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Retinal findings in hospitalised patients with severe COVID-19

British journal of ophthalmology, 2022-01, Vol.106 (1), p.102-105

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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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-R12

2017

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Acromegaly and pregnancy: a prospective study

European journal of endocrinology, 2014-02, Vol.170 (2), p.301-310

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

European journal of endocrinology, 2012-04, Vol.166 (4), p.631-640

2012

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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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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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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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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 and Metabolism, 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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Abnormal circadian rhythm and increased non-pulsatile secretion of thyrotrophin in Sheehan's syndrome

Clinical endocrinology (Oxford), 1999-10, Vol.51 (4), p.439-447

1999

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Increased thyrotrophin levels and loss of the nocturnal thyrotrophin surge in Sheehan's syndrome

Clinical endocrinology (Oxford), 1997-11, Vol.47 (5), p.515-522

1997

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Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

Arquivos brasileiros de endocrinologia e metabologia, 2007-10, Vol.51 (7), p.1097-1103

2007

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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

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

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

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

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

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

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

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

Abnormal circadian rhythm and increased non-pulsatile secretion of thyrotrophin in Sheehan's syndrome

Increased thyrotrophin levels and loss of the nocturnal thyrotrophin surge in Sheehan's syndrome

Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

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