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         Platelet Disorders:     more books (54)
  1. Bleeding disorders are behind approximately half of menorrhagia in adolescent girls. (Platelet Function Test).: An article from: Family Practice News by Mitchel L. Zoler, 2003-07-01
  2. Antiplatelet Therapy in Atherothrombosis: Supplement Issue: Cerebrovascular Diseases 2006
  3. Antiplatelet Therapy: Twenty Years Experience : Proceedings of a European Conference Florence, 26-28 March 1987 (Current Clinical Practice) by G.G. Neri Serneri, G.V.R. Born, 1987
  4. Platelet kinetics in normal subjects and in haematological disorders: With special reference to thrombocytopenia and to the role of the spleen (Scandinavian journal of haematology) by Martti Kotilainen, 1969
  5. Investigations in haemorrhagic disorders with prolonged bleeding time but normal number of platelets with special reference to platelet adhesiveness (Acta medica Scandinavica. Supplementum) by Stig Cronberg, 1968
  6. Blood cell aggregation in thrombotic processes: Cause and cure by Haim I Bicher, 1968
  7. Überlebenszeit und Abbau menschlicher Thrombozyten (Acta medica Scandinavica) by W Bleifeld, 1969
  8. Idiopathic thrombocytopenia purpura: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by L. Culvert, Rebecca, PhD Frey, 2006
  9. Terazosin cuts antidepressant-induced sweating.(Clinical Rounds): An article from: OB GYN News by Sherry Boschert, 2008-09-01
  10. Interactions of Blood and the Pulmonary Circulations (American Heart Association Monograph Series)
  11. USMLE Road Map Pathology (LANGE USMLE Road Maps) by George Wettach, Thomas Palmrose, et all 2009-06-12

61. Special Coagulation Lab
capabilities for congenital and acquired bleeding disorders, hyper coagulable evaluations, platelet disorders, and autoimmune coagulation disorders.
http://pathology.jhu.edu/N/n.web?EP=N&URL=/MCGI/SEND^WEBUTLTY(10291)

62. Hemic And Lymphatic Diseases
Syndrome Blood Coagulation Disorders - Blood platelet disorders - Blue Myeloproliferative Disorders - Neutropenia - Paraproteinemias - Platelet
http://www.mic.ki.se/Diseases/C15.html
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Diseases and Disorders Links pertaining to Hemic and Lymphatic Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Afibrinogenemia Afibrinogenemia Afibrinogenemia Anemia ... von Willebrand Disease
Hemic and Lymphatic Diseases BloodBook .com Human Blood [D O'Neil] - Palomar College (US) Normal Blood - HMDS (UK) Cells of the Blood [clickable map] - University of Leicester (UK) A Demo module Montandon et al. ] from HemoSurf/IMC About Erythrocytes , and Leukocytes - Encyclopedia.com About some Hematological Laboratory Tests - ASCLS An Educational Presentation of Basic Hematology - Puget Sound Blood C.(US) Haem.net [laboratory hematology] HemoSurf , an interactive hematology atlas [Woermann et al.] Morphological Cell Atlas [registration required, no charge] - CellaVision AB Some Blood Chemistry Definitions - Carbon Based Corp.

63. MeSH-D Terms Associated To MeSH-C Term Blood Platelet Disorders
MeSHD terms associated to MeSH-C term Blood platelet disorders, G2D Home of the association of the corresponding term to Blood platelet disorders.
http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Blood_Platelet_Disorders:unknown

64. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Blood_Disorders/Pl
bleeding caused by qualitative platelet disorders and many more topics. Platelet Disorder Support Association Information and support for those with
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Blood_Disor
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Trial At Jefferson Shows New Drug May Help Cancer Patients Who Need Stem Cell Transplants (September 8, 2005) full story Medication Reduces Risk Of Heart Attack And Cardiovascular Death Before And After Angioplasty (September 4, 2005) JAMA full story Cocoa Is The New Red Wine: Shows Benefits For Coronary Heart Disease (August 12, 2005) full story UNC Scientists Discover New Role For Protein As Fundamental Inhibitor Of Cell Movement (August 10, 2005) full story Anti-tumor Activity Also Plays A Critical Role During Eye Development In The Embryo (August 2, 2005) full story Gene Variants Predict Bleeding After Heart Surgery (May 4, 2005) full story OHSU Study Finds Ginkgo Beneficial For MS Symptoms (April 28, 2005) full story (April 11, 2005) full story [ More news about Platelet
Amazon.com's Price: Prices subject to change. Dental And Craniofacial Applications Of Platelet-Rich Plasma
by: Robert E. Marx

65. The Laboratory Diagnosis Of Platelet Disorders
platelet disorders can be associated with varying platelet appearances. platelet disorders may be divided into 3 major categories platelet dysfunction
http://arpa.allenpress.com/arpaonline/?request=get-document&doi=10.1043/0003-998

66. RFA-HL-05-020: Proteomic Studies Of Platelet Functions
It is also difficult to diagnose platelet disorders that increase the risk of As a result, most of the platelet disorders have remained qualitative.
http://grants.nih.gov/grants/guide/rfa-files/RFA-HL-05-020.html
Part I Overview Information Department of Health and Human Services Participating Organizations
National Institutes of Health (NIH), ( http://www.nih.gov Components of Participating Organizations
National Heart, Lung, and Blood Institute (NHLBI), ( http://www.nhlbi.nih.gov Title: Proteomic Studies of Platelet Functions Announcement Type
New Request For Applications (RFA) Number: RFA-HL-05-020 Catalog of Federal Domestic Assistance Number(s)
Key Dates
Release Date: July 8, 2005
Letters of Intent Receipt Date(s): December 12, 2005
Application Receipt Dates(s): January 12, 2006
Peer Review Date(s): June/July, 2006
Council Review Date(s): September 2006
Earliest Anticipated Start Date: September 2006 Additional Information To Be Available Date (Url Activation Date): Not applicable Expiration Date: January 13, 2006 Due Dates for E.O. 12372 Not Applicable Additional Overview Content Executive Summary
  • The National Heart, Lung, and Blood Institute (NHLBI) plans to support collaborative research on the application of proteomic tools to identify disorders of human platelet function. Support is intended for the adaptation and application of existing technology to study blood platelets and not for the development of new proteomic technology. We anticipate that such research will lead to more quantitative definitions of platelet disorders. The total amount to be awarded is $2.2 million over two years.

67. HighWire -- Browse Journals - Blood Platelet Disorders
Browse Journals publishing on Blood platelet disorders, (return to Topic List page) Platelet Storage Pool Deficiency Thrombocytosis
http://highwire.stanford.edu/lists/topic_dir/608683/608684/613947/613948/614082/
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Year: Vol: Page: Home Adv. Search For Institutions For Publishers ... Sign in or register for access to all HighWire Press customization features Browse Journals publishing on Blood Platelet Disorders: (return to Topic List page) Blood Platelet Disorders
Bernard-Soulier Syndrome
Thrombocytopenia Platelet Storage Pool Deficiency Thrombocytosis ... Hematologic Diseases Blood Platelet Disorders Home Adv. Search For Institutions For Publishers ... partners/suppliers

68. Entrez PubMed
The Quebec platelet disorder (QPD) is an autosomal dominant platelet disorder Blood platelet disorders/enzymology*; Blood platelet disorders/genetics
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

69. Entrez PubMed
and for coverage of surgical procedures in patients with platelet disorders. Cases include seven patients with congenital platelet disorders Glanzmann
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2

70. Guam Medical Libraries Digital Libraries Program
Chapter 135 Acquired Disorders of Platelet Function Access document Blood platelet disorders (MeSH browse) List of documents. Clinical Trials
http://guam-dl.slis.ua.edu/clinical/hematology/bleedingdisorders/plateletdisorde
Clinical Resources by Topic: Hematology
Acquired Platelet Dysfunction Clinical Resources
Emergency Pediatrics Geriatrics Pathology ... Miscellaneous Resources See also:

71. Platelet Disorders - General Practice Notebook
platelet disorders. The formation of the initial platelet plug is an important component platelet disorders that may interfere with this mechanism are
http://www.gpnotebook.co.uk/cache/-1389035490.htm
platelet disorders The formation of the initial platelet plug is an important component of normal haemostasis. Platelet disorders that may interfere with this mechanism are:
  • too few platelets - thrombocytopaenia abnormal platelet function - thrombocytopathy
Thrombocytopaenia accounts for the majority of cases.
Click here for more information...

72. Studies Of A Second Family With The Quebec Platelet Disorder: Evidence That The
CONGENITAL platelet disorders are rare but important causes of abnormal An inherited platelet disorder was suspected, because similar laboratory
http://www.bloodjournal.org/cgi/content/full/89/4/1243
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This Article Abstract Full Text (PDF) Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Rights and Permissions PubMed PubMed Citation Articles by Hayward, C. P.M. Articles by Rivard, G. E. Related Collections Hemostasis, Thrombosis, and Vascular Biology Blood , Vol. 89 No. 4 (February 15), 1997: pp. 1243-1253
Studies of a Second Family With the Quebec Platelet Disorder: Evidence That the Degradation of the -Granule Membrane and Its Soluble Contents Are Not Secondary to a Defect in Targeting Proteins to -Granules
By Catherine P.M. Hayward Elisabeth M. Cramer William H. Kane Shilun Zheng Madeleine Bouchard and Georges E. Rivard
ABSTRACT Abstract
Introduction
Methods
Results
Discussion
References We recently described a Quebec family with an autosomal dominant bleeding disorder characterized by mildly reduced-low normal platelet counts, an epinephrine aggregation defect, multimerin deficiency, and proteolytic degradation of several, soluble -granular proteins. Similar clinical features led us to investigate a second family with an unexplained, autosomal dominant bleeding disorder. The affected individuals had reduced to normal platelet counts, absent platelet aggregation with epinephrine, and multimerin deficiency. Their platelet

73. The Organization Of Microtubules And Microtubule Coils In Giant Platelet Disorde
Some of the cells from patients with giant platelet disorders are also diskshaped, but the majority of their huge platelets are spherical.
http://ajp.amjpathol.org/cgi/content/abstract/116/3/514

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HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Order Full text via Infotrieve Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by White, J. G. Articles by Sauk, J. J.
REGULAR ARTICLES
The organization of microtubules and microtubule coils in giant platelet disorders
JG White and JJ Sauk
Normal human platelets are characteristically discoid in shape. The lentiform appearance is supported by a circumferential band of microtubules lying just under the cell membrane along its greatest circumference. Some of the cells from patients with giant platelet disorders are also disk-shaped, but the majority of their huge platelets are spherical. In the present study platelets from patients with the Gray platelet syndrome (GPS), May-Hegglin anomaly (MHA), and Epstein's syndrome (ES) were examined in thin sections and negatively stained whole mounts, and by indirect immunofluorescence with a monoclonal antibody to tubulin for determination of the organization of their microtubule systems. Many GPS platelets and

74. NORD - National Organization For Rare Disorders, Inc.
A study of platelet disorders is being conducted at the National Institutes of Gray platelet syndrome is a rare bleeding disorder that causes excessive
http://www.rarediseases.org/research/clinicaltrials

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Many libraries, schools, universities, and hospitals subscribe to NORD's Rare Disease Database for unlimited access to reports on more than 1,150 diseases. Index of Rare Diseases
This is the list of diseases currently covered in the Rare Disease Database.
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This is the list of organizations in NORD's Organizational Database. Organizational Database
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Read about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC. Research NORD posts information on this page about current studies for which participants are being recruited. NORD does not promote, endorse, or encourage participation in any specific medical research. We post this page for informational purposes only, and we encourage individuals considering participating in any research project to discuss the matter with their physicians. Research Underway Cronkhite-Canada Syndrome Cronkhite-Canada syndrome (CCS) is a very rare disease with symptoms that include loss of taste, intestinal polyps, hair loss, and nail growth problems. It is difficult to treat because of malabsorption that accompanies the polyps. CCS occurs primarily in older people (average age 59) and it is not believed to have a genetic component. There have been fewer than 400 cases reported in the past 50 years, primarily in Japan but also in the U.S. and other countries.

75. Disease Category Listing (121): Platelet Disorders
CenterWatch Listing of Clinical Research Trials for platelet disorders.
http://www.centerwatch.com/studies/cat121.htm
Clinical Trials: Platelet Disorders
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76. Preface
platelet disorders include a case of platelet satellitism as well as thrombocytopenias and thrombocythemia. Blood parasites include babesiosis, filariosis,
http://www.ivis.org/advances/Camacho/camacho/chapter_frm.asp?LA=1

77. OHSU Division Of Hematology & Medical Oncology
An article by Thomas G. DeLoughery, Associate Professor of Medicine. platelet transfusion therapy and dysfunctional platelets are discussed.
http://www.ohsu.edu/som-hemonc/handouts/deloughery/bleed.shtml
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"The disease of cancer will be banished from life by calm, unhurrying, persistent men and women, working with every shiver of feeling controlled and suppressed in hospitals and laboratories, and the motive that will conquer cancer will not be pity or horror; it will be curiosity to know how and why."
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78. The HELLP Syndrome Society
International network for persons affected by the combined disorders of hemolysis, elevated liver enzymes and low platelet count.
http://hometown.aol.com/hellp1995/index.html
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79. Types Of Platelet Function Disorder
Hereditary platelet function disorders can be divided into five groups Three platelet function disorders involve platelet secretion.1) In Alpha Granule
http://www.hemophilia.ca/en/2.4.4.php

Platelet Function Disorders
Types of Platelet Function Disorder Platelet Function Disorders Types of Platelet Function Disorder

Hereditary Platelet function disorders Hereditary platelet function disorders can be divided into five groups depending on the type of abnormality.
Disorders of platelet adhesion This rare disorder is called Bernard-Soulier Syndrome. It is caused by a deficiency on the surface of the platelet in an area called Glycoprotein Ib/IX. As a result, platelets fail to stick and clump together at the site of the injury. (See Figure 1, stage 3.) The disorder is often first noticed during childhood. Children have frequent bruises, nose bleeds and bleeding in the mouth and gums. Some may experience gastrointestinal bleeding (bleeding in the gut). Women may experience heavy menstrual bleeding, or their menstruations (periods) last longer than normal. This is called menorrhagia. Blood tests show:
  • a prolonged bleeding time (bleeding time is a measure of the time it takes for a simple cut to stop bleeding)
  • a low platelet count (this means that there are fewer platelets than normal)
  • that the platelets appear larger than normal when seen through a microscope
  • that the platelets do not clump together in response to ristocetin.

80. Low Platelets
In the disorders described below, the immune system destroys platelets in the Cyclical thrombocytopenia is a rare platelet disorder characterized by
http://www.itppeople.com/lowplate.htm
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Low Platelet Disorders
(Adapted by the PDSA Staff from A Low Platelet Count Must Be ITP, Right?, by Jonathan G. Drachman M.D, Puget Sound Blood Center. The article appeared in The Platelet News, vol.4, no 4, winter 2002/2003, see www.pdsa.org/newsletter.htm A low platelet count is frequently assumed to represent ITP (immune thrombocytopenic purpura). However there are many other possible causes of thrombocytopenia, with clinical severity ranging from trivial to life threatening. ITP is a diagnosis of exclusion. This means that only after all other possible causes of low platelets have been ruled out, can a diagnosis of ITP be settled. This makes it important to know or at least be aware of the other common causes of low platelets that may be mistaken for or misdiagnosed as ITP. These other causes are either platelet production problems centered in the bone marrow or platelet destruction problems centered in the liver or spleen. Some low platelet conditions are characterized by both a low rate of production and a high rate of platelet destruction. The most common conditions or defects responsible for low platelets are listed below in the following categories:
I. Platelet Production Problems

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