81. Gaucher Disease Gaucher disease up. Gaucher disease / genetics Related topics other, NiemannPickdiseases. gauchers Association, A UK based charity for Gaucher disease. http://omni.ac.uk/browse/mesh/detail/C0017205L0017205.html

Gaucher Disease [up] Gaucher Disease / genetics Related topics: other Niemann-Pick Diseases Gauchers Association A UK based charity for Gaucher disease. Their web site provides comprehensive information about Gaucher disease (which is an inherited, enzyme deficiency disorder), aimed at patients and doctors. Information includes news items, information on bone disease, children and Gaucher disease, enzyme replacement therapy, gene therapy, fund raising, home infusions, new treatments, screening and nutritional analysis, tests, Type 2, and Type 3 Gaucher disease, and conference reports. The site is also available in Italian, German, and Spanish. Gaucher Disease Patient Education Neuronopathic Gaucher disease This leaflet, aimed at parents, provides information about Neuronopathic Gaucher disease (NGD), an inherited, enzyme deficiency, disorder. The prevalance, effects, symptoms and treatment are explained here for NGD types 2 and 3. Published on the Web by Great Ormond Street Children's Hospital (GOSH) and the Institute of Child Health (ICH). Also available in PDF requiring Adobe Acrobat Reader. Gaucher Disease Patient Education Handout [Publication Type] Neuronopathic Gaucher disease : special educational needs This leaflet, aimed at parents, provides information about the educational requirements of children with Neuronopathic Gaucher disease (NGD). It explains how NGD can affect learning and education, special provision at school, and what parents can do. A case study and list of useful addresses is also provided. Published on the Web by Great Ormond Street Children's Hospital (GOSH) and the Institute of Child Health (ICH). Also available in PDF requiring Adobe Acrobat Reader.

82. Avascular Necrosis injury; Longterm use of systemic corticosteroid drugs; Excessiveconsumption of alcohol; gauchers' disease; Pancreatitis; Radiation http://jhhs.client.web-health.com/web-health/topics/GeneralHealth/generalhealths

83. Gaucher Disease - Information And Support Resources , Breast Cancers Prevention and Resources. ?, Canavan disease. ?, Crohn'sdisease. Interactive ?. ?, Jewish Genetic diseases Boards. Gaucher's disease. http://www.mazornet.com/genetics/gauchers.asp

Jewish Genetic Diseases A Mazornet Guide VISIT MazorNet's other Jewish Guides The MazorNet-Jewish Celebrations Kosher Restaurant Guide The MazorNet- Jewish Celebrations Vendor Directory ( ... Photographers, Kosher Caterers, Bridal Gowns, and Much More) Important Information Home Page Genetic Counseling and Screening Genetic Screening Laboratories - A Directory A Brief Key to Basic Genetic ... s Select Disorder Bloom's Syndrome Breast and Ovarian Cancers Breast Cancers - Prevention and Resources Canavan Disease ... Ulcerative Colitis Recommended Reeading Genetic Diversity Among Jews - Diseases and Markers at the DNA Level Provides an authoritative, up-to-date account of the impact of molecular genetics on our understanding of genetic diseases prevalent among Jews. Jewish Genetic Disorders : A Layman's Guide Guide to genetic disorders that tend to affect the Jewish population more than the non-Jewish, including a short history of the Jews and basic facts concerning genetics and genetic disorders. Interactive Jewish Genetic Diseases Boards Gaucher's Disease Symptoms Incidence among People of Jewish Descent Treatment Resources and More Incidence and Carriers Gaucher's Disease is an inherited disease. An enzyme deficiency disorder. Gaucher Disease, also called cerebroside lipidosis and familial splenic anemia, is an autosomal-recessive condition named after French physician Philippe Gaucher. Gaucher Disease occurs at any age, but it is most dangerous and most severe in infants. In essence, Gaucher Disease results from the deposition of glucocerebroside in the liver, bone marrow, and spleen. The enzyme glucocerebrosidase normally breaks down glucocerebroside, but patients with Gaucher Disease do not manufacture enough of the enzyme, and deposition of glucocerebroside results.

84. The NTSAD Diseases Family: Gaucher Disease The Gaucher disease Home Page The UK gauchers Association Web Page TheGaucher disease Treatment Program at Massachusetts General Hospital http://www.ntsad.org/pages/gaucher.htm

Gaucher Disease IN 1882, PHILLIPE GAUCHER, A French physician, described the clinical disorder that now bears his name. Since his original description, many investigators have contributed to our understanding of Gaucher Disease. In the early 1900's, American physicians were the first to recognize its familial transmission and to characterize further the pathology of the disease. Although early investigations suggested that the disease was due to a metabolic disorder, it was not until 1965 that the specific metabolic defect, a deficiency in the enzyme glucocerebrosidase, was identified. We now recognize that the disease has three subtypes: Type I, II and III. A ll three types of Gaucher Disease are inherited storage diseases, and all result from the deficiency of an enzyme called glucocerebrosidase, which is necessary for the breakdown of a particular fatty substance, glucocerebroside. This fatty substance is normally present in very small amounts in all body cells, but in patients with Gaucher Disease, glucocerebroside is not broken down as it should be and becomes abnormally stored, primarily in unique cells called Gaucher cells. T he major disease manifestations are due to the progressive storage of glucocerebroside in Gaucher cells in the bone marrow, spleen and liver. Gaucher cells in the bone marrow can cause bone and joint pain, fractures and other orthopedic problems. Accumulation of Gaucher cells in the spleen and liver causes enlargement of these organs as well as blood abnormalities such as anemia, easy bruising and impaired blood clotting. In a small number of persons with Gaucher Disease, glucocerebroside also accumulates in the central nervous system, leading to neurological damage.

85. Nutrilinks diseases; Enfermedad de Gaucher Gaucher disease; gauchers Association;Gaucher disease Current Issues in Diagnosis and Treatment; Gaucher http://www.farmanet.com/nutrinet/meta.htm

Asociaciones Enfermos Nutrilinks Vademecum [Novedades] Diabetes Diabetic gourmet About ASPEN Diabetes Care Acute Glycemic Complications Diabetes-links ... Diabetes.com The British Inherited Metabolic Diseases Group and the Society for the Study of Inborn Errors of Metabolism Inborn Errors of Metabolism PATHWAY: Database of Inherited Metabolic Diseases Enfermedad de Gaucher Gaucher Disease Gauchers Association Gaucher Disease: Current Issues in Diagnosis and Treatment Gaucher Disease Discussions ... NINDS Gaucher's Disease Information Page Enfermedad de Fabry Fabry's Disease International Center for Fabry Disease Fabry Disease Home Page Enfermedad de Niemann-Pick Niemann-Pick Disease Niemann-Pick Disease Foundation NPC1 gene Hipoglucemia Hypoglycemia Support Foundation Hypoglycemia Hypoglycemia The Sugar Paradox Hiperlipidemia Hyperlipidemia Hyperlipidemia Management of Common Lipid Disorders Triglyceride, High Density Lipoprotein, and Coronary Heart Disease ... Drug Therapy for Lipid Disorders Desfase de Agua-Electrolito Hiperkalemia Hyperkalemia Dry Airplane Air Can Cause Dehydration Dehydration and Your Child Heat Stress Hipercalcemia Consistent with Hypercalcemia Hypercalcemia and Cancer Acute Hypercalcemia Hypercalcemia Bibliography, etc.

86. MPS Society Diseases Database gangliosidosis, 19, Fabrys disease, Trihexosylceramidosis, 20, Gauchersdisease, Glucosylceramidosis, 21, NiemannPicks disease, Sphingomyelinosis, http://www.mpssociety.ca/diseases.php3

Home The Society Members About MPS ... Supporters Common Name Alternate Name Hurler Syndrome MPS I-H Scheie Syndrome MPS I-S Hurler-Scheie Syndrome MPS I-HS Hunter Syndrome MPS II Sanfilippo Syndrome A,B,C,D MPS III Morquio Syndrome MPS IV Maroteaux-Lamy Syndrome MPS VI Sly Syndrome MPS VII Sialidosis ML I I-Cell Disease ML II Pseudo-Hurler Polydystrophy ML III ML IV ML IV Mannosidosis Fucosidosis Aspartylglycosaminuria AGU Multiple Sulfatase Deficiency MSD Landings Disease GM 1 gangliosidosis GM 2 gangliosidosis Fabrys Disease Trihexosylceramidosis Gauchers Disease Glucosylceramidosis Niemann-Picks Disease Sphingomyelinosis Metachromatic Leukodystrophy Sulfatidosis Krabbes Disease Galactosylceramidosis Farbers Disease Lipogranulomatosis

87. (almost) All The New Zealand Web Sites You Will Ever Want! - PIPERS Page Of New APECED Jeanette's Home Page. gauchers Association of New Zealand - gauchersDisease (or here). Genitals. Condoms - NZ Health Guide. Condoms - Medisafe. http://www.piperpat.co.nz/nz/medical.html

Bottom of Page PIPERSHome PIPERS New Zealand Pages Home Worldwide List ... Add a Link PIPERS New Zealand Pages This page is regularly updated. However, with over 20,000 links in our NZ pages, maintained on a part-time basis, it is impossible to keep up with all of them. If you find that any of the links are not working, or if you would like to suggest some useful new links, please let us know so that we can modify the listing. - Click here to Email us Headings on This Page Abortion Alcohol Allergies Alzheimer's ... Women Medical Information Links Abortion Abortion Supervisory Committee SPUC - Society for the Protection of the Unborn Child Inc. Alcohol ADANZ - Alcohol Drug Association New Zealand.. ALAC - Alcohol Advisory Council of New Zealand. Alcoholics Anonymous Alcoholics Anonymous - Auckland. Alcoholics Anonymous Auckland Service Centre Alcoholics Anonymous - Christchurch (or here Alcoholics Anonymous - Christchurch. Alcoholics Anonymous - Dunedin. Alcohol and Public Health Research Unit - Auckland. "Where's That Drink Taking You" - Game. Allergies Allergic rhinitis and hayfever - NZ Health Guide.

88. LEGG CALVE PERTHES DISEASE By Fred Lanting. Sickle cell disease. Thrombophilia (Protein C Protein S deficiencies). Gauchersdisease. Strong association but unproven Pregnancy/high dose estrogen therapy. http://siriusdog.com/legg.htm

Search SiriusDog.com CLASSIFIEDS Categories Sporting Group Hound Group Working Group Terrier Group ... Home Featured Bestseller! Interactive Polls What sport does your dog compete in? Agility Flyball Lure Coursing Obedience Ring Sport Schutzhund LEGG CALVE PERTHES DISEASE by Fred Lanting. by Fred Lanting SIGNS Radiographic features in NICO include: Poorly demarcated radiolucency or “moth eaten” appearance as seen on the radiograph, Irregular vertical trabeculae (a type of bone cell), A cotton wool or “ground glass” radiopacity, sometimes referred to as “ghost marrow”, Flecks and streaks radiating outward and giving rise to the term “eagle’s nest”, Soap bubble radiolucency, and more. CAUSE From “Etiologies for ischemic osteonecrosis”, as summarized by Dr. Bouquot:Local Factors: Trauma (mild or severe) or surgery Radiation therapy for cancer Strong association but unproven: Intraosseous inflammation/infection Rheumatoid arthritis Prosthetic obstruction of blood flow to marrow Intraosseous malignancy (especially lymphoma and metastatic carcinoma) S ystemic (more widespread throughout the body, some more genetic) Factors:

89. Disorders Of Energy Metabolism Metabolism Index. http://www.fpnotebook.com/END81.htm

Home About Links Index ... Editor's Choice Paid Advertisement (click above). Please see the privacy statement Endocrinology Metabolism Assorted Pages Inborn Errors of Metabolism Disorders of Energy Metabolism Lysosomal storage disease Inborn Error of Small Molecule Metabolism ... Tay-Sachs Disease Disorders of Energy Metabolism Glycogen Storage Disease 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 Endocrinology Index Adrenal Disease General Cardiovascular Medicine Diabetes Mellitus Examination Ophthalmology Geriatric Medicine Growth Hematology and Oncology Hypoglycemia Laboratory Metabolism Neonatology Obesity Obstetrics Parathyroid Disease Pediatrics Pharmacology Pituitary Disease Prevention Radiology Nephrology Sex Sports Medicine Surgery Symptom Evaluation Thyroid Disease Page Metabolism Index Background Class Energy Class Lysosomal Storage Class Small Molecules Fructose Intolerance Galactosemia Gauchers Disease Homocystinuria Tay-Sachs See Also Inborn Errors of Metabolism Types Oxidation defects Disorders of fatty acid mobilization and metabolism Glycogen storage diseases Type 3: Forbes Disease Type 6: Hers Disease Search other websites for this topic Search National Library of Medicine PubMed for related

90. Welcome To Mustafa's Hematology Lessons LymphomasHodgking disease Non Hodgkin lymphoma. Infilterative disorders, Gauchersdisease, Neimann Pick disease, Letterer –Swie disease. Infectious disease http://www.hematology.lastmaldives.com/pancytopenia.htm

Medscape WebMD MDConsult Medline ... View Guest book CAUSES OF PANCYTOPENIA Disorders infilterating the bone marrow Aleukemic leukemia Multiple Myeloma Matastatic carcinorma (leukoerythroblastic picture),lymphoma Myelofibrosis Myelosclerosis Agnogenic Myeloid Mataplasia Marble bone disease, osteopetrosis Disorders involving the spleen Cogestive splenomagaly Lymphomas:Hodgking disease Non Hodgkin lymphoma Infilterative disorders, Gauchers disease, Neimann Pick disease, Letterer –Swie disease Infectious disease: Kal-azar. Milliary tuberculosis, Syphilis, Primary splenic panhaematopenia Vitamin B 12 or folate deficiency:Pernecious anemia, Sprue Dissaminated Lupus Erythematosus Paroxysmal Nocturnal Haemoglobinuria Miscaellaniuos disorders ( with Cellular marrow) overwhelming infections. Mycobacterial infections, brucellosis,sarcoidosis,some refractory anemias, sideroblastic anemia (rarely) and perhaps drug sensitivity Pregnancy ( some cases) Aplastic or hypoplastic anemias Feed Back : Mustafa's Hematology Lessons

91. The Family Village / Gaucher Disease Library G H. Gaucher disease. The National Gaucher Foundation publishes a bi-monthlynewsletter, Gaucher disease Newsletter, at a cost of $35 Dollars a year. http://www.familyvillage.wisc.edu/lib_gauc.htm

Gaucher Disease Who to Contact Where to Go to Chat with Others Learn More About It Web Sites ... Search AltaVista for "Gaucher Disease" Who to Contact National Gaucher Foundation (NGF) 11140 Rockville Pike, Suite 350 Rockville, Maryland, USA 20852-3106 Fax: (301) 816-1516 e-mail: ngf@gaucherdisease.org The mission of The National Gaucher Foundation is to fund research, meet ever-increasing patients' needs, provide education and awareness, develop patient groups and eradicate Gaucher Disease. NGF has active local chapters in Philadelphia and Chicago, they will assist anyone who wishes to start a local support group in their locality. They do parent-to-parent matching through a directory of families who are interested in meeting other families with similar medical histories. The National Gaucher Foundation publishes a bi-monthly newsletter, Gaucher Disease Newsletter , at a cost of $35 Dollars a year. They also have a brochure that gives information on the organization, care and care+ program, and financial assistance program. There is a new parent packet that is free of charge and contains several pamphlets, fact sheets, brochure, and membership application. The Foundation has several videos that are available for loan to members. They collect information on physicians and researchers who treat/study the disease and make this information accessible to their members. The National Gaucher Foundation hosts a national conference; call for further details.

92. Thrombopoiesis And Thrombopoietins Thrombopoiesis and Thrombopoietins. Thrombopoiesis and ThrombopoietinsMolecular, Cellular, Preclinical and Clinical Biology David http://www.bloodline.net/stories/storyReader$1697

Bloodline Home About Call for Papers Free Membership ... Search Educational Features Image Atlas Case Studies Private Lectures Conference Reviews ... Glossary Resources Conference Calendar Hematology Links Full Text Journals Classifieds Specialties BMT/Stem Cell Cord Blood Thrombosis Hemostasis ... Veterinary News Hematology News BloodLink Newsletter Blood News Update Discussion Today's Discussion Create New Topic List by Topic Members Join Now Login Thrombopoiesis and Thrombopoietins Thrombopoiesis and Thrombopoietins Molecular, Cellular, Preclinical and Clinical Biology David J. Kuter, Pamela Hunt, William Sheridan and Dorothea Zucker-Franklin The story of the "discovery" of TPO illustrates well how such important milestones in science are often a combination of long painstaking work, the application of vision, and capitalizing on chance discoveries. For the student of megakaryocytopoiesis, as well as for those who wish to better understand the genesis of this fascinating area of hematopoiesis, this book is an excellent addition to the library. Reviewed for Bloodline by: John M. McCarty, M.D.

93. XTRAMSN: Health: Health Library: A To Z Conditions SEARCH WEB FOR BROWSE XTRAMSN Select -. http://www.xtramsn.co.nz/health/0,,8065--G,00.html

Advanced Search Home Hotmail Search ... Help navBG = '#336699'; navOverBG = '#6699FF'; casText = '#FFFFFF'; casTextOver = '#FFCC00'; casBG = '#6699FF'; casOverBG = '#336699'; Ask The Expert Beauty Fitness Health Library Natural Health Relationships Parenting SEARCH WEB FOR: BROWSE XTRAMSN: -Select - Academy Awards Auto/Bike/Boat Business Careers Entertainment Games Iraqi War 2003 Kids Money Motoring News Personals Shopping Sport Xtra Super 12 Travel Help SEARCH HEALTH RELATED ITEMS: XtraMSN Sport Contact Us You are here : XtraMSN Health Library A to Z Conditions Mon 31 March 2003 Pregnancy Alternative Health Ask the Expert A-Z Conditions ... Message Boards A - Z of Conditions Just click on the letters below to search our A to Z list of more than 300 diseases and conditions. These guides, written and reviewed by doctors, are regularly updated and the list is being expanded. A B C D ... P Q R S T U ... Y Z G Gallstones Gas gangrene Gastritis Gastro-Oesophageal Reflux Disease (GORD) ... Guillain-Barre Syndrome Learn About Cluster headache The majority of sufferers are men (tenfold) - especially between the ages of 20 to 40 Cluster headaches follow a classic pattern Alcohol is nearly always a trigger As these headaches start suddenly and seldom last long, they may be difficult to treat

94. New Page 1 Cirrhosis. 5.Inborn errors A1 antitrypsin def. -Haemochromatosis. -Gauchersdisease. -Haemophilia. -Cystic fibrosis. 6.Others -Biliary atresia. http://www.chills.co.uk/lz.htm

a b c d ... z Lung Cavitation 1.Staph pneumonia 2.PE 3.TB 4.Klebsiella 5.Rheumatoid nodules 6.Aspergillosis 7.Histoplasmosis 8.Cryptococcosis 9.Coccidiomycosis 10.Squamous cell ca 11.Wegeners Granulomatosis 12.Coal Workers Pneumoconiosis Lead poisoning ABCDEFG A naemia B asophilic stippling C olicky pain D iarrhoea E ncephalopathy F oot drop G um (lead line) lipid papers primary prevention pravastatin-give if cholesterol was above 7 men aged 45 to 64 reduced cholesterol by 20% reduced cardiovascular death by 33% screening should be done in ischaemic heart dosease, diabetes vascular disease, xanthoma anyone who requests corneal arcus at age less than 50 anyone w ith first degree relatives secondary prevention ssss 4444 patients aged 35-70 yrs angina or 6/12 post MI fasting cholesterol greater than 5.5

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