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         Gauchers Disease:     more books (38)
  1. Gaucher Disease
  2. The Official Parent's Sourcebook on Gaucher's Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09
  3. Gaucher Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-28
  4. Type 3 Gaucher Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  5. Gaucher Disease: A Century of Delineation and Research (Progress in Clinical & Biological Research)
  6. Type 2 Gaucher Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  7. Federal and private roles in the development and provision of alglucerase therapy for Gaucher disease (Background paper)
  8. Gaucher Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  9. Type 1 Gaucher Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-16
  10. Gaucher Disease by Claus Niederau,
  11. Lysosomal storage disease: Inborn Error of Metabolism, Lysosome, Organelle, Cell (biology), Tay-Sachs Disease, Gaucher's Disease, Cell Biology, Intracellular, ... Glycogen Storage Disease Type II, Enzyme.
  12. Genetic Disorders Sourcebook Basic Information About Heritable Diseases and Disorders Such As Down Synd Rome Pku Hemophilia Von Willebrand Disease Gaucher Disease Tay-Sachs d - 1996 publication. by unkn, 1996
  13. Biochemical and Morphological Studies of the Glycosphingolipidoses: Gaucher's Disease, Farby's Disease and Sandhoff's Disease by Susan Jane Desnick, 1972-01-01
  14. Psychosocial Aspects of Heart Failure / Gaucher Disease / Emergency: Digital Photographs in the ED (American Journal of Nursing, Volume 103, Number 12, December 2003)

61. Guardian Unlimited Archive Search
Oxford Glycosciences (OGS), a world leader in proteomics, already has a nearto-launchproduct, Vevesca, for gauchers disease - a $476m market - and has
http://www.guardian.co.uk/Archive/Article/0,4273,4096497,00.html

62. Avascular Necrosis
b. Non Traumatic. Caissons disease. “the bends” - seen with deep water diving.gauchers disease. Sickle cell anemia Local Radiotherapy. 2. Probable Cause.
http://www.arthritis.co.za/avn.htm
Avascular Necrosis / Osteonecrosis / AVN by drdoc on-line Index Definition
History

Epidemiology

Anatomy
...
Management
Definition: Osteonecrosis is defined as cell death in components of bone - The marrow fat and mineralized tissue.
It represents the final common pathway of several disease entities, which result in impaired blood supply to the bone tissue - causing necrosis or death of the bone. History It was first described in 1794 by James Russel , who wrote a book on bone necrosis, and full description of the entity followed in 1930 by Phemister et al. In 1962 the entity was revived with the description of 5 cases by Mankin and Brower.
Since then thousands of cases have been described, and it is estimated that there are 15000 cases per year in the USA alone. Epidemiology It is more common in young males.
Male : Female ratio is 8:1
Anatomy Commonest sites are the hip, the knees and shoulders as well as the wrist bones an feet.
In the case of the femoral neck - there is a precarious blood supply with blood supply coming from above and below, leaving a watershed area at risk -between the two main areas of supply - in the femoral head. The main blood supply is as follows: Medial Epiphyseal artery from Obturator via ligamentum teres.

63. Manuel Swaden Solicitors
He also chairs a national charity , the Gauchers Association which provides supportfor and advocacy on behalf of patients with gauchers disease , (a rare
http://www.manuelswaden.co.uk/team.html
The Team Jeremy Manuel Jeremy co-founded Manuel Swaden in 1989, with the aim of providing high quality personal service to all clients. He has extensive experience of the laws relating to property investment, development and trading. He serves a wide range of clients including major PLC's, property investment, development companies and individuals. In addition Jeremy is committed to the idea of effective dispute resolution and is a commercial mediator trained by and accredited with CEDR (centre for effective dispute resolution ). He is a panel mediator for Dispute Mediation Limited and a contributory author to "ADR and Commercial Disputes" , published by Sweet and Maxwell (2001). He also chairs a national charity , the Gauchers Association which provides support for and advocacy on behalf of patients with Gauchers disease , (a rare genetically inherited disorder) , for which he was awarded an O.B.E.

64. Private Psychiatry.co.uk Help Line Addresses And Telephone Numbers (helpline Inf
Fibromyalgia Fibromyalgia Association UK 8 Rochester Grove Stockport Cheshire SK74JD Tel 0161 483 3155 BACK TO TOP G gauchers disease Gauchers Association 25
http://www.privatepsychiatry.co.uk/psychiatry_000022.html
SITE SEARCH ENGINE HOMEPAGE BRIEF DETAILS ... FEEDBACK Helpline Addresses: The following alphabetical list contains helpline addresses and telephone numbers for organisations which deal with specific medical problems. NOTE:To add other useful addresses please email here MY ILLNESS/PROBLEM BEGINS WITH: A B C D ... Z or use the search engine click here to find additional information A Acoustic Neuroma British Acoustic Neuroma Association c/o 159 Main Street Cossington Leicestershire LE7 4UX TEL: 01509 813088 AIDS and HIV Foundation for AIDS Counselling Treatment and Support (FACTS) 23-25 Weston Park Crouch End London N8 9SYTel: 020 8348 9195 National AIDS Helpline PO Box 5000 Glasgow G12 9BL Helpline: 0800 567123 Alcoholism PrivatePsychiatry.co.uk Godden Green Clinic, Godden Green, Kent TN15 0JR. Clinics in Kent, Essex, Surrey and London Tel: 01732 763491 ex 508 Drinkline (National Alcohol Helpline)7th floor, Weddel House 13-14 West Smithfield London EC1A 9DL Helpline: 020 7332 0202 / 01345 320202 Allergies British Allergy Foundation Deepdene House 30 Bellgrove Road Welling Kent DA16 3BY Helpline: 020 8303 8583 Tel: 020 8303 8525 Food and Chemical Allergy Association 27 Ferringham Lane Ferring West Sussex Helpline: 01903 241178 National Society for Research into Allergy PO Box 45 Hinckley Leicestershire LE10 1JY Tel: 01455 851546 Alopecia Alopecia Patients' Society Lyons Court 168 High Street Knowle West Midlands B93 0LY Tel: 01564 775281 Amputees Limbless Association 31 The Mall Ealing London W5 2PX Tel: 020 8579 1758

65. DAXOR Corporation
Dr. Rosenthal has directed and performed extensive research on blood coagulation,hemorrhagic and thromboembolic diseases, leukemia and gauchers disease.
http://www.daxor.com/pressreleases/pr_5_06_02.html
DAXOR CORPORATION CREATES MEDICAL ADVISORY BOARD
New York, NY May 6, 2002 - Daxor Corporation (AMEX: DXR), the developer and manufacturer of the BVA-100, a semi-automated Blood Volume Analyzer, today announced that the following physicians and healthcare executives have agreed to join the Company’s newly created Medical Advisory Board. Robert L. Rosenthal, M.D. was the Chief of Hematology, Blood Bank Director, and attending physician at North General Hospital in New York City for 41 years. He was an Associate Clinical Professor of Medicine, Mt. Sinai School of Medicine. Dr. Rosenthal has directed and performed extensive research on blood coagulation, hemorrhagic and thromboembolic diseases, leukemia and Gauchers Disease. Dr. Rosenthal discovered Factor XI, and the hemorrhagic disease caused by its deficiency. He also published the first description of Acute Promyelocytic Leukemia. Dr. Rosenthal has published 70 papers. Eliezer Rachmilewitz, M.D. is Head of the Department of Hematology, Hadassah University in Jersusalem. Dr. Rachmilewitz has held a number of teaching assignments throughout the world including visiting professor at the University of Shanghai, China; Memorial Sloan Kettering Cancer Institute, New York; All-Union Scientific Center for Hematology of the USSR, Moscow, Soviet Union; and NIH, Bethesda, MD. He is an expert in many aspects of hematology and the author of over 200 papers. Dr. Rachmilewitz earned his undergraduate degrees at the Hebrew University in Israel and received his medical degree in 1961 from the Hadassah Medical School in Jerusalem.

66. Encyclopedia G-Gi (Search FastHealth.com) Encyclopedia G-Gi
Gastroparesis diabeticorum Gastroschisis closure Gastroschisis repair Gastrostomytube Gastrostomy tube insertion Gaucher disease gauchers disease GE reflux
http://www.jacksonfasthealth.com/encyclopedia/encyclopedia_G-Gi.php
Email This!
A-Am
An-Az B-Bm ... Z
G-Gi

G6PD Anemia

GAD

Gait/walking abnormalities

Galactorrhea
... Dead Links

67. Genzyme Partners Translational Research Grants
Ceredase®/Cerezyme®, protein therapies for the treatment of gauchers diseaseEpicel AM/and Carticel TM, autologous cell therapeutics Seprafilm® (a
http://research.bwh.harvard.edu/genzymegrant.htm

68. Exam #3 1998
Which of the following would NOT be characteristic of most sphingolipidstorage diseases, such as TaySachs and gauchers disease?
http://med.usd.edu/som/somdept/biochem/courses/bioc520/EXAM3X.htm
BIOCHEMISTRY 520 EXAM 3 October 2, 1998 Go to Next Bioc520 Exam
Go to Listing of Exams
Go to Bioc520 Home Page
jat

69. The Contact A Family Directory - GAUCHER DISEASE
age. The disease is associated with anaemia, fatigue, bruising andan increased tendency to bleed. article. gauchers ASSOCIATION.
http://www.cafamily.org.uk/Direct/g15.html
printer friendly GAUCHER DISEASE home more about us in your area conditions information ... how you can help search this site Gaucher Disease is a lysosomal storage disorder that is caused by an inherited deficiency of the enzyme glucocerebrosidase. In Type 1 symptoms may appear at any time from infancy to old age. The disease is associated with anaemia, fatigue, bruising and an increased tendency to bleed. An enlarged spleen and liver with abdominal distension may also occur as well as bone pain, fractures and skeletal degeneration. In the neuropathic forms of the condition (Types 2 and 3) involvement of the central nervous system is seen. Inheritance patterns
Autosomal recessive inheritance. The most common form (Type 1) affects under 1 in 100,000 of the general population but about 1 in 1,000 of Ashkenazi Jews. Not all these will show symptoms. Pre-natal diagnosis
Chorionic villus sampling at ten to twelve weeks allows the condition to be diagnosed in the early stages of pregnancy. Medical text last updated December 2001 by Dr A Velodi, Consultant Paediatrician and Honorary Senior Lecturer, Metabolic Unit, Great Ormond Street Hospital, London, UK.

70. Mature Megakaryocytes, Gauchers' Disease Marrow, PAS Stain
Mature megakaryocytes, gauchers' disease marrow, PAS stain. Two PAS positivemature megakaryocytes. gauchers' disease marrow. PAS stain 100X.
http://image.bloodline.net/stories/storyReader$322
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Mature megakaryocytes, Gauchers' disease marrow, PAS stain
Two PAS positive mature megakaryocytes. Gauchers' disease marrow. PAS stain - 100X Image ID: 2661-091 Carden Jennings Publishing Co., Ltd.

71. Disease: Megakaryocytic Leukemia In Relapse/Remission
Normal Mature Megakaryocyte, AML in Remission; Mature megakaryocytes,gauchers' disease marrow, PAS stain. sm_cjpLogo.gifCopyright
http://image.bloodline.net/ds19
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Disease: Megakaryocytic Leukemia in Relapse/Remission
Carden Jennings Publishing Co., Ltd.

72. Pathogenesis Of And Management For Chronic ITP
platelets. gauchers' disease marrow. PAS stain. gauchers' diseasemar; Huge mature megakaryocyte with some scattered nuclei. ITP
http://www.bloodline.net/stories/storyReader$1826
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Pathogenesis of and management for chronic ITP
Pathogenesis of and management for chronic idiopathic thrombocytopenic purpura: an update Renchi Yang and Zhong Chao Han International Journal of Hematology 2000;71:18-24 Yang.pdf Carden Jennings Publishing Co., Ltd. Related Content

73. BUBL LINK / 5:15 Internet Resources: Gaucher Disease
Author gauchers Association Subjects gaucher disease DeweyClass 616.042 ResourceTypedocuments, news Location uk Last checked 19990508 Laboratory
http://bubl.ac.uk/link/g/gaucherdisease.htm
BUBL LINK / 5:15 Catalogue of Internet Resources Home Search Subject Menus A-Z ... About
Gaucher disease
A-Z Index Titles Descriptions
  • Addenbrooke's Gaucher's Disease Service
  • Gaucher Disease: Current Issues in Diagnosis and Treatment
  • Gaucher Disease
  • Gauchers Association ...
  • National Tay-Sachs and Allied Diseases Association: Gaucher Disease Page last updated: 17 March 2003 Comments: bubl@bubl.ac.uk
    Addenbrooke's Gaucher's Disease Service
    An advisory service for patients and families with Gaucher's disease. The service includes full clinical assessment of Gaucher's patients, advice on general medical and specialist needs e.g. pregnancy, surgical procedures, and patient review.
    Author: Addenbrooke's Hospital
    Subjects: gaucher disease
    DeweyClass:
    ResourceType:
    documents
    Location: uk
    Last checked:
    Gaucher Disease: Current Issues in Diagnosis and Treatment
    Report on a Technology Assessment Conference evaluating the diagnosis and treatment of Gaucher disease. Screening, genetic counselling, and management are covered, as is the natural history of the disease, roles of current molecular and enzymatic assays, appropriate modes of therapy, goals for and consequences of treatment, genotype/phenotype correlation usage and appropriate directions for future research.
    Author: National Institutes of Health
    Subjects: gaucher disease
    DeweyClass:
    ResourceType:
    article Location: usa Last checked:
    Gaucher Disease
    Information about Gaucher disease, a lipid-storage disorder. Includes details of symptoms, prevalence, transmission, and therapy.
  • 74. GAUCHERS LINKS
    LINKS TO WEB RESOURCES ABOUT GAUCHER (gauchers) disease. Living withGaucher disease A guide for patients, parents, relatives, and
    http://www.not-for-profit.org.nz/gauchers/links.htm
    GAUCHERS
    HOME LINKS
    and

    RESOURCES
    LINKS TO WEB RESOURCES ABOUT
    GAUCHER (GAUCHERS) DISEASE
    The association is understood to have gone into recess however this links page has been retained as a service by not-for-profit. We cannot guarantee that any links are current. Living with Gaucher Disease: A guide for patients, parents, relatives, and friends:
    http://neuro-www2.mgh.harvard.edu/gaucher/living.html
    National and International Gaucher Disease Patient Organizations List:
    http://neuro-www2.mgh.harvard.edu/gaucher/orglist.html
    National Gaucher Foundation (USA):
    http://www.gaucherdisease.org/
    Gauchers Association (UK):
    http://www.gaucher.org.uk/first.htm
    Gaucher Association of Canada:
    http://www.gaucher.org
    The Gaucher Registry:
    http://www.gaucherregistry.com
    National Tay-Sachs and Allied Diseases of Ontario: http://www3.sympatico.ca/ntsad/ GAUCHER DISEASE: CURRENT ISSUES IN DIAGNOSIS AND TREATMENT http://text.nlm.nih.gov/nih/ta/www/16.html Mount Sinai School of Medicine Department of Human Genetics: http://academic.mssm.edu/gaucher/

    75. Climb - Providing Information And Support For Those Affected By A Metabolic Dise
    gauchers type 2. gauchers type 2 carrier Unspecified. gauchers type 2 Infantile.Gilberts disease. Gilberts disease Unspecified. Gitelman's Syndrome.
    http://www.climb.org.uk/Dislist.htm
    C hildren L iving with I nherited M eta b olic Diseases List of Currently Supported Diseases This list is currently being updated to include access to additional information on each Metabolic Disease. Where the symbol appears next to a disease this indicates that additional information is available. All additional information is correct at time of publishing and whilst this information has been fully research and checked Climb accepts no responsibility for any errors or omissions. 2 Methyl Acetoacetyl CoA Thiolase Deficiency 3 Hydroxybutyrate 3 Hydroxyl-Methyl Glutaryl CoAlyase Def 3 Methylglutaconic Aciduria 3 Methylglutaconic Aciduria type IV 4-Hydroxybutyric Aciduria 4-Hydroxybutyric Aciduria X Ref Succinic Semi Aldehyde Dehydrogenase 5 Alpha Reductase Def 5 Oxoprolinuria 5 Oxoprolinuria Unspecified Abetalipoprotinaemia Abetalipoprotinaemia and Autism Achondroplasia Achondroplasia - Pseudo Acrodermatitis Enteropathica ACTH Deficient Addison's Addison's - Unspecified ALD Adenosyl Cobalamin Receptor Defect ADHD - (Attention Deficit Hyperactive Disorder) Adrenal Hyperplasia Adrenal Hyperplasia - 11 Beta Hydro Adrenal Hyperplasia - 17 hydroxylas Adrenal Hyperplasia - 17 Ketosteroid Reductase Def Adrenal Hyperplasia - 17 Ketosteroid Reductase Def Unspecified Adrenal Hyperplasia - 20/22 Desmola Adrenal Hyperplasia - 21 Hydroxylase Def Adrenal Hyperplasia - Adreno Genital Syndrome Adrenal Hyperplasia - Congenital Adrenal Hyperplasia - late onset

    76. BUBL LINK: 616.04 Gaucher Disease
    Author gauchers Association Subjects gaucher disease DeweyClass 616.042 ResourceTypedocuments, news Location uk Living with Gaucher disease A guide for
    http://link.bubl.ac.uk/ISC8558
    BUBL LINK Catalogue of selected Internet resources Home Search Subject Menus A-Z ... About
    616.04 Gaucher disease
    Titles Descriptions
  • Addenbrooke's Gaucher's Disease Service
  • Gaucher Disease
  • National Tay-Sachs and Allied Diseases Association: Gaucher Disease
  • Gaucher Disease: Current Issues in Diagnosis and Treatment ...
  • Laboratory Diagnosis of and Genetic Counseling for Gaucher Disease
    All links checked August 2001 Comments: bubl@bubl.ac.uk
    Addenbrooke's Gaucher's Disease Service
    An advisory service for patients and families with Gaucher's disease. The service includes full clinical assessment of Gaucher's patients, advice on general medical and specialist needs e.g. pregnancy, surgical procedures, and patient review.
    Author: Addenbrooke's Hospital
    Subjects: gaucher disease
    DeweyClass:
    ResourceType:
    documents
    Location: uk
    Gaucher Disease
    Information about Gaucher disease, a lipid-storage disorder. Includes details of symptoms, prevalence, transmission, and therapy. Author: National Gaucher Foundation Subjects: gaucher disease DeweyClass: ResourceType: documents Location: usa
    National Tay-Sachs and Allied Diseases Association: Gaucher Disease
    Range of information about Gaucher Disease, first described by Phillipe Gaucher in 1882. The 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.
  • 77. Medicine Online Medical Reference, Cosmetic Plastic Surgery, Bid For Rx, Medicat
    Biotinidase Deficiency A site presenting the biotinidase deficiencydiseases LeschNyhan Syndrome and gauchers' disease. Links
    http://www.medicineonline.com/Default.asp?SubCatID=74&Main=1

    78. Pediatric Residents -- Adrenal Insufficiency: An Approach
    hypogonadism. ACTH Insensitivity (G) rare. Metabolic disease (GMA) suchas Wollman's and gauchers's disease. Secondary Panhypopituitarism
    http://www.cw.bc.ca/pediatricresidents/aiapprch.asp
    HOME Children's - Pediatric Residents Adrenal Insufficiency: an approach Upcoming Events Residency Information Resident Presentations and Teaching Files Useful Pediatric Internet Resources ... Welcome and Site Information Adrenal Insufficiency: an approach by Peter MacDougall The material below was written by the B.C. Residents for B.C. Pediatric Residents for educational purposes only. This material has not been subjected to any formal review process to guarantee accuracy or validity.This material is not intended as and should not be construed as a consultancy nor as advice on a particular patient or patient care. Please do not rely on these comments to make specific patient care decisions, and do not include printed versions of these comments in any patient's medical record. If you have any questions, please consult your own personal doctor. Definition: Deficiency of one or more adrenal hormones: most commonly glucocorticoids but also mineralocorticoids, and adrenal androgens.

    79. DiagnosisPro Medical Diagnostic Software
    biological drug (example) DRUG/Probably NOT safe/Pregnancy category C drug DRUG/Specializedusage medication (example) DRUG/Specific gauchers (Type 1) disease
    http://www.commercial-directory.com/diagnosispro/WRXimigl.htm

    80. Gaucher Disease
    gauchers Association UK Provides news, links, email list and chat, and physicianlist. Living With Gaucher disease A comprehensive online brochure from the
    http://rarediseases.about.com/cs/gaucherdisease/
    zfp=-1 About Rare/Orphan Diseases Search in this topic on About on the Web in Products Web Hosting
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    Gaucher disease
    Guide picks A hereditary disorder of glucocerebroside metabolism.
    Gauchers Association UK
    Provides news, links, email list and chat, and physician list. Living With Gaucher Disease A comprehensive online brochure from the Gaucher Disease Treatment Program at Massachusetts General Hospital in Boston. Lysosomal Diseases Australia Newsletter News and information about storage diseases. Requires Adobe Acrobat Reader for PDF files. Lysosomal Storage Diseases Support Group This group, based in New Zealand, provides information, newsletter, latest research, and links. National Gaucher Foundation Provides information, resources, and links. National Tay-Sachs and Allied Diseases Association Gives a disease profile, offers resources, services, and a reading list.

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