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  1. Aniridia and WAGR Syndrome: A Guide for Patients and Their Families

61. Www.ohsu.edu/cliniweb/C11/C11.250.60.html
www.dictionarybarn.com/WAGRSYNDROME.php SearchBug Directory Health Conditions_and_Diseases Search wagr syndrome, wagr syndrome - http//www.wagr.org Information forfamilies or physicians interested in learning more about wagr syndrome.
http://www.ohsu.edu/cliniweb/C11/C11.250.60.html

62. Health Library -
wagr syndrome. 3 affiliated groups. Founded 2000. Provides information andsupport to persons with wagr syndrome or aniridia, and their families.
http://healthlink.uhseast.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29w

63. Fablis Directory For /Health/Conditions_and_Diseases/Neurological_Disorders/Chro
wagr syndrome. Sponsors. Become a sponsor. See also NORD wagr syndrome Offers the synonyms, a general discussion and further resources.
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Health Chromosomal WAGR Syndrome Click here to list your site See also: This category needs an editor Last Updated: 2003-08-29 14:01:32 Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor
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64. Mioti: Diseases + Conditions
Diseases + Conditions wagr syndrome. Search Mioti
http://www.mioti.com/cat/condition/condition.asp?Cat=WAGRSyndrome

65. WAGR Syndrome
Google, WWW Medical.WebEnds.com. wagr syndrome. Google links. WAGR.org http//www.wagr.org/.wagr syndrome DESCRIPTION http//www.wagr.org/pages/432549/.
http://medical.webends.com/kw/WAGR Syndrome
Medical.WebEnds.com - Medical Terminology Dictionary
A B C D ... Z
WWW Medical.WebEnds.com
WAGR Syndrome
Contiguous Gene Syndrome, WAGR; Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome; WAGR Complex; WAGR Contiguous Gene Syndrome; Complices, WAGR; Syndrome, WAGR; Syndromes, WAGR; WAGR Complices; WAGR Syndromes A contiguous gene syndrome ANIRIDIA (A), genitourinary abnormalities (G), and MENTAL RETARDATION (R).
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66. Results Of The Search
wagr syndrome, Wilms tumor, aniridia, gonadoblastoma, mental retardation a reviewapropos of 2 cases MC Mochon T Philip Pediatrie 1987 ;42(4);24952.
http://invention.swmed.edu/trite/abstracts/user-1015659130/results.shtml
New This Month New This Year Submitted paragraph
[Molecular genetic study of the PAX6 gene in aniridia patients]
M Wolf ... G Wildhardt Ophthalmologe 1998 Dec;95(12);828-30.

Score: 0.57
Del11p13/nephroblastoma without aniridia.
C Turleau ... C Junien Hum Genet 1984 ;67(4);455-6.

Score: 0.56
Non-progressive mental retardation and peripheral neuropathy in a mother and her son.
C Longman ... R McWilliam Clin Dysmorphol 2001 Oct;10(4);273-6.

Score: 0.56
PAX6 mutations in aniridia.
I M Hanson ... V van Heyningen Hum Mol Genet 1993 Jul;2(7);915-20.

Score: 0.56
Wilms's tumour and aniridia: clinical and cytogenetic features.
R S Shannon ... A Herbert Arch Dis Child 1982 Sep;57(9);685-90.

Score: 0.56
Wilms tumour associated with unilateral dysplasia of the iris.
D G Harendra de Silva ... S Liyanaarachchi Ceylon Med J 1992 Mar;37(1);24-5.

Score: 0.54
Aniridia-Wilms' tumour syndromea case report.
M S Vidyasagar ... P Rao Indian J Ophthalmol 1992 Oct-Dec;40(4);122-3.

Score: 0.54
Aniridia: recent achievements in paediatric practice.
I Ivanov ... R Weitz Eur J Pediatr 1995 Oct;154(10);795-800.

67. Health Library -
wagr syndrome. Important It is possible that the main title of thereport wagr syndrome is not the name you expected. Please check
http://myhealth.barnesjewish.org/library/healthguide/illnessconditions/topic.asp

68. Health Library -
wagr syndrome. 3 affiliated groups. Founded 2000. Provides information andsupport to persons with wagr syndrome or aniridia, and their families.
http://myhealth.barnesjewish.org/library/healthguide/selfhelp/topic.asp?hwid=shc

69. Mental Retardation, Directory
wagr syndrome. wagr syndrome, OMIM wagr syndrome, NORD Waisman Syndrome. PARKINSONISM,EARLYONSET, WITH MENTAL RETARDATION, OMIM, Victor A. McKusick.
http://www.saunalahti.fi/kup/engl/webs_w.html
Finnish Information Center on Mental Retardation
English links
A B C D ... Z
Waardenburg Anophthalmia Syndrome
ANOPHTHALMOS WITH LIMB ANOMALIES (OMIM)
ophthalmo-acromelic syndrome, U.S. National Library of Medicine

Waardenburg Syndrome, NORD

Ophthalmo-Acromelic Syndrome, Orphanet
...
Waardenburg's syndrome III, Whonamedit
WAGR SYNDROME
WAGR SYNDROME, OMIM
WAGR SYNDROME, NORD
Waisman Syndrome
PARKINSONISM, EARLY-ONSET, WITH MENTAL RETARDATION, OMIM, Victor A. McKusick
Walker-Warburg Syndrome
Walker-Warburg syndrome (WWS), Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes, Steven Jablonski
Walker-Warburg, Case report, syndrome, Swiss Society of Neonatology

Warburg Syndrome, Walsh Laboratory, Christopher A. Walker

Cerebro-ocular dysplasia-muscular dystrophy (COD-MD) syndrome, PubMed
...
Pagon's syndrome Whonamedit
Watson Syndrome
WATSON SYNDROME, OMIM, Victor A. McKusick
Watson syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
Watson syndrome, Orphanet The patient is a 6-year-old male with multiple café au lait spots and a history of pulmonary stenosis, Radiology, University of Rochester Medical Center, Terry Chun and P-L Westesson ... Neurofibromatosis Resources - Photographs
Weaver Syndrome
WEAVER SYNDROME, OMIM

70. Wilms' Tumour - Genetics
Wilms tumor and wagr syndrome. Medline Search wagr syndrome (PubMed) Limit searchto Last Year Limit search to Last 2 Years Limit search to Reviews
http://www.cancerindex.org/geneweb/X210202.htm
Cancer Genetics Web
www.cancer genetics.org
Wilms' Tumour
Mutated Genes and Abnormal Protein Expression
Recurrent Chromosome Abnormalities
Overview of the Molecular Biology of Wilms' Tumour
Familial Wilms' Tumour
Wilms' tumor and WAGR syndrome
Wilms' Tumour and Beckwith-Wiedemann Syndrome
Denys-Drash Syndrome and Wilms' Tumour
Perlman Syndrome and Wilms' Tumour
LOH 16q in Wilms' Tumour LOH 19q in Familial Wilms' Tumour (FWT2 19q13.3-q13.4) Wilms' Tumour: Clinical and Epidemiological Resources Mutated Genes and Abnormal Protein Expression Gene Location Topics IGF2R Imprinting Errors in Wilms' Tumour CDKN2A Expression in Wilms' Tumour SET ( PHAPII , I2PP2A ) SET Expression in Wilms' Tumour WT1 and Wilms' Tumour WT2 and Wilms' Tumour (putative) IGF2 Imprinting and Overexpression in Wilms' Tumour ... GPC3 Expression in Wilms' Tumour Recurrent Chromosome Abnormalities LOH 16q in Wilms' Tumour LOH 19q in Familial Wilms' Tumour (FWT2 19q13.3-q13.4)
Related links:
Recurrent Chromosome Abnormalities - Wilms' tumor (Cancer Genome Anatomy Project)
Overview of the Molecular Biology of Wilms' Tumour Familial Wilms' tumour (defined as either bilateral disease or a family history of Wilms' tumour) account for approximately 5% of cases. For those with sporadic (unilateral) disease the risk of Wilms' tumour among their offspring is low: in a series of 179 children from 96 survivors of unilateral Wilms' (Li, 1988) non had developed the disease (upper 95% CI 2%). Children with

71. NodeWorks - Neurological Disorders: Chromosomal: WAGR Syndrome
mental retardation (R). 1. NORD wagr syndrome Offers the synonyms,a general discussion and further resources. thumbnail, 2. Reaching
http://dir.nodeworks.com/Health/Conditions_and_Diseases/Neurological_Disorders/C
in entire NodeWorks Directory in Health in Neurological Disorders in Chromosomal in ++ WAGR Syndrome Top Health Neurological Disorders Chromosomal WAGR Syndrome A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), ANIRIDIA (A), genitourinary abnormalities (G), and mental retardation (R). NORD: WAGR Syndrome Offers the synonyms, a general discussion and further resources. Reaching Out - The WAGR Network Parent support network for families and professionals looking for information about WAGR Syndrome/Aniridia. WAGR Syndrome Information for families or physicians interested in learning more about WAGR Syndrome. Yahoo! Groups : WAGR Syndrome A brief description of this support group. Join, post and read messages.
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72. New Page 1
wagr syndrome assoicated to Health Just The Best Results from the LinkspiderOrganization. Click here for wagr syndrome assoicated to Health Websites.
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73. Wauu.DE: Health: Conditions And Diseases: Neurological Disorders: Chromosomal: W
Wauu.DE Health Conditions and Diseases Neurological Disorders Chromosomal WAGRSyndrome. Groups wagr syndrome A brief description of this support group.
http://www.wauu.de/Health/Conditions_and_Diseases/Neurological_Disorders/Chromos
Home Health Conditions and Diseases Neurological Disorders ... Chromosomal : WAGR Syndrome Search DMOZ-Verzeichnis:
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  • NORD - WAGR Syndrome
    Offers the synonyms, a general discussion and further resources.
  • Reaching Out - The WAGR Network
    Parent support network for families and professionals looking for information about WAGR Syndrome/Aniridia.
    http://members.aol.com/ReachingOutNet/
  • WAGR Syndrome
    Information for families or physicians interested in learning more about WAGR Syndrome.
    http://www.wagr.org
  • Yahoo! Groups : WAGR Syndrome
    A brief description of this support group. Join, post and read messages. http://groups.yahoo.com/group/WAGR
© 1998- 2002 Ein Service von Wauu.de UserNet.DE Linktip: MnogoSearch.ORG Map TopTen TopTen eng Aktuelle Linktips Mozilla 1.7 RC 1 Basteln 0190 Warner Free Rund ums Rad ... Fantasy - Shop Webmaster-Links Webspace Free Subdomain Service Merchandise Fun SUMA - Forum ... Abmahnungen œber Wauu Regeln Webmasterservice Impressum b

74. Principal's Office: Welcome (University Of Dundee)
gene, WT1, was first identified in 1990 because of its involvement in chromosomaldeletions in children suffering from the wagr syndrome (Wilms tumour, aniridia
http://www.dundee.ac.uk/principalsoffice/discoverydays/fleming.html
Text only Principal's Office Home Principal Vice Principals ... General University Information (inc. maps)
DISCOVERY DAYS
Professor Stewart Fleming, Professor of Cellular and Molecular Pathology
The Wilms' tumour gene wt1 causes kidney failure and childhood cancer
"When I die and doctors know not why,
My friends' curiosity
Shall have me cut up to survey each part"
John Donne
WT1 kidney failure and cancer
Another similar disease is the WAGR syndrome, but rather than point mutation we have found that this is a contiguous gene syndrome, involving loss of extensive chromosomal material on chromosome 11 including the WT1 gene, resulting in a constitutional loss of one copy of WT1. Recently it has been shown that 38% of WAGR patients subsequently develop renal failure. In both, DDS and WAGR disease develops despite possession of one normal copy of WT1, although the rate of progress and precise nature of the disease differs between the two syndromes. We subsequently found that, in both syndromes, the development of a Wilms' tumour requires a second event at WT1, usually loss of the one remaining normal allele (gene). Transgenic models of WT1 associated disease
To study the disease processes further and to confirm the causal role of wt1 we needed experimental models. We have developed two transgenic models of DDS and WAGR syndrome, in both of which progressive glomerulosclerosis leading to terminal renal failure is seen.

75. Descripteur : WAGR Syndrome = WAGR, SYNDROME
Descripteur wagr syndrome = WAGR, SYNDROME Définition NLM A contiguous genesyndrome associated with hemizygous deletions of chromosome region 11p13.
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    Descripteur : WAGR Syndrome = WAGR, SYNDROME A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), ANIRIDIA (A), genitourinary abnormalities (G), and MENTAL RETARDATION (R).
      C - Diseases : Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Genetic Diseases, Inborn: Chromosome Disorders: WAGR Syndrome C - Diseases : Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Abnormalities: Chromosome Disorders: WAGR Syndrome C - Diseases : Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Abnormalities: Urogenital Abnormalities: WAGR Syndrome C - Diseases : Urologic and Male Genital Diseases: Urogenital Diseases: Urogenital Abnormalities: WAGR Syndrome C - Diseases : Eye Diseases: Uveal Diseases: Iris Diseases: Aniridia: WAGR Syndrome C - Diseases : Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Genetic Diseases, Inborn: Eye Diseases, Hereditary: Aniridia:

76. A To Z Encyclopedia Topic: Wilms` Tumor
wagr syndrome the acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored
http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Wilms` Tumor

77. Wilms Tumor - Lucile Packard Children's Hospital
wagr syndrome The acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored part
http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/oncology/wilms.html
Bone Marrow Transplantation
Hematology

Hematopoietic Stem Cell Transplantation

Oncology
...
Oncology
Oncology
Wilms Tumor
What is Wilms tumor?
Wilms tumor, also called nephroblastoma, is a malignant (cancerous) tumor originating in the cells of the kidney. It is the most common type of renal (kidney) cancer and accounts for about 6 percent of all childhood cancers. Approximately 400 children in the US are diagnosed with a Wilms tumor each year. The disease can occur at any age between infancy and 15 years, but, in most cases, the tumor is detected by the age of 3. This cancer affects males and females equally. The tumor can be very large and it may spread (metastasize) to other body tissues. The most common site for Wilms tumor to metastasize is the lungs. Lesions may also occur, however, in the liver, the other kidney, brain, and/or bones. In approximately 5 to 10 percent of children with Wilms tumor, both kidneys are involved. What causes Wilms tumor?

78. Wuup.de - /Health/Conditions_and_Diseases/Neurological_Disorders
Translate this page wagr syndrome. Siehe auch Links. » NORD wagr syndrome - Offers thesynonyms, a general discussion and further resources. » Reaching
http://wuup.de/index.php/Health/Conditions_and_Diseases/Neurological_Disorders/C

79. Oncology
wagr syndrome the acronym WAGR stands for the four diseases present in wagr syndrome,including Wilms tumor, aniridia (absence of the iris, the colored part
http://www.rush.edu/rumc/page-P02747.html
Oncology
Oncology (Pediatrics)
Wilms Tumor
Wilms Tumor
What is Wilms tumor?
Wilms tumor, also called nephroblastoma, is a malignant (cancerous) tumor originating in the cells of the kidney. It is the most common type of renal (kidney) cancer and accounts for about 6 percent of all childhood cancers. Approximately 500 children in the US are diagnosed with Wilms tumor each year. The disease can occur at any age between infancy and 15 years, but, in most cases, the tumor is detected by the age of 3. This cancer affects males and females equally. The tumor can be very large and it may spread (metastasize) to other body tissues. The most common site for Wilms tumor to metastasize is the lungs. Lesions may also occur, however, in the liver, the other kidney, brain, and/or bones. In approximately 5 to 10 percent of children with Wilms tumor, both kidneys are involved.
What causes Wilms tumor?
It is uncommon for Wilms tumor to run in families. Less than 2 percent of cases will have an affected relative. Most cases of Wilms tumor are considered sporadic (occur by chance) and are the result of genetic mutations that affect cell growth in the kidney. These mutations generally arise after birth, but, in some cases, children are born with a genetic alteration that predisposes them to cancer. A small percentage of patients with Wilms tumor have one of three genetic syndromes, including the following:

80. Aniridia
a fourth type associated with Wilms tumor, genital abnormalities, and deletionof 11p13 ( wagr syndrome ) term WAGR WAGR is a syndrome ..
http://ibis-birthdefects.org/start/aniridia.htm
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... Etchings Please Explore: 11p Chromosome Eye / Ocular WAGR S. Wilms Tumor ... Key Information Sources Topics include Title and An2 Paired Box Homeotic Gene; PAX6 Gillespie S. Special Resources Aniridia A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group ANIRIDIA; AN1 from OMIM ... A form of aniridia is not linked to markers on 2p as previously thought, ... There probably is no form of autosomal dominant aniridia other than that which maps to 11p13 and was designated AN2 ... Shaw et al. (1960) ascertained 176 cases of aniridia in the lower Michigan peninsula ... mutation rate about 4 x 10(-6) per gamete per generation. Affected persons may be visually handicapped because of nystagmus, cataract or glaucoma ... Undoubtedly more than one "cause" of aniridia exists ... Gove et al. (1961) identified 77 cases of aniridia descended from an affected woman born in 1824 ... Delleman and Winkelman (1973) emphasized that atypical colobomata and slitlike defects of the iris stroma may be partial expressions of aniridia ... a fourth type associated with Wilms tumor, genital abnormalities, and deletion of 11p13 ( WAGR syndrome ) ... PAIRED BOX GENE 6; PAX6

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