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Von Hippel-Lindau and hereditary pheochromocytoma/paraganglioma syndromes: Clinical features, genetics, and surveillance recommendations in childhood
Surya P. Rednam
, Ayelet Erez
, Harriet Druker
, Katherine A. Janeway
, Junne Kamihara
, Wendy K. Kohlmann
, Katherine L. Nathanson
, Lisa J. States
,
Gail E. Tomlinson
, Anita Villani
, Stephan D. Voss
, Joshua D. Schiffman
, Jonathan D. Wasserman
Department of Pediatrics
Research output
:
Contribution to journal
›
Article
›
peer-review
236
Scopus citations
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Medicine and Dentistry
Syndrome
100%
Pheochromocytoma
70%
Paraganglioma
70%
Neoplasm
60%
Von Hippel-Lindau Disease
40%
Screening
40%
Patient
30%
Surveillance
20%
Proteus Syndrome
20%
Gene
20%
Child
20%
Adult
20%
Childhood
20%
Urine
10%
Morbidity
10%
Disease Predisposition
10%
Central Nervous System
10%
Sequela
10%
Clinical Feature
10%
Kidney Cancer
10%
Familial Cancer
10%
Evaluation Study
10%
Mortality
10%
SDHB
10%
Gastrointestinal Stromal Tumor
10%
Disease Surveillance
10%
SDHD
10%
Magnetic Resonance Imaging of Neck
10%
Whole Body MRI
10%
Marker
10%
Plasma
10%
Abdomen
10%
Blood
10%