21. Picture Of Von Recklinghausen's Neurofibromatosis  *Otolaryngology Houston Pictures of von recklinghausen s Neurofibromatosis. http://www.ghorayeb.com/Neurofibromatosis.html

@import url(http://www.homestead.com/~media/elements/Text/font_styles.css); Otolaryngology Houston Bechara Y. Ghorayeb, MD 8830 Long Point, Suite 806 Houston, Texas 77055 Tel. 713 464 2614 Professional Information Office Information What is Otolaryngology? Post-Op Information ... Home This page was last updated: March 25, 2005 Pictures von Recklinghausen's Neurofibromatosis Pictures Ear Pictures Anatomy of the Pinna (Auricle) Home

22. Entrez PubMed A case of von recklinghausen s disease with duodenal somatostatinoma is reported.A search of the world s literature revealed 27 patients with Von http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7

23. Entrez PubMed von recklinghausen s disease associated with gastrointestinal carcinoid tumors.Hough DR, Chan A, Davidson H. The occurrence of both gastrointestinal http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=6

24. Von Recklinghausen's Disease - General Practice Notebook von recklinghausen s disease, or type I neurofibromatosis is an autosomal dominantlytransmitted disease in which the gene is located on the long arm of http://www.gpnotebook.co.uk/cache/1409679391.htm

von Recklinghausen's disease Von Recklinghausen's disease, or type I neurofibromatosis is an autosomal dominantly transmitted disease in which the gene is located on the long arm of chromosome 17. Click here for more information...

25. Von Recklinghausen's Disease Of Bone - General Practice Notebook von recklinghausen s disease of bone. Osteitis fibrosa cystica describes theadvanced bony changes seen in patients with primary or secondary http://www.gpnotebook.co.uk/cache/-409337818.htm

von Recklinghausen's disease of bone Osteitis fibrosa cystica describes the advanced bony changes seen in patients with primary or secondary hyperparathyroidism. It is now rare as hyperparathyroidism is usually discovered and treated at an earlier stage than before. Advancing hyperparathyroidism produces a sequence of bony changes: demineralisation osteitis fibrosa - increased osteoclastic activity with bone resorption and peritrabecular fibrosis osteitis fibrosa cystica is characterised by: extensive bone resorption accompanies marrow fibrosis with the development of cysts within the enlarged fibrotic marrow spaces brown tumours Skeletal changes are most prominent at the sites of highest bone activity - trabecular bones of vertebrae, phalanges, the ends of long bones, and parts of the skull. Osteitis fibrosa cystica is most common in severe primary hyperparathyroidism. Secondary hyperparathyroidism due to chronic renal failure usually produces renal osteodystrophy. Click here for more information...

26. Von Recklinghausen Gesell. - NF2-Group Neurofibromatosis Type II (NF2) is an hereditary disease (autosomaldominant).All of the symptoms go back to genetic predisposition. http://www.nf2.org/

27. Cerebral Aneurysms Associated With Von Recklinghausen's Neurofibromatosis: Repor Neurol India is an peerreviewed biomedical periodical of Neurological Societyof India. http://www.neurologyindia.com/article.asp?issn=0028-3886;year=2005;volume=53;iss

28. Cerebral Aneurysms Associated With Von Recklinghausen's Neurofibromatosis: Repor Neurol India is an peerreviewed biomedical periodical of Neurological Societyof India. http://www.neurologyindia.com/article.asp?issn=0028-3886;year=2005;volume=53;iss

29. Ophthalmologist And Eponyms - Von Recklinghausen Friedrich Daniel von recklinghausen first studied medicine in Bonn from 1852 to1855, von recklinghausen wrote one of the early descriptions of http://www.mrcophth.com/ophthalmologyhalloffame/vonrecklinghausen.html

Friedrich Daniel von Recklinghausen Recklinghausen's disease (neurofibromatosis) Biography: Friedrich Daniel von Recklinghausen von Recklinghausen wrote one of the early descriptions of haemochromatosis and introduced this term into the medical literature. In 1862, while still Virchow’s assistant, he published two important papers, one showing that connective tissue contained spaces which were drained by lymphatics and in which cells were present. He showed some of these cells had amoeboid movements and identified them as leukocytes. He established the method of using silver to stain the lines of junction of cells and his work led to Julius Friedrich Cohnheim’s (1839-1884) studies on leukocyte migration and inflammation. Cohnheim was a young assistant in the laboratory at the time. von Recklinghausen wrote both in German and Latin. Recklinghausen was widely known for his postgraduate teaching in the dissection room and the laboratory, attracting students from all over the world. Many of them later had great success and achieved high academic status. Still one of Recklinghausen's students in his memories said that his teacher had little contact with his candidates and rarely spoke to them. Recklinghausen was quite a colourful personality and pleasant colleague. He opposed Robert Koch’s concept that the tubercle bacillus was the cause of tuberculosis. He would argue that to say that tuberculous lesions contained Koch’s bacillus and therefore the bacillus was the cause of tuberculosis was like saying that the pyramid-like piles of horse manure (a frequent sight in Strassburg streets before the advent of the motor car) were du to sparrows which perched on top of them.

30. Neurofibromatosis Type 1 (NF-1) Neurofibromatosis type 1 (NF 1), also called von recklinghausen s disease, isa rare genetic disorder http://my.webmd.com/hw/raising_a_family/nord3.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Neurofibromatosis Type 1 (NF-1) Important It is possible that the main title of the report Neurofibromatosis Type 1 (NF-1) is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms neurofibroma, multiple neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome NF-1 peripheral neurofibromatosis Recklinghausen's phakomatosis Von Recklinghausen's disease Von Recklinghausen's neurofibromatosis Disorder Subdivisions segmental neurofibromatosis General Discussion Neurofibromatosis type 1 (NF-1), also called von Recklinghausen's disease, is a rare genetic disorder characterized by the development of multiple noncancerous (benign) tumors of nerves and skin (neurofibromas) and areas of abnormally decreased or increased coloration (hypo- or hyperpigmentation) of the skin. Areas of abnormal pigmentation typically include pale tan or light brown discolorations (cafe-au-lait spots) on the skin of the trunk and other regions as well as freckling, particularly under the arms (axillary) and in the groin (inguinal) area. Such abnormalities of skin pigmentation are often evident by one year of age and tend to increase in size and number over time.

31. NEJM -- Von Recklinghausen's Disease And Breast Cancer Images in Clinical Medicine from The New England Journal of Medicine VonRecklinghausen s Disease and Breast Cancer. http://content.nejm.org/cgi/content/short/352/17/1799

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Previous Volume 352:1799 April 28, 2005 Number 17 Next Von Recklinghausen's Disease and Breast Cancer Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings. Full Text PDF Add to Personal Archive Add to Citation Manager ... PubMed Citation View larger version [in this window] [in a new window] Full Text of this Article HOME SEARCH CURRENT ISSUE ... HELP Comments and questions? Please contact us The New England Journal of Medicine is owned, published, and Massachusetts Medical Society

32. NEJM -- Long-term Follow-up Of Von Recklinghausen Neurofibromatosis. Survival An Original Article from The New England Journal of Medicine Longterm follow-upof von recklinghausen neurofibromatosis. Survival and malignant neoplasms. http://content.nejm.org/cgi/content/abstract/314/16/1010

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Previous Volume 314:1010-1015 April 17, 1986 Number 16 Next Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms SA Sorensen, JJ Mulvihill, and A Nielsen Add to Personal Archive Add to Citation Manager Notify a Friend E-mail When Cited ... PubMed Citation Abstract This article has been cited by other articles: Varadarajalu, L., Khaneja, S., Niazi, M., Parithivel, V. S., Menon, L., Diaz-Fuentes, G. (2004). Adenocarcinoma masquerading as neurofibroma in a patient with von Recklinghausen's disease. Chest [Abstract] [Full Text] Reilly, K. M., Tuskan, R. G., Christy, E., Loisel, D. A., Ledger, J., Bronson, R. T., Smith, C. D., Tsang, S., Munroe, D. J., Jacks, T. (2004). Susceptibility to astrocytoma in mice mutant for Nf1 and Trp53 is linked to chromosome 11 and subject to epigenetic effects. Proc. Natl. Acad. Sci. U. S. A. [Abstract] [Full Text] Khosrotehrani, K., Bastuji-Garin, S., Zeller, J., Revuz, J., Wolkenstein, P. (2003). Clinical Risk Factors for Mortality in Patients With Neurofibromatosis 1: A Cohort Study of 378 Patients. Arch Dermatol [Abstract] [Full Text] Guillamo, J.-S., Creange, A., Kalifa, C., Grill, J., Rodriguez, D., Doz, F., Barbarot, S., Zerah, M., Sanson, M., Bastuji-Garin, S., Wolkenstein, P., for the Reseau NF France, (2002). Prognostic factors of CNS tumours in Neurofibromatosis 1 (NF1): A retrospective study of 104 patients.

33. Neurofibromatosis, Type I Neurofibromatosis, type I. Neurofibromatosis. NF1. von recklinghausen disease.217 images from 1 to 15 , 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 next http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=211

34. DermIS / Main Menu / DOIA / Neurofibromatosis Generalisata (von Recklinghausen) Neurofibromatosis Generalisata (von recklinghausen) / info. Do YOU sufferfrom Neurofibromatosis Generalisata (von recklinghausen) ? http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=237702&topic

35. DermIS / Main Menu / PeDOIA / Neurofibromatosis Generalisata (von Recklinghausen Translate this page / Neurofibromatosis Generalisata (von recklinghausen) / hyperlinks. description ,Die von recklinghausen Gesellschaft eV wurde 1987 von Eltern http://dermis.multimedica.de/doia/links.asp?zugr=p&lang=e&diagnr=237702

36. Vibewire.net von recklinghausen Profile Page Friends of von recklinghausen. witchita witchita Last 5 Forum posts by von recklinghausen. Re music game http://www.vibewire.net/2/index.php?option=com_comprofiler&task=userProfile&user

37. 2000 Collection - Margaretta Von Recklinghausen Hospice Mask Project, a charity art auction to benefit VNA Hospice of NorthernCalifornia, and their home hospice services. Ceramic masks decorated by http://www.maskproject.com/gallery2000/maskmakers/page3/487.htm

Mask Makers Page 1 Page 2 Page 3 Jim Plunkett Paul Pratchenko Linda Provenzale-Smilovitz Cherie Raciti ... Martin Wyatt Margaretta von Recklinghausen Bio Margaretta von Recklinghausen is an artist living and working in San Francisco. Reflection By the earth that is the body By the air that is the breath By the fire of her bright spirit By the waters of her living works We are ALL ONE in Her. The Mask Project is a registered trademark of Hospice Metro Denver.

38. NF1 - Neurofibromin 1 (neurofibromatosis, Von Recklinghausen Disease, Watson Dis Overview Neurofibromatosis Type 1 (aka. von recklinghausen disease) is a highlypenetrant autosomal dominant condition caused by mutations of the NF1 gene. http://www.cancerindex.org/geneweb/NF1.htm

Cancer Genetics Web www.cancer genetics.org ; Neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease) (17q11.2) NF1 Menu Summary Information - NF1 Gene Database Entries for NF1 Other NF1 Related Resources NF1 and Neurofibromatosis Type 1 ... Feedback / suggest a new topic for NF1 Search: Summary Information NF1; Neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease) Location: Overview: Neurofibromatosis Type 1 (aka. von Recklinghausen disease) is a highly penetrant autosomal dominant condition caused by mutations of the NF1 gene. The condition predisposes to cancer and malignancy is the most common cause of death in people with NF. A hetrogeneous range of NF1 mutations have been identified in NF patients and there is no clear relationship reported between specific NF1 mutations and the clinical variations of the disease. Return to NF1 Contents Gene Database Entries for NF1 OMIM GeneCard (Weizmann Institute) Atlas of Genetics and Cytogenetics in Oncology and Haematology Human Gene Mutation Database (Cardiff, UK) Swiss-Prot Locus Link UniGene GenAtlas ... Nomenclature (search for NF1) Return to NF1 Contents Other Related Resources International NF1 Genetic Mutation Analysis Consortium The consortium was established in 1992 and is managed by Dr Bruce Korf, Harvard Medical School, USA. The site is intended for scientists and a password is required to access the database.

39. Von Recklinghausen Disease (Neurofibromatosis, Type 1) von recklinghausen Disease (Neurofibromatosis, Type 1). Association Neurofibromatoseset Recklinghausen NF1 Gene and Neurofibromatosis Type 1 http://www.bdid.com/vrd.htm

HOME Von Recklinghausen Disease (Neurofibromatosis, Type 1) Association Neurofibromatoses et Recklinghausen NF1 Gene and Neurofibromatosis Type 1 Neurofibromatosis Generalisata (von Recklinghausen) (Includes Photos) Neurofibromatosis Type 1 NEUROFIBROMATOSIS (Type I) The Neurofibromatoses Neurofibroma ... HOME

40. Neurofibromatosis Type 1 (NF-1 Von Recklinghausen's) Definition of Neurofibromatosis Type 1 (NF1 von recklinghausen s) http://deafness.about.com/cs/earbasics/g/nfreck.htm

var zLb=4; var zIoa1 = new Array('Suggested Reading','Etiology','http://deafness.about.com/cs/etiology/index.htm'); zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a55' About Deafness / Hard of Hearing Deafness Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/7.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Deafness / Hard of Hearing newsletter! See Online Courses Search Deafness / Hard of Hearing Stay up to date! Compare Prices Email to a friend ... Print this page Suggested Reading Etiology Most Popular Sign Language Dictionaries Sign Word Reference Guide I Love You Handshape Learn Sign Language What's Hot James "Deaf" Burke ASL Poetry Thomas H. Gallaudet Mondini Syndrome ... Internet Relay Services Related Topics Parenting Special Needs Vision Senior Health Special Education ... Rare / Orphan Diseases adunitCM(150,100,'x55') Glossary Definition: group of inherited disorders in which noncancerous tumors grow on several nerves that may include the hearing nerve. The symptoms of NF-1 include coffee-colored spots on the skin, enlargement deformation of bones and neurofibromas. zau(256,420,100,'ri','http://z.about.com/5/o/c.htm?gs='+gs,'')

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