• 68 Ga-DOTANOC PET/CT in 2 Siblings With Von Hippel-Lindau Disease
• 68Ga-DOTANOC PET/CT in 2 Siblings With Von Hippel-Lindau Disease
• A Case of Bilateral Carotid Body Tumors
• A Cerebellar Tumor-to-Tumor Metastasis in a Patient With Von Hippel-Lindau Disease
• A comparative analysis of surgically excised hereditary and sporadic pheochromocytomas: Insights from a single-center experience
• A Von Hippel-Lindau Syndrome Case Diagnosed While Hospitalized for Major Depression
• An Unusual Case of Pheochromocytoma Associated with von Hippel-Lindau Disease and Lynch Syndrome During Pregnancy
• ANGPTL4 suppresses clear cell renal cell carcinoma via inhibition of lysosomal acid lipase
• Association Between Pancreatic Cysts and Diabetes Mellitus in Von Hippel-Lindau Disease
• Belzutifan for von Hippel-Lindau Disease: Pancreatic Lesion Population of the Phase 2 LITESPARK-004 Study
• Belzutifan-induced regression of retinal capillary hemangioblastoma: A case-series
• Belzutifan: a novel therapeutic for the management of von Hippel-Lindau disease and beyond
• Case Report of a Hemangioblastoma Originating from the T1 Spinal Nerve Treated with in Toto Resection, Hemicorporectomy and Pedicle Screw Stabilization
• Cauda equina myxopapillary ependymoma in von Hippel-Lindau disease: A case report
• Centralization of care for rare genetic syndromes associated with cancer: improving outcomes and advancing research on VHL disease
• Characteristics, aetiology and implications for management of multiple primary renal tumours: a systematic review
• Characterization of spinal hemangioblastomas in patients with and without von Hippel-Lindau, and YAP expression
• Clinical T1a Renal Cell Carcinoma with Solitary Diaphragmatic Metastasis in a Patient with von Hippel-Lindau Disease
• Clinicopathological features of BAP1 mutated clear cell renal cell carcinoma
• Comparison of 68 Ga-DOTATATE PET/CT and 123 I-MIBG SPECT/CT in the Imaging of Functional Pheochromocytoma in an Adolescent Patient With Von Hippel-Lindau Syndrome
• Comparison of 68Ga-DOTATATE PET/CT and 123I-MIBG SPECT/CT in the Imaging of Functional Pheochromocytoma in an Adolescent Patient With Von Hippel-Lindau Syndrome
• Comprehensive treatment of von Hippel-Lindau disease: A case report
• Computed tomography-guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients
• Concurrent multiple cerebral cavernous malformations and cauda equina paraganglioma: illustrative case
• Could Capsule Endoscopy Be Useful in Detection of Suspected Small Bowel Bleeding and IBD-10 Years of Single Center Experience
• CT-derived radiomics predict the growth rate of renal tumours in von Hippel-Lindau syndrome
• Deletion of endothelial IGFBP5 protects against ischaemic hindlimb injury by promoting angiogenesis
• Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype
• Diversities of Mechanism in Patients with VHL Syndrome and diabetes: A Report of Two Cases and Literature Review
• Endolymphatic sac tumor: An urgent case presenting acute intracranial hypertension successfully treated with suboccipital decompressive craniectomy - 8 years of follow-up
• Endolymphatic Sac Tumors Associated With von Hippel-Lindau: A Case Report Highlighting Opportunity for Novel Orphan Drug Therapy
• Epidemiology and economic burden of Von Hippel-Lindau Disease-associated central nervous system hemangioblastomas and pancreatic neuroendocrine tumors in the United States
• Evaluating the Urinary Exosome microRNA Profile of von Hippel Lindau Syndrome Patients with Clear Cell Renal Cell Carcinoma
• Exceptional and Sustained Response to Belzutifan in Von Hippel-Lindau Disease-Associated Central Nervous System Hemangioblastoma
• Expansion of targeted degradation by Gilteritinib-Warheaded PROTACs to ALK fusion proteins
• Exposure-Response Analyses for Belzutifan to Inform Dosing Considerations and Labeling
• Expression of somatostatin receptors in hemangioblastomas associated with von Hippel-Lindau disease as a novel diagnostic, therapeutic, and follow-up opportunity: A case report and literature review
• Gastrointestinal neuroendocrine tumors: update 2024
• Giant Cystic Pheochromocytoma Associated With Neurofibromatosis Type 1: A Case Report
• Hereditary Renal Cancer Syndromes
• Hereditary Syndromes Associated with Pancreatic and Lung Neuroendocrine Tumors
• IL-6-Producing Pheochromocytoma Associated With Von Hippel Lindau Disease: A Case Report With Literature Review
• Imaging of pancreatic serous cystadenoma and common imitators
• Indocyanine green-enhanced transpupillary thermotherapy for juxtapapillary retinal capillary hemangioblastoma
• Innovative solutions? Belzutifan therapy for hemangioblastomas in Von Hippel-Lindau disease: A systematic review and single-arm meta-analysis
• Insulinoma Unmasked Post Sleeve Gastrectomy With Incidental Renal Cell Carcinoma: A Rare Case
• Interpretation on genetic tumour syndromes in the 5th WHO classification of paediatric tumours: part Ⅱ
• LAT1 expression in colorectal cancer cells is unresponsive to HIF-1/2α accumulation under experimental hypoxia
• Late-Onset Manifestations of Von Hippel-Lindau Syndrome: A Case Report
• Malignant potential of neuroendocrine microtumor of the pancreas harboring high-grade transformation: lesson learned from a patient with von Hippel-Lindau syndrome
• Metabolomic landscape of renal cell carcinoma in von Hippel-Lindau syndrome in a Chinese cohort
• MITF regulates the subcellular location of HIF1α through SUMOylation to promote the invasion and metastasis of daughter cells derived from polyploid giant cancer cells
• Molecular classification and tumor microenvironment characteristics in pheochromocytomas
• Molecular mechanism of infectious spleen and kidney necrosis virus in manipulating the hypoxia-inducible factor pathway to augment virus replication
• Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
• Multiple and hereditary renal tumors: a review for radiologists
• Mutational profile of primary clear cell renal cell carcinoma predicts recurrence and potential candidacy for adjuvant immune checkpoint inhibition
• Neurosurgical Implications of Targeting Hypoxia-Inducible Factor 2α in Hemangioblastomas with Belzutifan
• Optic nerve and chiasm hemangioblastomas in von Hippel-Lindau disease: report of 12 cases and review of the literature
• Optic nerve haemangioblastoma in association with von Hippel-Lindau syndrome: case report and literature review
• Optical Coherence Tomography Angiography-Navigated Laser Photocoagulation of Retinal Hemangioblastomas in Patients With von Hippel-Lindau Disease
• Oral HIF-2alpha Inhibitor Belzutifan in Ocular von Hippel-Lindau Disease: Subgroup Analysis of the Single-Arm Phase 2 LITESPARK-004 Study
• Oral Hypoxia-Inducible Factor 2alpha Inhibitor Belzutifan in Ocular von Hippel-Lindau Disease: Subgroup Analysis of the Single-Arm Phase 2 LITESPARK-004 Study
• Pancreatic neuroendocrine tumor with solitary splenic metastasis and synchronous renal cell carcinoma: A rare case report
• Pancreatic neuroendocrine tumors in French VHL mutation carriers: a multicentric retrospective study
• Portal Venous Thrombosis after Percutaneous Cryoablation for Renal Cell Carcinoma
• Portuguese Pancreatic Club Perspectives on Pancreatic Neuroendocrine Neoplasms: Diagnosis and Staging, Associated Genetic Syndromes and Particularities of Their Clinical Approach
• Preclinical diagnostics of von Hippel-Lindau syndrome in a child
• Predicting tumor mutation burden and VHL mutation from renal cancer pathology slides with self-supervised deep learning
• Predictors of Progression in a Series of 81 Adult Patients Surgically Managed for an Intracranial Hemangioblastoma: Implications for the Postoperative Follow-Up
• Preparation of von Hippel-Lindau (VHL) E3 ubiquitin ligase ligands exploiting constitutive hydroxyproline for benzylic amine protection
• Prevalence of Neurological Symptoms and Imaging Findings in Von Hippel-Lindau Patients Referred to Rasool Akram Hospital, 2018-2021
• Prognostic Factors of Spinal Intramedullary Hemangioblastoma : Analysis of Surgical Outcomes and Tumor Characteristics
• Pronounced Conjunctival Vascular Engorgement in Von Hippel-Lindau Syndrome
• Recurrent Tuberous Sclerosis Complex/Mammalian Target of Rapamycin Mutations Define Primary Renal Hemangioblastoma as a Unique Entity Distinct From Its Central Nervous System Counterpart
• Saturation genome editing maps the functional spectrum of pathogenic VHL alleles
• Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease
• Single Stage Bilateral Adrenalectomy (Cortical-Sparing) and Pancreatectomy (Corpus-Sparing) in a Patient with Von Hippel-Lindau Disease
• SOCS domain targets ECM assembly in lung fibroblasts and experimental lung fibrosis
• Somatostatin receptor 2A expression in von Hippel-Lindau-related hemangioblastomas
• Surgical resection of double advanced pancreatic neuroendocrine tumors with multiple renal cell carcinoma associated with von Hippel-Lindau disease
• Targeting HIF-2α and anemia: A therapeutic breakthrough for clear-cell renal cell carcinoma
• Technical Considerations for the Surgical Management of a C2 Spinal Cord Hemangioblastoma and Subjacent Cervical Spondylotic Myelopathy: A 2-Dimensional Operative Video
• The genetic differences between types 1 and 2 in von Hippel-Lindau syndrome: comprehensive meta-analysis
• The Medical and Surgical Management of Recurrent Multicenter Insulinomatosis Without Known Genetic Predisposition
• The rare diagnosis of Von Hippel-Lindau disease in a 29-year-old patient
• The Role of the PAX Genes in Renal Cell Carcinoma
• Therapeutic Targeting of Hypoxia-Inducible Factors in Cancer
• Time course of tumorigenesis of a newly developed sporadic hemangioblastoma in an elderly patient: illustrative case
• Trigeminal nerve hemangioblastoma in the setting of undiagnosed von Hippel-Lindau disease: illustrative case
• Tumor-targeted PROTAC prodrug nanoplatform enables precise protein degradation and combination cancer therapy
• UFM1 inhibits hypoxia-induced angiogenesis via promoting proteasome degradation of HIF-1α
• Ultrasonographic characteristics of testicular renal cell carcinoma metastasis: A case report and literature review
• Understanding Adult Central Nervous System Hemangioblastomas: meta-analysis of meta-analysis
• Unusual Presentation of Von Hippel-Lindau Syndrome With Gastric Variceal Bleeding
• VHL mutation drives human clear cell renal cell carcinoma progression through PI3K/AKT-dependent cholesteryl ester accumulation
• von Hippel- Lindau syndrome-related congenital polycythemia and response to belzutifan
• von Hippel-Lindau Syndrome and Secondary Hypertension: A Case Report
• Von-Hipple Lindau syndrome with family history: a case report and seventeen years follow-up study
• When rare diseases crisscross within the same patient: von Hippel-Lindau and type 1 gastric neuroendocrine tumor