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Abetalipoproteinemia:     more detail

Abetalipoproteinemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS, CGC Polzin, 2005 Abetalipoproteinemia Abetalipoproteinemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19 Bassen-Kornzweig syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005

lists with details

41. Annual Reviews - Error
    Morphologic features of the liver in abetalipoproteinemia. abetalipoproteinemiatreated with parenteral and oral vitamins A, E, with medium chain  
    http://arjournals.annualreviews.org/doi/full/10.1146/annurev.nutr.20.1.663
    
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42. MedCirca.com | Lippincott Williams & Wilkins
    Index Search Results for abetalipoproteinemia What s an Index Search? abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an  
    http://www.medcirca.com/search/indexsearch.asp?root_id=3&index=yes

43. Abetalipoproteinemia - BlueRider.com
    abetalipoproteinemia listen domain availability. Dictionary and Thesaurusentries for. abetalipoproteinemia. Your search results  
    http://abetalipoproteinemia.bluerider.com/wordsearch/abetalipoproteinemia

44. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor
    News; Books; Links. More news about abetalipoproteinemia . Error We did notfind any matches for your request. More books about abetalipoproteinemia  
    http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica

45. Medicine Online Medical Reference Medical Information, Symptoms And Signs Medica
    Diseases and Conditions Blood Disorders - abetalipoproteinemia. Records found0, Number of Pages 1, Go to Page of 1. Add your site  
    http://www.medicineonline.com/Default.asp?SubSubCatID=958&Main=1

46. Penn State Faculty Research Expertise Database (FRED)
    , A disorder of lipid metabolism inherited asan autosomal recessive trait characterized by the near absence ofabetalipoproteinemia.  
    http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D000012

47. Abetalipoproteinemia: Metabolic, Endocrine, And Electron-microscopic Investigati
    Pediatrics, 4891, 1971, abetalipoproteinemia, SHORT STATURE, ENDOCRINE EVALUATION,LIPID STUDIES, DUODENAL HISTOLOGY.  
    http://pediatrics.aappublications.org/cgi/content/abstract/48/1/91
    
    Extractions: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Sperling, M. A. Articles by Drash, A. L. Pediatrics, Jul 1971, 91-102, Vol 48, No. 1 MA Sperling, F Hengstenberg, E Yunis, FM Kenny and AL Drash Department of Pediatrics, Harbor General Hospital, 1000 West Carson Street, Torrance, California 90509. ABSTRACT. Two siblings presenting with short stature and severely retarded skeletal maturation were found to have steatorrhea, retinitis pigmentosa, night blindness, and loss of posterior column function. The finding of acanthocytosis in the peripheral blood smear, low levels of all serum lipid fractions, and complete absence of betalipoproteins on electrophoresis

48. Normotriglyceridemic Abetalipoproteinemia In Infancy: An Isolated Apolipoprotein
    Normotriglyceridemic abetalipoproteinemia in infancy an isolated apolipoproteinB100 deficiency. Y Takashima, T Kodama, H Iida, M Kawamura, H Aburatani,  
    http://pediatrics.aappublications.org/cgi/content/abstract/75/3/541
    
    Extractions: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Takashima, Y. Articles by Kawade, M. Y Takashima, T Kodama, H Iida, M Kawamura, H Aburatani, H Itakura, Y Akanuma, F Takaku and M Kawade The plasma lipoproteins of a 1-year-old Japanese infant were studied because of malnutrition, severe decrease in plasma lipid level, and acanthocytosis. Plasma lipoprotein analysis revealed that low-density lipoproteins were deficient; however, low levels of triglyceride-rich lipoproteins were found in the plasma. On sodium dodecylsulfate (SDS) polyacrylamide gel electrophoresis, apoprotein B-48 and a faint band

49. HighWire -- Browse Journals - Abetalipoproteinemia
    Browse Journals publishing on abetalipoproteinemia, (return to Topic List page) Journals focusing on abetalipoproteinemia (in order by highest focus)  
    http://highwire.stanford.edu/lists/topic_dir/608683/608684/613947/613948/614082/
    
    Extractions: Sort by: Alphabet Frequency of articles in Abetalipoproteinemia Focus of journal on Abetalipoproteinemia What's this? Journals focusing on Abetalipoproteinemia (in order by highest focus) New England Journal of Medicine info Human Molecular Genetics info ... Blood Protein Disorders Abetalipoproteinemia Home Adv. Search For Institutions For Publishers ... partners/suppliers

50. Automated Web Directory: Abetalipoproteinemia
    root health medicine branches_of_medicine_and_dentistry conditions_and_diseases abetalipoproteinemia. Snowfox alphabetic index  
    http://www.snowfox.com/topictrees/English/root/health/medicine/branches_of_medic

51. Abetalipoproteinemia - Descipher Health
    abetalipoproteinemia. From Descipher Health External Links. Retrievedfrom http//www.descipher.com/health/info/abetalipoproteinemia . Views  
    http://www.descipher.com/health/info/LDL_deficiency

52. Abetalipoproteinemia - Descipher Health
    NEUROACANTHOCYTOSIS DISORDERS Contact a Family for families abetalipoproteinemia; Bassen-Kornzweig syndrome; Acanthocytosis; abetalipoproteinemia was first described by Dr FA Bassen and Dr AL Kornzweig in 1950.  
    http://www.descipher.com/health/info/Abetalipoproteinemia

53. Bassen-Kornzweig Syndrome
    diarrhea, failure to thrive in infancy, and problems with nerves. AlternativeNames. abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency  
    http://www.healthscout.com/ency/1/001666.html
    
    Extractions: Search HealthScout Web MEDLINE Special Offers TV Specials Chronic Pain Erectile Dysfunction GERD Diabetes ... High Tech Health Top Features Bipolar Disorder Resources Sleep Skin Cancer Migraines ... Diabetes Health Organizer Resources Healthscout News 3D Health Animations Health Videos Health Encyclopedia ... Drug Library Drug Information Drug Search Drug Interactions Image Database Pill Identifier Channels Home Today Women Men ... Drug Checker Medical Health Encyclopedia Injury Disease Nutrition Poison ... Prevention Definition: Bassen-Kornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. It results in fatty stools, diarrhea, failure to thrive in infancy, and problems with nerves. Causes, incidence, and risk factors: Bassen-Kornzweig syndrome is an autosomal recessive inherited disorder that affects both sexes, but predominantly males (70%). It is due to mutations in one of two genes: apolipoprotein B (APOB) or microsomal triglyceride transfer protein (MTP). The syndrome causes the body not to make lipoproteins (molecules of fat combined with protein ) including low-density lipoproteins ( LDL ), very-low-density lipoproteins (

54. Abetalipoproteinemia - Abetalipoproteinemia Information
    abetalipoproteinemia abetalipoproteinemia Information.  
    http://www.free-food-recipes.com/abetalipoproteinemia.htm
    
    Extractions: Cooking Glossary Abetalipoproteinemia can be defined as the rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels. Individuals with abetalipoproteinemia may be prescribed special vitamin E supplements by a physician to treat this disorder. Here are the list of some of the Abetalipoproteinemia Symptoms: Home Contact Us Resources This Page was last Modified: Sunday, 4th September 2005

55. MeSH-D Terms Associated To MeSH-C Term Abetalipoproteinemia
    MeSHD terms associated to MeSH-C term abetalipoproteinemia, G2D Home the strength of the association of the corresponding term to abetalipoproteinemia.  
    http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Abetalipoproteinemia:unknown

56. References For Hypobetalipoproteinemia, Familial, 2 With The MeSH
    References for Hypobetalipoproteinemia, familial, 2 with the MeSH termabetalipoproteinemia, G2D Home. PMID and date. Follow the link to see the  
    http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Abetalipoproteinemia

57. Tropes
    605552 3q27 Abdominal obesitymetabolic syndrome, 605552 (2) AOMS2 60557217p12 abetalipoproteinemia (3) APOB , FLDB 107730 2p24 abetalipoproteinemia,  
    http://freesense.free.fr/Diseases/d/0009.htm

58. Brain Diseases, Metabolic, Inborn
    605552 (2) AOMS2 605572 17p12 abetalipoproteinemia (3) APOB. , FLDB 1077302p24 abetalipoproteinemia, 200100 (3) MTP 157147 4q22q24 Acampomelic  
    http://freesense.free.fr/Diseases/c/404.htm
    
    Extractions: http://www.ncbi.nlm.nih.gov/htbin-post/Omim/getmorbid , AAS 305400 Xp11. 21 Abdominal obesity -metabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity -metabolic syndrome, 605552 (2) AOMS2 605572 17p12 Abetalipoproteinemia (3) APOB , FLDB 107730 2p24 Abetalipoproteinemia , 200100 (3) MTP 157147 4q22-q24 Acampomelic campolelic dysplasia (3) SOX9, CMD1, SRA1 http://www.ncbi.nlm.nih.gov/genome/guide/HsChrX.shtml Clusters Mouse Homologies for Human Chr. X_chromosome X Disease Genes Myelin stained section of brain in adrenoleukodystrophy Adrenoleukodystrophy Duchenne Muscular_dystrophy Lowe Syndrome Norrie Disease Rett_syndrome See OMIM or Genes and Disease for additional examples

59. Bassen-Kornzweig Syndrome (Disease) - Des Moines, Iowa Health Hospital
    abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency. Causes And Risk.BassenKornzweig syndrome is an autosomal recessive inherited disorder  
    http://www.iowahealth.org/12635.cfm
    
    Extractions: Search Health Information Talk To A Nurse: My Nurse Specialized Outpatient Services Patient Education Materials ... Contact A Nurse Search Health Information August 02, 2005 Back to Search Definition Bassen-Kornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. It results in fatty stools, diarrhea, failure to thrive in infancy, and problems with nerves. Alternative Names Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Causes And Risk Bassen-Kornzweig syndrome is an autosomal recessive inherited disorder that affects both sexes, but predominantly males (70%). It is due to mutations in one of two genes: apolipoprotein B (APOB) or microsomal triglyceride transfer protein (MTP). The syndrome causes the body not to make lipoproteins (molecules of fat combined with protein ) including low-density lipoproteins ( LDL ), very-low-density lipoproteins ( VLDL ), and chylomicrons (small molecules of fat in the blood).

60. OEDILF - Word Search
    www.absoluteastronomy.com/encyclopedia/a/ab/abetal abetalipoproteinemia Cause, Symptoms, Treatment and Cureabetalipoproteinemia Cause, Symptoms, Treatment and Cure. Deficiency is seen onlyin children with abetalipoproteinaemia and in patients on longterm  
    http://www.oedilf.com/db/Lim.php?Word=abetalipoproteinemia

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