These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
131 related articles for article (PubMed ID: 38195282)
1. Familial ApoB-specific familial hypobetalipoproteinemia in a patient with non-classical congenital adrenal hyperplasia. Ramos Bachiller B; Luque-Ramírez M; Rodríguez-Jiménez C; Arrieta Blanco FJ Clin Investig Arterioscler; 2024; 36(3):128-132. PubMed ID: 38195282 [TBL] [Abstract][Full Text] [Related]
2. Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations. Di Leo E; Magnolo L; Bertolotti M; Bourbon M; Carmo Pereira S; Pirisi M; Calandra S; Tarugi P Clin Genet; 2008 Sep; 74(3):267-73. PubMed ID: 18492086 [TBL] [Abstract][Full Text] [Related]
4. Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia. Conca P; Pileggi S; Simonelli S; Boer E; Boscutti G; Magnolo L; Tarugi P; Penco S; Franceschini G; Calabresi L; Gomaraschi M J Clin Lipidol; 2012; 6(3):244-50. PubMed ID: 22658148 [TBL] [Abstract][Full Text] [Related]
5. A Family with Familial Hypobetalipoproteinemia Caused by a c.1468C>T in APOB. Tada H; Kojima N; Nomura A; Takamura M Intern Med; 2024 Oct; 63(19):2637-2640. PubMed ID: 38369355 [TBL] [Abstract][Full Text] [Related]
6. [Familial hypobetalipoproteinemia: clinical characterization of a new mutation in the APOB gene]. Iglesias P; Díez JJ; Tarugi P Med Clin (Barc); 2009 Jun; 133(2):57-60. PubMed ID: 19442995 [TBL] [Abstract][Full Text] [Related]
7. Hypobetalipoproteinemia and abetalipoproteinemia. Welty FK Curr Opin Lipidol; 2014 Jun; 25(3):161-8. PubMed ID: 24751931 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B. Yilmaz BS; Mungan NO; Di Leo E; Magnolo L; Artuso L; Bernardis I; Tumgor G; Kor D; Tarugi P Clin Chim Acta; 2016 Jan; 452():185-90. PubMed ID: 26612772 [TBL] [Abstract][Full Text] [Related]
10. Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease. Peloso GM; Nomura A; Khera AV; Chaffin M; Won HH; Ardissino D; Danesh J; Schunkert H; Wilson JG; Samani N; Erdmann J; McPherson R; Watkins H; Saleheen D; McCarthy S; Teslovich TM; Leader JB; Lester Kirchner H; Marrugat J; Nohara A; Kawashiri MA; Tada H; Dewey FE; Carey DJ; Baras A; Kathiresan S Circ Genom Precis Med; 2019 May; 12(5):e002376. PubMed ID: 30939045 [TBL] [Abstract][Full Text] [Related]
11. In vivo metabolism of ApoB, ApoA-I, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the ApoB gene. Elias N; Patterson BW; Schonfeld G Arterioscler Thromb Vasc Biol; 2000 May; 20(5):1309-15. PubMed ID: 10807747 [TBL] [Abstract][Full Text] [Related]
12. Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia. Di Leo E; Magnolo L; Lancellotti S; Crocè L; Visintin L; Tiribelli C; Bertolini S; Calandra S; Tarugi P J Med Genet; 2007 Mar; 44(3):219-24. PubMed ID: 17158591 [TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of APOB, SAR1B, ANGPTL3, and MTTP in patients with primary hypocholesterolemia in a clinical laboratory setting: Evidence supporting polygenicity in mutation-negative patients. Blanco-Vaca F; Martin-Campos JM; Beteta-Vicente Á; Canyelles M; Martínez S; Roig R; Farré N; Julve J; Tondo M Atherosclerosis; 2019 Apr; 283():52-60. PubMed ID: 30782561 [TBL] [Abstract][Full Text] [Related]
14. High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent. Fouchier SW; Sankatsing RR; Peter J; Castillo S; Pocovi M; Alonso R; Kastelein JJ; Defesche JC J Med Genet; 2005 Apr; 42(4):e23. PubMed ID: 15805152 [TBL] [Abstract][Full Text] [Related]
15. [Familial hypobetalipoproteinemia secondary to a mutation in the apolipoprotein B gene]. Blanco-Rodríguez M; Muñoz-Calvo MT; Martos-Moreno GA; Abad-Pérez E; Argente-Oliver J An Pediatr (Barc); 2007 May; 66(5):535-7. PubMed ID: 17517208 [TBL] [Abstract][Full Text] [Related]
16. Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia. Katsuda S; Kawashiri MA; Inazu A; Tada H; Tsuchida M; Kaneko Y; Nozue T; Nohara A; Okada T; Kobayashi J; Michishita I; Mabuchi H; Yamagishi M Clin Chim Acta; 2009 Jan; 399(1-2):64-8. PubMed ID: 18848826 [TBL] [Abstract][Full Text] [Related]
17. Novel APOB nonsense variant related to familial hypobetalipoproteinemia and hepatic steatosis: A case report and review. Rodríguez de Vera-Gómez P; Del Pino-Bellido P; García-González JJ; Sánchez-Jiménez F; Oliva-Rodríguez R; Arrobas-Velilla T; Martínez-Brocca MA J Clin Lipidol; 2022; 16(5):601-607. PubMed ID: 35918255 [TBL] [Abstract][Full Text] [Related]
18. Non-alcoholic steatohepatitis-related cirrhosis in a patient with APOB L343V familial hypobetalipoproteinaemia. Heeks LV; Hooper AJ; Adams LA; Robbins P; Barrett PH; van Bockxmeer FM; Burnett JR Clin Chim Acta; 2013 Jun; 421():121-5. PubMed ID: 23694813 [TBL] [Abstract][Full Text] [Related]
19. The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations. Di Leo E; Eminoglu T; Magnolo L; Bolkent MG; Tümer L; Okur I; Tarugi P J Clin Lipidol; 2015; 9(3):400-5. PubMed ID: 26073401 [TBL] [Abstract][Full Text] [Related]
20. Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report. Cheng T; Liu J; Sun W; Song G; Ma H BMC Endocr Disord; 2022 Mar; 22(1):57. PubMed ID: 35255871 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]