Page last updated: 2024-10-28

ifosfamide and von Hippel-Lindau Disease

ifosfamide has been researched along with von Hippel-Lindau Disease in 1 studies

von Hippel-Lindau Disease: An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Keaney, CM1
Springate, JE1

Reviews

1 review available for ifosfamide and von Hippel-Lindau Disease

ArticleYear
Cancer and the kidney.
    Adolescent medicine clinics, 2005, Volume: 16, Issue:1

    Topics: Adolescent; Antineoplastic Agents; Antineoplastic Agents, Alkylating; Carcinoma, Renal Cell; Comorbi

2005