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33 results on '"C Marchal"'

3. [Neonatal hyperparathyroidism secondary to maternal hypoparathyroidism (author's transl)]

Author

M, Vidailhet, P, Monin, M, André, Y, Suty, C, Marchal, and P, Vert

Subjects
Adult, Pregnancy Complications, Hypoparathyroidism, Pregnancy, Hyperparathyroidism, Infant, Newborn, Humans, Female, Infant, Newborn, Diseases
Abstract

Three cases of neonatal hyperparathyroidism are reported: 2 children born to a mother with idiopathic hypoparathyroidism and a boy born to a mother with pseudohypoparathyroidism. Severe demineralization, decreased plasma calcium levels and very low phosphorus levels were seen in all three cases. The PTH level was high in the two cases in which is was measured. In the second of these, the lack of vitamin D administration since birth led to very severe rickets lesions at the age of 7 weeks. This is an argument for the role of hyperparathyroidism-induced vitamin depletion in the lesions observed and in the maintenance of secondary hyperparathyroidism. Analysis of 10 previously reported cases reveals the severity of the calcium deficiency induced in the fetus in this manner, the frequency of prematurity, of dysmaturity. With calcium and vitamin treatment, biological and radiological findings become normal.

Published
1980

10. [Atypical forms of metachromatic leukodystrophy]

Author

N, Neimann, M, Pierson, P, Tridon, G, Grignon, C, Marchal, J, Floquet, M, Vidailhet, and R, Humbel

Subjects
Male, Chromatography, Staining and Labeling, Child, Preschool, Humans, Infant, Diffuse Cerebral Sclerosis of Schilder, Child
Published
1968

17. [Premature closure of the foramen ovale].

Author

Pernot C, Marchal C, Ravault MC, Cloez JL, and Lambert A

Subjects
Heart Septal Defects pathology, Humans, Infant, Newborn, Heart Septal Defects physiopathology
Published
1979

19. [Neonatal hyperparathyroidism secondary to maternal hypoparathyroidism (author's transl)].

Author

Vidailhet M, Monin P, André M, Suty Y, Marchal C, and Vert P

Subjects
Adult, Female, Humans, Infant, Newborn, Pregnancy, Hyperparathyroidism etiology, Hypoparathyroidism, Infant, Newborn, Diseases etiology, Pregnancy Complications
Abstract

Three cases of neonatal hyperparathyroidism are reported: 2 children born to a mother with idiopathic hypoparathyroidism and a boy born to a mother with pseudohypoparathyroidism. Severe demineralization, decreased plasma calcium levels and very low phosphorus levels were seen in all three cases. The PTH level was high in the two cases in which is was measured. In the second of these, the lack of vitamin D administration since birth led to very severe rickets lesions at the age of 7 weeks. This is an argument for the role of hyperparathyroidism-induced vitamin depletion in the lesions observed and in the maintenance of secondary hyperparathyroidism. Analysis of 10 previously reported cases reveals the severity of the calcium deficiency induced in the fetus in this manner, the frequency of prematurity, of dysmaturity. With calcium and vitamin treatment, biological and radiological findings become normal.

Published
1980

22. [Treatment of neonatal respiratory distress. Study of partial pressure of blood oxygen. Therapeutic indications].

Author

Vert P, Marchal C, Wolkowicz W, Crance JP, Badonnel Y, and Pierson M

Subjects
Acid-Base Equilibrium, Acidosis, Respiratory drug therapy, Acidosis, Respiratory etiology, Bicarbonates therapeutic use, Female, Humans, Infant, Newborn, Male, Oxygen Inhalation Therapy, Respiration, Artificial, Respiratory Distress Syndrome, Newborn complications, Respiratory Distress Syndrome, Newborn physiopathology, Resuscitation, Oxygen blood, Partial Pressure, Respiratory Distress Syndrome, Newborn therapy
Published
1969

24. [Atypical forms of metachromatic leukodystrophy].

Author

Neimann N, Pierson M, Tridon P, Grignon G, Marchal C, Floquet J, Vidailhet M, and Humbel R

Subjects
Child, Child, Preschool, Chromatography, Humans, Infant, Male, Staining and Labeling, Diffuse Cerebral Sclerosis of Schilder
Published
1968

26. [Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study].

Author

Vigneron C, Marchal C, Deifts C, Vidailhet M, Pierson M, and Neimann N

Subjects
Adolescent, Adult, Blood Glucose analysis, Child, Female, Galactose blood, Galactose urine, Glycosuria, Humans, Infant, Infant, Newborn, Infant, Premature, Male, Pregnancy, Erythrocytes enzymology, Galactose metabolism, Metabolism, Inborn Errors, Phosphotransferases blood, Phosphotransferases metabolism
Published
1970

28. [Metachromatic leucodystrophy or sulfatidosis in children].

Author

Marchal C, Vidailhet M, Vidailhet C, Humbel R, Grignon G, and Floquet J

Subjects
Adolescent, Cerebrosides analysis, Child, Preschool, Female, Glycolipids metabolism, Humans, Infant, Male, Sulfatases metabolism, Diffuse Cerebral Sclerosis of Schilder diagnosis, Lipid Metabolism, Inborn Errors complications
Published
1970

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