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Journal Abstract Search

166 related items for PubMed ID: 36243606

  • 1. Guidance for the diagnosis and treatment of hypolipidemia disorders.
    Bredefeld C, Hussain MM, Averna M, Black DD, Brin MF, Burnett JR, Charrière S, Cuerq C, Davidson NO, Deckelbaum RJ, Goldberg IJ, Granot E, Hegele RA, Ishibashi S, Karmally W, Levy E, Moulin P, Okazaki H, Poinsot P, Rader DJ, Takahashi M, Tarugi P, Traber MG, Di Filippo M, Peretti N.
    J Clin Lipidol; 2022; 16(6):797-812. PubMed ID: 36243606
    [Abstract] [Full Text] [Related]

  • 2. Abetalipoproteinemia and homozygous hypobetalipoproteinemia: a framework for diagnosis and management.
    Lee J, Hegele RA.
    J Inherit Metab Dis; 2014 May; 37(3):333-9. PubMed ID: 24288038
    [Abstract] [Full Text] [Related]

  • 3. Lipids Responsible for Intestinal or Hepatic Disorder: When to Suspect a Familial Intestinal Hypocholesterolemia?
    Sissaoui S, Cochet M, Poinsot P, Bordat C, Collardeau-Frachon S, Lachaux A, Lacaille F, Peretti N.
    J Pediatr Gastroenterol Nutr; 2021 Jul 01; 73(1):4-8. PubMed ID: 33853111
    [Abstract] [Full Text] [Related]

  • 4. Update on primary hypobetalipoproteinemia.
    Hooper AJ, Burnett JR.
    Curr Atheroscler Rep; 2014 Jul 01; 16(7):423. PubMed ID: 24781598
    [Abstract] [Full Text] [Related]

  • 5. Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1.
    Wakabayashi T, Takahashi M, Okazaki H, Okazaki S, Yokote K, Tada H, Ogura M, Ishigaki Y, Yamashita S, Harada-Shiba M, Committee on Primary Dyslipidemia under the Research Program on Rare and Intractable Disease of the Ministry of Health, Labour and Welfare of Japan.
    J Atheroscler Thromb; 2024 Jul 01; 31(7):1005-1023. PubMed ID: 38710625
    [Abstract] [Full Text] [Related]

  • 6. Low cholesterol states: clinical implications and management.
    Gill PK, Hegele RA.
    Expert Rev Endocrinol Metab; 2023 May 01; 18(3):241-253. PubMed ID: 37089071
    [Abstract] [Full Text] [Related]

  • 7. New Classification and Management of Abetalipoproteinemia and Related Disorders.
    Bredefeld C, Peretti N, Hussain MM, Medical Advisory Panel.
    Gastroenterology; 2021 May 01; 160(6):1912-1916. PubMed ID: 33275938
    [No Abstract] [Full Text] [Related]

  • 8. Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects.
    Walsh MT, Di Leo E, Okur I, Tarugi P, Hussain MM.
    Biochim Biophys Acta; 2016 Nov 01; 1861(11):1623-1633. PubMed ID: 27487388
    [Abstract] [Full Text] [Related]

  • 9. Vitamin E and oxidative stress in abetalipoproteinemia and familial hypobetalipoproteinemia.
    Burnett JR, Hooper AJ.
    Free Radic Biol Med; 2015 Nov 01; 88(Pt A):59-62. PubMed ID: 26086616
    [Abstract] [Full Text] [Related]

  • 10. Current Diagnosis and Management of Abetalipoproteinemia.
    Takahashi M, Okazaki H, Ohashi K, Ogura M, Ishibashi S, Okazaki S, Hirayama S, Hori M, Matsuki K, Yokoyama S, Harada-Shiba M.
    J Atheroscler Thromb; 2021 Oct 01; 28(10):1009-1019. PubMed ID: 33994405
    [Abstract] [Full Text] [Related]

  • 11. Carotenoids in familial hypobetalipoproteinemia disorders: Malabsorption in Caco2 cell models and severe deficiency in patients.
    Bordat C, Cuerq C, Halimi C, Vairo D, Blond E, Restier L, Poinsot P, Duclaux-Loras R, Peretti N, Reboul E.
    J Clin Lipidol; 2024 Oct 01; 18(1):e105-e115. PubMed ID: 37989694
    [Abstract] [Full Text] [Related]

  • 12. Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature.
    Cefalù AB, Norata GD, Ghiglioni DG, Noto D, Uboldi P, Garlaschelli K, Baragetti A, Spina R, Valenti V, Pederiva C, Riva E, Terracciano L, Zoja A, Grigore L, Averna MR, Catapano AL.
    Atherosclerosis; 2015 Mar 01; 239(1):209-17. PubMed ID: 25618028
    [Abstract] [Full Text] [Related]

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  • 14. Hypobetalipoproteinemia and abetalipoproteinemia.
    Welty FK.
    Curr Opin Lipidol; 2014 Jun 01; 25(3):161-8. PubMed ID: 24751931
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  • 16. Hypobetalipoproteinemia and abetalipoproteinemia: liver disease and cardiovascular disease.
    Welty FK.
    Curr Opin Lipidol; 2020 Apr 01; 31(2):49-55. PubMed ID: 32039990
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  • 19. Fat accumulation in enterocytes: a key to the diagnosis of abetalipoproteinemia or homozygous hypobetalipoproteinemia.
    Desomer L, De Vos M, De Looze D.
    Endoscopy; 2015 Apr 01; 47 Suppl 1 UCTN():E223-4. PubMed ID: 26062159
    [No Abstract] [Full Text] [Related]

  • 20. 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 01; 61(4):891-902. PubMed ID: 24842304
    [Abstract] [Full Text] [Related]

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