61. ORPHANET® Von Hippel-Lindau Disease ORPHANET. Orphanet database access. von hippellindau disease. Direct access to data Clinical signs Ataxia/incoordination; Autosomal http://www.orpha.net/static/GB/vonhippellindaudisease.html

62. NEJM -- Sign In Next Next. Pheochromocytoma, Multiple Endocrine Neoplasia Type 2, and von hippellindau disease. von hippel-lindau disease a genetic study. http://content.nejm.org/cgi/content/full/330/15/1090-a

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63. NEJM -- Sign In PreviousPrevious, Volume 3401880, June 17, 1999, Number 24. Next Next. von Hippel–Lindau Disease. http://content.nejm.org/cgi/content/full/340/24/1880

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64. Learn More About Von Hippel-Lindau Disease In The Online Encyclopedia. You are here Online Encyclopedia von hippellindau disease. Enter a phrase or search word in the box below. see previous page. von hippel-lindau disease. http://www.onlineencyclopedia.org/v/vo/von_hippel_lindau_disease.html

You are here: Online Encyclopedia Enter a phrase or search word in the box below. You can enter multiple phrases at a time by putting a comma between each word.(e.g. cat ,dog ,lion ) Press the search button to start your search. Hint: Play with putting spaces before and after your words to see the different results you get. see previous page Von Hippel-Lindau Disease Von Hippel-Lindau Disease (VHL) is a rare inherited genetic condition involving the abnormal growth of tumors in parts of the body which are particularly rich in blood supply. In people with VHL little knots of capillaries sometimes occur called angiomatosis. The tumors of the central nervous system ( CNS ) are called hemangioblastomas These tumors, whether benign (usual) or malignant (rarer), may cause problems, for example angiomas in the brain or spinal cord may press on nerve or brain tissue. As an angioma grows, the walls of the blood vessels may weaken and leak, causing damage to surrounding tissues. Blood leakage from angiomas in the retina can interfere with vision. Cysts may also grow around angiomas.

65. Retinal Angioma Associated With Von Hippel-Lindau Disease » Clinical And Experi Retinal angioma associated with von hippellindau disease. Sanfilippo P, Troutbeck R, Vandeleur K. von hippel-lindau disease is a http://www.optometrists.asn.au/ceo/backissues/vol86/no3/2060

Home E-mail Alert Subscriptions Back Issues ... Contact Details Journal Search: All Author Title Journal of: Retinal angioma associated with von Hippel-Lindau disease Sanfilippo P, Troutbeck R, Vandeleur K Von Hippel-Lindau disease is a multi-system disorder that can produce hamartomas (benign tumour-like nodules) of the eyes, skin and nervous system. Retinal capillary angioma is a common ocular association of this congenital phakomatosis that may result in blinding sequelae, if not managed appropriately. We present a case of retinal angioma associated with von Hippel-Lindau disease and discuss the ocular and systemic signs, diagnosis and management. The optometrist is of particular importance in screening for this disorder, as it is often first detected in a routine eye examination. Download Full Text Internet Explorer: right-click (apple-click on the Mac) and choose 'Save Target As...'. right-click and select 'Save As...'

66. Ingenta: Article Summary -- Von Hippel-Lindau Disease With Bilateral Multiple Re von hippellindau disease with bilateral multiple renal cell carcinoma managed by right radical nephrectomy and left repeat partial nephrectomy International http://www.ingenta.com/isis/searching/ExpandTOC/ingenta?issue=pubinfobike://klu/

67. Nature Publishing Group Endolymphatic Sac Tumor Associated with a von hippellindau disease Patient An Immunohistochemical Study. Manifestations of von hippel-lindau disease. http://www.nature.com/cgi-taf/dynapage.taf?file=/modpathol/journal/v14/n7/full/3

68. UNC Radiology Teaching File Genito-Urinary Section Case #7 Case Material courtesy of J. Kevin Smith, MD, Ph.D. (jksmith@rad.uab.edu) Monica M. Colvin, MD. Diagnosis von hippellindau disease. Done. Other Links http://www.ibiblio.org/jksmith/UNC-Radiology-Webserver/Genito-Urinary/GU7.html

UNC Radiology Teaching File Genito-Urinary Section Case #7 History: This is a 44 year old white female with a history of von Hippel-Lindau syndrome. The patient is status post partial right nephrectomy and left total nephrectomy for renal cell cancer. Images: Comparison is made with a prior CT. The liver is normal in size and contains multiple small hepatic cysts. The gallbladder is well-distended with multiple calculi in it but no evidence of cholecystitis. The left kidney is surgically absent. Multiple simple renal cysts are noted in the right kidney. A complex septated cyst near the upper pole of the right kidney has slightly increased in size from 1.2 x 1.4 cm to 1.5 x 1.8 cm . Pre and post-contrast evaluation of the cyst measures 18 and 25 Hounsfields units respectively. However, at the inferior margin, it appears to enhance more. Multiple pancreatic cystic lesions are again noted. The largestof these contains multiple septations and is located in the region of the head of the pancreas. This may represent a serous cystadenoma. Discussion: von Hippel-Lindau disease is a rare autosomal dominant disorder with variable expressivity characterized by a variety of benign and malignant neoplasms widely dispersed throughout the body, the most characteristic being retinal angiomas and cerebellar hemangioblastomas. Abdominal neoplasms include multiple renal and pancreatic cysts, small renal adenomas, and frequent multiple and bilateral renal adenocarcinomas. These are best visualized using CT. Although CNS abnormalities usually predominate, renal cell carcinoma is a major cause of death. Renal carcinomas may be small and occur within the cysts making early detection difficult. Patients and their relatives should be screened periodically using CT.

69. Von Hippel-Lindau Disease The First Case Of Songklanagarind von hippellindau disease The first case of Songklanagarind Hospital Sarinya Puwanant, D. of Internal Medicine, F. of Medicine, PSU. http://www.clib.psu.ac.th/acad_43/psar1.htm

70. Von Hippel-Lindau Disease von hippellindau disease, Renal Tumor, and Bilateral Epididymal Masses. from Infections in Urology ® Adam J. Singer, MD. Introduction. http://www.medscape.com/viewarticle/410218

71. Qango : Health: Diseases And Conditions: V: Von Hippel-Lindau Disease category Options Help. Home Health Diseases and Conditions V von hippellindau disease, Suggest a Site. Health, etc. If you http://www.qango.com/dir/Health/Diseases_and_Conditions/V/von_Hippel-Lindau_Dise

Chat Forums Free Email Personals Classifieds ... Help Qango Directory von Hippel-Lindau Disease all of Qango only this category Options Help Home Health ... V > von Hippel-Lindau Disease Suggest a Site Health, etc If you would like to suggest a site for this category please click here Home Health Diseases and Conditions ... V > von Hippel-Lindau Disease Suggest a Site Home Suggest a Site Search ... Login

72. Project: Functionele Analyse Van Het Von Hippel-Lindau Tumor Suppressor-gen Midd SamenvattingEng, Background The von hippel-lindau disease is an hereditary cancer syndrome characterized by the development of vascular tumors in the central http://www.niwi.knaw.nl/nl/oi/nod/onderzoek/OND1270136/toon

Login NIWI (nl) Onderzoek Informatie NOD - Nederlandse Onderzoek Databank ... Powered by from "Project: Functionele ana..." entire NIWI site (nl) Project: Functionele analyse van het Von Hippel-Lindau tumor suppressor-gen middels conditionele gendisruptie. Titel-Eng Functional analysis of the Von Hippel-Lindau tumor suppressor gene using conditional gene disruption. Samenvatting-Eng Background: The von Hippel-Lindau disease is an hereditary cancer syndrome characterized by the development of vascular tumors in the central nervous system, kidneys, eyes, adrenals and the formation of cysts in liver, pancreas and epididymis. lnactivation of this gene is also a critical event in the pathogenesis of non-hereditary clear cell renal cancer. The current care of von Hippel-Lindau patients is based on early detection and timely management of the lesions. The mainstay of treatment is surgery (hemangioblastoma, renal cel cancer, pheochromocytoma) and laser photocoagulation (retinal angiomas). However, repetitive surgery has a significant impact on the quality of life of these patients. The development of novel treatment strategies are needed to prevent or to non-invasively treat clinical manifestations of von Hippel-Lindau disease. Purpose: Functional analysis of the von Hippel-Lindau gene is currently performed in von Hippel-Lindau deficient renal cell cancer lines. Because cancer cells have an unstable genome this may not be the best background for functional studies. The generation of homozygous von Hippel-Lindau deficient mice was hampered by an impaired placental vasculogenesis which lead to embryonic death. The purpose of this project is to generate a conditional von Hippel-Lindau knock-out mouse. This mouse will not only provide a system to perform studies on the function of the von Hippel-Lindau tumor suppressor gene in primary cells but may also serve as a model to test novel treatment strategies for von Hippel-Lindau disease and sporadic renal cell cancer.

73. NINDS Von Hippel-Lindau Disease Information Page More about NINDS von hippellindau disease Information Page. Content for this page. NINDS von hippel-lindau disease Information Page. Synonym(s) Angiomatosis. http://accessible.ninds.nih.gov/health_and_medical/disorders/vonhippe_doc.htm

Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Main sections of the NINDS web site Home About NINDS Disorders-you are in this section ... Find People Disorders section pages and search Image Description Science For the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Browse all disorders Browse all health organizations More about NINDS von Hippel-Lindau Disease Information Page Studies with patients Research literature Press release NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us Content for this page NINDS von Hippel-Lindau Disease Information Page Synonym(s): Angiomatosis Reviewed 05-09-2002 Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What is von Hippel-Lindau disease (VHL)? Is there any treatment? What is the prognosis? What research is being done? ... Organizations What is von Hippel-Lindau disease (VHL)? Is there any treatment?

74. Von Hippel-Lindau - Information / Diagnosis / Treatment / Prevention Web Directory ? Family Village Links to chat rooms, web sites and information about von Hippel Lindau s disease. ? Ocular Manifestations http://www.healthcyclopedia.com/genetic-disorders/von-hippel-lindau.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... genetic disorders > von hippel-lindau Von Hippel-Lindau Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Medical Definition Health News Web Directory: Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "hippel-lindau disease" Health News: Search millions of published articles for news on Von Hippel-Lindau Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: Family Village Links to chat rooms, web sites and information about Von Hippel Lindau's disease. Ocular Manifestations of Von Hippel-Lindau Disease An article by Emily Chew, M.D., National Eye Institute. Radiology: Von Hippel Lindau Disease Genetic, clinical and imaging features from the NIH.

75. Von Hippel-Lindau Syndrome the body. The gene for vonHippel Lindau disease (VHL) is found on chromosome 3, and is inherited in a dominant fashion. If one http://www.ncbi.nlm.nih.gov/disease/VHL.html

This Genes and Disease page has been moved to: Please update your bookmarks. If you are not automatically transported to the new page after 15 seconds, click on this link Genome View VHL on chromosome 3 Databases PubMed the literature LocusLink collection of gene-related information OMIM catalog of human genes and disorders Information Fact sheet from the National Institute of Neurological Disorders and Stroke, NIH VON HIPPEL-LINDAU SYNDROME is an inherited multi-system disorder characterized by abnormal growth of blood vessels. While blood vessels normally grow like trees, in people with VHL little knots of blood capillaries sometimes occur. These knots are called angiomas or hemangioblastomas. Growths may develop in the retina, certain areas of the brain, the spinal cord, the adrenal glands and other parts of the body.

76. Ophthalmic Images - Von Hippel-Lindau's Disease Retinal diseases von hippellindau s disease. von hippel-lindau S disease. FotoWeb - Ophthalmic Images. von hippel-lindau s disease. Retina (Other) - page 3. http://wmed.narod.ru/w_ophth/image_cl/diseases/ret_d/rd_32.htm

W Dr. Victor Zamyatin's Personal Web Site Catalogue of Ophthalmic Images World of Ophthalmology Catalogue of Ophthalmic Images Retinal Diseases Von Hippel-Lindau's Disease VON HIPPEL-LINDAU'S DISEASE FotoWeb - Ophthalmic Images Congenital/Hereditary diseases - page 1 Peripheral ischaemic retinopathy. Von Hippel-Lindau's Disease. Retina (Other) - page 3 Photocoagulated Von Hippel. Retina (Vascular disorders) - page 2 Peripheral ischaemic retinopathy. Von Hippel-Lindau's Disease. National Eye Institute /US/: Photograph and Image Catalog Eye Disease Anatomy Slit lamp photograph showing retinal detachment in Von Hippel-Lindau disease. New York Eye and Ear Infirmary, Robert Bendheim Digital Atlas of Ophthalmology Ocular Tumors - Retinal Tumors von Hipple Angioma Syndicat National des Ophtalmologistes de France ... About Me and My Site If you know of any links appropriate for page, please submit for inclusion We subscribe to the HONcode principles of the Health On the Net Foundation Verify here This symbol signifies that the Web site you are visiting has been reviewed by Healthlinks.Net

77. :: Ez2Find :: Von Hippel-Lindau Web Sites, Family Village Site Info - Translate - Open New Window Links to chat rooms, web sites and information about von Hippel Lindau s disease. http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Von Hippel-Lindau Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Von Hippel-Lindau ez2Find Home Directory Health Conditions and Diseases ... Genetic Disorders : Von Hippel-Lindau Web Sites Family Village [Site Info] [Translate] [Open New Window] Links to chat rooms, web sites and information about Von Hippel Lindau's disease. URL: http://www.familyvillage.wisc.edu/lib_vonh.htm The Human Gene Map [Site Info] [Translate] [Open New Window] Description of the characteristics and the development of Von Hippel-Lindau disease. URL: http://www.ncbi.nlm.nih.gov/cgi-bin/SCIENCE96/nph-gene?VHL Ocular Manifestations of Von Hippel-Lindau Disease [Site Info] [Translate] [Open New Window] An article by Emily Chew, M.D., National Eye Institute.

78. Radiology: Von Hippel Lindau Disease von Hippel Lindau disease Genetic, Clinical and Imaging Features. Peter L. Choyke, MD, Gladys M. Glenn, MD, Ph.D., McClellan M. Walther http://www.cc.nih.gov/ccc/papers/vonhip/toc.html

Von Hippel Lindau Disease: Genetic, Clinical and Imaging Features Peter L. Choyke, M.D., Gladys M. Glenn, M.D., Ph.D., McClellan M. Walther, M.D., Nicholas J. Patronas, M.D., W. Marston Linehan, M.D., Berton Zbar, M.D. Radiology (March) 146:629-642,1995 Table of Contents Abstract History Clinical Manifestations Genetics ... References Note: Figures 5-20 have been scanned at 50%. The full image can be viewed with an Helper Application that reads JPEG files and by double-clicking the image. From the: Diagnostic Radiology Department, Warren Grant Magnuson Clinical Center, Henry M. Jackson Foundation, National Institutes of Health, Bethesda, MD 20892 Cancer Diagnosis Branch, Division of Cancer Biology, Diagnosis and Centers, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892 Surgery Branch, Urologic Oncology Division, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892 Laboratory of Immunobiology, Frederick Cancer Research Facility, National Cancer Institute, National Institutes of Health, Frederick, MD 21701 Corresponding Author Peter L. Choyke, M.D.

79. Radiology: Von Hippel Lindau Disease This site has moved to http//www.cc.nih.gov/ccc/med_sci/staff_papers/vonhip/toc.html. Please update your bookmarks. http://www.cc.nih.gov/cc/vonhippel/toc.html

This site has moved to http://www.cc.nih.gov/ccc/med_sci/staff_papers/vonhip/toc.html Please update your bookmarks.

80. Von Hippel Lindau Disease von hippel lindau disease,. Print this article, Pancreatic lesions may be the only abdominal localization of von Hippel Lindau disease. http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 1/VON HIPPEL LIN

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Von hippel lindau disease, (Eugen von Hippel, 18671939, German ophthalmologist and Arvid Lindau, 18921958, Swedish pathologist), autosomal dominant hereditary disorder, linked to chromosome 3p, and characterized by angiomata of the retina and haemangioblastoma. Other features include hypertension due to phaeochromocytoma, hypernephroma-like tumours, polycythaemia due to the renal tumour or the haemangioblastoma, haemangiomas of the spinal cord, lungs and adrenals, cysts, microcystic adenomas and neuroendocrine tumours of the pancreas, kidneys and liver, and epdidymal cystadenoma. Pancreatic lesions may be the only abdominal localization of von Hippel Lindau disease. The extent of the cystic lesions of the pancreas varies from a few cysts to polycystic transformation of the enlarged organ ( Fig.1 ). Microcystic adenomas (serous cystadenomas) are more rare. The cysts always contain serous fluid. No mucinous cysts have been reported. In general, cystic pancreatic lesions in von Hippel Lindau disease are asymptomatic or associated with mild symptoms only. Imaging characteristics of both neoplasms are similar to those of other true cysts of the pancreas. Neuroendocrine tumours in von Hippel Lindau disease consist of a combination of MEN I and MEN II syndromes (see

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