Issue Special Issue 1/2012
Content (17 Articles)
Polyuria and polydipsia in a young child: diagnostic considerations and identification of novel mutation causing familial neurohypophyseal diabetes insipidus
Matthew D. Stephen, Raymond G. Fenwick, Patrick G. Brosnan
ACTH-producing remnants following apoplexy of an ACTH-secreting pituitary macroadenoma
Caroline Korsten Messer, Mary E. Fowkes, J. Lester Gabrilove, Kalmon D. Post, Honju Son, Alice C. Levine
Pituicytoma in a patient with Cushing’s disease: case report and review of the literature
K. Schmalisch, J. Schittenhelm, F. H. Ebner, F. Beuschlein, J. Honegger, R. Beschorner
Acromegaly as a cause of 1,25-dihydroxyvitamin D-dependent hypercalcemia: case reports and review of the literature
Reshma Shah, Angelo Licata, Nelson M. Oyesiku, Adriana G. Ioachimescu
Tamoxifen enhances the control of acromegaly treated with somatostatin analog lanreotide
Jean-Christophe Maiza, Stéphane Castillo-Ros, Maria Matta, Antoine Bennet, Philippe Caron
Distinctive growth pattern in a patient with a delayed diagnosis of Langerhans’ cell histiocytosis
Athanasios D. Anastasilakis, Gregory A. Kaltsas, Georgios Delimpasis, Ludwig Wilkens, George Kanakis, Polyzois Makras
Macrocorticotropinoma shrinkage and control of hypercortisolism under long-term cabergoline therapy: case report
Marcos Paulo Manavela, K. Danilowicz, O. D. Bruno
Cavernous sinus apoplexy presenting isolated sixth cranial nerve palsy: case report
Matteo Zoli, Diego Mazzatenta, Ernesto Pasquini, Paolo Ambrosetto, Giorgio Frank
Acute cortisol release during stereotactic fractionated radiotherapy to an ACTH-secreting pituitary macroadenoma
I. Shimon, Y. Manisterski, A. A. Kanner
Be careful …. She has a pituitary gland in her nose
N. M. Rabelink, P. Lips, J. A. Castelijns
Primary hypothyroidism presenting as pseudoacromegaly
K. V. S. Hari Kumar, Altamash Shaikh, Irfan Anwar, P. Prusty
Acromegaly due to an ectopic pituitary adenoma in the clivus: case report and review of literature
Julia Goulart Appel, Marvin Bergsneider, Harry Vinters, Noriko Salamon, Marilene B. Wang, Anthony P. Heaney
First demonstration of the effectiveness of peptide receptor radionuclide therapy (PRRT) with 111In-DTPA-octreotide in a giant PRL-secreting pituitary adenoma resistant to conventional treatment
S. Baldari, F. Ferraù, C. Alafaci, A. Herberg, F. Granata, V. Militano, F. M. Salpietro, F. Trimarchi, S. Cannavò
Genetic analysis in a patient presenting with meningioma and familial isolated pituitary adenoma (FIPA) reveals selective involvement of the R81X mutation of the AIP gene in the pathogenesis of the pituitary tumor
Federica Guaraldi, Valentina Corazzini, Gary L. Gallia, Silvia Grottoli, Karen Stals, Nadezhda Dalantaeva, Lawrence A. Frohman, Márta Korbonits, Roberto Salvatori
Desensitization treatment for hypersensitivity reaction to octreotide in an acromegalic patient
Daphne D. Dadzie, Esther J. Lee, Catherine A. Monteleone, Stephen H. Schneider
Variation of the baseline characteristics and treatment parameters over time: an analysis of 15 years of growth hormone replacement in adults in the German KIMS database
I. Kreitschmann-Andermahr, S. Siegel, F. Francis, M. Buchfelder, H. J. Schneider, P. H. Kann, H. Wallaschofski, M. Koltowska-Häggström, G. Brabant
Unilateral agenesis of internal carotid artery associated with congenital combined pituitary hormone deficiency and pituitary stalk interruption without HESX1, LHX4 or OTX2 mutation: a case report
Faïza Lamine, Faouzi Kanoun, Melika Chihaoui, Alexandru Saveanu, Emna Menif, Anne Barlier, Alain Enjalbert, Thierry Brue, Hédia Slimane