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Virchows Archiv, ISSN 0945-6317, 10/2019, Volume 475, Issue 4, pp. 533 - 533
It has been identified that one of the dosages listed within the above article was incorrectly abbreviated during the production process. This is now presented... 
Medicine & Public Health | Pathology | Intestine | Leukocytes (eosinophilic)
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2007, Volume 357, Issue 3, pp. 306 - 308
To the Editor: As many as 25% of pheochromocytomas — catecholamine-producing tumors located along the sympathetic nervous system, including the adrenals —... 
GERM-LINE MUTATIONS | GENE | MEDICINE, GENERAL & INTERNAL | Succinate Dehydrogenase - genetics | Urinary Bladder Neoplasms - genetics | DNA Mutational Analysis | Humans | Iron-Sulfur Proteins - genetics | Adult | Female | Pheochromocytoma - genetics | Loss of Heterozygosity
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 10/2018, Volume 179, Issue 4, p. G1
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing tumor with variable prognosis. The purpose of these guidelines is to... 
Histopathology | Surgery | Etoposide | Radiation measurement | Radiation therapy | Metastasis | Management | Doxorubicin | Patients | Cisplatin | Tumors | Metastases
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 607 - 612
Journal Article
Nederlands Tijdschrift voor Geneeskunde, ISSN 0028-2162, 2015, Volume 159, Issue 46
Journal Article
European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, 2012, Volume 39, Issue 12, pp. 1977 - 1995
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2011, Volume 108, Issue 1, pp. 314 - 318
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2009, Volume 10, Issue 8, pp. 764 - 771
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 05/2012, Volume 18, Issue 10, pp. 2828 - 2837
Journal Article
CANCERS, ISSN 2072-6694, 08/2019, Volume 11, Issue 8, p. 1070
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors that arise in the adrenal medulla and in extra-adrenal locations, such as the... 
pheochromocytoma | MARKERS | SDHB | paraganglioma | scoring system | MAX MUTATIONS | SPORADIC PHEOCHROMOCYTOMA | tumor classification | H-RAS | PASS | HEREDITARY | ONCOLOGY | PREDISPOSITION | GERMLINE MUTATIONS | GAPP | SPECTRUM | IMMUNOHISTOCHEMISTRY
Journal Article
The Journal of Nuclear Medicine, ISSN 0161-5505, 11/2015, Volume 56, Issue 11, p. 1647
  Pancreatic neuroendocrine tumors (NETs) are rare neoplasms for which surgery has almost the only potential for cure. When surgery is not possible because of... 
Nuclear medicine | Medical treatment | Metastasis | Pancreas | Tumors
Journal Article
Endocrine-Related Cancer, ISSN 1351-0088, 08/2015, Volume 22, Issue 4, pp. T123 - T133
Pathologists using their routine diagnostic tools can contribute both to the care of patients with pheochromocytoma/paraganglioma and to understanding the... 
Immunohistochemistry | Pathology | PASS | Oncology | Cancer Research | Histology | GAPP | Endocrinology, Diabetes and Metabolism | Endocrinology | pathology | NEUROENDOCRINE | CLINICAL-FEATURES | SDHD | TUMORS | SUSTENTACULAR CELLS | histology | GENE | ONCOLOGY | ENDOCRINOLOGY & METABOLISM | immunohistochemistry | MUTATIONS | NEUROFIBROMATOSIS TYPE-1 | S100 PROTEIN
Journal Article
Journal Article