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Hemophilia:     more books (100)

Hemophilia act of 1973: Hearing, Ninety-third Congress, first session, on S. 1326 by United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health., 1974-01-01 Hemophilia and Hemophilioid Diseases 21st Century Ultimate Medical Guide to Hemophilia - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-05-08 Encyclopedia of Family Health; Vol 5: Flotation Therapy - Hemophilia by Jacoby David B, 1998 Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.: An article from: Revista de Biología Tropical by Lizbeth Salazar-Sánchez, Guillermo Jiménez-Cruz, et all 2004-09-01 Gene therapy safe, feasible for patients with severe hemophilia A, Phase I study finds.(Brief Article): An article from: Transplant News Hemophilia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17 New Aspects of Hemophilia Treatment: 3rd Symposium, September 21-23, 1995 Copenhagen, Denmark (Haemostasis, Vol 26, Suppl 1) Vox Sanguinis (Viral Safety of Plasma-Derived Replacement Factors for Hemophilia , Vol 67, Suppl 4) by P. M. Mannucci, 1994-12 HEMOPHILIA: An entry from UXL's <i>UXL Complete Health Resource</i> Gale Encyclopedia of Nursing and Allied Health: Hemophilia by Jr., MD, DrPH L. Fleming Fallon, 2002-01-01 Von Willebrand's Disease and Hemophilia Clinical and Genetic Aspects by Kathelijne Peerlinck, 1994 Gene Therapy Promising for Hemophilia B.(Brief Article): An article from: Family Practice News by Bruce Jancin, 2000-09-15 Hemophilia by Inga Marie Nilsson, 1994

lists with details

81. Inheritance Of Hemophilia
    Xlinked Inheritance hemophilia. Legend hemophilia is a sex linked traitin humans, inherited in the same way white eye color in Drosophila.  
    http://www.accessexcellence.org/AB/GG/x-linked.html
    
    Extractions: Hemophilia is a sex linked trait in humans, inherited in the same way white eye color in Drosophila. Males are hemizygous, receiving their only X chromosome from their mother. Females are heterozygous, inheriting X chromosomes from both parents. If a female has a defective gene on one of her two X chromosomes, she will be protected from its effects by the normal gene on her second X chromosome. If a male has a mutant X and a normal Y chromosome, he will be affected by a X-linked disease. A heterozygous carrier mother and a normal father pass the gene for hemophilia on to possibly one- half of their children. Half the daughters will be carriers and half the sons will be hemophilic. The rest of the siblings will be normal. Daughters, as long as one parent is genotypically normal, can only be carriers. The normal gene on the second X chromosome counteracts the defect and the daughters do not suffer from the trait. If a son receives the defective gene from his mother, he will be hemophilic because the Y chromosome can not counteract the defective gene located on his X chromosome. Search Home Questions Email This Link

82. Hemophilia Association Of New Jersey - Hemophilia, Bleeding Disorders
    The hemophilia Association of New Jersey offers assistance to persons withhemophilia and their families from our office located in East Brunswick.  
    http://www.hanj.org/
    
    Extractions: All information that appears on the Hemophilia Association of New Jersey website, including links to other websites, is for your general information only. The Hemophilia Association of New Jersey makes no endorsements for or against medical treatments and/or therapies. Please consult your physician, or local treatment center before pursuing any course of treatment.

83. Hematology/Oncology - Hemophilia
    Hematology/Oncology. hemophilia. hemophilia A (Factor VIII deficiency)and hemophilia B (Factor IX deficiency) are bleeding disorders  
    http://www.mc.vanderbilt.edu/peds/pidl/hemeonc/hemophil.htm
    
    Extractions: PIDL Home/ Contents Development Nutrition Acute Illness ... Psychosocial Hematology/Oncology HEMOPHILIA Hemophilia A (Factor VIII deficiency) and hemophilia B (Factor IX deficiency) are bleeding disorders that are inherited as x- linked recessive traits. Thus, both affect males almost exclusively. The two disorders are clinically indistinguishable but can be easily differentiated by Factor VIII and Factor IX activity assays. In hemophilia A, the Factor VIII procoagulant moiety (Factor VIII:C) is deficient or abnormal, but other components of the Factor VIII/von Willebrand factor system (Von Willebrand's Factor antigen and Ristocetin Cofactor activity) are normal. In general, the severity of bleeding manifestations correlates well with the Factor VIII:C value. Hemophilia B (Christmas disease) is characterized by subnormal Factor IX activity, which may reflect a quantitative or qualitative abnormality in the Factor IX molecule. Both hemophilia A and hemophilia B are heterogeneous conditions with variable degrees of clinical expression. Hemophilia A is far more common, occurring in 1 in 10,000 males in the United States. In contrast, the incidence of hemophilia B is 0.25 in 10,000 males. More than 60% of patients will have a positive family history. Because of the high spontaneous mutation rate for this disease, as many as 1/3 of hemophiliacs have no significant family history.

84. MEDLINEplus: Hemophilia
    All Topics. hemophilia. Contents of this Children Teenagers. Search MEDLINEfor recent research articles on • hemophilia. You may also  
    http://www.nlm.nih.gov/medlineplus/hemophilia.html
    
    Extractions: Bleeding Disorders: Financial and Insurance Issues (National Hemophilia Foundation) Factor I Deficiency (Afibrinogenemia) (National Hemophilia Foundation) Factor II Deficiency (Prothrombin) (National Hemophilia Foundation) Factor V Deficiency (Mayo Foundation for Medical Education and Research) Factor VII Deficiency (Proconvertin or Stable Factor) (National Hemophilia Foundation) Hemophilia A (Factor VIII Deficiency) (National Hemophilia Foundation) Hemophilia B (Factor IX Deficiency) (National Hemophilia Foundation)

85. MEDLINEplus Medical Encyclopedia: Hemophilia
    hemophilia. Contents of this page This disease affects mostly males. Diseases inthis category include hemophilia A; hemophilia B; von Willebrand's disease.  
    http://www.nlm.nih.gov/medlineplus/ency/article/000537.htm
    
    Extractions: Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Blood clots Definition Return to top A sex-linked hereditary bleeding disorder in which it takes a long time for the blood to clot and abnormal bleeding occurs. This disease affects mostly males. Diseases in this category include: Update Date: 10/4/2001 Updated by: Victoria Kennedy, RN, A.D.A.M. editorial.

86. Hemophilia Treatment Center
    Harold R. Roberts. Comprehensive hemophilia Diagnostic and TreatmentCenter. Center for Thrombosis and Hemostasis School of Medicine  
    http://www.med.unc.edu/wrkunits/3ctrpgm/thromb/comprehe/

87. Gene Therapy For Hemophilia
    The International Symposium on Gene Therapy for hemophilia September 4 6, 1997, University of North Carolina at Chapel Hill, Chapel Hill, NC.  
    http://www.med.unc.edu/thromb/gene.htm

88. Hemophilia
    hemophilia resources, support groups, clinics with genetic counselors and geneticists.Image that's a link to Genetics Education Center Support Page hemophilia.  
    http://www.kumc.edu/gec/support/hemophil.html

89. MCG - Comprehensive Hemophilia Treatment Center
    Specialty section of larger website provides detailed information on hemophilia conditions, describing Category Regional North America United States Georgia Health The Medical College of Georgia Comprehensive hemophilia Treatment Center exists toimprove the quality of life for all affected by hemophilia, related bleeding  
    http://www.mcg.edu/centers/Hemo/

90. Northern Alberta Comprehensive Hemophilia Clinic
    Northern Alberta Comprehensive hemophilia Clinic. Welcome to our HomePage. Members of the Northern Alberta Comprehensive hemophilia Clinic.  
    http://www.ualberta.ca/~britchie/achcn.html
    
    Extractions: Last update 29 June 1999 The Northern Alberta Comprehensive Hemophilia Clinic has been in existence since 1978. It was formed by the Province of Alberta, under the leadership of the Minister of Health, the Alberta Chapter of the Canadian Hemophilia Society, and their medical consultant, Dr. Garner King. It was charged with the task of providing high quality comprehensive care for people with hemophilia, providing education to families and treaters of hemophilia, and performing research. The clinic has been successful in moving treatment of hemophilia to an outpatient setting, placing control of treatment in the hands of the patients, and providing comprehensive care to people with this disorder. This has resulted in dramatic improvement in efficiencies of care, improved management of hemophilia, improvements in the lifestyle of people with hemophilia, and better relationships between treaters and patients. Comprehensive Clinics are held once a month on the first Monday afternoon of the month in the General Clinics, on the first floor of the Walter McKenzie Center. Comprehensive Clinics are attended by the nurse coordinator, a physiotherapist, a social worker, a representative of the dental clinic, an orthopedic surgeon , and a hematologist. Surveillance clinics are held on intervening Mondays. Wilma McClure RN , Nurse Coordinator Dr. John Akabutu

91. MedWebPlus Subject Hemophilia
    A free service to help you find health sciences information quickly and easily. hemophilia Web Sites A, , GO, AHF the hemophilia disease management company.  
    http://www.medwebplus.com/subject/Hemophilia
    
    Extractions: A GO AHF : the hemophilia disease management company A GO BrighamRAD Teaching Case Database Hemophilic Arthropathy by David I Rose, Piran Aliabadi. May 3, 1996 A GO Canadian Hemophilia Society History of Hemophilia A GO A GO Haemophilia : official lournal of World Federation of Hemophilia (tables of contents) A GO Haemophilia Society (published three times a year by the National Center for Biotechnology Information) A GO Hemophilia Home Page maintained by Michael Davon A GO Hemophilia reports (Vol. 4, no. 6, 1998- ) A GO Hemophilia/von Willebrand's Disease by Matt Klimshuk A GO Hemophiliacure Home Page maintained by Paul Vess A GO World Federation of Hemophilia = Fédération Mondiale de L'Hémophilie = Federacion Mundial de Hemofilia

92. ::ÃÅÌÎÔÈËÈß Â ÐÎÑÑÈÈ::
    The summary for this Russian page contains characters that cannot be correctly displayed in this language/character set.  
    http://www.hemophilia.ru/

93. TKT Patient Information Hemophilia A
    hemophilia A It is important for your physician,family, and peers to understand hemophilia A.  
    http://www.tktx.com/patient/hemophilia.htm
    
    Extractions: What is Gene Therapy? Gene therapy can be categorized based on two relatively straightforward distinctions. The first is based on where the gene of interest is added to the patient's cell, whether it occurs in vivo (inside the body)or ex vivo (outside the body). The second category is based on how the gene is actually introduced to the cell, whether a viral or non-viral approach. In vivo gene therapies are based on the administration of DNA-based drugs directly to the patient. Ex vivo gene therapies are based on removing a small number of cells from a patient, introducing the gene into a cell and implanting the genetically- engineered cells into the patient. Viral gene therapy approaches use genetically modified viruses to introduce genes into human cells by infection. Non-viral approaches use non-infectious means to introduce the genes into human cells.

94. Hemophilia Research Society
    The hemophilia Research Society of North America is a fully charted, taxexemptresearch organization whose membership consists of nearly 200 physicians  
    http://www.uth.tmc.edu/xorgs/hrs/

95. This Domain Name Is Booked With Www.net4domains.com
    http://www.hemophiliaindia.org/

96. Welcome To Hemophilia Resources Of America (HRA): Home
    hemophilia Resources of America (HRA) is a full service provider of hemophilia coagulationproducts and services for adults and children living with hemophilia  
    http://www.hrahemo.com/
    
    Extractions: HRA is a full service provider of hemophilia coagulation products and services for adults and children living with hemophilia and von Willebrand disease. A word from our clients: "HRA found that my other home care company was filling the prescription at half the dose. Thank God there was no major problem that resulted from this." "Several head traumas have been prevented due to the protective headgear. If he had not had on the helmet a serious injury would certainly have occurred." "I have always been satisfied with your services, pleasant, professional, courteous, and knowledgeable." "There really is no way to improve something which has been perfected." "It is a pleasure to work with the HRA staff. Every Aspect is Great!" View All Quotes

97. Hemophilia Foundation Of Southern California
    hemophilia Carrier Testing at Orthopaedic Hospital Blood test for girls and womento see whether more, Important Message from Foundation President.  
    http://www.hemosocal.com/
    
    Extractions: Women's Issues Ricky Ray Program WON embraces all women in the [more] The Ricky Ray Program Office has established ... [more] Hemophilia Carrier Testing at Orthopaedic Hospital Events schedule Blood test for girls and women to see whether... [more] What is the Foundation? Special Events Our community consists of more than 1,200 men, women and children with hemophilia and other bleeding disorders in the Southern California area. Coming from a variety of ethnic, economic and professional backgrounds, our community works together to help one another solve many shared problems. [more] Sunday, June 30, 2002 - 2002 C.D. LeBlanc Polo Match This was a SENSATIONAL day at will Rodgers Park. The 2002 C.D. LeBlanc trophy cup w ent to .... [more] HemoGames Camp 2002 What a great time we had! Shooting hoops [more] Camp Blood Brothers and Sisters was held August 18 - 24, 2002 The Hemophilia Foundation of Southern California invites all children ages 7-14 with hemophilia and other bleeding disorders to join us for our week-long summer camp [more] Board Of Directors Links to Hemophilia related web sites

98. Hemophilia A
    PubMed the literature LocusLink collection of generelated information OMIM catalogof human genes and disorders Information National hemophilia Foundation a  
    http://www.ncbi.nlm.nih.gov/disease/hemoA.html

99. Hemophilia
    Library G H. hemophilia. National hemophilia Foundation (NHF) 110 Green Street,Suite 303 New York, NY, USA 10012 (800) 424-2634 Fax (212) 431-0906.  
    http://www.familyvillage.wisc.edu/lib_hemp.htm

100. Hemophilia
     hemophilia, hemophilia is the most common inherited bleeding disorder. Thereare about 20,000 people in the United States who have hemophilia.  
     http://www.ivillagehealth.com/library/onemed/content/0,7064,241012_245627,00.htm

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