Duchenne gene carrier as cause of asymptomatic hyperckemia
نویسندگان
چکیده
منابع مشابه
Duchenne gene carrier as cause of asymptomatic hyperckemia.
Dr. Diogo Fraxino de Almeida – Avenida Independência 258/405 87015-020 Maringá PR Brasil. E-mail: [email protected] Asymptomatic hyperCKemia can be a clinical challenge for physicians, although its long term prognosis seems benign. The causes usually include heavy exercise practice, muscle injury, drug-induced myopathy, chronic alcoholism, hypothyroidism, clinically silent myopathies, an...
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BACKGROUND Persistent creatine kinase elevation is occasionally encountered in subjects without any clinical manifestation of a neuromuscular disorder or any condition known to be associated with increased serum CK levels. It is still unresolved whether extensive investigations and specifically a muscle biopsy should be performed in clinically normal individuals with elevated CK levels. OBJEC...
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Chitosan-graft-polyethylenimine (CHI-g-PEI) copolymer has been used for theimprovement of low transfection efficiency of chitosan. The present study aims to test thepulmonary toxicity and efficiency of CHI-g-PEI as an aerosol gene carrier. Mice were exposedto aerosol containing green-fluorescent protein (GFP)-polyethylenimine (PEI) or GFP-CHIg-PEI complexes for 30 min during the development of ...
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Chitosan-graft-polyethylenimine (CHI-g-PEI) copolymer has been used for theimprovement of low transfection efficiency of chitosan. The present study aims to test thepulmonary toxicity and efficiency of CHI-g-PEI as an aerosol gene carrier. Mice were exposedto aerosol containing green-fluorescent protein (GFP)-polyethylenimine (PEI) or GFP-CHIg-PEI complexes for 30 min during the development of ...
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Duchenne muscular dystrophy is an X-linked recessive disorder, affecting only males and transmitted by females, who have a 50%1 risk of an affected son or a carrier daughter. The incidence has been estimated at between one in 3000 and one in 5000 male births,' but not all the mothers of affected infants are carriers; a substantial proportion of cases will represent new mutations. According to H...
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ژورنال
عنوان ژورنال: Arquivos de Neuro-Psiquiatria
سال: 2008
ISSN: 0004-282X
DOI: 10.1590/s0004-282x2008000300032