标题
Paraganglioma and phaeochromocytoma: from genetics to personalized medicine
作者
关键词
-
出版物
Nature Reviews Endocrinology
Volume 11, Issue 2, Pages 101-111
出版商
Springer Nature
发表日期
2014-11-11
DOI
10.1038/nrendo.2014.188
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- SDHBmutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paraganglioma
- (2014) Julien Hadoux et al. INTERNATIONAL JOURNAL OF CANCER
- The Clinical Phenotype ofSDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)
- (2014) Tobias Else et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- H-RAS Mutations Are Restricted to Sporadic Pheochromocytomas Lacking Specific Clinical or Pathological Features: Data From a Multi-Institutional Series
- (2014) Lindsey Oudijk et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Pitfalls in Genetic Analysis of Pheochromocytomas/Paragangliomas—Case Report
- (2014) Letizia Canu et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Phenotypic Variability and Risk of Malignancy inSDHC-Linked Paragangliomas: Lessons From Three Unrelated Cases With an Identical Germline Mutation (p.Arg133*)
- (2014) Julia K. Bickmann et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Rare Germline Mutations Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma
- (2014) Jenny Welander et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline
- (2014) Jacques W. M. Lenders et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- Mitochondrial complex II and genomic imprinting in inheritance of paraganglioma tumors
- (2013) Bora E. Baysal BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma
- (2013) Eric Letouzé et al. CANCER CELL
- Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas
- (2013) Aideen M. McInerney-Leo et al. CLINICAL ENDOCRINOLOGY
- Combined Inhibition of mTORC1 and mTORC2 Signaling Pathways Is a Promising Therapeutic Option in Inhibiting Pheochromocytoma Tumor Growth: In Vitro and In Vivo Studies in Female Athymic Nude Mice
- (2013) Alessio Giubellino et al. ENDOCRINOLOGY
- Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families
- (2013) Kory W. Jasperson et al. Familial Cancer
- Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas
- (2013) Luis Jaime Castro-Vega et al. HUMAN MOLECULAR GENETICS
- The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal function
- (2013) Y. Qin et al. HUMAN MOLECULAR GENETICS
- The Characterization of Pheochromocytoma and Its Impact on Overall Survival in Multiple Endocrine Neoplasia Type 2
- (2013) Sonali Thosani et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Somatic Mutations inH-RASin Sporadic Pheochromocytoma and Paraganglioma Identified by Exome Sequencing
- (2013) Joakim Crona et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Mosaicism inHIF2A-Related Polycythemia-Paraganglioma Syndrome
- (2013) Alexandre Buffet et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Long-Term Outcomes of Surgical Treatment for Hereditary Pheochromocytoma
- (2013) Elizabeth G. Grubbs et al. JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS
- Succinate Dehydrogenase Mutation Underlies Global Epigenomic Divergence in Gastrointestinal Stromal Tumor
- (2013) J. Keith Killian et al. Cancer Discovery
- Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma
- (2013) Joakim Crona et al. Endocrine Connections
- Phase 2 study of everolimus monotherapy in patients with nonfunctioning neuroendocrine tumors or pheochromocytomas/paragangliomas
- (2012) Do-Youn Oh et al. CANCER
- MAX and MYC: A Heritable Breakup
- (2012) A. Cascon et al. CANCER RESEARCH
- MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
- (2012) N. Burnichon et al. CLINICAL CANCER RESEARCH
- EANM 2012 guidelines for radionuclide imaging of phaeochromocytoma and paraganglioma
- (2012) David Taïeb et al. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
- A Decade (2001-2010) of Genetic Testing for Pheochromocytoma and Paraganglioma
- (2012) A. Buffet et al. HORMONE AND METABOLIC RESEARCH
- Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas
- (2012) Jenny Welander et al. HUMAN MOLECULAR GENETICS
- Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma
- (2012) Nelly Burnichon et al. HUMAN MOLECULAR GENETICS
- Epithelial to Mesenchymal Transition Is Activated in Metastatic Pheochromocytomas and Paragangliomas Caused bySDHBGene Mutations
- (2012) Céline Loriot et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Treatment with Sunitinib for Patients with Progressive Metastatic Pheochromocytomas and Sympathetic Paragangliomas
- (2012) Montserrat Ayala-Ramirez et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- TMEM127Screening in a Large Cohort of Patients with Pheochromocytoma and/or Paraganglioma
- (2012) Nassera Abermil et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Imaging Work-Up for Screening of Paraganglioma and Pheochromocytoma inSDHxMutation Carriers: A Multicenter Prospective Study from the PGL.EVA Investigators
- (2012) Anne-Paule Gimenez-Roqueplo et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Risk of malignant paraganglioma in SDHB-mutation and SDHD-mutation carriers: a systematic review and meta-analysis
- (2012) Leonie Theresia van Hulsteijn et al. JOURNAL OF MEDICAL GENETICS
- Staging and Functional Characterization of Pheochromocytoma and Paraganglioma by 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography
- (2012) Henri J. L. M. Timmers et al. JNCI-Journal of the National Cancer Institute
- Loss of expression of SDHA predicts SDHA mutations in gastrointestinal stromal tumors
- (2012) Andrew J Wagner et al. MODERN PATHOLOGY
- HIF2AMutations in Paraganglioma with Polycythemia
- (2012) NEW ENGLAND JOURNAL OF MEDICINE
- SomaticHIF2AGain-of-Function Mutations in Paraganglioma with Polycythemia
- (2012) Zhengping Zhuang et al. NEW ENGLAND JOURNAL OF MEDICINE
- von Hippel–Lindau disease: A clinical and scientific review
- (2011) Eamonn R Maher et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia
- (2011) C. Ladroue et al. HAEMATOLOGICA
- SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
- (2011) Esther Korpershoek et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Metastatic Pheochromocytoma/Paraganglioma Related to Primary Tumor Development in Childhood or Adolescence: Significant Link toSDHBMutations
- (2011) Kathryn S. King et al. JOURNAL OF CLINICAL ONCOLOGY
- Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status
- (2011) Chiara Bardella et al. JOURNAL OF PATHOLOGY
- Minimally invasive cortical-sparing surgery for bilateral pheochromocytomas
- (2011) Pier Francesco Alesina et al. LANGENBECKS ARCHIVES OF SURGERY
- Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
- (2011) Iñaki Comino-Méndez et al. NATURE GENETICS
- SDHA is a tumor suppressor gene causing paraganglioma
- (2010) Nelly Burnichon et al. HUMAN MOLECULAR GENETICS
- Prognostic Factors of Disease-Free Survival after Thyroidectomy in 170 Young Patients with a RET Germline Mutation: A Multicenter Study of the Groupe Français d'Etude des Tumeurs Endocrines
- (2010) V. Rohmer et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related Pheochromocytomas
- (2010) Elena López-Jiménez et al. MOLECULAR ENDOCRINOLOGY
- Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
- (2010) Yuejuan Qin et al. NATURE GENETICS
- Nebennierenresektion zum Erhalt der adrenokortikalen Funktion
- (2009) M.K. Walz CHIRURG
- Novel and Evolving Therapies in the Treatment of Malignant Phaeochromocytoma: Experience with the mTOR Inhibitor Everolimus (RAD001)
- (2009) M. R. Druce et al. HORMONE AND METABOLIC RESEARCH
- Comparison of18F-Fluoro-L-DOPA,18F-Fluoro-Deoxyglucose, and18F-Fluorodopamine PET and123I-MIBG Scintigraphy in the Localization of Pheochromocytoma and Paraganglioma
- (2009) Henri J. L. M. Timmers et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Isocitrate Dehydrogenase Mutations Are Rare in Pheochromocytomas and Paragangliomas
- (2009) José Gaal et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes
- (2009) B. Pasini et al. JOURNAL OF INTERNAL MEDICINE
- An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
- (2009) Francien H van Nederveen et al. LANCET ONCOLOGY
- The Warburg Effect Is Genetically Determined in Inherited Pheochromocytomas
- (2009) Judith Favier et al. PLoS One
- SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma
- (2009) H.-X. Hao et al. SCIENCE
- Medullary Thyroid Cancer: Management Guidelines of the American Thyroid Association
- (2009) Richard T. Kloos (Chair) et al. THYROID
- The kinesin KIF1B acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor
- (2008) S. Schlisio et al. GENES & DEVELOPMENT
- Rationale and Evidence for Sunitinib in the Treatment of Malignant Paraganglioma/Pheochromocytoma
- (2008) Anthony M. Joshua et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Use of the Tyrosine Kinase Inhibitor Sunitinib in a Patient with von Hippel-Lindau Disease: Targeting Angiogenic Factors in Pheochromocytoma and Other von Hippel-Lindau Disease-Related Tumors
- (2008) Camilo Jimenez et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Patient With Malignant Paraganglioma Responding to the Multikinase Inhibitor Sunitinib Malate
- (2008) Noah M. Hahn et al. JOURNAL OF CLINICAL ONCOLOGY
- Germline SDHB Mutations and Familial Renal Cell Carcinoma
- (2008) C. Ricketts et al. JNCI-Journal of the National Cancer Institute
- Health Supervision for Children With Neurofibromatosis
- (2008) J. H. Hersh et al. PEDIATRICS
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