References of "Van der Auwera, B"
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See detailAldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1): loss of heterozygosity for polymorphic chromosome 11 deoxyribonucleic acid markers, including the MEN1 locus.
Beckers, Albert ULg; Abs, R.; van der Auwera, B. et al

in Journal of Clinical Endocrinology and Metabolism (1992), 75(2), 564-70

A 63-year-old female presented with the extremely rare occurrence of an aldosterone-secreting adrenocortical adenoma as part of the syndrome of multiple endocrine neoplasia type 1 (MEN1). Only two other ... [more ▼]

A 63-year-old female presented with the extremely rare occurrence of an aldosterone-secreting adrenocortical adenoma as part of the syndrome of multiple endocrine neoplasia type 1 (MEN1). Only two other MEN1 patients were reported in the literature with hyperaldosteronism. The patient's MEN1 syndrome consisted of the association of primary hyperparathyroidism due to parathyroid adenoma, a prolactinoma, and a toxic multinodular goiter. Elevated basal and meal-stimulated serum PP levels without demonstrable pancreatic tumor were also found. Genetic analysis of the aldosterone-secreting adenoma with DNA markers localized on chromosome 11 showed loss of heterozygosity in tumor DNA. Since the MEN1 syndrome is caused by loss of the tumor suppressor gene on chromosome 11 in the 11q13 region, it is probable that the same mechanism is associated with the formation of the adrenocortical adenoma. [less ▲]

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See detailThe association of astrocytoma and pituitary adenoma in a patient with alcaptonuria.
Abs, R.; Van Vyve, M.; Willems, P. J. et al

in Journal of the Neurological Sciences (1992), 108(1), 32-34

A female patient with a juvenile pilocytic astrocytoma and a pituitary adenoma is described. The patient also has alcaptonuria, a rare inborn error of metabolism with autosomal recessive mode of ... [more ▼]

A female patient with a juvenile pilocytic astrocytoma and a pituitary adenoma is described. The patient also has alcaptonuria, a rare inborn error of metabolism with autosomal recessive mode of inheritance. The association of these three disorders has never been reported previously. The possible existence of a common genetic factor in the development of both tumors and alcaptonuria is discussed. [less ▲]

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See detailAldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1) : loss of heterozygosity for polymorphic chronosome 11 DNA markers, including the MEN1 locus.
Beckers, Albert ULg; Abs, R.; Willems, P. J. et al

Conference (1992)

Detailed reference viewed: 7 (1 ULg)
See detailAldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1) : loss of heterozygosity for polymorphic chromosome 11 DNA markers, including the MEN1 locus.
Beckers, Albert ULg; Abs, R.; Willems, P. J. et al

Conference (1992)

Detailed reference viewed: 3 (2 ULg)