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Recurrent Left Atrial Myxomas in Carney Complex: A Genetic Cause of Multiple Strokes that can be Prevented

Journal of stroke and cerebrovascular diseases, 2012-11, Vol.21 (8), p.914.e1-914.e8

2012

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Ectopic Adrenocorticotropic Hormone and Corticotropin-Releasing Hormone Co-Secreting Tumors in Children and Adolescents Causing Cushing Syndrome: A Diagnostic Dilemma and How to Solve It

The journal of clinical endocrinology and metabolism, 2015-01, Vol.100 (1), p.141-148

2015

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Growth hormone and risk for cardiac tumors in Carney complex

Endocrine-related cancer, 2016-09, Vol.23 (9), p.739-746

2016

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Does Somatostatin Have a Role in the Regulation of Cortisol Secretion in Primary Pigmented Nodular Adrenocortical Disease (PPNAD)? A Clinical and in Vitro Investigation

The journal of clinical endocrinology and metabolism, 2014-05, Vol.99 (5), p.E891-E901

2014

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Adrenal function in Smith-Lemli-Opitz syndrome

American journal of medical genetics. Part A, 2011-11, Vol.155A (11), p.2732-2738

2011

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Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing's syndrome and unusual histologic features

Journal of Pediatric Endocrinology and Metabolism, 2012-02, Vol.25 (1-2), p.213-219

2012

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An unusual presentation of pediatric Cushing disease: recurrent corticotropinoma of the posterior pituitary lobe

Journal of Pediatric Endocrinology and Metabolism, 2010-06, Vol.23 (6), p.607-612

2010

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SUN-917 Aggressive De Novo MEN1 Variant in a Child with Metastatic Pancreatic Acth and Crh Co-Secreting Neuroendocrine Tumor: Diagnosis and 10-Year Follow Up

Journal of the Endocrine Society, 2020-05, Vol.4 (Supplement_1)

2020

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Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with an ACTH-secreting pituitary adenoma, absence of stigmata of Cushing syndrome, and unusual histologic features

Journal of pediatric endocrinology & metabolism : JPEM, 2012-01, Vol.25 (1-2), p.213-219

2012

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Central Nervous System Abnormalities in Dyskeratosis Congenita and Fanconi Anemia: Correlation with Clinical Phenotype and Aplastic Anemia

Blood, 2007-11, Vol.110 (11), p.1682-1682

2007

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The growth hormone receptor (GHR) polymorphism in growth-retarded children with Cushing disease: lack of association with growth and measures of the somatotropic axis

Hormone and metabolic research, 2010-03, Vol.42 (3), p.194

2010

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Operative management of Cushing Syndrome secondary to micronodular adrenal hyperplasia

Surgery, 2008-06, Vol.143 (6), p.750-758

2008

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Cyclical Cushing Syndrome Presenting in Infancy: An Early Form of Primary Pigmented Nodular Adrenocortical Disease, or a New Entity?

The journal of clinical endocrinology and metabolism, 2004-07, Vol.89 (7), p.3173-3182

2004

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Surgical management of Cushing Syndrome secondary to micronodular adrenal hyperplasia

Surgery, 2008-06, Vol.143 (6), p.750-758

2008

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Cushing Syndrome - Diagnosis
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Recurrent Left Atrial Myxomas in Carney Complex: A Genetic Cause of Multiple Strokes that can be Prevented

Ectopic Adrenocorticotropic Hormone and Corticotropin-Releasing Hormone Co-Secreting Tumors in Children and Adolescents Causing Cushing Syndrome: A Diagnostic Dilemma and How to Solve It

Growth hormone and risk for cardiac tumors in Carney complex

Does Somatostatin Have a Role in the Regulation of Cortisol Secretion in Primary Pigmented Nodular Adrenocortical Disease (PPNAD)? A Clinical and in Vitro Investigation

Adrenal function in Smith-Lemli-Opitz syndrome

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing's syndrome and unusual histologic features

An unusual presentation of pediatric Cushing disease: recurrent corticotropinoma of the posterior pituitary lobe

SUN-917 Aggressive De Novo MEN1 Variant in a Child with Metastatic Pancreatic Acth and Crh Co-Secreting Neuroendocrine Tumor: Diagnosis and 10-Year Follow Up

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with an ACTH-secreting pituitary adenoma, absence of stigmata of Cushing syndrome, and unusual histologic features

Central Nervous System Abnormalities in Dyskeratosis Congenita and Fanconi Anemia: Correlation with Clinical Phenotype and Aplastic Anemia

The growth hormone receptor (GHR) polymorphism in growth-retarded children with Cushing disease: lack of association with growth and measures of the somatotropic axis

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in a large cohort of children and adolescents with pituitary adenomas

Operative management of Cushing Syndrome secondary to micronodular adrenal hyperplasia

Cyclical Cushing Syndrome Presenting in Infancy: An Early Form of Primary Pigmented Nodular Adrenocortical Disease, or a New Entity?

Surgical management of Cushing Syndrome secondary to micronodular adrenal hyperplasia

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