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Fanconi Anemia:     more books (21)

Fanconi Anemia: Clinical, Cytogenetic and Experimental Aspects C. elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair [An article from: DNA Repair] by S.J. Collis, L.J. Barber, et all 2006-11-08 Role of the Fancg gene in protecting cells from particulate chromate-induced chromosome instability [An article from: Mut.Res.-Genetic Toxicology and Environmental Mutagenesis] by L.C. Savery, E. Grlickova-Duzevik, et all 2007-01-10 Interstrand crosslink-induced radials form between non-homologous chromosomes, but are absent in sex chromosomes [An article from: DNA Repair] by A.E. Newell, Y.M.N. Akkari, et all 2004-05-04 Drosophila homologs of FANCD2 and FANCL function in DNA repair [An article from: DNA Repair] by L.R. Marek, A.E. Bale, 2006-11-08 FANCD2 monoubiquitination and activation by hexavalent chromium [Cr(VI)] exposure: Activation is not required for repair of Cr(VI)-induced DSBs [An article ... Toxicology and Environmental Mutagenesis] by S.K. Vilcheck, S. Ceryak, et all 2006-11-07 Influence of double-strand-break repair pathways on radiosensitivity throughout the cell cycle in CHO cells [An article from: DNA Repair] by J.M. Hinz, N.A. Yamada, et all

lists with details

21. Fanconi Anemia, Cincinnati Childrens Hospital Medical Center
    What is Known about fanconi anemia. fanconi anemia (FA) is one of the inheritedanemias that leads to bone marrow failure, or aplastic anemia.  
    http://www.cincinnatichildrens.org/Health_Topics/Your_Childs_Health/Hematology_a
    
    Extractions: Your Child's Health Hematology and Blood Overview Conditions and Diagnoses ... Hematology and Blood Disorders Fanconi Anemia Sickle Cell Anemia Tests and Procedures Home Care Fanconi Anemia (FA) is one of the inherited anemias that leads to bone marrow failure or aplastic anemia. Fanconi Anemia is an autosomal recessive disorder. 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: Children with Fanconi Anemia are usually diagnosed by age 12, when they may exhibit some or all of these symptoms: Long-Term Outlook Fanconi Anemia usually becomes more severe over time. There is also a risk that some patients may develop leukemia or other cancers.

22. Hope For Henry
    This web site is dedicated to helping people learn more about what a special young man Henry is and to educate everyone about the disease he is fighting, fanconi anemia.  
    http://www.hsg.org/
    
    Extractions: Publish Date June 30, 2001 Henry Strongin Goldberg was born on October 25, 1995. Henry knows all there is to know about Pokémon, believes that Disney World is the best place on earth, plays soccer, worships superheroes and wrestles with his younger brother Jack way past bedtime. Everything he does makes his parents smile. In these and so many other ways, Henry is a lot like other boys his age. But this lover of life and everything Batman is different from other kids because Henry has a horrible disease that threatens his life. After a scary and difficult five years of endless waiting rooms, doctor's visits, blood tests, EKG's, bone marrow aspirations, IV's, surgeries, transfusions, drugs, scars and a bone marrow transplant in July 2000 that met with innumerable complications, Henry faces a very uncertain future. This web site is dedicated to helping people learn more about what a special and brave young man Henry is and to educate everyone about the disease he is fighting, Fanconi anemia (FA). Through raising awareness and money for research and encouraging people to register to be a bone marrow donor, our family strives to give Hope for Henry and other children suffering from this killer. We welcome you to the site and encourage you to tell others about it and to bookmark this page so you can keep abreast of Henry's progress.

23. Fanconi Anemia Comprehensive Care Center, Cincinnati Childrens Hospital Medical
    fanconi anemia. Overview Together, Dr. Harris and Dr. Williams are leading a teamof caring experts at the first multidisciplinary fanconi anemia care center.  
    http://www.cincinnatichildrens.org/Services/Programs_And_Services/Fanconi_Anemia
    
    Extractions: Find Other Related Hematology/Oncology Programs and Services New Approach to Care, Renewed Hope for Patients and Families The Fanconi Anemia Comprehensive Care Center at Cincinnati Children's Hospital Medical Center is a first-of-its-kind center in the United States dedicated to compassionate, multidisciplinary care of children with Fanconi Anemia (FA) and other rare bone marrow failure syndromes. Distinguished experts Richard Harris, MD , and David Williams, MD , lead a team of specialists to deliver organized, outstanding medical, surgical and behavioral care at multiple levels. At the Fanconi Anemia Comprehensive Care Center, you'll discover a unique focus on care for children with Fanconi Anemia and support for their families. Multidisciplinary Approach Offers Patients Optimal Care The Fanconi Anemia Comprehensive Care Center provides a multidisciplinary approach to caring for children with Fanconi Anemia and other rare bone marrow failure syndromes. Collectively, experts from numerous areas of specialty can offer children and their families optimal care. The Fanconi Anemia Comprehensive Care Center designs personalized, ongoing treatment regimens for patients, delivered by specialists in the following areas:

24. Fanconi Anemia: The Frohnmayer Family's Experience
    The personal story of David and Lynn Frohnmayer whose three daughters were born with fanconi anemia, an inherited, usually fatal illness.  
    http://darkwing.uoregon.edu/~lfrohn/

25. Fanconi Anemia: The Frohnmayer Family's Experience
    http://oregon.uoregon.edu/~lfrohn/lynn.html

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

27. BMT InfoNet Home Page
    Breast Cancer. Cancer general. fanconi anemia. Graft-Versus-Host Disease. GriefCounselling. Immune Deficiency. Becoming a Donor. Finding a Donor. fanconi anemia.  
    http://www2.bmtnews.org/resource/index.cfm?Fuseaction=ResourceResults&Category=2

28. 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
    
    Extractions: 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. Though considered primarily a blood disorder, it may affect all systems of the body. Many patients develop acute myelgenous leukemia (AML). Older patients may develop other cancers. Many patients will not reach adulthood. Currently the only long-term cure for Fanconi Anemia is a bone marrow transplant. For additional information, please refer to

29. Aplastic Anemia
    fanconi anemia Fanconi's Anemia. Page, Marrow Index.  
    http://www.fpnotebook.com/HEM132.htm
    
    Extractions: Home About Links Index ... Editor's Choice Paid Advertisement (click above). Please see the privacy statement Hematology and Oncology Marrow Anemia Aplastic Anemia Fanconi Anemia Assorted Pages Macroglobulinemia Multiple Myeloma Myelofibrosis Polycythemia Rubra Vera ... Bone Marrow Aspiration Aplastic Anemia Book Home Page Cardiovascular Medicine Dental Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Hematology and Oncology Index Anemia Cancer Coagulopathy Cardiovascular Medicine Dermatology Endocrinology Otolaryngology Examination Gastroenterology Hematology and Oncology Hemoglobin Hemolysis Histiocytosis HIV Infectious Disease Laboratory Leukemia General Pulmonology Lymph Marrow Neurology Obstetrics Orthopedics Pediatrics Pharmacology Platelet Prevention Procedure Psychiatry Rheumatology Surgery Symptom Evaluation Vascular Page Marrow Index Anemia Aplastic Anemia Fanconi Macroglobulinemia Multiple Myeloma Myelofibrosis Polycythemia Epidemiology Median age of onset: 25 years Presentation: Symptoms Fatigue Fever Causes: Acquired Idiopathic (most common cause) Viral infection Infectious Mononucleosis Viral Hepatitis (non-A non-B non-C) Human Immunodeficiency Virus Medications Cancer Chemotherapy (common cause) Antileukemic medications Nitrogen mustard

30. Alex And Matt Pearl
    Personal stories of two children fighting fanconi anemia.  
    http://www.alexandmatt.com
    
    Extractions: 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. 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. Presentation (PPT) My little girl (PPT) ... more docs, click here Who knows, maybe you could be the perfect match that saves Matthew's or the 3,000 others in need. Thanks to all who have helped to add more than 17,000 people to the registry, that have resulted in at least 40 matches for others. It is a good start, but there is much work to be done. God Bless and Thank you

31. Kprones FA10001
    Karyotype evolution in the bone marrow of a patient with fanconi anemia breakpointsin clonal anomalies of this disease. fanconi anemia and DNA repair.  
    http://www.infobiogen.fr/services/chromcancer/Kprones/FA10001.html
    
    Extractions: Home Genes Leukemias Solid Tumours ... NA Identity Note Fanconi anaemia is a chromosome instability syndrome with progressive bone marrow failure and an increased risk of cancers Other names Fanconi pancytopenia Inheritance autosomal recessive; frequency is about 2.5/10 newborns Clinics Phenotype and clinics growth retardation (70% of cases) skin abnormalities: hyperpigmentation and/or café au lait spots in 80% squeletal malformations (60%), particularly radius axis defects (absent or hypoplastic thumb or radius...) no immune deficiency (in contrast with most other chromosome instability syndromes) progressive bone marrow failure; mean age of onset of anemia: 8 yrs; diagnosis made before onset of haematologic manifestations in only 30% other: renal anomalies, hypogonadism, mental impairment, heart defects, and perhaps diabetes mellitus, also occur in 10 to 30% of cases Neoplastic risk myelodysplasia (MDS) and acute non lyphocytic leukaemia (ANLL): 15% of cases; i.e. a 15000 fold increased risk of MDS and ANLL has been evaluated in FA, and it has been assumed that 'it is reasonable to regard the Fanconi anemia genotype as "preleukemia"'; mean age at diagnosis: 13-15 yrs hepatocarcinoma (androgen-therapy induced) in 10%; mean age at diagnosis: 16 yrs

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/
    
    Extractions: 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. Short Description Of Cell Lines. Pathology Fanconi Anemia
    Version 4.200205, Short description of cell lines. Pathology Fanconianemia OMIM Home. By selecting the cell line name, you will  
    http://www.biotech.ist.unige.it/cldb/pat32.html

34. MEDLINEplus: Anemia
    Blood Donor Anemia (Mayo Foundation for Medical Education and Research); WhatIs fanconi anemia and How Is It Diagnosed? (fanconi anemia Research Fund).  
    http://www.nlm.nih.gov/medlineplus/anemia.html

35. Center For Jewish Genetic Disorders | Fanconi Anemia
    Information about fanconi anemia and other genetic disorders which are unusuallycommon in Jews of eastern European descent, including symptoms, inheritance  
    http://www.jewishgenetics.org/fanane.htm
    
    Extractions: Fanconi anemia is a disorder characterized by a reduced production of all types of blood cells in the body. The most serious problem associated with this disorder is an increased risk for cancer. The underlying problem in this condition affects how the genetic information is copied in the cells of the body. The disorder can be seen in individuals from any ethnic background, but one specific gene alteration has been noted in individuals of Jewish ancestry. No effective treatment exists at this time. Disease frequency: Unknown Carrier frequency: Approximately 1 in 89 for a specific gene alteration noted in those of Jewish ancestry. Diagnosis: By a specialized type of chromosome testing or specific testing of one of the genes involved in Fanconi anemia. Inheritance: Autosomal Recessive Carrier testing: Available by testing for a specific gene alteration. Testing detects 95% of carriers for this specific type of Fanconi anemia. Prenatal diagnosis: Available through genetic testing in couples with a previous affected child or couples identified as being carriers.

36. HealthlinkUSA Fanconi Anemia Links
    medical and health related topics. FindWhat. Click here for page 1of fanconi anemia information from the HealthlinkUSA directory.  
    http://www.healthlinkusa.com/110ent.htm

37. Fanconi Anemia; Treatment, Prevention, Cure
    fanconi anemiaSearch information from many of the best fanconi anemia health sites. Clickhere to go to the next page of fanconi anemia links 1 2 3 4 5 Next  
    http://www.healthlinkusa.com/content/110.html

38. Nature Publishing Group
    p 1259 Cellular function of the fanconi anemia pathway Alan D. D'Andrea Harvard MedicalSchool Boston, Massachusetts, USA email alan_dandrea@dfci.harvard.edu.  
    http://www.nature.com/cgi-taf/DynaPage.taf?file=/nm/journal/v7/n12/full/nm1201-1

39. Nature Publishing Group
    doi10.1038/nm12011259b December 2001 Volume 7 Number 12 pp 1259 - 1260 Replyto 'Cellular function of the fanconi anemia pathway' Robert C. Cumming 1  
    http://www.nature.com/cgi-taf/DynaPage.taf?file=/nm/journal/v7/n12/full/nm1201-1

40. Fanconi Anemia
    fanconi anemia is an inherited disorder characterized by a reduced number ofall types of blood cells in the body, leading to bone marrow failure.  
    http://www.einstein.edu/e3front.dll?durki=7171

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