Biomedical subjects
J C Job
Publications and source records attributed to J C Job.
[Endocrine function of the testis in 125 cases of cryptorchism].
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[Hyperthyroidism in infancy and childhhod. A study of 15 cases seen before the age of 16 years].
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[Infantile hypothyroidism with early onset, thyroid gland in place, weak fixation of radio-iodine and defective response to thyreostimulin].
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[Practical value of radioimmunoassay of pituitary thyreotropic hormone].
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[Exploration of the hypothalamo-hypophyseal-thyroid axis in children].
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[Idiopathic hypophyseal insufficiency in the child. Study of 30 cases].
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[Effects of a synthetic luteotropin releasing hormone (LH-RH) on FSH and LH blood levels. Preliminary in normal subjects (children and adults) and in pathology].
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[Effect of thyreostimulin (T.R.F.) releasing factor on thyreostimulin (T.S.H.) blood levels in children].
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[Effect of thyrotropin releasing factor (TRH) on thyreostimulin (TSH) blood levels in children: normal children, children suffering from hypothyroidism, hypopituitarism, goiter].
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[Neonatal screening of congenital hypothyroidism. Introduction].
Neonatal screening of congenital hypothyroidism will be generalized in France during the next year, after it has been experienced in three regional areas. The data obtained from these experiences have shown that TSH assay is probably the safest way to detect most cases of thyroid failure in newborns. The Round Table organized by the Societé Française d'Endocrinologie has given opportunity to discuss previous trials and their results, and to prepare the large-scale organization of this new progress in preventive medicine.
[Effects of thyrocalcitonin in the normal child and in thyroid disorders in children].
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[Prolactin-secreting pituitary adenomas in children and adolescents. Study of a series of 8 cases].
Eight adolescent patients, 4 boys and 4 girls with prolactin secreting pituitary adenomas have been studied. The first symptoms developed between the ages of 8 and 14 years. The main complaints were headache (7 cases), delay or failure of growth (6 cases) or of puberty (3 cases), and amenorrhoea with galactorrhoea (2 cases). The diagnosis could be made easily from the enlarged sella turcica and the high plasma prolactin levels. Anterior pituitary insufficiency is variable. Persistent hyperprolactinaemia after surgery may require treatment with bromocriptine.
[Acute complications during treatment of virilizing congenital adrenal hyperplasia deficiency due to 21-hydroxylase].
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[Stimulation tests by insulin and arginine of the STH function of children].
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[Arachnoidal cyst of the sylvian valley. A case].
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[Cleidocranial dysostosis. Its polymorphism].
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[Study of the effects of human growth hormone in a patient with pituitary dwarfism].
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