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Medullary thyroid carcinoma with extremely rare presentation in a child: Considerations for management

Pediatric blood & cancer, 2024-03, Vol.71 (3), p.e30823-n/a

2024

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Lymph node thyroglobulin in the diagnosis of metastases of thyroid carcinoma with the thyroid in situ: A prospective intraoperative study

European journal of surgical oncology, 2023-04, Vol.49 (4), p.760-763

2023

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Germinal defects of SDHx genes in patients with isolated pituitary adenoma

European journal of endocrinology, 2020-10, Vol.183 (4), p.369

2020

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The Evolving Role of Succinate in Tumor Metabolism: An ^sup 18^F-FDG-Based Study

The Journal of nuclear medicine (1978), 2017-11, Vol.58 (11), p.1749

2017

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The Evolving Role of Succinate in Tumor Metabolism: An 18 F-FDG-Based Study

Journal of Nuclear Medicine, 2017-11, Vol.58 (11), p.1749-1755

2017

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The Evolving Role of Succinate in Tumor Metabolism: An 18F-FDG-Based Study

The Journal of nuclear medicine (1978), 2017-11, Vol.58 (11), p.1749-1755

2017

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The Evolving Role of Succinate in Tumor Metabolism: An 18 F-FDG–Based Study: succinate and [18F]-FDG

The Journal of nuclear medicine (1978), 2017-11, Vol.58 (11), p.1749-1755

2017

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18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma

The journal of clinical endocrinology and metabolism, 2018-04, Vol.103 (4), p.1574-1582

2018

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Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation

Endocrine pathology, 2017-12, Vol.28 (4), p.302-307

2017

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Characterization of adrenocortical tumors by F-18-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Surgical oncology, 2018-06, Vol.27 (2), p.231-235

2018

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Characterization of adrenocortical tumors by 18F-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Surgical oncology, 2018-06, Vol.27 (2), p.231-235

2018

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Hürthle Cell Neoplasms: A New Differential Diagnosis for 18F-FDOPA-avid Thyroid Nodules?

The journal of clinical endocrinology and metabolism, 2013-03, Vol.98 (3), p.865-866

2013

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Sinonasal Paraganglioma With Long-Delayed Recurrence and Metastases: Genetic and Imaging Findings

The journal of clinical endocrinology and metabolism, 2013-11, Vol.98 (11), p.4262-4266

2013

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Peribiliary cysts

Hepatology (Baltimore, Md.), 2011-12, Vol.54 (6), p.2272-2273

2011

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Targeting Dopamine Receptors Subtype 2 (D2DR) in Pheochromocytomas: Head-to-Head Comparison Between In Vitro and In Vivo Findings

The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.E1951-E1955

2013

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Characterization of adrenocortical tumors by 18 F-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Surgical oncology, 2018-06, Vol.27 (2), p.231

2018

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Une tumeur ovarienne peut en cacher une autre

Annales de pathologie, 2017-12, Vol.37 (6), p.479-483

2017

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Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation

Endocrine pathology, 2017-12, Vol.28 (4), p.302-307

2017

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Implications of SDHB genetic testing in patients with sporadic pheochromocytoma

Langenbeck's archives of surgery, 2017-08, Vol.402 (5), p.787-798

2017

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An ovarian tumor can hide another one

Annales de pathologie, 2017-12, Vol.37 (6), p.479-483

2017

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Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2[alpha] mutation: A case report.(Case overview)(Case study)

Oncology letters, 2017-03, Vol.13 (3), p.1083

2017

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Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2 α mutation: A case report

Oncology letters, 2017-03, Vol.13 (3), p.1083-1086

2017

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Medullary thyroid carcinoma with extremely rare presentation in a child: Considerations for management

Pediatric blood & cancer, 2024, Vol.71 (3), p.e30823-e30823

2024

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Amylose pyélo-urétérale

Progrès en urologie (Paris), 2004-06, Vol.14 (3), p.406-410

2004

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Pyelo-ureteric amyloidosis

Progrès en urologie (Paris), 2004-06, Vol.14 (3), p.406-410

2004

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Medullary thyroid carcinoma with extremely rare presentation in a child: Considerations for management

Lymph node thyroglobulin in the diagnosis of metastases of thyroid carcinoma with the thyroid in situ: A prospective intraoperative study

Germinal defects of SDHx genes in patients with isolated pituitary adenoma

The Evolving Role of Succinate in Tumor Metabolism: An ^sup 18^F-FDG-Based Study

The Evolving Role of Succinate in Tumor Metabolism: An 18 F-FDG-Based Study

The Evolving Role of Succinate in Tumor Metabolism: An 18F-FDG-Based Study

The Evolving Role of Succinate in Tumor Metabolism: An 18 F-FDG–Based Study: succinate and [18F]-FDG

18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma

Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation

Characterization of adrenocortical tumors by F-18-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Characterization of adrenocortical tumors by 18F-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Hürthle Cell Neoplasms: A New Differential Diagnosis for 18F-FDOPA-avid Thyroid Nodules?

Sinonasal Paraganglioma With Long-Delayed Recurrence and Metastases: Genetic and Imaging Findings

Peribiliary cysts

Targeting Dopamine Receptors Subtype 2 (D2DR) in Pheochromocytomas: Head-to-Head Comparison Between In Vitro and In Vivo Findings

Characterization of adrenocortical tumors by 18 F-FDG PET/CT: Does steroid hormone hypersecretion status modify the uptake pattern?

Une tumeur ovarienne peut en cacher une autre

Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation

Implications of SDHB genetic testing in patients with sporadic pheochromocytoma

An ovarian tumor can hide another one

Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2[alpha] mutation: A case report.(Case overview)(Case study)

Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2 α mutation: A case report

Medullary thyroid carcinoma with extremely rare presentation in a child: Considerations for management

Amylose pyélo-urétérale

Pyelo-ureteric amyloidosis

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