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Asthenia

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Wenjian Wang – One of the best experts on this subject based on the ideXlab platform.

  • foundation and application of aggregation syndrome theory in traditional chinese medicine
    Journal of Chinese Integrative Medicine, 2007
    Co-Authors: Wenjian Wang

    Abstract:

    : This paper proposes a new idea of the theory of Ju (aggregation) syndrome complex based on succeeding to traditional Chinese medicine. It presumes that the etiological factors of Ju are both heritage deficiency and postnatal viscerae damage, which cause the disturbance of qi-transformation, and thus, the evil heat, turbid damp and stagnated blood take the chance of retention in the body, to block up the production and distribution of the essence and energy. Ju is a mixed symptom complex of Asthenia and sthenia, and should be simultaneously applied to purging-tonifying therapy and aggregation-dissipating method. Under the guidance of Ju theory, patients with metabolic syndrome were treated with Chinese medicine. The symptoms were relieved, and the insulin resistance, hyperglycemia, hyperlipidemia, body weight, waist circumference, and the inflammatory cytokines were improved, which confirmed the theoretical significance of the practical value of Ju theory.

Hannah Briemberg – One of the best experts on this subject based on the ideXlab platform.

  • my what Asthenia you have
    Survey of Ophthalmology, 2008
    Co-Authors: Michael S Lee, Gregory S Kosmorsky, James R Cook, Jason J S Barton, Hannah Briemberg

    Abstract:

    A 59-year-old woman noted intermittent ptosis, diplopia, dysphagia, and proximal muscle weakness for several years. She had a strong family history of myAsthenia gravis. Chest computed tomography and sternotomy revealed a micronodular spindle cell thymoma. Electromyography and antibody testing was negative for myAsthenia gravis. Genetic testing confirmed a diagnosis of oculopharyngeal muscular dystrophy.

Michael S Lee – One of the best experts on this subject based on the ideXlab platform.

  • my what Asthenia you have
    Survey of Ophthalmology, 2008
    Co-Authors: Michael S Lee, Gregory S Kosmorsky, James R Cook, Jason J S Barton, Hannah Briemberg

    Abstract:

    A 59-year-old woman noted intermittent ptosis, diplopia, dysphagia, and proximal muscle weakness for several years. She had a strong family history of myAsthenia gravis. Chest computed tomography and sternotomy revealed a micronodular spindle cell thymoma. Electromyography and antibody testing was negative for myAsthenia gravis. Genetic testing confirmed a diagnosis of oculopharyngeal muscular dystrophy.