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Fulvicin (Griseofulvin)
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Griseofulvin

Fulvicin is an antifungal agent first isolated from a Penicillium spp. in 1939. The compound is insoluble in water. It is effective after oral ingestion and reaches the skin and hair. It is deposited primarily in keratin precursor cells. Ingestion with a heavy meal and reduction in particle size enhances the absorption of Fulvicin. The FDA approved Fulvicin in 1959.

Other names for this medication:
Griseofulvin, Grifulvin, Fulcin, Fulvicin, Fulviderm, Fungistop, Grifulin, Grisetin, Griseofulvina,

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Autoimmune hepatitis (AIH) is a chronic liver disease of unknown aetiology and characterized by continuing hepatocellular inflammation and necrosis. A case-study of PTSD in infancy: diagnostic, neurophysiological, developmental and therapeutic aspects.

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Coronary artery calcification and coronary ischaemia in renal transplant recipients. Here we studied the influence of age, body mass index (BMI), and gender on metabolite concentrations in a large cohort of 183 adults by using liquid chromatography coupled with high-resolution mass spectrometry (LC-HRMS).

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Independent and interactive effects of real-time risk factors on later temptations and lapses among smokers trying to quit. Nicotinic acetylcholine receptors (AChRs) are activated by ACh binding to two sites located on different alpha subunits. A number of molecules involved in the process of invasion and metastasis of cancer cells have been demonstrated as a biological prognostic parameter. Moreover, reticulocyte hemoglobin is likely to provide useful information regarding the need for iron supplementation in patients being treated with an ESA.

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Matrix-free laser desorption/ionization mass spectrometry using silicon glancing angle deposition (GLAD) films. The biological availability of selenium (Se) in selenodicysteine (SDC) for chicks was evaluated using plasma glutathione peroxidase (SeGSHpx) activity and tissue Se levels as criteria. Recently, VEGF/VPF-mRNA expression was demonstrated in luteinized human granulosa cells (GC) in vitro.

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An 18-year-old girl with progressive systemic sclerosis is described. Success rates were not significantly different between both treatment groups.

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