SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

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Phaeochromocytoma

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Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

Astuti, D., Latif, F., Dallol, A., Dahia, P. L. M., Douglas, F., George, E., Sköldberg, F., Husebye, E. S., Eng, C., & Maher, E. R. (2001) · The American Journal of Human Genetics · doi:10.1086/321282 · Cited by 1,087

Mutations in SDHC cause autosomal dominant paraganglioma, type 3

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Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

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SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma

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SDHA is a tumor suppressor gene causing paraganglioma

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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

van Nederveen, F. H., Gaal, J., Favier, J., Korpershoek, E., Oldenburg, R. A., de Bruyn, E. M., Sleddens, H. F. B. M., Derkx, P., Rivière, J., Dannenberg, H., et al. (2009) · The Lancet Oncology · doi:10.1016/s1470-2045(09)70164-0 · Cited by 554

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

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Succinate dehydrogenase and fumarate reductase from Escherichia coli

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Recent developments in eosinophilic renal neoplasms: what's new, true and important?

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Diagnosis and Management of Hereditary Phaeochromocytoma and Paraganglioma

Lalloo, F. I. (2016) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-319-29998-3_7 · Cited by 6

Renal Cell Tumors: Molecular Findings Reshaping Clinico-pathological Practice

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SDHx mutation and pituitary adenoma: can in vivo 1H-MR spectroscopy unravel the link?

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Familial endocrine tumours: pheochromocytomas and extra-adrenal paragangliomas – an update

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Histopathology of Parasellar Neoplasms

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Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas

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Heritable and Syndromic Pheochromocytoma and Paraganglioma

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First-positive surveillance screening in an asymptomatic SDHA germline mutation carrier

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Molecular pathology of endocrine gland tumors: genetic alterations and clinicopathologic relevance

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A Pathologist’s View: Molecular Profiles for Diagnosing Pheochromocytomas and Paragangliomas

Kimura, N. (2015) · International Journal of Endocrine Oncology · doi:10.2217/ije.15.16 · Cited by 5

Neuroendocrine Neoplasms, Olfactory Neuroblastomas and Paragangliomas of the Head and Neck

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Outcomes of Carotid Body Tumor Management with Active Surveillance

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Données récentes sur l’hypertension endocrine

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Progressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum

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Syndromes that link the endocrine system and genitourinary tract

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Hereditary Neuroendocrine Tumor Syndromes

Faggiano, A., Ramundo, V., Circelli, L., & Colao, A. (2013) · InTech eBooks · doi:10.5772/53841 · Cited by 4

Implications of SDHB genetic testing in patients with sporadic pheochromocytoma

Maignan, A., Guérin, C., Julliard, V., Paladino, N. C., Kim, E., Roche, P., Castinetti, F., Essamet, W., Mancini, J., Impériale, A., et al. (2017) · Langenbeck s Archives of Surgery · doi:10.1007/s00423-017-1564-y · Cited by 4

Successful response to pegylated interferon alpha in a patient with recurrent paraganglioma

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Neue WHO-Klassifikation 2022: Harnblasenkarzinom

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Diagnosis, Genetics, and Management of 24 Patients With Cardiac Paragangliomas: Experience From a Single Center

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Paraganglioma of the tongue with SDHB gene mutation in a patient with Graves’ disease

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Somatic SDHA mutations in paragangliomas in siblings

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Feocromocitoma-Paraganglioma: revisión de tema

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A case of Carney triad complicated by renal cell carcinoma and a germline SDHA pathogenic variant

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Pheochromocytoma and Paraganglioma

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Consultation génétique des phéochromocytomes et paragangliomes

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Síndrome de feocromocitoma-paraganglioma tipo 5 asociado a mutación en el complejo de la succinato deshidrogenasa tipo A (SDHA), a propósito de un caso

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Molecular uropathology: what a practising pathologist should know

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Mitochondrial Respiratory Chain Complex II

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Apport du pathologiste dans les prédispositions héréditaires aux paragangliomes et phéochromocytomes

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Pathology of Pheochromocytoma and Paraganglioma

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A Novel Germline SDHA Gene Mutation and Co-Occurring Somatic KIT Activating Mutation in a Patient With Pediatric Central Nervous System Germ Cell Tumor: Case Report

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Genetic Alterations in Pheochromocytoma and Paraganglioma

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Paragangliomas of the head and neck region

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Carney-Stratakis Syndrome presenting as occult mediastinal paraganglioma

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A Case for Genetic Testing in Isolated Tympanic Paragangliomas

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Impact of compound heterozygous SDHA variants on mitochondrial function in pediatric with neurological disease

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Soft-Tissue Tumors of the Head and Neck

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Bilateral Pheochromocytoma with Germline MAX Variant without Family History

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Exome sequencing and SDH (A, B) immunohistochemistry of canine Pheochromocytomas

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Back to Biochemistry

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Translating Genetic Data into Actionable Clinical Guidelines: Succinate Dehydrogenase Subunit A Variants of Unknown Significance in Gastrointestinal Stromal Tumors

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SDHB mutated paraganglioma imitating thyroid tumor: A case report and review of literature

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Paragangliomas and Pheochromocytomas

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Pheochromocytomas, Paragangliomas, and Pituitary Adenomas (3PAs) and Succinate Dehydrogenase Defects

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SDH assembly in S. cerevisiae: focus on the functional role of SDH6

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La génétique des paragangliomes

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Genetic and molecular background of pheochromocytoma and paraganglioma

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Hereditary Paraganglioma and Pheochromocytoma

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Paragangliomas carotídeos: hacia un tratamiento personalizado que reduzca la morbilidad

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Pheochromocytomas and Paragangliomas: Genetics and Pathophysiology

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Familial Head and Neck Paraganglioma and Genetic Testing

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The Role of TMEM127 in mTOR Pathway and Cancer Suppression

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Pheochromocytomas, Paragangliomas, and Pituitary Adenomas (3PAs) and Succinate Dehydrogenase Defects

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Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma

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Succinate Dehydrogenase Mutation and Paraganglioma Syndromes: A Review Article

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Pheochromocytoma and Adrenal Medullary Hyperplasia

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Familial and Syndrome-Related Pheochromocytoma and Paraganglioma

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Case report of a succinate dehydrogenase-deficient renal cell carcinoma

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Current Understanding of Carotid Body Paraganglioma Management

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Pheochromocytoma & Paraganglioma

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Potential Pitfalls of SDH Immunohistochemical Detection in Paragangliomas and Phaeochromocytomas Harbouring Germline SDHx Gene Mutation

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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

van Nederveen, F. H., Gaal, J., Favier, J., Korpershoek, E., Oldenburg, R. A., de Bruyn, E. M., Sleddens, H. F. B. M., Derkx, P., Rivière, J., Dannenberg, H., et al. (2009) · The Lancet Oncology · doi:10.1016/s1470-2045(09)70164-0 · Cited by 554

SDHD Immunohistochemistry: A New Tool to ValidateSDHxMutations in Pheochromocytoma/Paraganglioma

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Usefulness of Negative and Weak–Diffuse Pattern of SDHB Immunostaining in Assessment of SDH Mutations in Paragangliomas and Pheochromocytomas

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