04.26.2004

HEMIC AND LIMPHATIC DISEASES

• von Willebrand Factor-Mutations Database
• Evans Syndrome-primary thrombocytopenic purpura
• Hereditary Spherocytosis-minireview
• Methemoglobinemia-minireview
• Myelodysplastic Syndromes-by B.Cheson -1998 (Medscape,Inc)
• Factor V Leiden Thrombophilia - GeneClinics 1999
• GeneClinics Factor V Leiden-review by J Kujovich,S Goonight-GeneClinics1999

General Aspects

• Blood Coagulation-Medical Biochemistry Page
• Bleeding Disorders-Virtual Hospital
• Atlas of Hematology
• Hematopoiesis-Encyclopedia of Cancer(art)
• Hematologic Disorders - Handbook online
• Hematologically Important Mutations
• Hematology Clinical Medical Education-Kanzas University
• HEMATOLOGY DATABASES
• Globin Gene Server home page (USA)
• Hemorrhagic Disease of the Newborn-review
• Hypercoagulable States in Children-minireview
• Neonatal Hematologic Disorders-Virtual Hospital
• Heme and Porphyrin Biosynthesis-Medical Biochemistry Page

Anemias

• Congenital spherocytic anemia - fact sheet, WWW links
• Congenital Hemolytic Anemia-review
• Fanconi Anemia Mutation Database
• X-Linked Sideroblastic Anemia

Sickle Cell Anemia

• Sickle Cell Information Center Home Page
• Sickle Cell Anemia
• Sickle Cell Anemia-a guide for parents
• Sickle Cell Defiers [ defiers.com ]
• Sickle Cell Disease-Baby Net
• Joint Center for Sickle Cell and Thalassemia
• Sickle Cell Syndromes-review
• Sickle Cell Syndromes II-minireview
• Sickle Cell Anemia-Virtual Hospital
• Sickle-Cell Genetics- educational (facts sheets, slide)
• New Hope for People with Sickle Cell Anemia (.
• Sickle Cell Anemia - Handbook online
• Sickle cell anemia - Pediatric Encyclopedia
• Sickle Cell Disease (Clinical Guideline)
• Evolution of a Retinal Hemorrhage in a Patient With Sickle Cell-Hemoglobin C Disease... [Fulltext, Aug Arch Ophthalmol. 1995)
• First Unaffected Pregnancy Using Preimplantation Genetic Diagnosis for Sickle Cell Anemia-article, JAMA.1999
• SICKLE CELL ANEMIA - JAMA Patient Page
• Health Supervision for Children With Sickle Cell Diseases and Their Families (RE9631)
• Acute Chest Syndrome in Sickle Cell Disease-Correspondence-NEJM 2000

Hemophilia

• The World Federation of Hemophilia (haemophilia)
• Swedish Hemophilia Society
• South African Haemophilia Foundation
• Northern California Hemophilia Foundation Web Page
• National Hemophilia Foundation
• National Hemophilia Foundation Northern Ohio Chapter
• Manitoba Hemophilia Society's New Page
• Hemophilia-South Carolina Home Page
• Hemophilia-personal
• Hemophilia Ontario
• Hemophilia of Georgia, Inc.. Home Page
• Hemophilia Foundation of Michigan
• FAMOHIO Hemophilia Home Page
• DNA Testing for Haemophilia
• HAEMOPHILIA CARRIERS-guide
• Hemophilia-review
• Hemophilia - StudyWeb
• HAMSTeRS - The Haemophilia A Mutation Database
• Haemophilia B Mutation Database
• Hemophilia and von Willebrand's disease 2. Management
• Hemophilia and von Willebrand's disease 1. Diagnosis, comprehensive care and assessment
• Indivinar Crystalluria-A 33-year-old man with hemophilia-NEJM 1999
• GeneClinics - Hemophilia B
• GeneClinics - Hemophilia A
• Hemophilia Home Page

Thalassemias

• Thalassemia - Atlas of Hematology
• Successful Treatment of Severe Thalassemia - Images in Clinical Medicine-NEJM 1999; 341 92
• DNA Testing for the Thalassaemias
• Cooley's Anemia Foundation - Thalassemia
• Screening for Hemoglobinopathies-review
• Single gene disorders or complex traits-lessons from the thalassaemias and other monogenic diseases-article by Weatherall,2000
• Hepatic Iron Concentration and Total Body Iron Stores in Thalassemia Major-Corresponde