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Abnormalities of hypothalamic-pituitary-thyroid axis in patients with primary empty sellaCANNAVO, S; CURTO, L; VENTURINO, M et al.Journal of endocrinological investigation (Testo stampato). 2002, Vol 25, Num 3, pp 236-239, issn 0391-4097Article

Subjective health status in Norwegian patients with Addison's diseaseLØVAS, Kristian; LOGE, Jon Hovard; HUSEBYE, Eystein S et al.Clinical endocrinology (Oxford. Print). 2002, Vol 56, Num 5, pp 581-588, issn 0300-0664Article

Female sexual dysfunctionFREEDMAN, Murray A.International journal of fertility and women's medicine. 2002, Vol 47, Num 1, pp 18-21, issn 1534-892XConference Paper

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The natural history of incidentally discovered adrenocortical adenomas: A retrospective evaluationGROSSRUBATSCHER, E; VIGNATI, F; POSSA, M et al.Journal of endocrinological investigation (Testo stampato). 2001, Vol 24, Num 11, pp 846-855, issn 0391-4097Article

Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1ACHERMANN, John C; SILVERMAN, Bernard L; HABIBY, Reema L et al.The Journal of pediatrics. 2000, Vol 137, Num 6, pp 878-881, issn 0022-3476Article

Circulating adrenomedullin is increased in patients with corticotropin-dependent Cushing's syndrome due to pituitary adenomaLETIZIA, C; DI LORIO, R; DE TOMA, G et al.Metabolism, clinical and experimental. 2000, Vol 49, Num 6, pp 760-763, issn 0026-0495Article

Expression of menin in parathyroid tumorsBHUIYAN, M. M. R; SATO, M; MURAO, K et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 7, pp 2615-2619, issn 0021-972XArticle

A new heterozygous mutation (L338N) in the human Gsα (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophyPOHLENZ, Joachim; AHRENS, Wiebke; HIORT, Olaf et al.European journal of endocrinology. 2003, Vol 148, Num 4, pp 463-468, issn 0804-4643, 6 p.Article

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L'imagerie hypophysaire dans la maladie de Cushing = Pituitary gland imaging in Cushing's diseaseBONNEVILLE, J.-F; CATTIN, F; BONNEVILLE, F et al.Feuillets de radiologie. 2003, Vol 43, Num 1, pp 55-66, issn 0181-9801, 12 p.Article

High risk of adrenal insufficiency in adults previously treated for idiopathic childhood onset growth hormone deficiencyLANGE, Martin; FELDT-RASMUSSEN, Ulla; SVENDSEN, Ole Lander et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 12, pp 5784-5789, issn 0021-972X, 6 p.Article

Low plasma bicarbonate level in hyponatremia related to adrenocorticotropin deficiencyDECAUX, G; MUSCH, W; PENNINCKX, R et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 11, pp 5255-5257, issn 0021-972X, 3 p.Article

Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHβ-subunit genePOHLENZ, Joachim; DUMITRESCU, Alexandra; AUMANN, Ulrich et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 1, pp 336-339, issn 0021-972XArticle

Growth hormone deficiency and replacement in hypopituitary patients previously treated for acromegaly or Cushing's diseaseFELDT-RASMUSSEN, Ulla; ABS, Roger; BENGTSSON, Bengt-Ake et al.European journal of endocrinology. 2002, Vol 146, Num 1, pp 67-74, issn 0804-4643Article

Two novel variants in the thyroxine-binding globulin (TBG) gene behind the diagnosis of TBG deficiencyDOMINGUES, Rita; BUGALHO, Maria Joao; GARRAO, Antonio et al.European journal of endocrinology. 2002, Vol 146, Num 4, pp 485-490, issn 0804-4643Article

Cavernous sinus sampling in selected cases of Cushing's diseaseFLITSCH, J; LÜDECKE, D. K; KNAPPE, U. J et al.Experimental and clinical endocrinology & diabetes. 2002, Vol 110, Num 7, pp 329-335, issn 0947-7349, 7 p.Article

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