Results 111 to 120 of about 4,444,377 (217)

Generation of TWO iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC)

Stem Cell Research
VHL disease is an inherited and autosomal dominant disorder affecting 1 in 36,0000 individuals worldwide. It is caused by von Hippel-Lindau (VHL) gene mutations and can affect both genders and all ethnic backgrounds (Nordstrom-O’Brien et al., 2009; Maher,
Liani G. Devito, Eugénie S. Lim, Samuel M. O’Toole, Scott T.C. Shepherd, Daqi Deng, Hugang Feng, Taja Barber, William M. Drake, Samra Turajlic, Lyn Healy   +9 more
doaj   +1 more source

Von Hippel Lindau Disease [PDF]

The Journal of Pediatrics, 2019
Deniz, Hos, Claus, Cursiefen, Claudia, Dahlke   +2 more
openaire   +2 more sources

Von Hippel Lindau Disease Pathology of Mini Hemangioblastoma

, 1976
Von Hippel Lindau Disease. Pathologic appearance of flat preparation of retina from necropsy study. Trypsin digestion study of retinal vascular bed with a mini VHL lesion. Anatomy: Retina. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau
William F. Hoyt, MD
core  

Pancreatic Cysts Causing Biliary Obstruction in von Hippel Lindau Syndrome

, 2020
Context Extrahepatic biliary obstruction secondary to pancreatic cysts is rare in patients with von Hippel Lindau syndrome. We describe a patient with von Hippel Lindau syndrome who had biliary obstruction due to pancreatic cysts who was initially ...
Radha Krishan Dhiman, Ajay Duseja, Amod Gupta, Rahul Gupta, Yogesh Kumar Chawla, Arun Sharma, Arunanshu Behera, Deepak Chettri, Naveen Kalra   +8 more
core  

Von Hippel-Lindau Disease and Gadolinium MRI

, 1991
Gadolinium-enhanced MRI was used to determine the frequency and distribution of CNS lesions in 50 patients with Von Hippel-Lindau Disease (VHL) at the National Institutes of Health, Bethesda, MD; University of Louisville, KY; and the Massachusetts ...
J Gordon Millichap, Millichap, J. Gordon
core   +1 more source

Von Hippel-Lindau disease (VHLD)

Acta Médica del Centro, 2009
Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the
Jorge Luis González Jara
doaj  

VHL-gene deletion in single renal tubular epithelial cells and renal tubular cysts: further evidence for a cyst-dependent progression pathway of clear cell renal carcinoma in von Hippel-Lindau disease

, 2010
Inheritance of a mutant allele of the von Hippel-Lindau tumor suppressor gene predisposes affected individuals to develop renal cysts and clear cell renal cell carcinoma.
Rudolph, T, Moch, H, von Teichman, Adriana, Perren, A, Moch, Holger, Rudolph, Thomas, Heinimann, Karl, Montani, Matteo, Heinimann, K, Montani, M, Perren, Aurel, von Teichman, A, Montani M, Moch H, Perren A, von Teichman A, Heinimann K, Rudolph T, Thomas Rudolph, Matteo Montani, Karl Heinimann, Aurel Perren, Adriana von Teichman, Holger Moch   +23 more
core   +1 more source

Masive enterorrhagia in patients suffering from hippel-lindau disease

Acta Médica del Centro, 2008
The Von Hippel Lindau disease is an autosomic-dominant neoplasia syndrome produced by a delection or mutation of tumor suppressor gene of chromosome 3p25. It was descripted by the German pathologist Arvid Lindau and the ophthalmologist Eugene Von Hippel,
Jorge Luis González Jara, Oliver Martín García, Gustavo A. Pérez Zavala   +2 more
doaj  

Clinical and Genetic Characterization of Russian Patients with von Hippel-Lindau Syndrome. [PDF]

Int J Mol Sci
Mikhaylenko DS, Vasserman NN, Kuryakova NB, Kuznetsova EB, Gorban NA, Stepanova AA, Shchagina OA, Polyakov AV, Zaletaev DV, Kutsev SI, Strelnikov VV.   +10 more
europepmc   +1 more source

Regenerative potential of von Hippel-Lindau tumor suppressor protein. [PDF]

World J Biol Chem
Kanno H, Nakahara K.
europepmc   +1 more source