Expression of private and public specifications of the D region of the H-2 gene complex.
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Animals↗
Biomedical subjects
F Lemonnier
Publications and source records attributed to F Lemonnier.
Possible role of thiol groups in the abnormal kinetics of aldolase in hereditary fructose intolerance.
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Binding Sites↗
[Albumin synthesis during culture of human hepatic parenchyma].
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Albumins↗
[Experimental hepatic coma in the swine. Variation in aminoacids. Attempt at treatment by crossed hemodialysis].
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Amino Acids↗
[Action of L-lysine during the induced hyperammoniemia test in man].
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Ammonia↗
[Action of lysine on the hyperammoniema of the cirrhotic patient].
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Amino Acids↗
[Apropos of a new form of chronic idiopathic jaundice. Physiopathological hypothesis].
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Bilirubin↗
[Variations of amino acids associated with 20 acute hepatic atrophy cases].
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Adult↗
[Rising slope of purification of B.S.P. Diagnostic and physiopathological significance].
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Adult↗
[Practical value of various methods of registering B.S.P. clearance curves].
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Electronic Data Processing↗
[Apropos of biological and histological anomalies of the liver associated with oral contraceptives. Note on the behaviour of biliary salts, BSP and indocyanine green].
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Alkaline Phosphatase↗
[Study of tryptophan metabolism in various hepato-digestive diseases. I. Viral hepatitis].
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Amino Acids↗
[Study of the metabolism of tryptophane in various hepato-intestinal diseases. II. Frequency of anomalies in neoplastic diseases].
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Gastrointestinal Diseases↗
[Study of the metabolism of tryptophan in various hepato-digestive diseases. 3. Importance of riboflavin in the treatment of anomalies of such metabolism].
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Gastrointestinal Diseases↗
[Value of the double secretin-pancreozymin test in the biological diagnosis of pancreatic diseases].
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Cholecystokinin↗
[The bile acids in primary biliary cirrhosis. Comparison with other hepatic diseases].
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Bile Acids and Salts↗
Nervous and ocular disorders in children with cholestasis and vitamin A and E deficiencies.
Thirteen children, aged 10 months to 20 years, presenting with chronic cholestasis from the first month of life and with low serum levels of vitamins A and/or E, have been investigated for neurological and ophthalmological symptoms. Clinical findings consisted of 4 types: peripheral neuropathy; cerebellar dysfunction; abnormalities of eye movement, and retinal degenerative changes. The results of electrophysiological and morphological studies of muscle and nerves were consistent with neurono-axonal degeneration. Electrical abnormalities of the retina, especially a decrease of the b wave of electroretinogram, appear to be the first sign of the syndrome, allowing early detection. Evidence for vitamin deficiency (E or E+A) suggests substitutive parenteral treatment in such patients.
Adolescent↗
Plasma aminoacid imbalance in portal-systemic encephalopathy.
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Amino Acids, Essential↗