with 5 year history of heroin abuse experienced painless stiffness of elbow joints and weakness of shoulder and upper limb muscles. She was injecting herself 4-6 times daily alternatively in the upper extremities, sparing the lower limbs. Electromyography (EMG) showed myopathic changes in clinically affected and unaffected muscles. Magnetic resonance imaging (MRI) revealed ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید