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7. Asymptomatic elevation of aminotransferase levels and fatty liver secondary to heterozygous hypobetalipoproteinemia. Ahmed A; Keeffe EB Am J Gastroenterol; 1998 Dec; 93(12):2598-9. PubMed ID: 9860439 [No Abstract] [Full Text] [Related]
8. Familial heterozygous hypobetalipoproteinemia and breast cancer risk: A systematic review and suggestions for further research. Lima Pessoa E; Costa Vilella Dos Reis M; Sayuri Yamamoto T; Ribeiro Neto M; Ferraro O; Alves MJ; Guedes Coelho Lopes R Breast J; 2019 Jul; 25(4):763-765. PubMed ID: 31111608 [No Abstract] [Full Text] [Related]
9. Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease. Gutiérrez-Cirlos C; Ordóñez-Sánchez ML; Tusié-Luna MT; Patterson BW; Schonfeld G; Aguilar-Salinas CA Ann Hepatol; 2011; 10(2):155-64. PubMed ID: 21502677 [TBL] [Abstract][Full Text] [Related]
10. Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia. Rimbert A; Pichelin M; Lecointe S; Marrec M; Le Scouarnec S; Barrak E; Croyal M; Krempf M; Le Marec H; Redon R; Schott JJ; Magré J; Cariou B Atherosclerosis; 2016 Jul; 250():52-6. PubMed ID: 27179706 [TBL] [Abstract][Full Text] [Related]
12. SPG11 mutation in a Turkish familial hypobetalipoproteinemia family with hereditary spastic paraplegia. Hooper AJ; Akinci B; Davis MR; Burnett JR Clin Chim Acta; 2015 May; 445():1. PubMed ID: 25769290 [No Abstract] [Full Text] [Related]
13. 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]
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. Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote. Hooper AJ; Robertson K; Champain D; Hua J; Song S; Parhofer KG; Barrett PHR; van Bockxmeer FM; Burnett JR Clin Biochem; 2016 Jun; 49(9):720-722. PubMed ID: 26916057 [TBL] [Abstract][Full Text] [Related]
16. 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]
18. Absence of fatty liver in familial hypobetalipoproteinemia linked to chromosome 3p21. Yue P; Tanoli T; Wilhelm O; Patterson B; Yablonskiy D; Schonfeld G Metabolism; 2005 May; 54(5):682-8. PubMed ID: 15877300 [TBL] [Abstract][Full Text] [Related]
19. [Extreme degree familial hypobetalipoproteinemia caused by hypothetic double heterozygosity in a subject with severe mental deficiency]. Acocella M; Cossio M; Barucci M; Ciardetti A; Archi G; Rossini R; Bassini E; Lusetti W Pediatr Med Chir; 1984; 6(6):843-52. PubMed ID: 6545600 [TBL] [Abstract][Full Text] [Related]
20. Acanthocytosis in a patient with homozygous familial hypobetalipoproteinemia due to a novel APOB splice site mutation. Hegele RA; Miskie BA Clin Genet; 2002 Feb; 61(2):101-3. PubMed ID: 11940084 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]