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         Ollier Disease:     more detail
  1. Molecular Profiling of Solitary and Ollier Disease-related Central Chondrosarcomas: An Investigation of DNA Aberrations, mRNA and Protein Expression by Leida B. Rozeman, 2005
  2. Allergy: The Facts (Oxford Medical Publications) by Robert J. Davies, Susan Ollier, 1989-05-18

61. Ollier's Disease - General Practice Notebook
medical information from General Practice Notebook. ollier's disease.This is a familial cause of multiple, unilateral chondromata.
http://www.gpnotebook.co.uk/cache/-1449525246.htm
Ollier's disease This is a familial cause of multiple, unilateral chondromata.
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62. AAOS On-Line Service - Scientific Program Ollier's Disease: Correction Of Angula
American Academy of Orthopaedic Surgeons 1994 Annual Meeting Scientific Program.ollier's disease Correction of Angular Deformities and Limb Lengthening.
http://www.aaos.org/wordhtml/anmeet94/sciprog/224.htm
American Academy of Orthopaedic Surgeons
1994 Annual Meeting - Scientific Program
Ollier's Disease: Correction of Angular Deformities and Limb Lengthening
Paper No. 224 FRIDAY, FEBRUARY 25, 1994
3:30-5:30 PM Location: CONVENTION CENTER ROOMS 58-60 Maurizio A. Catagni, MD , Lecco, ITALY
Roberto Cattaneo, MD, Lecco, ITALY
Francesco Guerreschi, MD, Lecco, ITALY Seventeen limb segments representing eight femora, six tibia and three humeri in nine patients with Ollier's disease were treated using the Ilizarov method. The mean lengthening achieved was 7.0 cm in the femur, 6.8 cm in the tibia and 7.5 cm in the humerus. The average duration of treatment was 7.5 months. Equal limb length was achieved in six of seven lower limbs. Multiplanar angular deformities were corrected in all the limb segments. With a mean follow-up of 4.3 years, the tissue transformation and corrections achieved are observed to be maintained. The corticotomy and tissue manipulation through the sites of the lesions achieved angular correction and lengthening and tissue transformation of the lesions. Moderator(s):Henry J. Mankin, MD, Boston, MA

63. Ollier's Disease
one click … For Medical Professionals only. ollier's disease,, Printthis article, (Louis ollier, 1830–1900, French orthopaedic
http://www.amershamhealth.com/medcyclopaedia/Volume VII/OLLIERS DISEASE.asp
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*For Medical Professionals only, registration required Ollier's disease, (Louis Ollier, 1830–1900, French orthopaedic surgeon), enchondromatosis multiple
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64. Ollier's Disease
only one click … For Medical Professionals only. ollier's disease,,Print this article, Leopold Louis Xavier Edouard ollier, 1830
http://www.amershamhealth.com/medcyclopaedia/Volume III 1/OLLIERS DISEASE.asp
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*For Medical Professionals only, registration required Ollier's disease, Leopold Louis Xavier Edouard Ollier, 1830–1900, French surgeon), see enchondromatosis
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65. Foot Problems > Diseases Of The Foot > Ollier's Disease
diseases of the foot ollier's disease. ollier's disease is usuallyassociated with a bony prominence under the toenail. Some form
http://www.mid-michiganfootandankle.com/prob_diseases_ollier.php
4224 State St, Saginaw, MI 48602
612 N. Euclid Ave, Bay City, MI 48706
Foot Problems Diseases of the foot Ollier's Disease Arthritis Cancer ... Sever's Disease Diseases of the foot - Ollier's Disease
Ollier's Disease is usually associated with a bony prominence under the toenail.
Some form of injury or trauma to the toe results in the formation of the bony irregularity or prominence.
Officite
There are 250,000 sweat glands in a pair of feet. Sweat glands in the feet excrete as much as a half-pint of moisture a day.

66. Wheeless' Textbook Of Orthopaedics
Main Menu Home Page Multiple Enchodromatosis (ollier's disease). Discussion - originally was described by ollier in late 1800's
http://wheeless.orthoweb.be/o6/93.htm
Main Menu Home Page
Multiple Enchodromatosis (Ollier's Disease)
- Discussion: - originally was described by Ollier in late 1800's; - characterized by multiple enchondroma lesions primarily located w/ in the metaphyseal regions of tubular bones; - usually diagnosed in childhood; - pts w/ Ollier's dz have increased risk of a secondary chondrosarcoma developing later in life; - risk is about 25% by age 40 yrs; - Clinical Findings: - most pts have bilateral involvement, w/ predominance on one side; - enchondromas most frequently involve the short tubular bones of hands The malignant potential of enchondromatosis Ollier's Disease. An assessment of angular deformity, shortening, and pathological fracture in twenty-one patients.

67. Health Library - Ollier's Disease
SEARCH. ollier's disease. Founded 1985.Mutual support and exchange of ideas forpersons with ollier's or Maffucci's disease, their families and physicians.
http://www.muskogeehealth.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29o

68. Bilateral Presentation Of The Ollier's Disease.A Case Report, And Literature Rev

http://www.medigraphic.com/ingles/i-htms/i-h-gral/i-hg2001/i-hg01-3/im-hg013f.ht

69. Bilateral Presentation Of The Ollier's Disease. A Case Report, And Literature Re
Bilateral presentation of the ollier's disease.A case report, and literaturereview. Key words Enchondromas, osteochondromas, ollier´s disease.
http://www.medigraphic.com/ingles/i-htms/i-h-gral/i-hg2001/i-hg01-3/ir-hg013f.ht
Pacheco LRC, Torres GB, Ugalde VJA,Vecchyo CC
Bilateral presentation of the Ollier's disease.
A case report, and literature review
Original title: Enfermedad de Ollier de presentación bilateral.
Reporte de un caso y revisión de la literatura
Rev Med Hosp Gen Mex 2001; 64 (3): 152-156

ABSTRACT Key words: Enchondromas, osteochondromas, Ollier´s disease.

70. Pediatric Orthopaedics Of Children's Hospital Of New York
dystrophy, severs disease, skeletal dysplasias, bone tumors, soft tissue tumors,bone cyst, chondrosarcoma, enchondroma, ollier's disease, ewing tumor
http://www.childrensorthopaedics.com/
March 31, 2003 site developed by databean HOME OUR TEAM THE FUTURE OF MEDICINE ... USFUL LINKS

71. Malignant Progression In Multiple Enchondromatosis (Ollier's Disease): An Autops
Malignant progression in multiple enchondromatosis (ollier's disease)an autopsybased molecular genetic study. Bovee JV, van Roggen
http://www.isols.com.br/content/basic_sciences/3n/article248.html
Malignant progression in multiple enchondromatosis (Ollier's disease): an autopsy-based molecular genetic study.
Bovee JV, van Roggen JF, Cleton-Jansen AM, Taminiau AH, van der Woude HJ, Hogendoorn PC.
Department of Pathology, Leiden University Medical Center, The Netherlands.
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72. SpringerLink: Child's Nervous System - Abstract Volume 15 Issue 5 (1999) Pp 222-
Abstract Volume 15 Issue 5 (1999) pp 222225. brief communication Diffuse brainstem tumor in an adolescent with multiple enchondromatosis (ollier's disease).
http://link.springer-ny.com/link/service/journals/00381/bibs/9015005/90150222.ht
Child's Nervous System
ISSN: 0256-7040 (printed version)
ISSN: 1433-0350 (electronic version) Table of Contents Abstract Volume 15 Issue 5 (1999) pp 222-225
brief communication : Diffuse brain stem tumor in an adolescent with multiple enchondromatosis (Ollier's disease)
D. Frappaz (1), A. C. Ricci (2), R. Kohler (3), P. Bret (2), C. Mottolese (2)
Received: 13 November 1998 Abstract Among patients with enchondromatosis, those with Ollier's disease are usually considered to be at a lower risk for extra-osseous malignancy than those with Maffucci's disease. However, several reports suggest that Ollier's disease may also be associated with gliomas. We report here the youngest patient in the literature (16 years) to be detected with a brain tumor and Ollier's disease. This is also the first case with diffuse brain stem involvement. Thus, counselling of patients with Ollier's disease may become more difficult than initially thought. Key words Article in PDF format (104 KB) Online publication: May 17, 1999
SpringerLink Helpdesk

73. Abstract
Case Report. ollier's disease in association with adjacent fibromatosis. ollier'sdisease (enchondromatosis) is a nonhereditary disorder of mesodermal dysplasia.
http://link.springer-ny.com/link/service/journals/00256/contents/02/00483/s00256
Case Report
Ollier's disease in association with adjacent fibromatosis
Khalid Al-Ismail , William C. Torreggiani , Peter L. Munk , John X. O'Connell , Savvakis Nicolaou and Bassam A. Masri Department of Radiology, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Department of Pathology, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Department of Orthopaedics, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Abstract. Ollier's disease (enchondromatosis) is a nonhereditary disorder of mesodermal dysplasia. It is characterized by the presence of multiple enchondromas that typically affect the metaphyseal ends of bones. The association of Ollier's disease with adjacent fibromatosis has, to our knowledge, not been previously described. We report a case of Ollier's disease in association with soft tissue fibromatosis adjacent to the involved upper arm. Key words.

74. Chondrosarcoma, Secondary To Enchondroma
Site The most common precursor is multiple enchondroma or ollier's disease. Thisphenomenon is rare in solitary enchondroma or synovial chondromatosis.
http://imc.gsm.com/demos/mskdemo/mspath/enneking/sect14/secencho.html
About Table of Contents Malignant Lesions of Bone Help
Chondrosarcoma, Secondary to Enchondroma
Definition Demographics Clinical Presentation Natural History ... References
Definition
Chondrosarcoma secondary to enchondroma is a primary neoplasm of cartilaginous histogenesis arising from a pre-existing benign enchondroma.
Demographics
Age: 30 - 50 Site: The most common precursor is multiple enchondroma or Ollier's disease. This phenomenon is rare in solitary enchondroma or synovial chondromatosis.
Clinical Presentation
The patient presents with pain at the site of a previously-painless enchondroma.
Natural History
Slow, displacing growth is characteristic of this tumor with very late transition to a high-grade lesion and risk of metastasis. The survival rate is excellent with adequate treatment prior to transition.
Radiographic Features
On radiograph, there is an expanding, radiolucent zone surrounding a calcified enchondroma with endosteal scalloping and periosteal, cortical thickening. [X-Ray] This radiograph shows the original enchondroma at first presentation. The patient was asymptomatic at this time. [X-Ray] This radiograph was made fourteen years later when the patient presented with a secondary chondrosarcoma.

75. Rockford Register Star Online - Special Reports
Amber suffers from ollier's disease, which causes tumors to grow at the jointson the right side of her body and prevents her arm and leg from growing.
http://www.rrstar.com/specialreports/amber/index.shtml
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Rockford Register Star Special Report
Amber's story:
From pain comes hope A three-part series by Register Star reporter Christine Byers
Amber Cornford of Roscoe has endured a life of surgeries, hospitals, doctors' appointments and pain just to be able to do one thing walk.
At 11 months old, Amber was diagnosed with a rare bone disease. The disorder causes tumors to form at the joints on the right side of her body. The tumors, made of cartilage, keep her limbs from growing.

76. Rockford Register Star Online - Special Reports
Eighthgrader at Prairie Hill Elementary School Her disease Amber was diagnosedwith a rare bone disorder called ollier's disease when she was 11 months old.
http://www.rrstar.com/specialreports/amber/breakout1.shtml
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Rockford Register Star Special Report
Amber's story: From pain comes hope
E-mail to a friend
From pain
comes hope
Homepage of Amber's story
Effect of Ollier's and Amber's first surgery
Amber's first and second Ilizarov ‘The only time to do this’ ... Amber's war box Amber's bio Age: 13 Family: parents, Vicki and Dave; sisters, Ashley, 6, and Jessica, 16.

77. Extended Possibilities For Patient With Leg Length Discrepancy
Daniel Bowen, a 22year-old resident of League City, Texas, enjoys a normal familylife after growing up with a condition called ollier's disease, which caused
http://www.shrinershq.org/shc/houston/olliers1-01.html

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Extended possibilities for patient with leg length discrepancy
Local resident successful graduate of Shriners Hospitals
January 2001 Daniel Bowen, a 22-year-old resident of League City, Texas, enjoys a normal family life after growing up with a condition called Ollier's disease, which caused a significant leg length discrepancy in his right leg. At 5 feet 6 1/2 inches, Daniel Bowen has no problem standing his ground when it comes to his Great Dane, Brutus. After observing him throughout the following day, they realized that Daniel skipped everywhere he went. Daniel's parents and grandparents finally asked him to simply walk across the room, and that's when they noticed that Daniel limped when he walked. After a closer look at his legs, they found that his right leg was shorter then his left leg. "After discovering my lower limb length discrepancy, my parents took me to several doctors before I was finally diagnosed with Ollier's Disease," explained Daniel. Ollier's disease is a non-hereditary congenital defect (present from birth) that causes tumors in the bones of usually just one extremity, affecting not only the long bones, but also those of the foot. The tumors affect the growth plates, which over time causes a lower limb length discrepancy.

78. Multiple Enchondromatosis: Ollier’s Disease
International Pediatrics. Volume 17, Number 4. Clinical Article. Multiple EnchondromatosisOllier’s disease. Neal P. Simon, MD; Michael W. Simon, MD, PhD, FAAP.
http://www.int-pediatrics.org/newip/volumes/volume 17/17-4/case/simon.htm
International Pediatrics Volume 17, Number 4 Clinical Article Multiple Enchondromatosis: Ollier’s Disease Neal P. Simon, MD; Michael W. Simon, MD, PhD, FAAP Address reprint requests to Neal P. Simon, MD, 699 West Drive, RR208, Indianapolis, IN 46202. Abstract Multiple enchondromatosis may cause devastating disfigurement and even adversely affect the growth and function of an extremity. Radiographs show typical changes and are generally diagnostic. Surgical intervention is usually warranted and should be sought as soon as the diagnosis is suspected. Approximately 50% of cases of untreated multiple enchondromas undergo malignant sarcomatous transformation. Int Pediatr. 2002;17(4):231-232. Full Article in PDF

79. Tumors ChondrosarcID5063.txt
While most enchondromas are solitary, patients with ollier's disease and Maffucci'ssyndrome demonstrate multiple enchondromas.A minority (15%) of
http://www.infobiogen.fr/services/chromcancer/Tumors/chondrosarcID5063.html
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Home Genes Leukemias Solid Tumours ... NA
Chondrosarcoma
Identity Figure 1: En bloc resection specimen of the proximal fibula of a 43 year old female, containing a lobulated bluish white, translucent tumour (4.5 x 2 x 1.9 cm) located centrally within the medullary cavity, consistent with central chondrosarcoma
Figure 2: Corresponding macro-slice showing a lobular architecture, and endosteal cortical thinning. Cytonucle ar appearance can be more readily appreciated in figure 3 Classification Note approximately 90% of chondrosarcomas are histologically of the conventional type; in addition to conventional chondrosarcoma, some rare variants with distinctive microscopic and clinical features are discerned: clear cell chondrosarcoma (1%), mesenchymal chondrosarcoma (2%), juxtacortical chondrosarcoma (2%) and extra-skeletal myxoid chondrosarcoma (5%). Furthermore, dedifferentiated chondrosarcoma is a relatively rare high grade sarcoma next to a low-grade conventional malignant cartilage-forming tumor, comprising 6-10% of all chondrosarcomas. Conventional chondrosarcomas can be categorized according to their location in bone. The majority of chondrosarcomas (75%) are located centrally within the medullary cavity (central chondrosarcoma), a small percentage of which arise within a preexisting benign precursor (enchondroma). While most enchondromas are solitary, patients with Ollier's disease and Maffucci's syndrome demonstrate multiple enchondromas.A minority (15%) of chondrosarcomas develops from the surface of bone (peripheral chondrosarcoma) as a result of malignant transformation within the cartilaginous cap of a solitary or hereditary pre-existent osteochondroma.

80. IComm: File Not Found!
ollier's disease .. ollier's diseaseSelf Help Group http//uhsweb.edu/olliers/olliers.htm. ollier's
http://www.icomm.ca/geneinfo/o.htm
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