Pheochromocytoma and paraganglioma syndromes: genetics and management update.
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Energy metabolism in neuroblastoma and Wilms tumorA Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Recurrent benign adrenal pheochromocytomas associated with hemihypertrophy.Diagnosis and management of multiple paragangliomas of the head and neck.Recurrence of Phaeochromocytoma and Abdominal Paraganglioma After Initial Surgical InterventionFrom arterial hypertension complications to von Hippel-Lindau syndrome diagnosis.Pheochromocytoma Screening Initiation and Frequency in von Hippel-Lindau Syndrome.A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGLGiant Cystic Pheochromocytoma with Low Risk of Malignancy: A Case Report and Literature Review.A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes.Clinical characteristics of adrenal tumors in children: a retrospective review of a 15-year single-center experience.A comprehensive characterization of rare mitochondrial DNA variants in neuroblastoma.Malignant paraganglioma in children treated with embolization prior to surgical excision.DDA: A Novel Network-Based Scoring Method to Identify Disease-Disease Associations.Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.Inherited predisposition to endometrial cancer: Moving beyond Lynch syndromeTumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.Pheochromocytoma and Paraganglioma in Neurofibromatosis type 1: frequent surgeries and cardiovascular crises indicate the need for screening.Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients
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Pheochromocytoma and paraganglioma syndromes: genetics and management update.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2014
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@en
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@nl
type
label
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@en
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@nl
prefLabel
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@en
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
@nl
P2860
P356
P1433
P1476
Pheochromocytoma and paraganglioma syndromes: genetics and management update
@en
P2093
W D Foulkes
P2860
P304
P356
10.3747/CO.21.1579
P577
2014-02-01T00:00:00Z