| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Craig G Rogers, Adam M Blatt, George E Miles, W Marston Linehan, Peter A Pint. Concurrent robotic partial adrenalectomy and extra-adrenal pheochromocytoma resection in a pediatric patient with von Hippel-Lindau disease. Journal of endourology. vol 22. issue 7. 2008-10-27. PMID:18690816. |
we present a case of a pediatric patient with von hippel-lindau disease (vhl) and both an adrenal pheochromocytoma and an extra-adrenal pheochromocytoma, who underwent concurrent partial adrenalectomy and extra-adrenal pheochromocytoma resection utilizing robotic assistance. |
2008-10-27 |
2023-08-12 |
Not clear |
| Margit Rosner, Michaela Hanneder, Nicol Siegel, Alessandro Valli, Christiane Fuchs, Markus Hengstschläge. The mTOR pathway and its role in human genetic diseases. Mutation research. vol 659. issue 3. 2008-10-14. PMID:18598780. |
mutations in the mtor pathway component genes tsc1, tsc2, lkb1, pten, vhl, nf1 and pkd1 trigger the development of the syndromes tuberous sclerosis, peutz-jeghers syndrome, cowden syndrome, bannayan-riley-ruvalcaba syndrome, lhermitte-duclos disease, proteus syndrome, von hippel-lindau disease, neurofibromatosis type 1, and polycystic kidney disease, respectively. |
2008-10-14 |
2023-08-12 |
human |
| John A Butman, W Marston Linehan, Russell R Lonse. Neurologic manifestations of von Hippel-Lindau disease. JAMA. vol 300. issue 11. 2008-09-24. PMID:18799446. |
von hippel-lindau disease (vhl) is an autosomal-dominant neoplasia syndrome that is the result of a germline mutation of the vhl tumor suppressor gene on the short arm of chromosome 3. |
2008-09-24 |
2023-08-12 |
Not clear |
| William G Kaeli. Von Hippel-Lindau disease. Annual review of pathology. vol 2. 2008-08-21. PMID:18039096. |
von hippel-lindau disease, which is characterized by an increased risk of hemangioblastomas, clear cell renal carcinomas, and pheochromocytomas, is caused by inactivating mutations of the vhl tumor suppressor gene. |
2008-08-21 |
2023-08-12 |
Not clear |
| Catherine B Meyerle, Sam S Dahr, Nicholas M Wetjen, Guy V Jirawuthiworavong, John A Butman, Russell R Lonser, Edward Oldfield, Hanna Rodriguez-Coleman, Wai T Wong, Emily Y Che. Clinical course of retrobulbar hemangioblastomas in von Hippel-Lindau disease. Ophthalmology. vol 115. issue 8. 2008-08-19. PMID:18395800. |
to report clinical findings of rare retrobulbar optic nerve hemangioblastomas associated with von hippel-lindau disease (vhl). |
2008-08-19 |
2023-08-12 |
Not clear |
| A Marinozzi, N Papapietro, S A Barnaba, A Di Martino, G Tonini, V Denar. Chondrosarcoma of the iliac wing in Von Hippel-Lindau disease. Journal of experimental & clinical cancer research : CR. vol 26. issue 4. 2008-08-11. PMID:18365559. |
von hippel-lindau disease is a rare autosomic dominant hereditary tumoral syndrome characterized by mutation of the vhl gene. |
2008-08-11 |
2023-08-12 |
Not clear |
| Hidenori Karasaki, Akira Ishizaki, Nobuyuki Yanagawa, Yasuhiro Nakano, Jyunpei Sasajima, Yusuke Mizukami, Satoshi Tanno, Yoshihiko Tokusashi, Naoyuki Miyokawa, Mitsuhiro Obara, Junichi Goto, Shuichi Kino, Toru Kono, Shinichi Kasa. [Two cases of pancreatic tumor with von Hippel-Lindau disease]. Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology. vol 105. issue 5. 2008-07-02. PMID:18460863. |
von hippel-lindau disease (vhl disease) is an inherited neoplasia syndrome. |
2008-07-02 |
2023-08-12 |
Not clear |
| Libero Santarpia, Nicholas J Sarlis, Mariacarmela Santarpia, Steven I Sherman, Francesco Trimarchi, Salvatore Benveng. Mosaicism in von Hippel-Lindau disease: an event important to recognize. Journal of cellular and molecular medicine. vol 11. issue 6. 2008-06-18. PMID:18205710. |
von hippel-lindau disease (vhl) is an autosomal dominant, familial neoplastic disorder with variable interfamilial and intrafamilial expression. |
2008-06-18 |
2023-08-12 |
human |
| Russell R Lonser, Martin Baggenstos, H Jeffrey Kim, John A Butman, Alexander O Vortmeye. The vestibular aqueduct: site of origin of endolymphatic sac tumors. Journal of neurosurgery. vol 108. issue 4. 2008-05-09. PMID:18377255. |
to determine the precise topographic origin of elsts, the authors analyzed the imaging, operative, and pathological findings in patients with von hippel-lindau disease (vhl) and elsts. |
2008-05-09 |
2023-08-12 |
Not clear |
| Attila Patocs, Peter Gergics, Katalin Balogh, Miklos Toth, Ferenc Fazakas, Istvan Liko, Karoly Rac. Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family. BMC medical genetics. vol 9. 2008-05-08. PMID:18416845. |
von hippel-lindau disease (vhl) is a rare autosomal dominant disease characterized by development of cystic and tumorous lesions at multiple sites, including the brain, spinal cord, kidneys, adrenals, pancreas, epididymis and eyes. |
2008-05-08 |
2023-08-12 |
human |
| Koichi Masunaga, Akito Inadome, Yutaka Sugiyama, Yoshihiro Maeda, Yo Satoji, Wataru Takahashi, Masaki Yoshida, Shoichi Ueda, Kazuyoshi Ikeda, Yuichi Takano, Junji Yatsud. [Bilateral pheochromocytomas with von Hippel-Lindau disease: a case report]. Nihon Hinyokika Gakkai zasshi. The japanese journal of urology. vol 98. issue 7. 2008-02-04. PMID:18062217. |
a case of bilateral pheochromocytomas with von hippel lindau disease (vhl) is reported. |
2008-02-04 |
2023-08-12 |
Not clear |
| Joseph A Blansfield, Lynda Choyke, Shane Y Morita, Peter L Choyke, James F Pingpank, H Richard Alexander, Geoffrey Seidel, Yvonne Shutack, Nargiza Yuldasheva, Michelle Eugeni, David L Bartlett, Gladys M Glenn, Lindsay Middelton, W Marston Linehan, Steven K Libutt. Clinical, genetic and radiographic analysis of 108 patients with von Hippel-Lindau disease (VHL) manifested by pancreatic neuroendocrine neoplasms (PNETs). Surgery. vol 142. issue 6. 2008-01-04. PMID:18063061. |
clinical, genetic and radiographic analysis of 108 patients with von hippel-lindau disease (vhl) manifested by pancreatic neuroendocrine neoplasms (pnets). |
2008-01-04 |
2023-08-12 |
Not clear |
| Mohammad K Zia, Khaled A Rmali, Gareth Watkins, Robert E Mansel, Wen G Jian. The expression of the von Hippel-Lindau gene product and its impact on invasiveness of human breast cancer cells. International journal of molecular medicine. vol 20. issue 4. 2007-12-11. PMID:17786294. |
the von hippel-lindau (vhl) gene is located on the short arm of chromosome 3, the mutations of which lead to the development of von hippel-lindau disease. |
2007-12-11 |
2023-08-12 |
human |
| Mahmoud R Hussei. Central nervous system capillary haemangioblastoma: the pathologist's viewpoint. International journal of experimental pathology. vol 88. issue 5. 2007-12-07. PMID:17877533. |
most haemangioblastomas are sporadic but up to one quarter are associated with von hippel-lindau disease (vhl). |
2007-12-07 |
2023-08-12 |
Not clear |
| Esther Korpershoek, Bart-Jeroen Petri, Francien H van Nederveen, Winand N M Dinjens, Albert A Verhofstad, Wouter W de Herder, Sonja Schmid, Aurel Perren, Paul Komminoth, Ronald R de Krijge. Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma. Endocrine-related cancer. vol 14. issue 2. 2007-11-20. PMID:17639058. |
according to the literature, between 15 and 25% of apparently sporadic adrenal pcc and spgl are caused by germline mutations in ret, von hippel-lindau disease (vhl), succinate dehydrogenase subunit b (sdhb), or subunit d sdhd. |
2007-11-20 |
2023-08-12 |
Not clear |
| b' B R Stanojevic, P Lohse, G G Neskovic, S M Damjanovic, T B Novkovic, S P Jovanovic-Cupic, B B Dimitrijevi\\xc4\\x8. Germline VHL gene mutations in three Serbian families with von Hippel-Lindau disease. Neoplasma. vol 54. issue 5. 2007-10-24. PMID:17688370.' |
germline vhl gene mutations in three serbian families with von hippel-lindau disease. |
2007-10-24 |
2023-08-12 |
Not clear |
| Chel Hun Choi, Kyung-Mee Lee, Jung-Joo Choi, Tae-Joong Kim, Woo Young Kim, Jeong-Won Lee, Sun-Joo Lee, Je-Ho Lee, Duk-Soo Bae, Byoung-Gie Ki. Hypermethylation and loss of heterozygosity of tumor suppressor genes on chromosome 3p in cervical cancer. Cancer letters. vol 255. issue 1. 2007-10-15. PMID:17467893. |
we examined the promoter methylation status and loh of the chromosome 3p genes, von hippel-lindau disease (vhl), retinoic acid receptor beta (rar-beta), ras association domain family 1a (rassf1a), and fragile histidine triad (fhit), in 37 samples of cervical squamous cell carcinoma and corresponding noncancerous tissues. |
2007-10-15 |
2023-08-12 |
Not clear |
| J S Huang, C J Huang, S K Chen, C C Chien, C W Chen, C M Li. Associations between VHL genotype and clinical phenotype in familial von Hippel-Lindau disease. European journal of clinical investigation. vol 37. issue 6. 2007-09-27. PMID:17537157. |
associations between vhl genotype and clinical phenotype in familial von hippel-lindau disease. |
2007-09-27 |
2023-08-12 |
Not clear |
| Deric M Park, Zhengping Zhuang, Ling Chen, Nicholas Szerlip, Irina Maric, Jie Li, Taesung Sohn, Stephanie H Kim, Irina A Lubensky, Alexander O Vortmeyer, Griffin P Rodgers, Edward H Oldfield, Russell R Lonse. von Hippel-Lindau disease-associated hemangioblastomas are derived from embryologic multipotent cells. PLoS medicine. vol 4. issue 2. 2007-09-26. PMID:17298169. |
to determine the origin of the neoplastic cell in central nervous system (cns) hemangioblastomas in von hippel-lindau disease (vhl) and its role in tumor formation and distribution, we characterized and differentiated neoplastic cells from hemangioblastomas removed from vhl patients. |
2007-09-26 |
2023-08-12 |
Not clear |
| Lindsay Fraser, Sally Watts, Anna Cargill, Stephen Sutton, Shirley Hodgso. Study comparing two types of screening provision for people with von Hippel-Lindau disease. Familial cancer. vol 6. issue 1. 2007-09-13. PMID:17160432. |
patients diagnosed with von hippel-lindau disease (vhl) require life-long surveillance for this multi-system disease. |
2007-09-13 |
2023-08-12 |
Not clear |