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The epidemiology of von Hippel-Lindau disease
Rachel S. van Leeuwaarde
*
,
Reut Halperin
*
Corresponding author for this work
Internal Medicine
Utrecht University
Research output
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Chapter in Book/Report/Conference proceeding
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Chapter
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peer-review
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Keyphrases
Autosomal Dominant Disorder
25%
Benign Tumor
25%
Broad Ligament
25%
Central Nervous System
25%
Clear Cell Renal Cell Carcinoma (ccRCC)
25%
Cyst
75%
Diagnostic Criteria
25%
Disease Classification
25%
Endolymphatic Sac Tumor
25%
Epidemiology
100%
Epididymis
25%
Hemangioblastoma
25%
Malignant Tumor
25%
Pancreatic Neuroendocrine Tumors (pNETs)
25%
Paraganglioma
25%
Penetrance
25%
Pheochromocytoma
25%
Retina
25%
Von Hippel-Lindau Disease
100%
Medicine and Dentistry
Autosomal Dominant Inheritance
25%
Benign Tumor
25%
Broad Ligament
25%
Cancer
25%
Central Nervous System
25%
Clear Cell Renal Cell Carcinoma
25%
Cohort Effect
100%
Cyst
75%
Diseases
50%
Endolymphatic Sac Tumor
25%
Hemangioblastoma
25%
Nosology
25%
Pancreas Islet Cell Tumor
25%
Paraganglioma
25%
Penetrance
25%
Pheochromocytoma
25%
Prevalence
25%
Von Hippel-Lindau Disease
100%