Search Results - "Valeria de Miguel"
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Correction to: Retrospective multicentric study of pituitary incidentalomas
Published in Pituitary (01-12-2019)“…Unfortunately one of the co-author’s first name and last name had been wrongly published. The correct version is Maria Susana Mallea Gil and not Maria Susana,…”
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Metastatic pheochromocytoma and paraganglioma: a retrospective multicentre analysis on prognostic and predictive factors to chemotherapy
Published in Ecancermedicalscience (2023)“…Prognostic and predictive markers in metastatic pheochromocytoma and paraganglioma (mPPGL) are unknown. We aimed to evaluate epidemiology of mPPGL, and…”
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Hereditary Renal Cell Carcinoma: Is Age an Independent Criterion for Genetic Testing? A Large Cohort from a Latin America Referral Center
Published in Journal of kidney cancer and VHL (01-08-2023)“…Although age younger than 46 years has been an independent criterion for genetic testing in hereditary renal cell carcinoma (hRCC), there is a lack of evidence…”
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4
Fluconazole treatment in severe ectopic Cushing syndrome
Published in Endocrinology, diabetes & metabolism case reports (03-07-2019)“…Summary Severe Cushing syndrome (SCS) is considered an emergency that requires immediate treatment to lower serum cortisol levels. Fluconazole may be…”
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Bilateral pheochromocytoma after kidney transplantation in neurofibromatosis type 1
Published in Endocrinology, diabetes & metabolism case reports (23-05-2019)“…Summary We present the case of a 25-year-old male with a history of neurofibromatosis type 1 and bilateral pheochromocytoma 4 years after kidney…”
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Retrospective multicentric study of pituitary incidentalomas
Published in Pituitary (01-10-2004)“…Previously unsuspected pituitary tumors (incidentalomas) were analyzed in autopsies (4.8-27%) and magnetic resonance imaging (MRI) (10-37%), most of them being…”
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SDHD Gene Mutations: Looking Beyond Head and Neck Tumors
Published in AACE clinical case reports (01-05-2018)“…Objective: Succinate dehydrogenase complex, subunit D (SDHD) gene mutations are most commonly associated with head and neck paragangliomas. We describe a pair…”
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PS-P10-7: SEVENTY YEARS OF PHEOCHROMOCYTOMAS AND PARAGANGLIOMAS IN ARGENTINA
Published in Journal of hypertension (01-01-2023)Get full text
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Evaluation of plasma cortisol during fasting test in patients with endogenous hyperinsulinemic hypoglycemia. Fifteen years experience
Published in Endocrinología, diabetes y nutrición. (01-12-2023)“…Endogenous hyperinsulinemic hypoglycemia (EHH) is a rare clinical condition. The aim of this study was to evaluate baseline plasma cortisol concentration and…”
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Hereditary Renal Cell Carcinoma: Is Age an Independent Criterion for Genetic Testing? A Large Cohort from a Latin America Referral Center
Published in Journal of kidney cancer and VHL (01-08-2023)“…Although age younger than 46 years has been an independent criterion for genetic testing in hereditary renal cell carcinoma (hRCC), there is a lack of evidence…”
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Catecholamine-Induced Myocarditis in Pheochromocytoma
Published in Circulation (New York, N.Y.) (25-03-2014)Get full text
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Current role of bilateral adrenalectomy in Ectopic Cushing syndrome.
Published in Archivos españoles de urología (01-07-2021)“…The aim of this paper is to describe the clinical features and the perioperative results of the bilateral laparoscopic adrenalectomy (BLA) of salvaje in 5…”
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Carney complex review: Genetic features
Published in Endocrinologia, diabetes y nutricion (01-01-2018)“…Carney complex is a multiple neoplasia syndrome having endocrine and non-endocrine manifestations. Diagnostic criteria include myxoma, lentigines, and primary…”
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Carney complex review: Genetic features
Published in Endocrinología, diabetes y nutrición. (01-01-2018)“…Abstract Carney complex is a multiple neoplasia syndrome having endocrine and non-endocrine manifestations. Diagnostic criteria include myxoma, lentigines, and…”
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Carney complex review: Genetic features
Published in Endocrinología, diabetes y nutrición. (01-01-2018)Get full text
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Aberrant expression of glucagon receptors in adrenal glands of a patient with Cushing's syndrome and ACTH-independent macronodular adrenal hyperplasia
Published in Medicina (Buenos Aires) (2010)“…Adrenocorticotropin (ACTH) independent bilateral macronodular adrenal hyperplasia (AIMAH) is a rare cause of Cushing's syndrome, characterized by bilateral…”
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Erratum to: Retrospective multicentric study of pituitary incidentalomas
Published in Pituitary (01-06-2011)Get full text
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