Results 161 to 170 of about 9,530,886 (208)
Von hippel-lindau disease - a chromosomal study
Indian Journal of Ophthalmology, 1969 Jain I, Das K, Mahajan B
doaj
When is belzutifan the right option for von Hippel-Lindau disease-associated hemangioblastomas?-a critical review of LITESPARK-004 results. [PDF]
Transl Cancer ResSener U, Galloway T.
europepmc +1 more source
Pancreatic Involvement by Mixed Serous Neuroendocrine Neoplasm Detected by Endosonography With Fine-Needle Tissue Acquisition in Von Hippel-Lindau Disease. [PDF]
CureusOrsini-Arman AC +5 more
europepmc +1 more source
Gross total resection is associated with improvement and prognosis even in von Hippel-Lindau disease-related hemangioblastomas: Nationwide registry in Japan. [PDF]
Neurooncol PractTakayanagi S +11 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
International Ophthalmology Clinics, 2001
In recent years advances have been made in the clinical and genetic aspects of von Hippel-Lindau disease (VHL). Retinal capillary hemangioma is the most common manifestation of VHL disease and, therefore, ophthalmologists are frequently involved in the care of patients with this disease.
D, Gauthier, D J, D'Amico, S, Mukai
+6 more sources
In recent years advances have been made in the clinical and genetic aspects of von Hippel-Lindau disease (VHL). Retinal capillary hemangioma is the most common manifestation of VHL disease and, therefore, ophthalmologists are frequently involved in the care of patients with this disease.
D, Gauthier, D J, D'Amico, S, Mukai
+6 more sources
Microscopy Research and Technique, 2003
AbstractVon Hippel‐Lindau (VHL) disease is an uncommon, autosomal dominant hereditary multitumor syndrome caused by germline alterations of the VHL gene, which has been cloned recently and identified as a tumor suppressor gene. The major lesions in VHL disease include hemangioblastomas in the central nervous system and retina, clear cell renal cell ...
Toshiaki, Sano, Hidehisa, Horiguchi
+6 more sources
AbstractVon Hippel‐Lindau (VHL) disease is an uncommon, autosomal dominant hereditary multitumor syndrome caused by germline alterations of the VHL gene, which has been cloned recently and identified as a tumor suppressor gene. The major lesions in VHL disease include hemangioblastomas in the central nervous system and retina, clear cell renal cell ...
Toshiaki, Sano, Hidehisa, Horiguchi
+6 more sources
Pregnancy in von Hippel-Lindau disease
American Journal of Obstetrics and Gynecology, 1999We retrospectively evaluated maternal and fetal outcomes in a series of women with von Hippel-Lindau disease. Data resulted from 56 pregnancies in 30 women. Symptoms related to von Hippel-Lindau disease occurred in 3 of 56 pregnancies. In this unselected group of patients with von Hippel-Lindau disease, most pregnancies had a favorable outcome with a ...
Philippe Grimbert +2 more
exaly +3 more sources