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 *

299 related articles for article (PubMed ID: 18940129)

  • 1. Familial chylomicronemia in a nine months old infant.
    Lone SW; Imdad A; Billoo AG
    J Coll Physicians Surg Pak; 2008 Oct; 18(10):655-6. PubMed ID: 18940129
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial chylomicronemia syndrome.
    Sugandhan S; Khandpur S; Sharma VK
    Pediatr Dermatol; 2007; 24(3):323-5. PubMed ID: 17542893
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial chylomicronemia syndrome.
    Mohandas MK; Jemila J; Ajith Krishnan AS; George TT
    Indian J Pediatr; 2005 Feb; 72(2):181. PubMed ID: 15758547
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Chylomicronemia syndrome].
    Francis A; Levy Y
    Harefuah; 2002 Feb; 141(2):201-3, 221, 220. PubMed ID: 11905095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Encephalopathy in type I hyperlipidemia.
    Onal H; Atugluzeybek C; Alhaj S; Altun G
    Indian Pediatr; 2007 Apr; 44(4):306-8. PubMed ID: 17468530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The familial hyperchylomicronaemia syndrome.
    Bijvoet SM; Bruin T; Kastelein JJ
    Neth J Med; 1993 Feb; 42(1-2):36-44. PubMed ID: 8446222
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Chylomicronemia].
    Yamamoto T; Kawakami M
    Nihon Rinsho; 1990 Nov; 48(11):2526-31. PubMed ID: 2270016
    [No Abstract]   [Full Text] [Related]  

  • 8. Lipoprotein abnormalities in compound heterozygous lipoprotein lipase deficiency after treatment with a low-fat diet and orlistat.
    Blackett P; Tryggestad J; Krishnan S; Li S; Xu W; Alaupovic P; Quiroga C; Copeland K
    J Clin Lipidol; 2013; 7(2):132-9. PubMed ID: 23415432
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry.
    Foubert L; Bruin T; De Gennes JL; Ehrenborg E; Furioli J; Kastelein J; Benlian P; Hayden M
    Hum Mutat; 1997; 10(3):179-85. PubMed ID: 9298816
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Chylomicronemia Syndrome Is Most Often Multifactorial: A Narrative Review of Causes and Treatment.
    Chait A; Eckel RH
    Ann Intern Med; 2019 May; 170(9):626-634. PubMed ID: 31035285
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial Chylomicronemia Syndrome: A Clinical Guide For Endocrinologists.
    Falko JM
    Endocr Pract; 2018 Aug; 24(8):756-763. PubMed ID: 30183397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Primary hyperchylomicronemia].
    Yamashita S
    Nihon Rinsho; 2013 Sep; 71(9):1578-83. PubMed ID: 24205717
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular basis of familial chylomicronemia.
    Ameis D; Schotz C; Greten H
    Z Gastroenterol Verh; 1991 Mar; 26():102-3. PubMed ID: 1714114
    [No Abstract]   [Full Text] [Related]  

  • 14. Building a better understanding of the burden of disease in familial chylomicronemia syndrome.
    Ahmad Z; Halter R; Stevenson M
    Expert Rev Clin Pharmacol; 2017 Jan; 10(1):1-3. PubMed ID: 27771961
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
    Kim KY; Heo YJ; Ko JM; Lee YA; Shin CH; Ki CS; Lee YJ
    BMC Endocr Disord; 2024 Apr; 24(1):47. PubMed ID: 38622573
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Familial lipoprotein lipase deficiency].
    Yoshida T; Gotoda T
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):84-7. PubMed ID: 9645014
    [No Abstract]   [Full Text] [Related]  

  • 17. Challenges in familial chylomicronemia syndrome diagnosis and management across Latin American countries: An expert panel discussion.
    Santos RD; Lorenzatti A; Corral P; Nogueira JP; Cafferata AM; Aimone D; Lourenço CM; Izar MC; Lima JG; Lottenberg AM; Alonso R; Garay K; Morales AR; Vargas-Uricoechea H; Peña CAC; Roman-González A
    J Clin Lipidol; 2021; 15(5):620-624. PubMed ID: 34920815
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lipoprotein lipase deficiency in an infant.
    Nampoothiri S; Radhakrishnan N; Schwentek A; Hoffmann MM
    Indian Pediatr; 2011 Oct; 48(10):805-6. PubMed ID: 22080683
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial chylomicronemia syndrome: pediatric experience in Argentina].
    Araujo MB; Eiberman G; Etcheverry N; Pacheco G
    Arch Argent Pediatr; 2022 Jun; 120(3):e123-e127. PubMed ID: 35533124
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chylomicronemia syndrome.
    Chait A; Brunzell JD
    Adv Intern Med; 1992; 37():249-73. PubMed ID: 1557997
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.