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Retinal findings in hospitalised patients with severe COVID-19

British journal of ophthalmology, 2022-01, Vol.106 (1), p.102

2022

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Short- and Long-Term Efficacy of Combined Cabergoline and Octreotide Treatment in Controlling IGF-I Levels in Acromegaly

Neuroendocrinology, 2010-01, Vol.92 (2), p.120-127

2010

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Brazilian multicenter study on pegvisomant treatment in acromegaly

Archives of Endocrinology and Metabolism, 2019-07, Vol.63 (4), p.328-336

2019

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Pituitary metastasis of lung neuroendocrine carcinoma: case report and literature review

Archives of Endocrinology and Metabolism, 2015-12, Vol.59 (6), p.548-553

2015

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Prolactin Response to Metformin in Cabergoline-Resistant Prolactinomas: A Pilot Study

Neuroendocrinology, 2022-01, Vol.112 (1), p.68-73

2022

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Criteria for the definition of Pituitary Tumor Centers of Excellence (PTCOE): A Pituitary Society Statement

Pituitary, 2017-10, Vol.20 (5), p.489-498

2017

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MANAGEMENT OF ENDOCRINE DISEASE: Acromegaly and pregnancy: a contemporary review

European journal of endocrinology, 2017-07, Vol.177 (1), p.R1

2017

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Acromegaly and pregnancy: a prospective study

European journal of endocrinology, 2014-02, Vol.170 (2), p.301

2014

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Effect of central hypothyroidism on Doppler-derived myocardial performance index

Journal of the American Society of Echocardiography, 2004-06, Vol.17 (6), p.622-629

2004

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Detecting and solving the interference of pregnancy serum, in a GH immunometric assay

Growth hormone & IGF research, 2013-02, Vol.23 (1), p.13-18

2013

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Diagnosis of subclinical central hypothyroidism in patients with hypothalamic-pituitary disease by Doppler echocardiography

European journal of endocrinology, 2012-04, Vol.166 (4), p.631

2012

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Long-Term Remission of Acromegaly after Octreotide Withdrawal Is an Uncommon and Frequently Unsustainable Event

Neuroendocrinology, 2017-01, Vol.104 (3), p.273-279

2017

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Evidence for Thyroid Hormone as a Positive Regulator of Serum Thyrotropin Bioactivity

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.3108-3113

2007

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Growth Hormone Replacement Improves Thyroxine Biological Effects: Implications for Management of Central Hypothyroidism

The journal of clinical endocrinology and metabolism, 2007-11, Vol.92 (11), p.4144-4153

2007

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Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome : Characterization of TSH carbohydrate content and bioactivity

The journal of clinical endocrinology and metabolism, 2001-04, Vol.86 (4), p.1694-1699

2001

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Changes in serum thyroid hormones levels and their mechanisms during long-term growth hormone (GH) replacement therapy in GH deficient children

Clinical endocrinology (Oxford), 2000-08, Vol.53 (2), p.183-189

2000

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Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

The journal of clinical endocrinology and metabolism, 2003-01, Vol.88 (1), p.38-44

2003

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Children with Cushing's syndrome: primary pigmented nodular adrenocortical disease should always be suspected

Pituitary, 2011-03, Vol.14 (1), p.61-67

2011

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Bilateral nonarteritic anterior ischemic neuropathy following acute angle-closure glaucoma in a patient with iridoschisis: case report

Arquivos brasileiros de oftalmologia, 2011-01, Vol.74 (1), p.61-63

2011

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Conservative management of pituitary apoplexy : a prospective study

The journal of clinical endocrinology and metabolism, 1995-07, Vol.80 (7), p.2190-2197

1995

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Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Clinical endocrinology (Oxford), 2003-06, Vol.58 (6), p.756-762

2003

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Central precocious puberty associated with pituitary duplication and midline defects

Journal of pediatric endocrinology & metabolism : JPEM, 2007-10, Vol.20 (10), p.1141

2007

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Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation

Pituitary, 2006-03, Vol.9 (1), p.47-52

2006

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Endoscopic transnasal approach to sellar tumors

Brazilian journal of otorhinolaryngology, 2007-07, Vol.73 (4), p.463-475

2007

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Controversial issues in the management of hyperprolactinemia and prolactinomas - An overview by the Neuroendocrinology Department of the Brazilian Society of Endocrinology and Metabolism

Retinal findings in hospitalised patients with severe COVID-19

Short- and Long-Term Efficacy of Combined Cabergoline and Octreotide Treatment in Controlling IGF-I Levels in Acromegaly

Brazilian multicenter study on pegvisomant treatment in acromegaly

Pituitary metastasis of lung neuroendocrine carcinoma: case report and literature review

Prolactin Response to Metformin in Cabergoline-Resistant Prolactinomas: A Pilot Study

Criteria for the definition of Pituitary Tumor Centers of Excellence (PTCOE): A Pituitary Society Statement

MANAGEMENT OF ENDOCRINE DISEASE: Acromegaly and pregnancy: a contemporary review

Acromegaly and pregnancy: a prospective study

Effect of central hypothyroidism on Doppler-derived myocardial performance index

Detecting and solving the interference of pregnancy serum, in a GH immunometric assay

Diagnosis of subclinical central hypothyroidism in patients with hypothalamic-pituitary disease by Doppler echocardiography

Long-Term Remission of Acromegaly after Octreotide Withdrawal Is an Uncommon and Frequently Unsustainable Event

Evidence for Thyroid Hormone as a Positive Regulator of Serum Thyrotropin Bioactivity

Growth Hormone Replacement Improves Thyroxine Biological Effects: Implications for Management of Central Hypothyroidism

Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome : Characterization of TSH carbohydrate content and bioactivity

Changes in serum thyroid hormones levels and their mechanisms during long-term growth hormone (GH) replacement therapy in GH deficient children

Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

Children with Cushing's syndrome: primary pigmented nodular adrenocortical disease should always be suspected

Bilateral nonarteritic anterior ischemic neuropathy following acute angle-closure glaucoma in a patient with iridoschisis: case report

Conservative management of pituitary apoplexy : a prospective study

Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred

Central precocious puberty associated with pituitary duplication and midline defects

Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation

Endoscopic transnasal approach to sellar tumors

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