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	41.	Criteria for the cure of acromegaly: comparison between basal growth hormone and somatomedin C plasma concentrations in active and non-active acromegalic patients. [electronic resource] by Giannella-Neto, D Wajchenberg, B L Mendonça, B B Almeida, S F Macchione, M Spencer, E M Producer: 19880609 In: Journal of endocrinological investigation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene. [electronic resource] by Mendonça, B B Barbosa, A S Arnhold, I J McElreavey, K Fellous, M Moreira-Filho, C A Producer: 19941129 In: American journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Growth hormone receptor messenger ribonucleic acid in normal and pathologic human adrenocortical tissues--an analysis by quantitative polymerase chain reaction technique. [electronic resource] by Lin, C J Mendonca, B B Lucon, A M Guazzelli, I C Nicolau, W Villares, S M Producer: 19970828 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant rickets. [electronic resource] by Mechica, J B Leite, M O Mendonca, B B Frazzatto, E S Borelli, A Latronico, A C Producer: 19971125 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain. [electronic resource] by Murono, K Mendonca, B B Arnhold, I J Rigon, A C Migeon, C J Brown, T R Producer: 19951214 In: Human mutation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [electronic resource] by Bachega, T A Billerbeck, A E Marcondes, J A Madureira, G Arnhold, I J Mendonca, B B Producer: 20000801 In: Clinical endocrinology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene. [electronic resource] by Mendonca, B B Osorio, M G Latronico, A C Estefan, V Lo, L S Arnhold, I J Producer: 19990413 In: The Journal of clinical endocrinology and metabolism vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis. [electronic resource] by Ottolenghi, C Moreira-Filho, C Mendonça, B B Barbieri, M Fellous, M Berkovitz, G D McElreavey, K Producer: 20010705 In: The Journal of clinical endocrinology and metabolism vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Zinc acutely and temporarily inhibits adrenal cortisol secretion in humans. A preliminary report. [electronic resource] by Brandão-Neto, J de Mendonça, B B Shuhama, T Marchini, J S Pimenta, W P Tornero, M T Producer: 19910220 In: Biological trace element research vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Spironolactone-reversible rickets associated with 11 beta-hydroxysteroid dehydrogenase deficiency syndrome. [electronic resource] by Batista, M C Mendonça, B B Kater, C E Arnhold, I J Rocha, A Nicolau, W Bloise, W Producer: 19861229 In: The Journal of pediatrics vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Hyperandrogenism due to 3 beta-hydroxysteroid dehydrogenase deficiency with accessory adrenocortical tissue: a hormonal and metabolic evaluation. [electronic resource] by Paula, F J Dick-de-Paula, I Pontes, A Schmitt, F C Mendonça, B B Foss, M C Producer: 19950120 In: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	52.	Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction. [electronic resource] by Costa, E M Bedecarrats, G Y Mendonca, B B Arnhold, I J Kaiser, U B Latronico, A C Producer: 20010705 In: The Journal of clinical endocrinology and metabolism vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Genotyping of the type II 3beta-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated delta(5)-steroids. [electronic resource] by Marui, S Russell, A J Paula, F J Dick-de-Paula, I Marcondes, J A Mendonca, B B Producer: 20001010 In: Fertility and sterility vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Leydig cell hypoplasia causing male pseudohermaphroditism: case report and review of the literature. [electronic resource] by Arnhold, I J de Mendonça, B B Toledo, S P Madureira, G Nicolau, W Bisi, H Bloise, W Producer: 19880901 In: Revista do Hospital das Clinicas vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	55.	[Sex reversal in a case of male pseudohermaphroditism (Reifenstein syndrome)]. [electronic resource] by Lodovici, O Salvatore, C A Bloise, W Sarmiento, O Gemperli, R de Mendonça, B B Travi, M E Producer: 19810709 In: Revista do Hospital das Clinicas vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	56.	Ectopic ACTH syndrome caused by pheochromocytoma: computed tomography-guided percutaneous ethanol injection as an alternative treatment. [electronic resource] by Danilovic, D L Brandão Neto, R A D'Abronzo, H Menezes, M R Lucon, A M Mendonca, B B Producer: 20080205 In: Journal of endocrinological investigation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Ovarian resistance to luteinizing hormone: a novel cause of amenorrhea and infertility. [electronic resource] by Arnhold, I J Latronico, A C Batista, M C Carvalho, F M Chrousos, G P Mendonça, B B Producer: 19970314 In: Fertility and sterility vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Somatomedin levels in the diagnosis and therapy of growth hormone deficiency. [electronic resource] by Giannella-Neto, D Wajchenberg, B L Mendonca, B B Liberman, B Nery, M Macchione, M Spencer, E M Producer: 19880804 In: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Mutation analysis of the follicle-stimulating hormone receptor gene in girls with gonadotropin-independent precocious puberty resulting from autonomous cystic ovaries. [electronic resource] by Batista, M C Kohek, M B Frazzatto, E S Fragoso, M C Mendonça, B B Latronico, A C Producer: 20000309 In: Fertility and sterility vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome. [electronic resource] by Melo, K F Latronico, A C Costa, E M Billerbeck, A E Mendonca, B B Arnhold, I J Producer: 19991007 In: Human mutation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 139 results.