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1
High Frequency of SDHB Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic Testing
High Frequency of SDHB Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic Testing
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High Frequency of SDHB Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic Testing

Brouwers, Frederieke M ; Eisenhofer, Graeme ; Tao, Jessica J ; Kant, Jeffrey A ; Adams, Karen T ; Linehan, W. Marston ; Pacak, Karel

The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4505-4509 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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2
Age at Diagnosis of Pheochromocytoma Differs According to Catecholamine Phenotype and Tumor Location
Age at Diagnosis of Pheochromocytoma Differs According to Catecholamine Phenotype and Tumor Location
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Age at Diagnosis of Pheochromocytoma Differs According to Catecholamine Phenotype and Tumor Location

Eisenhofer, Graeme ; Timmers, Henri J ; Lenders, Jacques W.M ; Bornstein, Stefan R ; Tiebel, Oliver ; Mannelli, Massimo ; King, Kathryn S ; Vocke, Cathy D ; Linehan, W. Marston ; Bratslavsky, Gennady ; Pacak, Karel

The journal of clinical endocrinology and metabolism, 2011-02, Vol.96 (2), p.375-384 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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3
Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes
Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes
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Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes

Eisenhofer, Graeme ; Walther, Mcclellan M ; Huynh, Thanh-Truc ; Li, Sheng-Ting ; Bornstein, Stefan R ; Vortmeyer, Alexander ; Mannelli, Massimo ; Goldstein, David S ; Linehan, W. Marston ; Lenders, Jacques W. M ; Pacak, Karel

The journal of clinical endocrinology and metabolism, 2001-05, Vol.86 (5), p.1999-2008 [Periódico revisado por pares]

Endocrine Society

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4
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes
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Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

EISENHOFER, Graeme ; WALTHER, Mcclellan M ; PACAK, Karel ; HUYNH, Thanh-Truc ; LI, Sheng-Ting ; BORNSTEIN, Stefan R ; VORTMEYER, Alexander ; MANNELLI, Massimo ; GOLDSTEIN, David S ; LINEHAN, W. Marston ; LENDERS, Jacques W. M

The journal of clinical endocrinology and metabolism, 2001-05, Vol.86 (5), p.1999-2008 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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5
Germline- and Somatic-Inactivating FLCN Variants in Parathyroid Cancer and Atypical Parathyroid Tumors
Germline- and Somatic-Inactivating FLCN Variants in Parathyroid Cancer and Atypical Parathyroid Tumors
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Germline- and Somatic-Inactivating FLCN Variants in Parathyroid Cancer and Atypical Parathyroid Tumors

Jha, Smita ; Welch, James ; Tora, Rana ; Lack, Justin ; Warner, Andrew ; del Rivero, Jaydira ; Sadowski, Samira M ; Nilubol, Naris ; Schmidt, Laura S ; Linehan, W Marston ; Weinstein, Lee S ; Simonds, William F ; Agarwal, Sunita K

The journal of clinical endocrinology and metabolism, 2023-09, Vol.108 (10), p.2686-2698 [Periódico revisado por pares]

US: Oxford University Press

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6
Hereditary Leiomyomatosis Associated with Bilateral, Massive, Macronodular Adrenocortical Disease and Atypical Cushing Syndrome: A Clinical and Molecular Genetic Investigation
Hereditary Leiomyomatosis Associated with Bilateral, Massive, Macronodular Adrenocortical Disease and Atypical Cushing Syndrome: A Clinical and Molecular Genetic Investigation
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Hereditary Leiomyomatosis Associated with Bilateral, Massive, Macronodular Adrenocortical Disease and Atypical Cushing Syndrome: A Clinical and Molecular Genetic Investigation

Matyakhina, Ludmila ; Freedman, Reneé J ; Bourdeau, Isabelle ; Wei, Ming-Hui ; Stergiopoulos, Sotirios G ; Chidakel, Aaron ; Walther, McClellan ; Abu-Asab, Mones ; Tsokos, Maria ; Keil, Meg ; Toro, Jorge ; Linehan, W. Marston ; Stratakis, Constantine A

The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3773-3779 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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7
Predictive Value of Preoperative Tests in Discriminating Bilateral Adrenal Hyperplasia from an Aldosterone-Producing Adrenal Adenoma
Predictive Value of Preoperative Tests in Discriminating Bilateral Adrenal Hyperplasia from an Aldosterone-Producing Adrenal Adenoma
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Predictive Value of Preoperative Tests in Discriminating Bilateral Adrenal Hyperplasia from an Aldosterone-Producing Adrenal Adenoma

Phillips, John L ; Walther, McClellan M ; Pezzullo, John C ; Rayford, Walter ; Choyke, Peter L ; Berman, Arlene A ; Linehan, W. Marston ; Doppman, John L ; Gill Jr, John R

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4526-4533 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
p53 mutations in human adrenocortical neoplasms: immunohistochemical and molecular studies
p53 mutations in human adrenocortical neoplasms: immunohistochemical and molecular studies
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p53 mutations in human adrenocortical neoplasms: immunohistochemical and molecular studies

Reincke, M ; Karl, M ; Travis, W H ; Mastorakos, G ; Allolio, B ; Linehan, H M ; Chrousos, G P

The journal of clinical endocrinology and metabolism, 1994-03, Vol.78 (3), p.790-794 [Periódico revisado por pares]

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9
p53 Mutations in human adrenocortical neoplasms : immunohistochemical and molecular studies
p53 Mutations in human adrenocortical neoplasms : immunohistochemical and molecular studies
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p53 Mutations in human adrenocortical neoplasms : immunohistochemical and molecular studies

REINCKE, M ; KARL, M ; TRAVIS, W. H ; MASTORAKOS, G ; ALLOLIO, B ; LINEHAN, H. M ; CHROUSOS, G. P

Journal of Clinical Endocrinology and Metabolism, 1994-03, Vol.78 (3), p.790-794 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
In silico VHL Gene Mutation Analysis and Prognosis of Pancreatic Neuroendocrine Tumors in von Hippel–Lindau Disease
In silico VHL Gene Mutation Analysis and Prognosis of Pancreatic Neuroendocrine Tumors in von Hippel–Lindau Disease
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In silico VHL Gene Mutation Analysis and Prognosis of Pancreatic Neuroendocrine Tumors in von Hippel–Lindau Disease

Tirosh, Amit ; el Lakis, Mustapha ; Green, Patience ; Nockel, Pavel ; Patel, Dhaval ; Nilubol, Naris ; Gara, Sudheer Kumar ; Keutgen, Xavier M ; Linehan, W Marston ; Kebebew, Electron

The journal of clinical endocrinology and metabolism, 2018-04, Vol.103 (4), p.1631-1638 [Periódico revisado por pares]

Washington, DC: Endocrine Society

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