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Cytogenetic and p53 Profiles in Congenital Cystic Adenomatoid Malformation: Insights into its Relationship with Pleuropulmonary Blastoma.
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- Pediatric & Developmental Pathology, 2006, v. 9, n. 3, p. 190, doi. 10.2350/06-01-0025.1
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- Article
Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics.
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- 2019
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- Publication type:
- journal article
Metabolomics, machine learning and immunohistochemistry to predict succinate dehydrogenase mutational status in phaeochromocytomas and paragangliomas.
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- Journal of Pathology, 2020, v. 251, n. 4, p. 378, doi. 10.1002/path.5472
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- Article
The mTORC1 Complex Is Significantly Overactivated in SDHX -Mutated Paragangliomas.
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- Neuroendocrinology, 2017, v. 105, n. 4, p. 384, doi. 10.1159/000455864
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- Article
Catecholamine-Synthesizing Enzymes Are Expressed in Parasympathetic Head and Neck Paraganglioma Tissue.
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- Neuroendocrinology, 2015, v. 101, n. 4, p. 289, doi. 10.1159/000377703
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- Article
Conditional Pten knock-out mice: a model for metastatic phaeochromocytoma.
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- Journal of Pathology, 2009, v. 217, n. 4, p. 597, doi. 10.1002/path.2492
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- Article
Assessment of VAV2 Expression Refines Prognostic Prediction in Adrenocortical Carcinoma.
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- 2017
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- journal article
Identification of Mutations in Cell-Free Circulating Tumor DNA in Adrenocortical Carcinoma: A Case Series.
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- 2017
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- journal article
DNA Methylation Is an Independent Prognostic Marker of Survival in Adrenocortical Cancer.
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- 2016
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- journal article
Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis.
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- 2016
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- journal article
Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.
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- 2015
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- journal article
H-RAS Mutations Are Restricted to Sporadic Pheochromocytomas Lacking Specific Clinical or Pathological Features: Data From a Multi-Institutional Series.
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- 2014
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- Publication type:
- Journal Article
SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas.
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- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. E1472, doi. 10.1210/jc.2011-1043
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- Article
Heat Shock Protein 90 as a Prognostic Marker and Therapeutic Target for Adrenocortical Carcinoma.
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- Frontiers in Endocrinology, 2019, p. 1, doi. 10.3389/fendo.2019.00487
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- Article
Vascular Pattern Analysis for the Prediction of Clinical Behaviour in Pheochromocytomas and Paragangliomas.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0121361
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- Article
Isocitrate Dehydrogenase Mutations Are Rare in Pheochromocytomas and Paragangliomas.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 3, p. 1274, doi. 10.1210/jc.2009-2170
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- Article
Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.
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- 2009
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- Publication type:
- journal article
Frequent Genetic Changes in Childhood Pheochromocytomas.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 166, doi. 10.1196/annals.1353.017
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- Article
The Occurrence of SDHB Gene Mutations in Pheochromocytoma.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 177, doi. 10.1196/annals.1353.018
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- Article
Molecular Alterations in Dog Pheochromocytomas and Paragangliomas.
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- Cancers, 2019, v. 11, n. 5, p. 607, doi. 10.3390/cancers11050607
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- Article
Treatment of inoperable or metastatic paragangliomas and pheochromocytomas with peptide receptor radionuclide therapy using <sup>177</sup>Lu-DOTATATE.
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- European Journal of Endocrinology, 2019, v. 181, n. 1, p. 45, doi. 10.1530/EJE-18-0901
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- Article
False-positive findings on 6-[<sup>18</sup>F]fluor-l-3,4- dihydroxyphenylalanine PET (18F-FDOPA-PET) performed for imaging of neuroendocrine tumors.
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- European Journal of Endocrinology, 2018, v. 179, n. 2, p. 125, doi. 10.1530/EJE-18-0321
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- Article
Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC-PGL syndromes: a clinicopathological and molecular analysis.
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- European Journal of Endocrinology, 2014, v. 170, n. 1, p. 1, doi. 10.1530/EJE-13-0623
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- Article
Neurofibromas in LZTR1 schwannomatosis.
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- Clinical Genetics, 2022, v. 101, n. 5/6, p. 571, doi. 10.1111/cge.14121
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- Article
Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma.
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- Frontiers in Endocrinology, 2023, v. 14, p. 01, doi. 10.3389/fendo.2022.1070074
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- Article
Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas.
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- PLoS ONE, 2022, v. 17, n. 9, p. 1, doi. 10.1371/journal.pone.0274478
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- Article
Nonmosaic somatic HIF2A mutations associated with late onset polycythemia‐paraganglioma syndrome: Newly recognized subclass of polycythemia‐paraganglioma syndrome.
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- Cancer (0008543X), 2019, v. 125, n. 8, p. 1258, doi. 10.1002/cncr.31839
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- Article
Nonmosaic somatic HIF2A mutations associated with late onset polycythemia-paraganglioma syndrome: Newly recognized subclass of polycythemia-paraganglioma syndrome.
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- 2019
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- Publication type:
- journal article
High‐yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing.
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- Human Mutation, 2022, v. 43, n. 12, p. 2130, doi. 10.1002/humu.24487
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- Article
Murine Models and Cell Lines for the Investigation of Pheochromocytoma: Applications for Future Therapies?
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- Endocrine Pathology, 2012, v. 23, n. 1, p. 43, doi. 10.1007/s12022-012-9194-y
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- Article
Expression of GAD67 and Novel GAD67 Splice Variants During Human Fetal Pancreas Development.
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- Endocrine Pathology, 2007, v. 18, n. 2, p. 31, doi. 10.1007/s12022-007-0003-y
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- Article
New developments in the detection of the clinical behavior of pheochromocytomas and paragangliomas.
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- Endocrine Pathology, 2006, v. 17, n. 2, p. 137, doi. 10.1385/EP:17:2:137
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- Article
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.
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- BMC Medical Genetics, 2014, v. 15, n. 1, p. 2, doi. 10.1186/s12881-014-0111-8
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- Article