4.7 Article

Inherited Mutations in Pheochromocytoma and Paraganglioma: Why All Patients Should Be Offered Genetic Testing

Related references

Note: Only part of the references are listed.
Article Oncology

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Nelly Burnichon et al.

CLINICAL CANCER RESEARCH (2012)

Review Endocrinology & Metabolism

Perioperative Management of Pheochromocytoma/Paraganglioma: Is There a State of the Art?

M. Mannelli et al.

HORMONE AND METABOLIC RESEARCH (2012)

Article Oncology

SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma

Henricus P. M. Kunst et al.

CLINICAL CANCER RESEARCH (2011)

Article Endocrinology & Metabolism

Germline Mutations of the TMEM127 Gene in Patients with Paraganglioma of Head and Neck and Extraadrenal Abdominal Sites

Hartmut P. H. Neumann et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)

Article Endocrinology & Metabolism

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

Esther Korpershoek et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)

Review Peripheral Vascular Disease

Cardiovascular manifestations of phaeochromocytoma

Aleksander Prejbisz et al.

JOURNAL OF HYPERTENSION (2011)

Article Genetics & Heredity

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Inaki Comino-Mendez et al.

NATURE GENETICS (2011)

Article Biochemistry & Molecular Biology

SDHA is a tumor suppressor gene causing paraganglioma

Nelly Burnichon et al.

HUMAN MOLECULAR GENETICS (2010)

Article Medicine, General & Internal

Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas

Li Yao et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)

Article Oncology

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

Jean-Pierre Bayley et al.

LANCET ONCOLOGY (2010)

Article Genetics & Heredity

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

Yuejuan Qin et al.

NATURE GENETICS (2010)

Review Oncology

Clinical aspects of SDHx-related pheochromocytoma and paraganglioma

Henri J. L. M. Timmers et al.

ENDOCRINE-RELATED CANCER (2009)

Article Endocrinology & Metabolism

Genetics of Pheochromocytoma and Paraganglioma in Spanish Patients

Alberto Cascon et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)

Article Endocrinology & Metabolism

Clinically Guided Genetic Screening in a Large Cohort of Italian Patients with Pheochromocytomas and/or Functional or Nonfunctional Paragangliomas

Massimo Mannelli et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)

Article Endocrinology & Metabolism

The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas

Nelly Burnichon et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)

Review Endocrinology & Metabolism

Current progress and future challenges in the biochemical diagnosis and treatment of pheochromocytomas and paragangliomas

G. Eisenhofer et al.

HORMONE AND METABOLIC RESEARCH (2008)

Article Otorhinolaryngology

Malignant head and neck paragangliomas in SDHB mutation carriers

Carsten Christof Boedeker et al.

OTOLARYNGOLOGY-HEAD AND NECK SURGERY (2007)

Review Genetics & Heredity

Guidelines for the diagnosis and management of individuals with neurofibromatosis 1

Rosalie E. Ferner et al.

JOURNAL OF MEDICAL GENETICS (2007)

Article Endocrinology & Metabolism

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas:: Implications for genetic testing

Frederieke M. Brouwers et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)

Article Endocrinology & Metabolism

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes

DE Benn et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)

Article Oncology

Genetic testing in pheochromocytoma or functional paraganglioma

L Amar et al.

JOURNAL OF CLINICAL ONCOLOGY (2005)

Review Oncology

SDHC mutations in hereditary paraganglioma/pheochromocytoma

U Muller et al.

FAMILIAL CANCER (2005)

Article Medicine, General & Internal

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

HPH Neumann et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)

Correction Medicine, General & Internal

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations (vol 292, pg 943, 2004)

HPH Neumann

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)

Article Medicine, General & Internal

Germ-line mutations in nonsyndromic pheochromocytoma.

HPH Neumann et al.

NEW ENGLAND JOURNAL OF MEDICINE (2002)

Article Genetics & Heredity

Mutations in SDHC cause autosomal dominant paraganglioma, type 3

S Niemann et al.

NATURE GENETICS (2000)

Article Multidisciplinary Sciences

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

BE Baysal et al.

SCIENCE (2000)