{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T05:00:19Z","timestamp":1780894819128,"version":"3.54.1"},"reference-count":8,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,6,7]]},"DOI":"10.7759\/cureus.110423","type":"journal-article","created":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T04:53:55Z","timestamp":1780894435000},"source":"Crossref","is-referenced-by-count":0,"title":["Radiologically Probable Late-Onset Von Hippel\u2013Lindau Syndrome: A Case Report"],"prefix":"10.7759","author":[{"given":"Venkatesh","family":"Y","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bheru Dan","family":"Charan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hemanth Kumar","family":"G R","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tarikjot","family":"Singh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Archit","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1038\/ejhg.2010.175","article-title":"von Hippel-Lindau disease: a clinical and scientific review","volume":"19","author":"Maher ER","year":"2011","unstructured":"Maher ER, Neumann HP, Richard S. von Hippel-Lindau disease: a clinical and scientific review. Eur J Hum Genet. 2011, 19:617-623. 10.1038\/ejhg.2010.175","journal-title":"Eur J Hum Genet"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(03)13643-4","article-title":"von Hippel-Lindau disease","volume":"361","author":"Lonser RR","year":"2003","unstructured":"Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, Oldfield EH. von Hippel-Lindau disease. Lancet. 2003, 361:2059-2067. 10.1016\/S0140-6736(03)13643-4","journal-title":"Lancet"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.28.7.443","article-title":"Von Hippel-Lindau disease: a genetic study","volume":"28","author":"Maher ER","year":"1991","unstructured":"Maher ER, Iselius L, Yates JR, et al.. Von Hippel-Lindau disease: a genetic study. J Med Genet. 1991, 28:443-447. 10.1136\/jmg.28.7.443","journal-title":"J Med Genet"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2796.1998.00337.x","article-title":"Haemangioblastoma of the central nervous system in von Hippel-Lindau disease","volume":"243","author":"Richard S","year":"1998","unstructured":"Richard S, Campello C, Taillandier L, Parker F, Resche F. Haemangioblastoma of the central nervous system in von Hippel-Lindau disease. J Intern Med. 1998, 243:547-553. 10.1046\/j.1365-2796.1998.00337.x","journal-title":"J Intern Med"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1002\/cncr.33978","article-title":"Management recommendations for pancreatic manifestations of von Hippel-Lindau disease","volume":"128","author":"Laks S","year":"2022","unstructured":"Laks S, van Leeuwaarde R, Patel D, et al.. Management recommendations for pancreatic manifestations of von Hippel-Lindau disease. Cancer. 2022, 128:435-446. 10.1002\/cncr.33978","journal-title":"Cancer"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2022.104538","article-title":"von Hippel-Lindau disease: updated guideline for diagnosis and surveillance","volume":"65","author":"Louise M Binderup M","year":"2022","unstructured":"Louise M Binderup M, Smerdel M, Borgwadt L, et al.. von Hippel-Lindau disease: updated guideline for diagnosis and surveillance. Eur J Med Genet. 2022, 65:104538. 10.1016\/j.ejmg.2022.104538","journal-title":"Eur J Med Genet"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.7759\/cureus.62756","article-title":"Late-onset manifestations of Von Hippel-Lindau syndrome: a case report","volume":"16","author":"Kalekar T","year":"2024","unstructured":"Kalekar T, Kumar SP, Pachva A. Late-onset manifestations of Von Hippel-Lindau syndrome: a case report. Cureus. 2024, 16:e62756. 10.7759\/cureus.62756","journal-title":"Cureus"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.3340\/jkns.2025.0018","article-title":"Von Hippel-Lindau disease: a comprehensive review of diagnosis, genetics, clinical challenges, and surveillance","volume":"68","author":"Jung NY","year":"2025","unstructured":"Jung NY, Park JB. Von Hippel-Lindau disease: a comprehensive review of diagnosis, genetics, clinical challenges, and surveillance. J Korean Neurosurg Soc. 2025, 68:338-349. 10.3340\/jkns.2025.0018","journal-title":"J Korean Neurosurg Soc"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/498844-radiologically-probable-late-onset-von-hippel-lindau-syndrome-a-case-report","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T04:53:56Z","timestamp":1780894436000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/498844-radiologically-probable-late-onset-von-hippel-lindau-syndrome-a-case-report"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,6,7]]},"references-count":8,"URL":"https:\/\/doi.org\/10.7759\/cureus.110423","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2026,6,7]]}}}