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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

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

82. Abetalipoproteinemia - English Dictionary Meaning
    Free Online ICD9/ICD9CM codes and Medical Dictionary abetalipoproteinemia Apolipoprotein B Deficiency Disease BassenKornzweig Syndrome Betalipoprotein Deficiency Disease Microsomal Triglyceride Transfer  
    http://www.realdictionary.com/A/dir/abetalipoproteinemia.asp

83. Role Of Apolipoprotein E-containing Lipoproteins In Abetalipoproteinemia
    Clin Invest. 1982 December; 70 (6) 1157 1169 Role of ApolipoproteinEcontaining Lipoproteins in abetalipoproteinemia. Conrad B. Blum  
    http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=370332

84. Abnormalities Of High Density Lipoproteins In Abetalipoproteinemia*
    Investigation J Clin Invest. 1967 July; 46 (7) 1151 1161 Abnormalitiesof High Density Lipoproteins in abetalipoproteinemia *. John W. Jones  
    http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=297114

85. NodeWorks - Brain Diseases: Metabolic: Abetalipoproteinemia
    disease. thumbnail, 1. people involved in abetalipoproteinemia we are people who have this disorder annd /or family involved.  
    http://dir.nodeworks.com/Health/Conditions_and_Diseases/Neurological_Disorders/B
    
    Extractions: in entire NodeWorks Directory in Health in Neurological Disorders in Brain Diseases in Metabolic in ++ Abetalipoproteinemia Top Health Neurological Disorders Brain Diseases ... Metabolic Abetalipoproteinemia A disorder of lipid metabolism characterized by fat malabsorption, acanthocytosis, retinopathy, and progressive neurologic disease. people involved in abetalipoproteinemia we are people who have this disorder annd /or family involved. group help with information, support and investigation WebMD/Lycos A definition of Bassen-Kornzweig syndrome, followed by a look at the alternate names, causes, symptoms, tests, treatment, prognosis and complications.

86. Abetalipoproteinemia Medical Definition Of Abetalipoproteinemia In The Medical D
    Definition of abetalipoproteinemia in the Medical Dictionary and Thesaurus. Providessearch by definition of abetalipoproteinemia.  
    http://medical-dictionary.thefreedictionary.com/Abetalipoproteinemia

87. Abetalipoproteinemia Legal Definition Of Abetalipoproteinemia. What Is Abetalipo
    Definition of abetalipoproteinemia in the Ledal Dictionary and Thesaurus. abetalipoproteinemia.Word Word.  
    http://legal-dictionary.thefreedictionary.com/Abetalipoproteinemia

88. Abetalipoproteinemia Definition Of Abetalipoproteinemia In Computing. What Is Ab
    Computer term of abetalipoproteinemia in the Computing Dictionary andThesaurus. Provides search by definition of abetalipoproteinemia.  
    http://computing-dictionary.thefreedictionary.com/Abetalipoproteinemia

89. Disease - Bassen-Kornzweig Syndrome, North Carolina
    with nerves. Alternative Names abetalipoproteinemia; Acanthocytosis;Apolipoprotein B deficiency. Causes And Risk BassenKornzweig  
    http://www.uhseast.com/12127.cfm
    
    Extractions: Back Email Us Search Centers of Excellence ... Disease Management 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).

90. Abetalipoproteinemia
    http://medical.webends.com/kw/Abetalipoproteinemia
    
    Extractions: WWW Medical.WebEnds.com Apolipoprotein B Deficiency Disease; Bassen-Kornzweig Syndrome; Betalipoprotein Deficiency Disease; Microsomal Triglyceride Transfer Protein Deficiency Disease; Bassen-Kornzweig Disease; Deficiency Disease, Apolipoprotein B A disorder of lipid metabolism inherited as an autosomal recessive trait characterized by the near absence of APOLIPOPROTEINS B and apoB-containing lipoproteins in plasma. Microsomal triglyceride transfer protein is deficient or absent in enterocytes . Clinical and laboratory findings include acanthocytosis, hypocholesterolemia, peripheral neuropathy, posterior column degeneration, ataxia , and steatorrhea. Intellectual abilities may also be impaired. (Menkes, Textbook of Child Neurology , 5th ed, p118; Curr Opin Lipidol 1994 Apr;5(2):81-6)

91. Redirect
    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?200100

92. ► Síndrome De Bassen-Kornzweig
    de apolipoproteína B. Causas, incidencia y factores de riesgo  
    http://www.umm.edu/esp_ency/article/001666.htm
    
    Extractions: Toggle English Spanish Informaci³n general S­ntomas Tratamiento Prevenci³n Definici³n: Es una enfermedad cong©nita rara, que se caracteriza por la incapacidad de absorber por completo las grasas de la dieta a trav©s del intestino. Lo anterior produce heces grasosas, diarrea, retraso en el desarrollo infantil y problemas con los nervios. Causas, incidencia y factores de riesgo: El s­ndrome de Bassen-Kornzweig es un trastorno cong©nito autos³mico recesivo que afecta ambos sexos, pero de manera predominante a los hombres (70%). Este es causado por mutaciones en uno de dos genes: la apolipoprote­na B (APOB) o la prote­na de transferencia de triglic©rido micros³mico (MTP). El s­ndrome hace que el organismo no produzca lipoprote­nas (mol©culas de grasa combinadas con prote­na ) que incluyen lipoprote­nas de baja densidad ( LDL ), lipoprote­nas de muy baja densidad (

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