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2. 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 [TBL] [Abstract][Full Text] [Related]
3. 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; 320(24):1604-10. PubMed ID: 2725600 [No Abstract] [Full Text] [Related]
4. Novel mutation (c.G1124A) in exon 9 of the APOB gene causes aberrant splicing and familial hypobetalipoproteinemia. Homer VM; George PM Clin Chem; 2007 Jun; 53(6):1165-7. PubMed ID: 17517592 [No Abstract] [Full Text] [Related]
5. 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 [TBL] [Abstract][Full Text] [Related]
7. Fatty liver in a case with heterozygous familial hypobetalipoproteinemia. Ogata H; Akagi K; Baba M; Nagamatsu A; Suzuki N; Nomiyama K; Fujishima M Am J Gastroenterol; 1997 Feb; 92(2):339-42. PubMed ID: 9040220 [TBL] [Abstract][Full Text] [Related]
8. A clinical and neurophysiological investigation of a Danish kindred with heterozygous familial hypobetalipoproteinemia. Andersen GE; Trojaborg W; Lou HC Acta Paediatr Scand; 1979 Mar; 68(2):155-9. PubMed ID: 419983 [TBL] [Abstract][Full Text] [Related]
9. Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia. Di Costanzo A; Di Leo E; Noto D; Cefalù AB; Minicocci I; Polito L; D'Erasmo L; Cantisani V; Spina R; Tarugi P; Averna M; Arca M J Clin Lipidol; 2017; 11(5):1234-1242. PubMed ID: 28733173 [TBL] [Abstract][Full Text] [Related]
10. Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100. Young SG; Bertics SJ; Curtiss LK; Dubois BW; Witztum JL J Clin Invest; 1987 Jun; 79(6):1842-51. PubMed ID: 3473077 [TBL] [Abstract][Full Text] [Related]
12. 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 [TBL] [Abstract][Full Text] [Related]
13. Low plasma cholesterol levels caused by a short deletion in the apolipoprotein B gene. Young SG; Northey ST; McCarthy BJ Science; 1988 Jul; 241(4865):591-3. PubMed ID: 3399894 [TBL] [Abstract][Full Text] [Related]
14. [Familial hypobetalipoproteinemia: description of a heterozygous form with important biochemical alterations]. Muñoz Torres M; Cano Romera A; Domínguez S; Cano Parra MD; Lobón JA; Escobar Jiménez F Rev Clin Esp; 1991 Feb; 188(2):81-2. PubMed ID: 2041905 [TBL] [Abstract][Full Text] [Related]
15. Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins. Young SG; Hubl ST; Smith RS; Snyder SM; Terdiman JF J Clin Invest; 1990 Mar; 85(3):933-42. PubMed ID: 2312735 [TBL] [Abstract][Full Text] [Related]
17. Spontaneous regression of hepatocellular carcinoma. Grossmann M; Hoermann R; Weiss M; Jauch KW; Oertel H; Staebler A; Mann K; Engelhardt D Am J Gastroenterol; 1995 Sep; 90(9):1500-3. PubMed ID: 7544955 [TBL] [Abstract][Full Text] [Related]
18. Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia. Whitfield AJ; Marais AD; Robertson K; Barrett PH; van Bockxmeer FM; Burnett JR Hum Mutat; 2003 Aug; 22(2):178. PubMed ID: 12872264 [TBL] [Abstract][Full Text] [Related]
19. Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB gene. Florkowski C; Hedley J; Bickley V; Hooper AJ; Burnett JR; George P N Z Med J; 2010 Mar; 123(1310):98-100. PubMed ID: 20360784 [No Abstract] [Full Text] [Related]
20. Heterozygous familial hypobetalipoproteinemia associated with fatty liver. Tarugi P; Lonardo A Am J Gastroenterol; 1997 Aug; 92(8):1400-2. PubMed ID: 9260828 [No Abstract] [Full Text] [Related] [Next] [New Search]