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Immunohistochemistry for SDHB triages genetic testing of SDHB , SDHC , and SDHD in paraganglioma-pheochromocytoma syndromes

Human pathology, 2010-06, Vol.41 (6), p.805-814

2010

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Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors

The American journal of surgical pathology, 2013-02, Vol.37 (2), p.226-233

2013

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Breast cancer-associated fibroblasts induce epithelial-to-mesenchymal transition in breast cancer cells

Endocrine-related cancer, 2013-02, Vol.20 (1), p.1-12

2013

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TERT structural rearrangements in metastatic pheochromocytomas

Endocrine-related cancer, 2018-01, Vol.25 (1), p.1-9

2018

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Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

The New England journal of medicine, 2011-03, Vol.364 (9), p.885-886

2011

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Pheochromocytoma: Current Approaches and Future Directions

The oncologist (Dayton, Ohio), 2008-07, Vol.13 (7), p.779-793

2008

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Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma

BMC cancer, 2017-07, Vol.17 (1), p.497-497, Article 497

2017

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MicroRNA profiling of benign and malignant pheochromocytomas identifies novel diagnostic and therapeutic targets

Endocrine-related cancer, 2010-09, Vol.17 (3), p.835-846

2010

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Utility of the succinate:fumarate ratio for assessing SDH dysfunction in different tumor types

Molecular genetics and metabolism reports, 2017-03, Vol.10 (C), p.45-49

2017

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Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Nature reviews. Endocrinology, 2017-04, Vol.13 (4), p.233-247

2017

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Outcomes of SDHB Pathogenic Variant Carriers

The journal of clinical endocrinology and metabolism, 2024-08, Vol.109 (9), p.2400-2410

2024

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The Utility of Metaiodobenzylguanidine Single Photon Emission Computed Tomography/Computed Tomography (MIBG SPECT/CT) for the Diagnosis of Pheochromocytoma

Annals of surgical oncology, 2010-02, Vol.17 (2), p.392-400

2010

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Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients

The American journal of surgical pathology, 2014-12, Vol.38 (12), p.1588-1602

2014

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Surveillance Improves Outcomes for Carriers of SDHB Pathogenic Variants: A Multicenter Study

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.e1907-e1916

2022

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Familial SDHA Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma

The journal of clinical endocrinology and metabolism, 2013-06, Vol.98 (6), p.E1103-E1108

2013

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A Clinicopathologic and Molecular Analysis of Fumarate Hydratase-deficient Pheochromocytoma and Paraganglioma

The American journal of surgical pathology, 2023-01, Vol.47 (1), p.25-36

2023

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Bayesian approach to determining penetrance of pathogenic SDH variants

Journal of medical genetics, 2018-11, Vol.55 (11), p.729-734

2018

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Renal tumors associated with germline SDHB mutation show distinctive morphology

The American journal of surgical pathology, 2011-10, Vol.35 (10), p.1578-1585

2011

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Functional significance of germline EPAS1 variants

Endocrine-related cancer, 2021-02, Vol.28 (2), p.97-109

2021

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Distortion in transmission of pathogenic SDHB- and SDHD-mutated alleles from parent to offspring

Endocrine-related cancer, 2023-05, Vol.30 (5), p.1

2023

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Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

Oncogene, 2003-03, Vol.22 (9), p.1358-1364

2003

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Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types

The American journal of surgical pathology, 2010-05, Vol.34 (5), p.636-644

2010

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Genetic Testing in Pheochromocytoma- and Paraganglioma-Associated Syndromes

Annals of the New York Academy of Sciences, 2006-08, Vol.1073 (1), p.104-111

2006

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Clinical Presentation and Penetrance of Pheochromocytoma/Paraganglioma Syndromes

The journal of clinical endocrinology and metabolism, 2006-03, Vol.91 (3), p.827-836

2006

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Succinate dehydrogenase deficiency is rare in pituitary adenomas

The American journal of surgical pathology, 2014-04, Vol.38 (4), p.560-566

2014

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Immunohistochemistry for SDHB triages genetic testing of SDHB , SDHC , and SDHD in paraganglioma-pheochromocytoma syndromes

Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors

Breast cancer-associated fibroblasts induce epithelial-to-mesenchymal transition in breast cancer cells

TERT structural rearrangements in metastatic pheochromocytomas

Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

Pheochromocytoma: Current Approaches and Future Directions

Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma

MicroRNA profiling of benign and malignant pheochromocytomas identifies novel diagnostic and therapeutic targets

Utility of the succinate:fumarate ratio for assessing SDH dysfunction in different tumor types

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Outcomes of SDHB Pathogenic Variant Carriers

The Utility of Metaiodobenzylguanidine Single Photon Emission Computed Tomography/Computed Tomography (MIBG SPECT/CT) for the Diagnosis of Pheochromocytoma

Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients

Surveillance Improves Outcomes for Carriers of SDHB Pathogenic Variants: A Multicenter Study

Familial SDHA Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma

A Clinicopathologic and Molecular Analysis of Fumarate Hydratase-deficient Pheochromocytoma and Paraganglioma

Bayesian approach to determining penetrance of pathogenic SDH variants

Renal tumors associated with germline SDHB mutation show distinctive morphology

Functional significance of germline EPAS1 variants

Distortion in transmission of pathogenic SDHB- and SDHD-mutated alleles from parent to offspring

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types

Genetic Testing in Pheochromocytoma- and Paraganglioma-Associated Syndromes

Clinical Presentation and Penetrance of Pheochromocytoma/Paraganglioma Syndromes

Succinate dehydrogenase deficiency is rare in pituitary adenomas

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