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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 34091928)

  • 1. Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASH.
    Buryska S; Ahn JC; Allen AM; Simha V; Simonetto DA
    Hepatology; 2021 Nov; 74(5):2897-2898. PubMed ID: 34091928
    [No Abstract]   [Full Text] [Related]  

  • 2. Phenotypic Differences Between Polygenic and Monogenic Hypobetalipoproteinemia.
    Rimbert A; Vanhoye X; Coulibaly D; Marrec M; Pichelin M; Charrière S; Peretti N; Valéro R; Wargny M; Carrié A; Lindenbaum P; Deleuze JF; Genin E; Redon R; Rollat-Farnier PA; Goxe D; Degraef G; Marmontel O; Divry E; Bigot-Corbel E; Moulin P; Cariou B; Di Filippo M
    Arterioscler Thromb Vasc Biol; 2021 Jan; 41(1):e63-e71. PubMed ID: 33207932
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel APOB mutation in familial hypobetalipoproteinemia.
    Domenech M; Llano-Rivas I; Arroyo V; Ortega E
    J Clin Lipidol; 2022; 16(1):28-32. PubMed ID: 34852964
    [No Abstract]   [Full Text] [Related]  

  • 4. Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia.
    Di Filippo M; Moulin P; Roy P; Samson-Bouma ME; Collardeau-Frachon S; Chebel-Dumont S; Peretti N; Dumortier J; Zoulim F; Fontanges T; Parini R; Rigoldi M; Furlan F; Mancini G; Bonnefont-Rousselot D; Bruckert E; Schmitz J; Scoazec JY; Charrière S; Villar-Fimbel S; Gottrand F; Dubern B; Doummar D; Joly F; Liard-Meillon ME; Lachaux A; Sassolas A
    J Hepatol; 2014 Oct; 61(4):891-902. PubMed ID: 24842304
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New Classification and Management of Abetalipoproteinemia and Related Disorders.
    Bredefeld C; Peretti N; Hussain MM;
    Gastroenterology; 2021 May; 160(6):1912-1916. PubMed ID: 33275938
    [No Abstract]   [Full Text] [Related]  

  • 6. Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB)--Update 2014.
    Burnett JR; Bell DA; Hooper AJ; Hegele RA
    Eur J Hum Genet; 2015 Jun; 23(6):890-. PubMed ID: 25335495
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 11. Familial hypobetalipoproteinemia associated with hypothyroidism.
    Moriyama K; Takada Y; Araki K; Matsunaga A; Sasaki J; Arakawa K
    Intern Med; 1995 Sep; 34(9):879-82. PubMed ID: 8580561
    [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]  

  • 17. Recurrent familial hypobetalipoproteinemia-induced nonalcoholic fatty liver disease after living donor liver transplantation.
    Harada N; Soejima Y; Taketomi A; Yoshizumi T; Uchiyama H; Ikegami T; Saibara T; Nishizaki T; Maehara Y
    Liver Transpl; 2009 Jul; 15(7):806-9. PubMed ID: 19562718
    [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]
    of 7.