Von Hippel-Lindau’s Disease

von Hippel-Lindau syndrome (VHL) is a hereditary condition associated with tumors arising in multiple organs. Tumors in VHL include hemangioblastomas, which are blood vessel tumors of the brain, spinal cord, and eye. Here is the latest research.

May 30, 2020

Significance of PI3K signalling pathway in clear cell renal cell carcinoma in relation to VHL and HIF status

Journal of Clinical Pathology
Raviprakash Tumkur SitaramBörje Ljungberg
June 27, 2020

Ubiquitination of PPAR-gamma by pVHL inhibits ACLY expression and lipid metabolism, is implicated in tumor progression

Metabolism: Clinical and Experimental
Kyung Hee NohCho-Rok Jung
June 25, 2020

Retinal Artery Macroaneurysm Associated With Retinal Hemangioblastoma

Ophthalmic Surgery, Lasers & Imaging Retina
Nora C ElsonBasil K Williams
July 11, 2020

Pheochromocytoma: A three-decade clinical experience in a multicenter study

Revista clínica española
P IglesiasJ J Díez
July 15, 2020
Open Access

Phacomatoses in the pediatric age group

Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery
Shlomi Constantini, Martin U Schuhmann
July 17, 2020
Case Report
Open Access


AACE Clinical Case Reports
Michael GoldsteinGary D Rothberger
May 12, 2020
Case Report

Spinal paraganglioma as unusual finding in von Hippel-Lindau disease

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
Jan-Helge KlinglerChristine Steiert
July 1, 2020
Open Access

The pVHL neglected functions, a tale of hypoxia-dependent and -independent regulations in cancer

Open Biology
Giovanni MinerviniSilvio C E Tosatto
June 9, 2020
Comment / Editorial
Open Access

History of the multiple endocrine neoplasia workshops and overview of MEN2019

Endocrine-related Cancer
Elizabeth G GrubbsRobert F Gagel
May 9, 2020
Open Access

Complementary role of 18 F-FDG and 68 Ga-DOTATATE PET/CT in the surveillance of patients with von Hippel-Lindau syndrome

Annals of Gastroenterology : Quarterly Publication of the Hellenic Society of Gastroenterology
Georgios Z PapadakisCorina Millo
July 22, 2020

E3 Ubiquitin Ligase Von Hippel-Lindau Protein Promotes Th17 Differentiation

The Journal of Immunology : Official Journal of the American Association of Immunologists
Alisha ChitrakarLauren A Zenewicz
July 9, 2020

Spinal hemangioblastoma: surgical procedures, outcomes and review of the literature

Acta neurologica Belgica
Huanyu WangQuanfeng Ma
July 2, 2020
Open Access

Von Hippel-Lindau Disease: Current Challenges and Future Prospects

OncoTargets and Therapy
Sven GläskerAlexander O Vortmeyer

Sign up to follow this feed and discover related papers.

Related Feeds

22q11 Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a congenital disorder caused as a result of a partial deletion of chromosome 22. Here is the latest research.

4H Leukodystrophy

4H Lekodystrophy involves hypomyelination, hypogonadotropic hypogonadism and hypodontia. It is also known as POLR-3Related Leukodystrophy. 4H syndrome symptoms include delayed or abnormal puberty, issues with central nervous system signal transmission, abnormal development of teeth, and symptoms tend to progressively get worse over time. There is not yet a known cure.


Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS here.

Adenomatous Polyposis Coli

Adenomatous polyposis coli is a protein encoded by the APC gene and acts as a tumor suppressor. Discover the latest research on adenomatous polyposis coli here.

Adult Polyglucosan Body Disease

Adult polyglucosan body disease (APBD) is a rare autosomal recessive disease characterized by defects in the glycogen brancher enzyme 1 (GBE1) gene. Discover the latest research on APBD here.

Alzheimer's Disease: Abeta

Alzheimer's disease (AD) is a chronic neurodegenerative disease associated with accumulation of amyloid plaques, which are comprised of amyloid beta. Here is the latest research in this field.

Angelman Syndrome

Angelman syndrome is a neurogenetic imprinting disorder caused by loss of the maternally inherited UBE3A gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. Here is the latest research.


Autism spectrum disorder is associated with challenges with social skills, repetitive behaviors, and often accompanied by sensory sensitivities and medical issues. Here is the latest research.

Bullous Pemphigoid

Bullous pemphigoid is a chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. Discover the latest research on bullous pemphigoid here.

CLOVES Syndrome

Congenital, Lipomatous, Overgrowth, Vascular Malformations, Epidermal Nevi and Spinal/Skeletal Anomalies and/or Scoliosis (CLOVES) syndrome is a rare genetic disorder caused by mutations in the PIK3CA gene. Symptoms include blood vessel abnormalities, small tissue tumors, skin legions and spinal abnormalities. Here is the latest research.

© 2020 Meta ULC. All rights reserved