81. Abnormalities Of High Density Lipoproteins In Abetalipoproteinemia* Abnormalities of High Density Lipoproteins in abetalipoproteinemia*. John W.Jones† and Peter Ways‡. Williams Research Laboratories and Medical Service, http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=297114

82. A Study Of The Abnormal Lipoproteins In Abetalipoproteinemia. The serum lipoproteins of five patients with abetalipoproteinemia (ABL) were Whether the abetalipoproteinemia previously described and noted in the http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=301487

83. JAMA -- Abstract: Abetalipoproteinemia. New Insights Into Lipoprotein Assembly A abetalipoproteinemia is a rare genetic disease that has provided important new abetalipoproteinemia Caused by Maternal Isodisomy of Chromosome 4q http://jama.ama-assn.org/cgi/content/abstract/270/7/865

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 270 No. 7, August 18, 1993 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Rader DJ Brewer HB Articles that cite this article Contact me when this article is cited Abetalipoproteinemia. New insights into lipoprotein assembly and vitamin E metabolism from a rare genetic disease D. J. Rader and H. B. Brewer Jr Molecular Disease Branch, National Heart, Lung, and Blood Institute, Bethesda, Md. 20892. Abetalipoproteinemia is a rare genetic disease that has provided important new insights into the physiology of lipoprotein assembly and vitamin E metabolism. Forty-two years after its initial description, a molecular etiology of ABL has been reported to be a deficiency of a microsomal transfer protein, thus suggesting that this protein plays a key role in

84. CMAJ -- Please Take Our Questionnaire Arrest of neuropathy and myopathy in abetalipoproteinemia with highdose vitaminE therapy. RA Hegele and A. Angel. A 16-year-old girl, one of dizygotic http://www.cmaj.ca/cgi/content/abstract/132/1/41

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85. ► Síndrome De Bassen-Kornzweig apolipoproteína B. Causas, incidencia y factores de riesgo http://www.umm.edu/esp_ency/article/001666.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Enfermedades Nutrici³n Cirugia Sintomas Lesiones ... Encyclopedia (Spanish) Toggle English Spanish S­ndrome de Bassen-Kornzweig 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. Nombres alternativos: Abetalipoproteinemia; acantocitosis; deficiencia de apolipoprote­na B 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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