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341por Buffet, Alexandre, Calsina, Bruna, Flores, Shahida, Giraud, Sophie, Lenglet, Marion, Romanet, Pauline, Deflorenne, Elisa, Aller, Javier, Bourdeau, Isabelle, Bressac-de Paillerets, Brigitte, Calatayud, María, Dehais, Caroline, De Mones Del Pujol, Erwan, Elenkova, Atanaska, Herman, Philippe, Kamenický, Peter, Lejeune, Sophie, Sadoul, Jean Louis, Barlier, Anne, Richard, Stephane, Favier, Judith, Burnichon, Nelly, Gardie, Betty, Dahia, Patricia L, Robledo, Mercedes, Gimenez-Roqueplo, Anne-Paule“…BACKGROUNDS: The incidence of germline mutations in the newly discovered cryptic exon (E1’) of VHL gene in patients with von Hippel-Lindau (VHL) disease and in patients with paraganglioma or pheochromocytoma (PPGL) is not currently known. …”
Publicado 2020
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342“…BACKGROUND: Hemangioblastoma is a benign tumor of the central nervous system and may appear as a component of von Hippel-Lindau (VHL) disease. At present, approximately 40 cases of optic nerve HGBs have been reported in the literature. …”
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343“…Through case-control study, only found that the von Hippel-Lindau gene rs1642742 (G>A) may be associated with the occurrence and metastasis of HCC. …”
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344por Akioka, Takahiro, Terada, Naoki, Takamori, Hiroki, Kamimura, Toshio, Mukai, Shoichiro, Kamoto, Toshiyuki“…von Hippel–Lindau (VHL) disease is an autosomal dominant hereditary disease with benign and malignant tumors occurring in various organs including the kidneys. …”
Publicado 2021
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345por Remenyi, Gyula, Bereczky, Zsuzsanna, Gindele, Réka, Ujfalusi, Aniko, Illes, Arpad, Udvardy, Miklos“…Secondary erythrocytosis may also be congenital due to different gene mutations of hemoglobin, hemoglobin stabilization proteins, EPO receptors, or oxygen sensing pathways. Von Hippel- Lindau gene mutation causes altered tissue oxygen sensation in VHL disease, usually with normal hemoglobin. …”
Publicado 2021
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346por Chia, Tan Yong, Gan, Chee Yuen, Murugaiyah, Vikneswaran, Hashmi, Syed F., Fatima, Tabinda, Ibrahim, Lazhari, Abdulla, Mohammed H., Alswailmi, Farhan Khashim, Johns, Edward James, Ahmad, AshfaqEnlace del recurso
Publicado 2021
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347por Gościniak, Piotr, Larysz, Michał, Sagan, Leszek, Larysz, Barbara, Syrenicz, Anhelli, Kurzyna, Marcin“…Von Hippel–Lindau (VHL) disease along with chronic thromboembolic pulmonary hypertension (CTEPH) is a unique and unusual severe complication of ventriculoatrial (VA) shunt implantation in the treatment of hydrocephalus. …”
Publicado 2022
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348“…CASE PRESENTATION: A 34-year-old monocular male patient complained decreased visual acuity (20/100) without pain and redness in the left eye five years ago. Von Hippel-Lindau syndrome were diagnosed with genetic testing. …”
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349por Dantas, François, Raso, Jair Leopoldo, Braga, Patrícia Salomé Gouvea, Botelho, Ricardo Vieira, Dantas, Fernando Luiz Rolemberg“…Multiple central nervous system (CNS) HBs are usually associated with von Hippel–Lindau disease, and leptomeningeal dissemination of sporadic HBs is extremely rare. …”
Publicado 2022
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350“…BACKGROUND: Clinacanthus nutans (Burm.f.) Lindau (C. nutans) has been used in the therapy of hepatitis B (HB) and is effective; however, the mechanism of action has not been elucidated. …”
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351por Patocs, Attila, Gergics, Peter, Balogh, Katalin, Toth, Miklos, Fazakas, Ferenc, Liko, Istvan, Racz, Karoly“…Von Hippel-Lindau disease (VHL) is a rare autosomal dominant disease characterized by development of cystic and tumorous lesions at multiple sites, including the brain, spinal cord, kidneys, adrenals, pancreas, epididymis and eyes. …”
Publicado 2008
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353por Feijóo-Cuaresma, Monica, Méndez, Fernando, Maqueda, Alfredo, Esteban, Miguel A., Naranjo-Suarez, Salvador, Castellanos, Maria C., del Cerro, Mercedes Hernández, Vazquez, Silvia N., García-Pardo, Angeles, Landázuri, Manuel O., Calzada, Maria J.“…The von Hippel-Lindau (VHL) tumor suppressor gene regulates extracellular matrix deposition. …”
Publicado 2008
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354por Kim, Won Tae, Ham, Won Sik, Ju, Hee Jeong, Lee, Jin Sun, Lee, Jin Sung, Choi, Young Deuk“…This study was done to analyze the clinical characteristics of renal cell carcinoma (RCC) in Korean patients with von Hippel-Lindau (VHL) disease. Between January 1996 and July 2008, 1,514 patients were diagnosed with RCC and 24 patients were diagnosed with VHL disease at our institute. …”
Publicado 2009
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355por Rahma, Osama E, Ashtar, Ed, Ibrahim, Ramy, Toubaji, Antoun, Gause, Barry, Herrin, Vincent E, Linehan, W Marston, Steinberg, Seth M, Grollman, Frank, Grimes, George, Bernstein, Sarah A, Berzofsky, Jay A, Khleif, Samir N“…The identification of the von Hippel-Lindau (VHL) gene mutations in RCC patients provided the potential for developing a novel targeted vaccine for RCC. …”
Publicado 2010
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356por Pagoulatos, Dionysios, Pharmakakis, Nikolaos, Lakoumentas, John, Assimakopoulou, Martha“…The purpose of this study was to investigate the co-expression patterns of transcription factor HIF-1α and von Hippel Lindau protein (pVHL)—which normally acts to keep levels of HIF-1α activity low under normoxic conditions—in pterygium and normal conjunctival human samples. …”
Publicado 2014
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357por Baldewijns, Marcella M., van Vlodrop, Iris J. H., Smits, Kim M., Vermeulen, Peter B., Van den Eynden, Gert G., Schot, Fiona, Roskams, Tania, van Poppel, Hein, van Engeland, Manon, de Bruïne, Adriaan P.“…Background: von Hippel–Lindau (VHL) inactivation is common in sporadic clear cell renal cell carcinomas (ccRCC). pVHL is part of the ubiquitin ligase complex that targets the alpha subunits of hypoxia-inducible transcription factor (HIF) for degradation under well-oxygenated conditions. …”
Publicado 2009
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358por Iwamoto, Hideki, Nakamura, Toru, Koga, Hironori, Izaguirre-Carbonell, Jesus, Kamisuki, Shinji, Sugawara, Fumio, Abe, Mitsuhiko, Iwabata, Kazuki, Ikezono, Yu, Sakaue, Takahiko, Masuda, Atsutaka, Yano, Hirohisa, Ohta, Keisuke, Nakano, Masahito, Shimose, Shigeo, Shirono, Tomotake, Torimura, Takuji“…In this study, we focused on von Hippel-Lindau protein (pVHL) in hepatocellular carcinoma (HCC) and investigated the effects of sulfoquinovosyl-acylpropanediol (SQAP), a novel synthetic sulfoglycolipid, for HCC. …”
Publicado 2015
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359“…von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited neoplastic syndrome that increases susceptibility to a variety of benign and malignant neoplasms. …”
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360por Che Sulaiman, Intan Soraya, Basri, Mahiran, Fard Masoumi, Hamid Reza, Chee, Wei Jian, Ashari, Siti Efliza, Ismail, Maznah“…BACKGROUND: Clinacanthus nutans Lindau is a well-known plant, native to tropical Asian countries. …”
Publicado 2017
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