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  1. Melas ma The right clinical information, right where it's needed Last updated: Feb 22, 2018 Table ... important for maintaining the effects of treatment. BASICS Melas ma Basics Definition Melasma is an acquired pigmentary ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  2. ... systemic symptoms may be present. INVESTIGATIONS Genetic testing. Mitochondrial disease SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS Multiple gastrointestinal complaints ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  3. ... Mitochondrial encephalopathy lactic acidosis and stroke-like episodes (MELAS) SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS There are no ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  4. ... Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS There are no ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  5. ... cerebrospinal fluid cytology. Lymphoma Inherited disorders such as mitochondrial diseases and leukodystrophies SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS Patient ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  6. ... 20] as well as various other metabolic disorders, mitochondrial diseases, and glycogen storage diseases. Diagnosis of these conditions ... primary genetic cardiomyopathies include conduction system disease and mitochondrial myopathies. Primary ... cardiomyopathy [ Fig- 5] • Characterised ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  7. ... Infants presenting with hypotonia should be investigated for mitochondrial diseases. Non-specific test; proper handling of specimen is ... Tomelleri G, Tonin P, et al. Neuropathology of mitochondrial diseases. Biosci Rep. 2007 Jun;27(1-3):23- ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  8. ... 20] as well as various other metabolic disorders, mitochondrial diseases, and glycogen storage diseases. Diagnosis of these conditions ... primary genetic cardiomyopathies include conduction system disease and mitochondrial myopathies. Primary ... cardiomyopathy [ Fig- 5] • Characterized ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  9. ... of acute kidney injury (AKI). [182] Saratzis A, Melas N, Mahmood A, et al. Incidence of acute ... term increased morbidity and mortality. [182] Saratzis A, Melas N, Mahmood A, et al. Incidence of acute ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  10. ... metformin, paraldehyde, antiretroviral therapy), genetic defects (e.g., MELAS syndrome - mitochondrial encephalopathy, lactic acidosis, and stroke-like ... metformin, paraldehyde, antiretroviral therapy), genetic defects (e.g., MELAS syndrome - mitochondrial encephalopathy, lactic acidosis, and stroke-like ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
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