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Journal Abstract Search
118 related items for PubMed ID: 9357195
1. Persistent transaminase elevation due to heterozygous (familial) apolipoprotein B deficiency. Mehta NN, Desai HG. Indian J Gastroenterol; 1997 Oct; 16(4):158-9. PubMed ID: 9357195 [Abstract] [Full Text] [Related]
2. Fatty liver with elevated transaminase levels due to heterozygous apolipoprotein B deficiency. Artekar TM, Desai HG. Trop Gastroenterol; 2003 Oct; 24(1):35-6. PubMed ID: 12974215 [Abstract] [Full Text] [Related]
7. Unusual presentation of three siblings with familial heterozygous hypobetalipoproteinaemia. Kairamkonda V, Dalzell M. Eur J Pediatr; 2003 Mar; 162(3):129-131. PubMed ID: 12655413 [Abstract] [Full Text] [Related]
8. Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B. Tarugi P, Lonardo A, Ballarini G, Grisendi A, Pulvirenti M, Bagni A, Calandra S. Gastroenterology; 1996 Oct; 111(4):1125-33. PubMed ID: 8831609 [Abstract] [Full Text] [Related]
12. Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46). Young SG, Hubl ST, Chappell DA, Smith RS, Claiborne F, Snyder SM, Terdiman JF. N Engl J Med; 1989 Jun 15; 320(24):1604-10. PubMed ID: 2725600 [No Abstract] [Full Text] [Related]
14. Acanthocytosis in a patient with homozygous familial hypobetalipoproteinemia due to a novel APOB splice site mutation. Hegele RA, Miskie BA. Clin Genet; 2002 Feb 15; 61(2):101-3. PubMed ID: 11940084 [Abstract] [Full Text] [Related]
19. Apoprotein B-100 production is decreased in subjects heterozygous for truncations of apoprotein B. Aguilar-Salinas CA, Barrett PH, Parhofer KG, Young SG, Tessereau D, Bateman J, Quinn C, Schonfeld G. Arterioscler Thromb Vasc Biol; 1995 Jan 15; 15(1):71-80. PubMed ID: 7749818 [Abstract] [Full Text] [Related]