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Tangier Disease:     more detail

Tangier disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Lisa, MS, CGC Andres, 2005 Tangier Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19 Tangier Disease Tonsils and apolipoproteins;: Lessons about plasma lipoproteins derived from Tangier disease and other mutants (Jiménez Díaz memorial lecture) by Donald S Fredrickson, 1976

lists with details

101. JAX®Mice Database - Mouse/Human Gene Homologs: Tangier's Disease
     JAX®MICE Database Mouse/Human Gene Homologs tangier s disease List.  
     http://jaxmice.jax.org/jaxmicedb/html/model_1548.shtml
     
     Extractions: (link to Data Sheet) Strain Type Standard Supply DBA/1- /J Repository-Live. No age specifications accepted. Colony sized to produce minimal quantities (typically up to 6 mice) upon order receipt; one order per strain. Expected delivery: 1-3 months. Larger quantities or custom orders arranged upon request. (1 stocks) Back to top Back to Top Research Research Resources ... The Jackson Laboratory

102. Log In Problems
     Patients with tangier s disease have a markedly reduced level of HDL. They havean enlarged liver and spleen, and have an increased risk of cardiovascular  
     http://www.medscape.com/viewarticle/474936_12

103. Lymphocytic Interstitial Pneumonitis In A Woman With Tangier's Disease -- Kenney
     We report the first case of LIP in a patient with tangier’s disease. tangier’sdisease is an extremely rare, autosomal recessive metabolic disorder,  
     http://meeting.chestjournal.org/cgi/content/abstract/126/4/977S
     
     Extractions: This Article Full Text (PDF) Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Kenney, L. Articles by Aoun, N. Y. Tuesday, October 26, 2004 4:15 PM - 5:45 PM Lawrence Kenney, MD Eduardo Velez, MD and Naim Y. Aoun, MD* St. Elizabeth Medical Center, Brighton, MA INTRODUCTION: Lymphocytic Interstitial Pneumonitis is often seen in conjunction with systemic diseases whether auto-immune, inflammatory or infectious. We report the first case of LIP is an extremely rare, autosomal recessive metabolic disorder, characterized by a severe deficiency in HDL cholesterol and accumulation of foamy macrophages in different tissues. Affected patients present with enlarged yellow/orange tonsils, hepatosplenomegaly, polyneuropathy, and an increased risk for coronary heart disease. A mutation in the ABC1 gene on chromosome 9q31 is believed to be responsible for the disease.

104. HNRCA : Subpopulations Of High Density Lipoproteins In Homozygous And Heterozygo
     Subpopulations of high density lipoproteins in homozygous and heterozygous Tangierdisease. Atherosclerosis 2001;156(1)217225.  
     http://hnrc.tufts.edu/publications/detail.php?id=825

105. References For Hypoalphalipoproteinemia, Primary With The MeSH
     References for Hypoalphalipoproteinemia, primary with the MeSH term TangierDisease, G2D Home. PMID and date. Follow the link to see the corresponding  
     http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Tangier_Disease:U568

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