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The triad of paragangliomas, gastric stromal tumours and pulmonary chondromas (Carney triad), and the dyad of paragangliomas and gastric stromal sarcomas (Carney–Stratakis syndrome): molecular genetics and clinical implications

Journal of internal medicine, 2009-07, Vol.266 (1), p.43-52

2009

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SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes

Journal of internal medicine, 2009-07, Vol.266 (1), p.19-42

2009

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Functional screen analysis reveals miR-26b and miR-128 as central regulators of pituitary somatomammotrophic tumor growth through activation of the PTEN–AKT pathway

Oncogene, 2013-03, Vol.32 (13), p.1651-1659

2013

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Carney complex syndrome manifesting as cardioembolic stroke: a case report and review of the literature

International journal of neuroscience, 2022-07, Vol.132 (7), p.1-655

2022

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

Clinical genetics, 2010-11, Vol.78 (5), p.457-463

2010

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Vandetanib Successfully Controls Medullary Thyroid Cancer-Related Cushing Syndrome in an Adolescent Patient

The journal of clinical endocrinology and metabolism, 2014-09, Vol.99 (9), p.3055-3059

2014

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Lipoprotein Particles in Adolescents and Young Women With PCOS Provide Insights Into Their Cardiovascular Risk

The journal of clinical endocrinology and metabolism, 2015-11, Vol.100 (11), p.4291-4298

2015

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GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

Hormone and metabolic research, 2016-06, Vol.48 (6), p.389-393

2016

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Dependence of the Excitability of Pituitary Cells on Cyclic Nucleotides

Journal of neuroendocrinology, 2012-09, Vol.24 (9), p.1183-1200

2012

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Threat bias in mice with inactivating mutations of Prkar1a

Neuroscience, 2013-06, Vol.241, p.206-214

2013

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Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion

European journal of endocrinology, 2014-01, Vol.170 (1), p.151-160

2014

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Age-dependent effects of Armc5 haploinsufficiency on adrenocortical function

Human molecular genetics, 2017-09, Vol.26 (18), p.3495-3507

2017

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Multiple endocrine neoplasias: advances and challenges for the future

Journal of internal medicine, 2009-07, Vol.266 (1), p.1-4

2009

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Association of a COL1A1 polymorphism with lumbar disc disease in young military recruits

Journal of medical genetics, 2005-07, Vol.42 (7), p.e44-e44

2005

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Pituitary macroadenoma in a 5-year-old : An early expression of multiple endocrine neoplasia type 1

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4776-4780

2000

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Protein kinase A and its role in human neoplasia: the Carney complex paradigm

Endocrine-related cancer, 2004-06, Vol.11 (2), p.265-280

2004

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The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis

Journal of Medical Genetics, 2005-11, Vol.42 (11), p.801-810

2005

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Bone Formation, Growth, and Repair

Hormone and metabolic research, 2016-11, Vol.48 (11), p.687-688

2016

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Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005

Clinical genetics, 2005-09, Vol.68 (3), p.215-221

2005

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Phosphodiesterases and adrenal Cushing in mice and humans

Hormone and metabolic research, 2014-11, Vol.46 (12), p.863-868

2014

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From β-catenin to ARM-repeat proteins in adrenocortical disorders

Hormone and metabolic research, 2014-11, Vol.46 (12), p.889-896

2014

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Molecular mechanisms of medullary thyroid carcinoma: current approaches in diagnosis and treatment

Histology and histopathology, 2008-01, Vol.23 (1), p.109

2008

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Multiple Endocrine Neoplasia – Introduction

Journal of internal medicine, 2005-01, Vol.257 (1), p.2-5

2005

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Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

Annals of internal medicine, 1999-10, Vol.131 (8), p.585

1999

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Chromosome 2 (2p16) abnormalities in Carney complex tumours

Journal of medical genetics, 2003-04, Vol.40 (4), p.268-277

2003

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The triad of paragangliomas, gastric stromal tumours and pulmonary chondromas (Carney triad), and the dyad of paragangliomas and gastric stromal sarcomas (Carney–Stratakis syndrome): molecular genetics and clinical implications

SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes

Functional screen analysis reveals miR-26b and miR-128 as central regulators of pituitary somatomammotrophic tumor growth through activation of the PTEN–AKT pathway

Carney complex syndrome manifesting as cardioembolic stroke: a case report and review of the literature

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

Vandetanib Successfully Controls Medullary Thyroid Cancer-Related Cushing Syndrome in an Adolescent Patient

Lipoprotein Particles in Adolescents and Young Women With PCOS Provide Insights Into Their Cardiovascular Risk

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

Dependence of the Excitability of Pituitary Cells on Cyclic Nucleotides

Threat bias in mice with inactivating mutations of Prkar1a

Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion

Age-dependent effects of Armc5 haploinsufficiency on adrenocortical function

Multiple endocrine neoplasias: advances and challenges for the future

Association of a COL1A1 polymorphism with lumbar disc disease in young military recruits

Pituitary macroadenoma in a 5-year-old : An early expression of multiple endocrine neoplasia type 1

Protein kinase A and its role in human neoplasia: the Carney complex paradigm

The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis

Bone Formation, Growth, and Repair

Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005

Phosphodiesterases and adrenal Cushing in mice and humans

From β-catenin to ARM-repeat proteins in adrenocortical disorders

Molecular mechanisms of medullary thyroid carcinoma: current approaches in diagnosis and treatment

Multiple Endocrine Neoplasia – Introduction

Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

Chromosome 2 (2p16) abnormalities in Carney complex tumours

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