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The Journal of Pediatrics, ISSN 0022-3476, 06/2019, Volume 209, pp. 252 - 252
Journal Article
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2018, Volume 1085, pp. 201 - 203
Phakomatoses (phakoma = birthmark) are a group of diseases or syndromes that have hamartomas (tumorous malformations composed of tissues normally present at... 
Phakomatoses | von Hippel-Lindau disease | MEDICINE, RESEARCH & EXPERIMENTAL | OPHTHALMOLOGY | GENETICS & HEREDITY | CELL BIOLOGY
Journal Article
Original Article - Pancreatic involvement in Von Hippel-Lindau disease, 10/2004
BACKGROUND: Involvement of the pancreas in Von Hippel-Lindau disease that is a tumor predisposing syndrome mentioned in literature with some morbid and mortal... 
Botany | Von Hippel-Lindau, pancreatic, involvement, cysts, renal cell carcinoma. cn04030
Journal
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 06/2011, Volume 19, Issue 6, pp. 617 - 623
The autosomal dominantly inherited disorder von Hippel-Lindau disease (VHL) is caused by germline mutations in the VHL tumour suppressor gene (TSG). VHL... 
renal cysts | phaeochromocytoma | renal carcinoma | VHL | von Hippel-Lindau | haemangioblastoma | SPARING SURGERY | GENOTYPE-PHENOTYPE CORRELATIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR-SUPPRESSOR GENE | ENDOCRINE NEOPLASIA TYPE-2 | NATURAL-HISTORY | RETINAL HEMANGIOBLASTOMA | RENAL-CELL CARCINOMA | RECEPTOR INHIBITOR SU5416 | GENETICS & HEREDITY | CENTRAL-NERVOUS-SYSTEM | ENDOLYMPHATIC SAC TUMORS | Genetic Predisposition to Disease | Carcinoma, Renal Cell - pathology | Pheochromocytoma - diagnosis | Pheochromocytoma - etiology | Hemangioblastoma - etiology | Humans | Carcinoma, Renal Cell - genetics | Hemangioblastoma - diagnosis | von Hippel-Lindau Disease - complications | von Hippel-Lindau Disease - genetics | von Hippel-Lindau Disease - diagnosis | Magnetic Resonance Imaging | von Hippel-Lindau Disease - pathology | Hemangioblastoma - pathology | Mass Screening | Genes, Dominant | Hemangioblastoma - genetics | Carcinoma, Renal Cell - diagnosis | Germ-Line Mutation | Pheochromocytoma - pathology | Pheochromocytoma - genetics | Von Hippel-Lindau Tumor Suppressor Protein - genetics | Adrenal Gland Neoplasms | Carcinoma, Renal Cell - etiology | Biomedical research | Medical imaging | Central nervous system | Retina | Nervous system | Family medical history | Preventive medicine | Patients | Von Hippel-Lindau disease | Reviews | Cysts | Genetics | VHL protein | Mutation | Neoplasia | Clear cell-type renal cell carcinoma | Cancer | Tumors | Practical Genetics | von Hippel–Lindau
Journal Article
Current Molecular Medicine, ISSN 1566-5240, 12/2004, Volume 4, Issue 8, pp. 833 - 842
Journal Article
The Lancet, ISSN 0140-6736, 2004, Volume 363, Issue 9416, pp. 1231 - 1234
Journal Article
The Lancet Oncology, ISSN 1470-2045, 10/2018, Volume 19, Issue 10, pp. 1267 - 1269
Journal Article
The Japanese Journal of Urology, ISSN 0021-5287, 2012, Volume 103, Issue 3, pp. 557 - 561
Journal Article
Postgraduate Medical Journal, ISSN 0032-5473, 04/2019, Volume 95, Issue 1122, pp. 223 - 223
[...]the diagnosis of Von Hippel-Lindau disease (VHL) was considered. VHL is an autosomal-dominant disease with variable penetrance due to mutation in VHL gene... 
dysphagia | pheochromocytoma | hemangioblastoma | syrinx | von hippel -lindau disease | MEDICINE, GENERAL & INTERNAL | Spinal cord | Dysphagia | Brain research | Cysts
Journal Article
The Lancet Oncology, ISSN 1470-2045, 10/2018, Volume 19, Issue 10, pp. 1351 - 1359
No approved systemic therapy exists for von Hippel-Lindau disease, an autosomal dominant disorder with pleiotropic organ manifestations that include clear cell... 
RETINAL CAPILLARY HEMANGIOBLASTOMA | THERAPY | EFFICACY | GENE | ONCOLOGY | SAFETY | SUNITINIB | TUMOR | INTRAVITREAL BEVACIZUMAB | CANCER | RENAL-CELL CARCINOMA | Medicine, Experimental | Medical research | Angiogenesis inhibitors
Journal Article