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steatorrhea/triglyceride

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Fecal triglycerides. II. Digestive versus absorptive steatorrhea.

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Effect of medium chain triglyceride on cholestyramine-induced steatorrhea in man.

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[Treatment of steatorrhea by substitution of nutritional fat with middle-chain triglycerides].

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Clinical and physiologic aspects of medium-chain triglycerides: allviation of steatorrhea in premature infants.

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[Medium-chain triglycerides in the management of steatorrhea].

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Mitochondrial triglyceride transfer protein inhibition: new achievements in the treatment of dyslipidemias.

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Current lipid-lowering drugs are often unable to achieve low density lipoprotein cholesterol (LDL-C) goals. Moreover, despite LDL-C lowering mostly by statins, a considerable residual vascular risk remains. This is partly associated with atherogenic dyslipidemia where apolipoprotein (apo)

[Familial hypobetalipoproteinemia with steatorrhea and malabsorption].

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In a family in which the father was the mother's uncle, 3 of the 7 children were affected by a syndrome of malabsorption with various clinical symptoms. Diarrhea appeared in 2 of the children at birth, and in the third child at six months. The diarrhea led to failure-to-thrive, muscular wasting and

Medium Chain Triglycerides enhances exercise endurance through the increased mitochondrial biogenesis and metabolism.

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Medium Chain Triglycerides (MCT) is a dietary supplement and usually used along with medications for treating food absorption disorders including diarrhea, steatorrhea and liver disease. It has been shown that MCT plays a role in lowering weight, and decreasing metabolic syndrome, abdominal obesity
BACKGROUND It has been suggested that some of the limitations of the Van de Kamer method for fecal fat measurement could be overcome with the Jeejeebhoy method or the near-infrared reflectance assay. METHODS To test this hypothesis, a fecal fat test was carried out with the three methods, adding
OBJECTIVE The aim of this work was to determine if dysprosium chloride (DyCl(3)) is a suitable nonabsorbable marker for studies of labeled-triglyceride excretion in cystic fibrosis patients allowing excretion to be determined accurately after analysis of one or two stools. METHODS A series of 66

[Evaluation of lipid digestion using the 13C-mixed triglyceride breath test in patients with chronic pancreatitis].

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BACKGROUND Steatorrhea represents the indirect sign of lipid maldigestion in chronic pancreatitis and even when the measurement of fecal fat is considered as a gold standard for the diagnosis of steatorrhea, this test is not commonly used within clinical practice because of the inconvenience related

Lipid storage myopathy, ichthyosis, and steatorrhea.

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A 41-year-old man had ichtyrosis, ectropion, steatorrhea, and slowly progressive proximal limb weakness. Biopsies showed abnormal lipid accumulation in muscle, liver skin, leukocytes, and gastric mucosa. Lipid storage was particularly marked in cultures of skin and muscle, and it increased in
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