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         Enchondromatosis:     more detail

41. Encyclopædia Britannica
Topic enchondromatosis. Encyclopædia Britannica Related Articles. occurrence ofenchondromas Go to Index Browse List of Abbreviations
http://www.britannica.com/eb/topic?idxStructId=186498&typeId=13

42. Annals Of Plastic Surgery - UserLogin
enchondromatosis of the Hand Severe and Mild Forms, and Treatment Modalities enchondromatosis is a nonhereditary benign growth of cartilage that arises
http://www.annalsplasticsurgery.com/pt/re/annps/fulltext.00000637-200108000-0002
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43. Penn State Faculty Research Expertise Database (FRED)
, Benign growths of cartilage in the metaphyses ofseveral bones. Related Terms. Enchondroma, Multiple, Enchondrosis, Multiple......enchondromatosis.
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D004687

44. Orthoguide.com EnchondromatosisEnchondroma Enchondroma 4-3114 To See Images Firs
Search results for enchondromatosis . Orthoguide Matches 1 1 of 1. Related FieldsRadiology Search AltaVista for more on enchondromatosis
http://www.orthoguide.com/ortho/Enchondromatosis.php3
Can't open file: 'adviews.MYI'. (errno:

45. Medical Image Database, Radiology Teaching Files And Cases, MedPix™: Single
enchondromatosis (Ollier s disease) Factoid 3472 Created 2001-12-05 Clinical manifestations of enchondromatosis include deformities of the bones
http://rad.usuhs.mil/medpix/medpix.html?mode=single&comebackto=mode=cat_browse&r

46. Medical Image Database, Radiology Teaching Files And Cases, MedPix™: Factoid Im
TOPIC enchondromatosis (Ollier s disease) Magnify enchondromatosis (Ollier sdisease). enchondromatosis (Ollier s disease)
http://rad.usuhs.mil/medpix/medpix.html?mode=factoid_images&recnum=3472

47. 166000 ENCHONDROMATOSIS, MULTIPLE
A number sign ( ) is used with this entry because enchondromatosis was found by The combination of enchondromatosis and multiple exostoses characterizes
http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:166000] -e

48. %271550 SPONDYLOENCHONDRODYSPLASIA
(1976) described enchondromatosis, similar to that of Ollier disease, in associationwith (1978) identified 6 types of enchondromatosis Ollier disease,
http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:271550] -e

49. All Showcase - Enchondromatosis
MAFFUCCI’S SYNDROME REPORT OF A CASEenchondromatosis is a nonhereditary skeletal disorder, characterized by enchondromatosis (Ollier’s disease) and ovarian juvenile granulosa cell tumor.
http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/E/Enchondr
All Showcase Enchondromatosis
List of Enchondromatosis information, links and web resources. Discount Shopping Collectibles Coupons Clickbank ... Advertise Search for: All Showcase This Category
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Enchondromatosis All Showcase
NORD: Ollier Disease
Sample report, plus links to organisations. [Fee required for full report]
Virtual Children's Hospital: Enchondromatosis

Clinical presentation, etiology and imaging findings.
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50. ENCHONDROMATOSIS
medicaldictionary.thefreedictionary.com/enchondro Rarelink.net - Diagnoselisten enchondromatosis, MultipleDu er her Hjem Diagnoselisten enchondromatosis, Multiple enchondromatosis,Multiple, enchondromatosis, Multiple, Mafucci syndrom
http://www.websters-online-dictionary.org/definition/english/En/Enchondromatosis
Philip M. Parker, INSEAD.
ENCHONDROMATOSIS
Specialty Definition: ENCHONDROMATOSIS
Domain Definition
Health
Benign growths of cartilage in the metaphyses of several bones. ( references Source: compiled by the editor from various references ; see credits. Top
Frequency of Internet Keywords: ENCHONDROMATOSIS
The following statistics estimate the number of searches per day across the major English-language search engines as identified by various trade publications. Hyperlinks lead to commercial use of the expression at Amazon.com
Expression Frequency
per Day
enchondromatosis
Source: compiled by the editor from various references ; see credits. Top
Modern Translation: ENCHONDROMATOSIS
Language Translations for "ENCHONDROMATOSIS"; alternative meanings/domain in parentheses.
French
enchondromatose various references
German
Enchondromatose various references
Pig Latin
enchondromatosisay
Spanish
encondromatosis
various references Source: compiled by the editor from various translation references Top
Anagrams: ENCHONDROMATOSIS
Words within the letters "a-c-d-e-h-i-m-n-n-o-o-o-r-s-s-t" -3 letters : chondriosomes.

51. Rarelink.net - Diagnoslistan Enchondromatosis, Multiple
Du är här Hem Diagnoslistan enchondromatosis, Multiple enchondromatosis,Multiple, enchondromatosis, Multiple, Mafucci syndrom
http://www.rarelink.se/diagnosedetail.jsp?diagnoseId=162

52. Radiology Case 438-3114
Neurosurgery Fulltext Volume 34(5) May 1994 p 903-906 Identical Only 13 cases of multiple enchondromatosis associated with intracranial gliomas enchondromatosis is a rare, nonhereditary condition first described by
http://www.sbu.ac.uk/~dirt/museum/438-3114.html
no history available
Analysis
There are defects in the phalanges with some elevation of the edges, indicating expanding lesions in the bone. The lesions have well demarcated endosteal margins. Diagnosis: Enchondromatosis, acroform, distal, expression. ian@idmhome.demon.co.uk

53. Neurosurgery - UserLogin
Both are congenital but not hereditary enchondromatosis (a mesodermal dysplasia Bendel CJA, Gelmers HJ Multiple enchondromatosis(Ollier s disease)
http://www.neurosurgery-online.com/pt/re/neurosurg/fulltext.00006123-199707000-0
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54. Exostoses, Multiple
enchondromatosis is a rare disorder that affects males and females equally. enchondromatosis is characterized by slow growing tumors of cartilage cells
http://hw.healthdialog.com/kbase/nord/nord973.htm
document.write(''); var hwPrint=1; var hwDocHWID="nord973"; var hwDocTitle="Exostoses, Multiple"; var hwRank="1"; var hwSectionHWID="nord973"; var hwSectionTitle=""; var hwSource="us6.0"; var hwProdCfgSerNo="wsh_html_003_s"; var hwDocType="NORD";
National Organization for Rare Disorders, Inc.
Exostoses, Multiple
Important
It is possible that the main title of the report 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
  • Diaphyseal Aclasis EXT External Chondromatosis Syndrome Multiple Cartilaginous Exostoses Multiple Exostoses Multiple Exostoses Syndrome Multiple Osteochondromatosis
Disorder Subdivisions
  • None
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Enchondromatosis Epiphysealis Hemimelica Dysplasia Metachondromatosis Maffucci Syndrome
General Discussion
Hereditary Multiple Exostoses (HME) is a rare skeletal disorder that is inherited in an autosomal dominant fashion. As the name suggests, this disorder is characterized by multiple bony growths or tumors (exostoses), often on the growing end (epiphysis) of the long bones of the legs, arms, and digits. These bony growths are covered by cartilage and usually continue to grow until shortly after puberty. They may cause deformities, especially of the ankle, knee, and wrist.
Symptoms
Multiple Exostoses is a rare disorder that affects bone growth. Bony tumors (exostoses), covered with cartilage, typically (but not exclusively) appear in the growth zones (metaphyses) of the long bones adjacent to the areas where tendon and muscles attach to the bone. These growths vary in size and number among affected individuals. Some individuals will present with a few large "lumps" while others will show several small growths.

55. International Journal Of Gynecological Pathology - UserLogin
Spindle Cell Vulvar Hemangiomatosis Associated With enchondromatosis A RareVariant of Maffucci s Syndrome. FernándezAguilar, Sergio MD; Fayt,
http://www.intjgynpathology.com/pt/re/intgynpath/fulltext.00004347-200401000-000
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56. International Journal Of Gynecological Pathology - Abstract: Volume 23(1) Januar
Spindle Cell Vulvar Hemangiomatosis Associated With enchondromatosis A RareVariant of Maffucci s Syndrome. International Journal of Gynecological
http://www.intjgynpathology.com/pt/re/intgynpath/abstract.00004347-200401000-000
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Fulltext
PDF (233 K) Spindle Cell Vulvar Hemangiomatosis Associated With Enchondromatosis: A Rare Variant of Maffucci's Syndrome.
International Journal of Gynecological Pathology. 23(1):68-70, January 2004.
Fernandez-Aguilar, Sergio M.D.; Fayt, Isabelle M.D.; Noel, Jean-Christophe Ph.D. Abstract:
Summary: Spindle cell hemangioma is a rare vascular tumor that most frequently involves the distal extremities, especially the hand. We report a case of spindle cell hemangiomatosis of the vulva in an 18-year-old woman with Maffucci's syndrome, the first report of such a case, to the best of our knowledge. The vascular lesions, present from the age of 2, were located in the right olecranon, the third left toe, and the vulva. Spindle cell hemangiomas are either benign neoplasms or hamartomatous malformations. (C)2004International Society of Gynecological Pathologists
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57. Ollier's Disease (Dyschondroplasia, [Multiple] Enchodromatosis, Osteochondromato
a further variant of multiple enchondromatosis with vertebral involvement?Diffuse brain stem tumor in an adolescent with multiple enchondromatosis
http://www.bdid.com/ollier.htm

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Ollier's Disease (Dyschondroplasia, [Multiple] Hereditary Enchodromatosis, Osteochondromatosis)

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58. Connective Tissue Oncology Society - Poster
enchondromatosis CAUSED BY A MUTANT TYPE I PTH/PTHRP RECEPTOR When they occurin multiple locations in enchondromatosis (Ollier’s disease),
http://www.ctos.org/meeting/2001/posters/poster75.html
Connective Tissue Oncology Society
2001 CTOS Annual Meeting Posters— Biology ENCHONDROMATOSIS CAUSED BY A MUTANT TYPE I PTH/PTHRP RECEPTOR
Sevan Hopyan , Nalan Gokgoz , Raymond Poon , Robert S. Bell , William G. Cole , Irene L. Andrulis , Benjamin A. Alman , Jay S. Wunder
Musculoskeletal Oncology Unit and Program in Molecular Biology and Cancer, Mount Sinai Hospital, Program in Developmental Biology, The Hospital for Sick Children OBJECTIVE: METHODS: RESULTS: We showed that key IHH-PTHrP pathway members are expressed in enchondromas and chondrosarcomas. The IHH and PTHrP signalling pathways were functional, but the feedback loop regulating IHH was dysregulated in these lesions. We identified a mutant PTHR1 in two patients with enchondromatosis. This mutant lowered baseline cAMP level and abolished IP3 accumulation in vitro. Expression of the mutant, but not WT, PTHR1 in the growth plates of transgenic mice resulted in the appearance of multiple enchondromas. These enchondromas were likely caused by abnormal proliferation and not abnormal resorption, since growth plate zonal architecture was altered, but the number of TRAP positive cells, which resorb the growth plate, were not.

59. Enchondromatosis
Base de données sur les maladies rares et les médicaments orphelins.
http://www.orpha.net/static/GB/enchondromatosis.html
Orphanet database access
Enchondromatosis
Direct access to data Summary
Full text
Clinical signs
  • Asymmetry of the body
  • Autosomal dominant inheritance
  • Bowed diaphysis
  • Haemangioma-cavernous
  • Restricted joint mobility
  • Visceral angiomatosis
  • Mutiple fractures
  • Neoplasia/cancer
  • Decreased skin pigmentation irregular
  • Lymphoedema/oedema
Update : 04/09/2005
Orphanet database access

60. Multiple Enchondroma Diseases / Family Village
Related Disorders Ollier s Disease, Multiple enchondromatosis, Multiple Cartilaginous, Enchondroma and enchondromatosis from eMedicine
http://www.familyvillage.wisc.edu/Lib_olli.htm
Multiple Enchondroma Diseases
Related Disorders: Ollier's Disease, Multiple Enchondromatosis, Multiple Cartilaginous, Ollier Osteochondromatosis, Unilateral Chrondromatosis, or Maffucci Syndrome.
Who to Contact
Where to Go to Chat with Others

Learn More About It

Web Sites
...
Search Google for "Multiple Enchondroma Diseases"
Who to Contact
American Association of Multiple Enchondroma Diseases (previously Ollier/Maffucci Self-Help Group)
357 Redwood Road
Venice, FL 34293
Web: http://www.aamed.net/ Founded in 1998, incorporated in 2002 as a not-for-profit corporation and registered as a tax exempt organization with the US Internal Revenue Service, AAMED is comprised of individuals with Ollier's disease, Maffucci's syndrome, enchondromatosis, their families, and physicians. AAMED is THE source for news and information about bone tumor diseases, research and services for adults and children with Enchondromatosis, Multiple Enchondroma, Ollier's disease, Maffucci's syndrome, and their families.On this site, you'll find links to our quarterly newsletters, message board, pen-pal program for children, latest research information, and much more. We invite interested persons to become part of group. Click on the membership link for more information on joining us.
Where to Go to Chat with Others
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