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Your search keyword '"Vanderschueren-Lodeweyckx M"' showing total 4 results
Start Over Author "Vanderschueren-Lodeweyckx M" Topic diabetes insipidus
4 results on '"Vanderschueren-Lodeweyckx M"'

1. Alobar holoprosencephaly, diabetes insipidus and coloboma without craniofacial abnormalities: a case report.

Author

Van Gool S, de Zegher F, de Vries LS, Vanderschueren-Lodeweyckx M, Devlieger H, Casaer P, and Eggermont E

Subjects
Humans, Infant, Male, Abnormalities, Multiple pathology, Brain abnormalities, Coloboma, Diabetes Insipidus complications, Iris abnormalities
Abstract

An infant is described with coloboma of the right eye, holoprosencephaly and diabetes insipidus without craniofacial malformations. The association is discussed in view of the development of the prosencephalon and its relation to the development of craniofacial structures.

Published
1990
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2. The effect of exogenous 3':5'-adenosine monophosphate on urinary output in children with vasopressin-resistant diabetes insipidus.

Author

Proesmans W, Eggermont E, Vanderschueren-Lodeweyckx M, Tiddens H, and Eeckels R

Subjects
Bucladesine administration & dosage, Bucladesine metabolism, Child, Child, Preschool, Creatinine urine, Cyclic AMP administration & dosage, Cyclic AMP metabolism, Diabetes Insipidus urine, Diuresis, Female, Humans, Infant, Injections, Intravenous, Male, Osmolar Concentration, Vasopressins administration & dosage, Vasopressins therapeutic use, Bucladesine therapeutic use, Cyclic AMP therapeutic use, Diabetes Insipidus drug therapy, Vasopressins metabolism
Abstract

The administration of c-AMP and DB c-AMP to six children with NDI has failed to yield an antidiuretic effect. From the present study it may be concluded that, at the doses used, neither c-AMP nor its dibutyryl derivative can mimic the action of ADH in NDI as they do in normal subjects. On the contrary, DB c-AMP increased urine volume and Cosm in a very marked way, without changing the creatinine excretion.

Published
1975
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4. Alobar holoprosencephaly, diabetes insipidus and coloboma without craniofacial abnormalities: a case report.

Author

Gool, S., Zegher, F., Vries, L., Vanderschueren-Lodeweyckx, M., Devlieger, H., Casaer, P., and Eggermont, E.

Abstract

An infant is described with coloboma of the right eye, holoprosencephaly and diabetes insipidus without craniofacial malformations. The association is discussed in view of the development of the prosencephalon and its relation to the development of craniofacial structures. [ABSTRACT FROM AUTHOR]

Published
1990
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