| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| I Y Pita-Ortiz, J N Jaurrieta-Hinojo, I Espinosa-Soto, A Ramirez-Estudill. Primary and secondary retinal capillary haemangioma in Mexico. Archivos de la Sociedad Espanola de Oftalmologia. vol 96. issue 6. 2021-10-15. PMID:34092289. |
there were seven primary haemangioblastomas, and nine due to von hippel-lindau disease (vhl). |
2021-10-15 |
2023-08-13 |
Not clear |
| Kristin Huntoon, Matthew J Shepard, Rimas V Lukas, Ian E McCutcheon, Anthony B Daniels, Ashok R Asthagir. Hemangioblastoma diagnosis and surveillance in von Hippel-Lindau disease: a consensus statement. Journal of neurosurgery. 2021-10-01. PMID:34598132. |
hemangioblastomas are a frequent underlying cause of neurological morbidity and death in patients with von hippel-lindau disease (vhl). |
2021-10-01 |
2023-08-13 |
Not clear |
| Nesrettin Fatih Turgut, Rosa Crunkhorn, Javed Iqbal, Soumit Dasgupt. Vestibular Function in Children With Von Hippel-Lindau Disease. The journal of international advanced otology. vol 17. issue 4. 2021-09-27. PMID:34309559. |
von hippel-lindau disease (vhl) is a rare autosomal dominant disorder. |
2021-09-27 |
2023-08-13 |
Not clear |
| Juan Francisco Sánchez-Ortega, Marta Claramonte, Mónica Martín, Juan Calatayud-Pére. Sporadic supratentorial hemangioblastoma with meningeal affection: A case report and literature review. Surgical neurology international. vol 12. 2021-09-14. PMID:34513160. |
supratentorial hemangioblastomas are extremely rare and are generally associated with von hippel-lindau disease (vhl). |
2021-09-14 |
2023-08-13 |
Not clear |
| P-L Vérot, P-Y Rabattu, O Chabre, A Gayot, H Sartelet, R Faguet, Y Robert, C Piola. Pediatric pheochromocytoma in association with Von Hippel-Lindau disease: Focus on screening strategies. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. vol 27. issue 8. 2021-08-23. PMID:33067065. |
von hippel-lindau disease (vhl) is a syndrome of familial predisposition to the development of malignant and benign tumours, due to mutations in the vhl tumour suppressor gene. |
2021-08-23 |
2023-08-13 |
Not clear |
| Takashi Kokumai, Masamichi Mizuma, Katsuya Hirose, Hideaki Karasawa, Masaharu Ishida, Hideo Ohtsuka, Kei Nakagawa, Takanori Morikawa, Takashi Kamei, Atsushi Masamune, Toru Furukawa, Michiaki Unn. A long-term survivor of metachronous liver metastases of pancreatic serous cystic neoplasm associated with von Hippel-Lindau disease. Surgical case reports. vol 7. issue 1. 2021-07-21. PMID:34191152. |
von hippel-lindau disease (vhl) manifests a dominantly inherited systemic syndrome accompanied by several benign or malignant tumors, including cystic tumors, in various organs. |
2021-07-21 |
2023-08-13 |
Not clear |
| Reinier Alvarez, Panagiotis Mastorakos, Elizabeth Hogan, Gretchen Scott, Russell R Lonser, Henry E Wiley, Emily Y Chew, Prashant Chittiboin. Retrobulbar Hemangioblastomas in von Hippel-Lindau Disease: Clinical Course and Management. Neurosurgery. vol 88. issue 5. 2021-07-02. PMID:33442737. |
retrobulbar hemangioblastomas involving the optic apparatus in patients with von hippel-lindau disease (vhl) are rare, with only 25 reported cases in the literature. |
2021-07-02 |
2023-08-13 |
Not clear |
| Lu Wang, Yi Feng, Lu-Yang Jian. Anesthetic management of bilateral pheochromocytoma resection in Von Hippel-Lindau syndrome: A case report. World journal of clinical cases. vol 9. issue 15. 2021-05-30. PMID:34046474. |
von hippel-lindau disease (also known as vhl syndrome), is an autosomal dominant inherited disease. |
2021-05-30 |
2023-08-13 |
Not clear |
| Nathan S Rubalcava, R Elliott Overman, Tanvi T Kartal, Steven W Bruch, Tobias Else, Erika A Newma. Laparoscopic adrenal-sparing approach for children with bilateral Pheochromocytoma in Von Hippel-Lindau disease. Journal of pediatric surgery. 2021-05-21. PMID:34016427. |
von hippel-lindau disease (vhl) is a rare cause of hereditary bilateral pheochromocytomas (pheo). |
2021-05-21 |
2023-08-13 |
Not clear |
| Ziao Li, Jin Zhang, Lei Zhang, Lin Yao, Cuijian Zhang, Zhisong He, Xuesong Li, Liqun Zho. Natural history and growth kinetics of clear cell renal cell carcinoma in sporadic and von Hippel-Lindau disease. Translational andrology and urology. vol 10. issue 3. 2021-04-16. PMID:33850741. |
to evaluate and compare the natural history and growth kinetics of sporadic clear cell renal cell carcinoma (ccrcc) with those of ccrcc in von hippel-lindau disease (vhl). |
2021-04-16 |
2023-08-13 |
Not clear |
| Songbiao Zhu, Wenxi Ding, Yuling Chen, Weixuan Wang, Renhua Xu, Chongdong Liu, Xiaohui Liu, Haiteng Den. High VHL Expression Reverses Warburg Phenotype and Enhances Immunogenicity in Kidney Tumor Cells. Genomics, proteomics & bioinformatics. 2021-03-01. PMID:33647481. |
von hippel-lindau disease tumor suppressor (vhl), a known tumor suppressor, is frequently mutated in about 50% of patients with ccrcc. |
2021-03-01 |
2023-08-13 |
Not clear |
| Amit Tirosh, Jonathan Keith Killian, David Petersen, Yuelin Jack Zhu, Robert L Walker, Jenny E Blau, Naris Nilubol, Dhaval Patel, Sunita K Agarwal, Lee Scott Weinstein, Paul Meltzer, Electron Kebebe. Distinct DNA Methylation Signatures in Neuroendocrine Tumors Specific for Primary Site and Inherited Predisposition. The Journal of clinical endocrinology and metabolism. vol 105. issue 10. 2021-02-19. PMID:32706863. |
to compare the deoxyribonucleic acid (dna) methylation signature of neuroendocrine tumors (nets) by primary tumor site and inherited predisposition syndromes von hippel-lindau disease (vhl) and multiple endocrine neoplasia type 1 (men1). |
2021-02-19 |
2023-08-13 |
Not clear |
| Koen M A Dreijerink, Rachel S van Leeuwaarde, Wenzel M Hackeng, Rachel H Giles, Wendy W J de Leng, Paul C Jutte, Albert J H Suurmeijer, Bernadette P M van Nesselrooij, Lodewijk A A Brosen. Clear cell chondrosarcoma in Von Hippel-Lindau disease. Familial cancer. vol 19. issue 1. 2021-02-08. PMID:31673890. |
a diagnosis of clear cell chondrosarcoma of the ulna was made in a patient with von hippel-lindau disease (vhl). |
2021-02-08 |
2023-08-13 |
Not clear |
| Z Zibly, Z R Cohen, A Peled, L Zach, U Nissim, Moshe Attia, Christian Graves, K Camphausen, R Spiegelma. Linear accelerator stereotactic radiosurgery can modulate the clinical course of Hemangioblastoma: Case series and review of the literature. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 82. issue Pt A. 2021-01-25. PMID:33317726. |
often associated with von hippel lindau disease (vhl), the lesions are often multifocal requiring complex resection and are difficult to control. |
2021-01-25 |
2023-08-13 |
Not clear |
| Francisco R Fields, Niraja Suresh, Morgan Hiller, Stefan D Freed, Kasturi Haldar, Shaun W Le. Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein. PloS one. vol 15. issue 11. 2020-12-21. PMID:33151962. |
von hippel-lindau disease (vhl) is an autosomal dominant rare disease that causes the formation of angiogenic tumors. |
2020-12-21 |
2023-08-13 |
Not clear |
| A M Cuesta, V Albiñana, E Gallardo-Vara, L Recio-Poveda, I de Rojas-P, K Villar Gómez de Las Heras, D T Aguirre, L M Botell. The β2-adrenergic receptor antagonist ICI-118,551 blocks the constitutively activated HIF signalling in hemangioblastomas from von Hippel-Lindau disease. Scientific reports. vol 9. issue 1. 2020-11-09. PMID:31296894. |
one of the major consequences of the lack of a functional vhl protein in von hippel-lindau disease, a rare cancer, is the constitutive activation of the hif pathway. |
2020-11-09 |
2023-08-13 |
Not clear |
| Zhen Liu, Jingcheng Zhou, Liang Li, Zhiqiang Yi, Runchun Lu, Chunwei Li, Kan Gon. Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel-Lindau disease: case report. BMC medical genetics. vol 21. issue 1. 2020-11-02. PMID:33004005. |
intronic mutation of the vhl gene associated with central nervous system hemangioblastomas in two chinese families with von hippel-lindau disease: case report. |
2020-11-02 |
2023-08-13 |
Not clear |
| Daniela Alosi, Marie Luise Bisgaard, Sophie Nowak Hemmingsen, Lotte Nylandsted Krogh, Hanne Birte Mikkelsen, Marie Louise Mølgaard Binderu. Management of Gene Variants of Unknown Significance: Analysis Method and Risk Assessment of the Current genomics. vol 18. issue 1. 2020-10-01. PMID:28503092. |
this is especially so in phenotypically variable diseases, such as von hippel-lindau disease (vhl). |
2020-10-01 |
2023-08-13 |
Not clear |
| Beatriz González-Rodríguez, Karina Villar Gómez de Las Heras, Daniel T Aguirre, Luis Rodríguez-Padial, Virginia Albiñana, Lucía Recio-Poveda, Angel M Cuesta, Luisa Mª Botella, Rosa María Jiménez-Escriban. Evaluation of the safety and effectiveness of oral propranolol in patients with von Hippel-Lindau disease and retinal hemangioblastomas: phase III clinical trial. BMJ open ophthalmology. vol 4. issue 1. 2020-10-01. PMID:31245608. |
von hippel-lindau disease (vhl) is a multisystem cancer syndrome caused by mutations in the |
2020-10-01 |
2023-08-13 |
Not clear |
| Evelynn Vergauwen, Anne-Marie Vanbinst, Carola Brussaard, Peter Janssens, Dieter De Clerck, Michel Van Lint, Anne C Houtman, Olaf Michel, Kathelijn Keymolen, Bieke Lefevere, Susanne Bohler, Dirk Michielsen, Anna C Jansen, Vera Van Velthoven, Sven Gläske. Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes. Hereditary cancer in clinical practice. vol 16. 2020-09-30. PMID:29312473. |
to explore the prevalence and rate of gadolinium accumulation in different subgroups, we retrospectively analyzed mris of patients with von hippel-lindau disease (vhl) and tuberous sclerosis complex (tsc). |
2020-09-30 |
2023-08-13 |
Not clear |