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European Journal of Endocrinology, ISSN 0804-4643, 10/2016, Volume 174, Issue 10, p. 311
Background Genetic aetiology of pheochromocytoma (PCC) and paraganglioma (PGL) is increasingly being studied; however, Asian Indian data on this aspect are... 
Genotype & phenotype | Phenotypes | Pheochromocytoma | Paraganglioma | VHL protein | Metastasis | Mutation | Genotypes | Tumors | Metastases
Journal Article
Cancer Biology & Therapy, ISSN 1538-4047, 12/2017, Volume 18, Issue 12, pp. 944 - 947
In this study, we report here a rare case of polycythemia and cRCC in the same patient, which may be helpful in understanding clinical features and molecular... 
polycythemia | renal carcinoma | VHL | HIF2A | GENE | ONCOLOGY | EXON-12 | Index Medicus
Journal Article
The Journal of Nuclear Medicine, ISSN 0161-5505, 05/2018, Volume 59, p. 1306
Background: Pheochromocytomas/paragangliomas (PHEO/PGL) are extremely rare and their evaluation and management is very challenging. Currently, 68Ga-DOTATATE... 
Nuclear medicine | Evaluation | Succinate dehydrogenase | Pheochromocytoma | Positron emission | Paraganglioma | Males | Patients | Subgroups | Incidence | Histopathology | Magnetic resonance imaging | Computed tomography | Cysts | Kidney cancer | Tomography | VHL protein | Mutation | Lesions | Neoplasia | Females | Clear cell-type renal cell carcinoma | Tumors
Journal Article
Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 12/2016, Volume 20, Issue 12, pp. 771 - 776
Journal Article
Human Mutation, ISSN 1059-7794, 1995, Volume 5, Issue 1, pp. 66 - 75
Journal Article
Journal Article
Journal Article