Search Results - "Lovicu, R. M."

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  1. 1

    Giant prolactinomas in men: efficacy of cabergoline treatment by Corsello, S. M., Ubertini, G., Altomare, M., Lovicu, R. M., Migneco, M. G., Rota, C. A., Colosimo, C.

    Published in Clinical endocrinology (Oxford) (01-05-2003)
    “…Summary objective The term ‘giant prolactinoma’ can be used for tumours larger than 4 cm in diameter and/or with massive extrasellar extension. Cabergoline…”
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    Journal Article
  2. 2

    Long-term results of treatment in patients with ACTH-secreting pituitary macroadenomas by CANNAVO, S, ALMOTO, B, D'ALLASTA, C, CORSELLO, S, LOVICU, R. M, DE MENIS, E, TRIMARCHI, F, AMBROSI, B

    Published in European journal of endocrinology (01-09-2003)
    “…Since Cushing's disease due to large pituitary tumors is rare, we evaluated biochemical characteristics at entry and the results of first surgical approach and…”
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    Journal Article
  3. 3

    Levothyroxine therapy in preventing nodular recurrence after hemithyroidectomy: A retrospective study by Alba, M., Fintini, D., Lovicu, R. M., Paragliola, R. M., Papi, G., Rota, C. A., Pontecorvi, A., Corsello, S. M.

    Published in Journal of endocrinological investigation (01-04-2009)
    “…Aim : To determine the effect of levothyroxine (L-T 4 ) therapy on the recurrence rate of nodular disease in patients previously treated with lobectomy for…”
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    Journal Article
  4. 4

    Medical therapy of benign thyroid diseases by Corsello, S M, Migneco, M G, Lovicu, R M

    Published in Rays (01-04-1999)
    “…Main guide-lines of medical therapy of benign thyroid diseases are reviewed. The most common drug therapy of the various forms of hyperthyroidism is…”
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  5. 5

    Diagnostic approach, genetic screening and prognostic factors of medullary thyroid carcinoma by Corsello, S M, Lovicu, R M, Migneco, M G, Rufini, V, Summaria, V

    Published in Rays (01-04-2000)
    “…Medullary thyroid carcinoma is the least frequent thyroid neoplasm; it originates in thyroid parafollicular cells (calcitonin secreting C cells). In 80% of…”
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  6. 6

    First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy by Concolino, Paola, Corsello, Salvatore, Carrozza, Cinzia, Minucci, Angelo, Santonocito, Concetta, Lovicu, Rosa Maria, Santini, Stefano Angelo, Ameglio, Franco, Zuppi, Cecilia, Capoluongo, Ettore

    Published in Clinical biochemistry (01-12-2007)
    “…To report a first case of 21-hydroxylase deficiency associated with a new genotype determined by V281+I172N/V281L mutations of the CYP21A2 gene. Direct genetic…”
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    Journal Article