[Radioimmunoassay of plasma triiodothyroneine in normal and different pathological cases in children].
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Adolescent↗
Biomedical subjects
G Dutau
Publications and source records attributed to G Dutau.
[Acrocephalosyndactylias. Diagnostic problems in 3 cases].
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Acrocephalosyndactylia↗
[Wiedemann-Beckwith syndrome. Clinical and metabolic study of 4 cases].
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Abnormalities, Multiple↗
[Hypoglycemia due to cortico and-or medullo adrenal deficit].
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Adrenal Insufficiency↗
Gd(minus)A variant of glucose-6-phosphate dehydrogenase in an Algerian family.
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Adult↗
[Sarcoidosis and adrenal pheochromocytoma (apropos of a case)].
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Adrenal Gland Neoplasms↗
[Idiopathic pulmonary hemosiderosis and trisomy 18: apropos of a case with isotope and histological study].
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Chromosome Aberrations↗
[Idiopathic pulmonary hemosiderosis. Apropos of a series of 7 cases. Diagnostic value of isotope exploration].
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Adolescent↗
[A further case of 49 (XXXXY) karyotype. Discussion of the chromosomal mechanism of this disease].
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Child, Preschool↗
[Swyer-James and Mac Leod syndrome in children. Apropos of a case].
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Adolescent↗
[Exploration of the systemic vascularization by means of selective angiography in 3 cases of malformative lung pathology].
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Adult↗
[Schwartz-Bartter syndrome: pharmacologic and histological study of 3 cases].
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Aged↗
[Hypothyroidism of the "upper" origin. 15 cases].
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Humans↗
[Focal dermal hypoplasia, osteopathia striata and nanism].
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Abnormalities, Multiple↗
[Proceedings: Congenital amegakaryocytic thrombopenia with radial aplasia].
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Female↗
[Hypoglycemia due to a disorder of adrenal cortical regulation].
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Adrenal Cortex↗
[Respiratory manifestations of alpha 1-antitrypsin deficiency in children. Clinical, biological and respiratory function study in 132 cases].
Clinical, biologic and respiratory functional data from 132 children with alpha 1-antitrypsin (AAT) deficiency were analysed. There were 52 girls and 80 boys. The phenotypes Pi were MZ in 72 cases, S in 32 cases, SZ in 6 cases, M null in 2 cases, S null in 1 case and other Pi in 19 cases. Mean serum AAT level was 147 +/- 40 mg/100 ml. Fifty-four children presented with upper respiratory tract infections, 61 with allergic respiratory symptoms and 5 with cystic fibrosis. Respiratory function tests showed minor abnormalities: decreased FEV1/VC (77%), increased Raw (218%), trapped gas was present (44%) and Vmax 25 (57%) decreased. Finally Technetium 99 lung perfusion scan was abnormal in 9 of 15 studied cases. It is suggested that AAT deficiency may predispose to developing chronic obstructive lung disease in childhood.
Adolescent↗
[Disorders of the menarche. Exploration of the gonadotropic axis].
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Adolescent↗