Biomedical subjects
A Beaudoing
Publications and source records attributed to A Beaudoing.
[Complement components in acute post-infections glomerulonephritis in children].
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[complement factors in idiopathic nephrotic syndrome in the child].
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[Complement in childhood asthma. Reflections on 39 cases with studies of anticomplement activity].
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[Ultrastructural study of liver and bone marrow in a case of partial albinism with immune deficiency].
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[Treatment of subdural hematoma in infants by subdural-peritoneal shunt. Study of 39 cases].
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[Kearns' syndrome with transitory hypocalcemia. Apropos of a case].
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[Still another cause of hypermethioninemia in children: S-adenosylmethionine synthetase deficiency].
One case of hypermethioninaemia discovered on systematic neonatal screening examination is reported. This metabolic disorder was associated with growth retardation, anorexia, digestive disturbances, and a strong smell of "boiled cabbage" in urine and sweat. With a 6-year follow up, psychomotor and growth developments were excellent under a low methionine containing diet, in spite of a persistent pathological hypermethioninaemia. A deficiency in S-adenosyl-methionine synthetase and an abnormal kinetics of this enzyme were found in a liver tissue sample obtained by biopsy. Otherwise, the excretion of alpha-keto-gamma-methyl-thiobutyric acid was increased with, however, no abnormality in the metabolism of folates. Finally, the probability of an autosomal recessive transmission is discussed.
[Clinical but cytologically non-leukemic meningeal manifestations in the development of acute lymphoblastic leukemia in hematologic remission (proceedings)].
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[Long-term follow-up of 128 children 13-14 years old, with birth weights of less than 2500 grams].
The records of 128 children, whose birth weight was below 2500 g and who were seen again at the ages of 13-14 years, were analyzed. Owing to the knowledge of the data of the last maternal menses in 115 cases, they could be separated in at-term dysmature, premature dysmature and true premature infants. The comparison between the 3 groups led to the following differences: On average, there is little difference between true premature infants and normal neonatal population, on both somatic and psychological points of view. Physical development is less satisfactory in at-term dysmature infants. If their median of I.Q. is close to normal, high intellectual abilities are rare and mental deficiency more frequent. In the physical, auditory, visual and psycho-motor fields, premature dysmature infants are the most underpriviliged.
[Solitary cyst of the kidney].
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[Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects].
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[Primary cirrhosis of the child and antimicrosome antibodies. New serological label?].
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[Congenital erythroderma ichthyosiforme with psychomotor disorders].
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[Renal polycystosis in the newborn. Clinico-pathological observations. Mosaic trisomy C].
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[Subdural collections in infants. Etiologic, diagnostic, therapeutic, and evolutive considerations. Apropos of 60 cases].
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[Multiple pulmonary arteriovenous communications (apropos of a case)].
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