21. Targeted Disruption Of Exons 1 To 6 Of The Fanconi Anemia Group A Targeted disruption of exons 1 to 6 of the fanconi anemia group A gene leads to growth retardation, strainspecific microphthalmia, meiotic defects http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

22. Heterozygosity For P53 (Trp53+/-) Accelerates Epithelial Tumor Heterozygosity for p53 (Trp53+/) Accelerates Epithelial Tumor Formation in fanconi anemia Complementation Group D2 (Fancd2) Knockout Mice http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. OMIM - FANCONI ANEMIA; FA http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650

24. Gonadotropin-Releasing Hormone Regulates Expression Of The DNA GonadotropinReleasing Hormone Regulates Expression of the DNA Damage Repair Gene, fanconi anemia A, in Pituitary Gonadotroph Cells1 http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

25. Entrez PubMed fanconi anemia is a polygenic trait hypothesized to be a DNA damage repair disease.We show that all three fanconi anemia loci that have been cloned are http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

26. WELCOME TO FANCONI CANADA Canadian charity whose mission is to fund medical research into finding a cure for fanconi anemia and to serve as a support network for affected Canadian families. http://www.fanconicanada.org

Home 2006 Toronto Fundraiser 2005 National Anemia Patient Conference Fanconi Anemia ... Donate Now FAMILIES Families Welcome Page PHYSICIANS/RESEARCHERS Sitemap Home Virtual Office of Janelle Redekop April 25, 1990 - June 9th, 2004 GIVE THEM TOMORROW Fanconi Canada is a registered charity whose mission is to fund research in Canada into an effective treatment and, ultimately, a cure for Fanconi Anemia and to serve as a support network for affected Canadian families. Canada Revenue Agency reg'n no. 868951724 RR 0001 Pour francais, pousser ici OVER $50,000 RAISED FOR FA RESEARCH 2005 Fundraiser Sponsors Thanks for Visiting! Canadian Fanconi Anemia Research Fund / La Fondation Canadienne de Recherche de L'Anemie de Fanconi Home 2006 Toronto Fundraiser 2005 National Anemia Patient Conference Fanconi Anemia ... Families Welcome Page

27. USATODAY.com - Early Genetic Testing Allays Fears, Ignites Ethics leukemia or aplastic anemia. The first reported case of this dual use of PGD involved Molly Nash, a Denver girl born with fanconi anemia, which http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

28. Fanconi Anemia Web fanconi anemia Web has documented Medical information downloads for this rareterminal childhood disease and support for patients and their families. http://lt.tripod.com/tr/directory/_h_/members.tripod.com/fanconianemiaweb/

var TlxPgNm='index'; setAdGroup('67.18.104.18'); var cm_role = "live" var cm_host = "tripod.lycos.com" var cm_taxid = "/memberembedded" Search: Lycos Tripod TV, Movie News Share This Page Report Abuse Edit your Site ... Next Quality Web Site Design that is helping to save terminally ill kids lives by donating 15% of their web design fee to The Fanconi Anemia Research Fund! FastCounter by bCentral (View Maximized to display correctly) Pages may load slowly, Thank you for your patience! Welcome to the: "Fanconi Anemia Web" WEB SITE Fanconi Anemia is a rare and terminal genetic childhood disease that results in death due to Bone marrow failure. See Tucker's "Tucker Time!" photo page My baby boy Tucker's fatal Fanconi Anemia diagnosis totally devastated and encompassed my life with despair...Never have I experienced such a profound weeping of my soul... The only way I Knew that I was going to be able to break the paralyzing depression I was in, was to try to turn my despair into Hope . By devoting myself to "Taking Action" And doing all I can to offer help and resources to others dealing with this heartbreaking disease, and to provide up to date access to medical documentation for Doctors, researchers, medical students and anyone seeking knowlege on this very rare genetic childhood disease. I pray there is a "Miracle" behind the tragedy of this disease...for it is well documented that researchers world wide are learning more and more that equal to the extreme rareness of Fanconi Anemia is counter matched by concentrated properties and similarities that with continued research could unveil a cure for cancer and Leukemia as well. That truly would be a breakthrough for all mankind not just the rare several thousand Fanconi Anemia cases reported globally. The urgency of continued research is also why I created this Web Site to generate a comradery of Fundraising efforts, volunteers and contributions to The Fanconi Anemia Research Fund. I also donate 20% of my web site design fee to the Research Fund as well at my other site:

29. B+ Home A charitable organization providing assistance to children with fanconi anemia within the St. Louis and St. Charles Missouri metro areas. http://www.bpositiveinc.com

B Positive! Bone Marrow Drive Schedule UPDATE B Positive, Inc. P.O. Box 533 Chesterfield, Mo. 63006-0533 (314) 503-BPOS (2767) In December, 2000, two St. Louis area siblings, Matthew Pearl, age 4, and Alexandra Pearl, age 6, were diagnosed with Fanconi Anemia . At the same time, they discovered that each child had B+ blood types and that their only hope for finding a cure was successful bone marrow transplant. The odds of any given individual, other than an immediate family member, being a perfect match is about one in a million. Alex received her bone marrow transplant in May, 2001 and is recovering well... however, no match for Matt has been found yet. We need your help! For more about Alex and Matt, visit their web site at www.alexandmatt.com Welcome to the B Positive, Inc. Web Site! For those who do not know exactly what Fanconi Anemia is, it is a genetic, life-threatening, inherited blood disorder that leads to bone marrow failure. It occurs equally in males and females and is found in all ethnic groups.

30. Alex And Matt Pearl Personal stories of two children fighting fanconi anemia. http://www.alexandmatt.com

PHOTO GALLERY UPDATED!! OVER 500 PHOTOS!! Hi, most of you may know our story; we are Alexandra and Matthew Pearl In December 2000 and January 2001 we were both diagnosed with a rare, life threatening blood disease called Fanconi anemia. It causes bone marrow failure; our bodies cannot make the blood we need to survive. Our only hope is a bone marrow transplant. Cardinals Help With Bone Marrow Drive For Eureka Child Read Press Release Alex has found a perfect match and is recovering from her May 31, 2001 transplant in Cincinnati, Ohio. There is no perfect match for Matthew, in any registry throughout the entire world. We need your help, please consider getting added to the National Bone Marrow Registry through the Pearl Million-Donor March. Refer to the ' How You Can Help ' section.

31. Fanconi Anemia: The Frohnmayer Family's Experience http://darkwing.uoregon.edu/~lfrohn/

32. Adam Day Learn about a boy who passed away after a fight with fanconi anemia. Find out how to make a donation to the fanconi anemia Research Fund. http://www.adam.interactiveinc.com/

Posted by Darla on February 28, 1997 at 03:02:11: Soaring with angels Greetings All: We, again would like to thank everyone for their sincere and heartfelt support. We literally could not have come as far as we did without all of you. We regretfully inform you all that Adam passed away at 9:11 PM, Minnesota time, on February 27, 1997. He was peaceful and pain-free when he passed. His family was with him, as was most of the staff from 4A, who have care for him in the entire duration of our stay here. We will happily inform everyone, though that Adam is now soaring with the angels, watching down protectively on all of us. We're sure he is having go-cart races with Mark Muellen and showing his knife collection to Joey Adamson and fishing with John Dumouchel. We will miss him but we know he is in a better place. May God bless all of you and shower you with goodness, health and many miracles. Thank you again. The Day Family Adam's Uncle Bob went to Minnesota during 1/30-2/3 and took some photos. Adam was in great spirits despite the constant interruptions by a wide variety of physicians and assistants. Go to: http://www.geocities.com/Heartland/Hills/2219/

33. Fanconi's Anemia Links to articles, information and support for fanconi anemia. http://rarediseases.about.com/cs/fanconisanemia/

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases 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/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Fanconi anemia Guide picks An inherited anemia that leads to bone marrow failure (aplastic anemia). Fanconi Anemia "Crossing the Line in Baby-Making?" looks at a family who selected an embryo and had a baby specifically for his ability to donate bone marrow to his older sister with Fanconi anemia. Describes symptoms, diagnosis, and treatment of Fanconi anemia. Fanconi's Anemia: Definition Brief definition of the disorder, with links, from the National Organization for Rare Disorders. Fanconi Anemia Research Fund Lists information, events, and offers support. Hope for Henry Personal story and photos of a boy's struggle with the disorder. Back to index of blood disorders Topic Index Email to a Friend Our Story ... Patent Info.

34. Key Protein For Fanconi Anemia Isolated Researchers at the Oregon Health Science University have discovered a newprotein involved with fanconi anemia. When this protein, called PHF9, http://rarediseases.about.com/b/a/031779.htm

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases 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/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Key protein for Fanconi anemia isolated Rare/Orphan Diseases Blog Main October 03, 2003 Key protein for Fanconi anemia isolated Fanconi anemia . When this protein, called PHF9, is inactivated, it disables the function of a network of proteins critical to cell life. The Fanconi Anemia Research Fund and the National Institutes of Health funded portions of the research. Email a Friend Display Latest Headlines Read Archives Advertisement Most Popular Muscular Dystrophy ALD and Lorenzo's Oil Progeria Syndromes Leprosy (Hansen's Disease) ... The Elephant Man What's Hot Muscular Dystrophy Autoimmune Kidney Disease Minamata Disease Charcot-Marie-Tooth Disease ... Meckel-Gruber Syndrome adunitCM(150,100,'x55') Topic Index Email to a Friend Our Story Be a Guide ... Patent Info.

35. Fanconi Anemia - Wikipedia, The Free Encyclopedia fanconi anemia (FA) is a rare genetic disease that affects children and adultsfrom all ethnic backgrounds. Named for Swiss pediatrician, Guido Fanconi, http://en.wikipedia.org/wiki/Fanconi_anemia

You did it! Over US$240,000 was donated in the 21 day fund drive. Thank you for your generosity! You are still welcome to make a donation or purchase Wikimedia merchandise Fanconi anemia From Wikipedia, the free encyclopedia. Fanconi anemia (FA) is a rare genetic disease that affects children and adults from all ethnic backgrounds. Named for Swiss pediatrician, Guido Fanconi , it is one of the inherited anemias that leads to bone marrow failure ( aplastic anemia FA is primarily a autosomal recessive genetic condition. There are at least 8 genes for which mutations in are known to cause FA: A, C, D1, D2, F, G, L, and B. FANCB is the one exception to FA being autosomal recessive, as this gene is on the X chromosome. For an autosomal recessive disorder, both parents must be carriers in order for a child to inherit the condition. If both parents are carriers, there is a 25% risk with each pregnancy for the mother to have an affected child. Approximately 1,000 persons worldwide presently suffer from the disease. The carrier frequency in the Ashkenazi Jewish population is about 1/90. Genetic counseling and genetic testing is recommended for families that may be carriers of Fanconi anemia.

36. Fanconi Anemia Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/GB/fanconi_anemia.html

Orphanet database access Fanconi anemia Direct access to data Summary in situ somatic hybridization, followed by the search for complementation for the cytotoxic response to DNA cross-linking agents, using lymphoblastoid cell lines, led to the identification of 8 complementation groups (FANCA-FANCH), each of which was thought to represent a unique gene. To date, 6 FANC genes have been cloned. A unified and precise understanding of the biochemical events responsible for FA is still lacking. The functions of the different FANC genes remain unknown. *Author: Dr E. Moustacchi (October 2003)*. Full text http://www.orpha.net/data/patho/GB/uk-FA.pdf Clinical signs Autosomal recessive inheritance Chromosome breakage Haematological system Increased skin pigmentation diffuse Short stature/dwarfism Thumb anomalies (other than hypoplasia) Abnormal urinary tract/renal function Cardiac septal defect Mental retardation(degree not assessed) Microcephaly Agenesis/hypoplasia of kidneys Blepharophimosis/short palp. fissures Cafe-au-lait spot Cleft palate Clinodactyly of fifth finger Dilated cerebral ventricles Dislocated hip Duodenum atresia/sten./annular pancreas

37. Fanconi Anemia Definition - Medical Dictionary Definitions Of Popular Medical Te Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=9616

38. Fanconi Anemia: Definition And Much More From Answers.com fanconi anemia fanconi anemia A genetic disease that affects all of the bonemarrow elements, is associated with a great diversity of malformations. http://www.answers.com/topic/fanconi-anemia

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Medical Term Medical WordNet Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Fanconi anemia Medical Term Fanconi anemia Fanconi anemia A genetic disease that affects all of the bone marrow elements, is associated with a great diversity of malformations as well as pigmentary changes of the skin, and predisposes to malignancy. Malignancy : Fanconi anemia predisposes particularly to a disturbance of bone marrow growth called myelodysplasia and to acute myeloid leukemia . Patients tend also to develop cancers in areas of the body where cells normally reproduce rapidly, such as the mouth, esophagus, the intestinal and urinary tracts, and the reproductive organs. Clinical features : Children with Fanconi anemia usually have low birth weight, are smaller than average at birth and tend to have the following birth defects Skin pigment changes (65% of cases) Caf©-au-lait spots (coffee-with-milk spots) on the skin Brownish pigmentation of the body so it has a suntanned look Large freckles Short stature (60% of cases) Upper limb malformations (50% of cases): Underdeveloped or missing radius (a forearm bone) Misshapen or missing thumbs Clinodactyly (curved fingers), polydactyly (extra fingers), absent finger bones, short fingers

39. Fanconi Anemia, Cincinnati Children's Hospital Medical Center fanconi anemia (FA) signs, symptoms and longterm outlook information by CincinnatiChildren s Hospital Medical Center. http://www.cincinnatichildrens.org/health/info/blood/diagnose/fanconi-anemia.htm

Home Contact Us Site Map Go to Advanced Search ... Conditions and Diagnoses Fanconi Anemia Hemophilia Sickle Cell Anemia von Willebrand Disease Home Care ... Tests and Procedures Conditions and Diagnoses Fanconi Anemia: Signs, Symptoms, Long-Term Outlook Related Services Blood Disease Center Fanconi Anemia Center Bone Marrow Failure Clinic Fanconi Anemia (FA) is one of the inherited anemias that leads to bone marrow failure or aplastic anemia. If both parents carry a defect (mutation) in the same Fanconi Anemia gene, and if their children inherit the defective gene from both parents, the child will be born with Fanconi Anemia. Signs and Symptoms Fanconi Anemia may be evident at birth by a combination of the following physical traits: Short stature Thumb, arm and skeletal anomalies in the hips, spine and ribs Kidney problems Skin discoloration Small head and eyes Learning disabilities Low birth weight Gastrointestinal difficulties Small reproductive organs in males Heart defects Children with Fanconi Anemia are usually diagnosed by age 12, when they may exhibit some or all of these symptoms: Sudden and extreme fatigue Recurrent infections Frequent nosebleeds Easy bruising Long-Term Outlook Fanconi Anemia usually becomes more severe over time. There is also a risk that some patients may develop leukemia or other

40. Fanconi Anemia, Cincinnati Children's Hospital Medical Center Cincinnati Children s Hospital Medical Center presents fanconi anemia clinicaltrials information. http://www.cincinnatichildrens.org/svc/alpha/c/cancer/trials/fanconi/

Home Contact Us Site Map Go to Advanced Search ... Fanconi Anemia Overview Hodgkin's Lymphoma Neuroblastoma Neurofibromatosis and Neoplasia Non-Hodgkin's Lymphoma ... News Releases Fanconi Anemia Overview Find detailed information on a selected Phase I or Phase II clinical trial for Fanconi Anemia at Cincinnati Children's Hospital Medical Center. There are two versions of some of the trials. While they contain the same basic information, one version is geared toward healthcare professionals and the other is geared toward families. Trial Healthcare Professional Version Family-Friendly Version Collection of Hematopoietic Cells from Patients with Fanconi Anemia (FA) for Future Autologous Reinfusion and Research Professional Family Friendly Non-Genoidentical Donor Stem Cell Transplantation for Fanconi Anemia: Good Risk Regimen Professional Not Available Non-Genoidentical Donor Stem Cell Transplantation for Fanconi Anemia: Good Risk Regimen: Cord Blood Professional Not Available Reinfusion of Autologous Bone Marrow, Cord Blood and Peripheral Blood Progenitor Cells from Patients with Fanconi Anemia Professional Family Friendly Repository of Tissue Samples and Data from Patients with Fanconi Anemia Professional Not Available A Pilot Trial of Oxandrolone for the Treatment Of Bone Marrow Aplasia in Patients with Fanconi Anemia Professional Family Friendly Gene Transfer for Patients with Fanconi Anemia, Genotype A: A Pilot Study

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