Lipoprotein lipase deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lipoprotein lipase deficiency" in English language version.

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cbc.ca

newsinteractives.cbc.ca

Crowe, Kelly (17 November 2018). "The million-dollar drug". CBCNews. CBC (Canadian Broadcasting Corporation). Retrieved 17 November 2018.

doi.org

Santamarina-Fojo, S (1998). "Familial lipoprotein lipase deficiency". Endocrinol Metab Clin North Am. 27 (3): 551–567. doi:10.1016/S0889-8529(05)70025-6. PMID 9785052.
Santamarina-Fojo, S; Brewer HB, Jr (20 February 1991). "The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects". JAMA. 265 (7): 904–8. doi:10.1001/jama.1991.03460070086049. PMID 1992190.

medlineplus.gov

"Familial lipoprotein lipase deficiency: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 17 April 2019.

nih.gov

pubmed.ncbi.nlm.nih.gov

Santamarina-Fojo, S (1998). "Familial lipoprotein lipase deficiency". Endocrinol Metab Clin North Am. 27 (3): 551–567. doi:10.1016/S0889-8529(05)70025-6. PMID 9785052.
Santamarina-Fojo, S; Brewer HB, Jr (20 February 1991). "The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects". JAMA. 265 (7): 904–8. doi:10.1001/jama.1991.03460070086049. PMID 1992190.
Burnett, John R.; Hooper, Amanda J.; Hegele, Robert A. (June 22, 2017). "Familial Lipoprotein Lipase Deficiency". In Adam, MP; Ardinger, HH; Pagon, RA; et al. (eds.). GeneReviews. Seattle: University of Washington. PMID 20301485.

ncbi.nlm.nih.gov

Burnett, John R.; Hooper, Amanda J.; Hegele, Robert A. (June 22, 2017). "Familial Lipoprotein Lipase Deficiency". In Adam, MP; Ardinger, HH; Pagon, RA; et al. (eds.). GeneReviews. Seattle: University of Washington. PMID 20301485.
A.D.A.M. Editorial Board (2011-05-29). Dugdale, III, David C.; Zieve, David (eds.). Familial lipoprotein lipase deficiency. National Center for Biotechnology Information (published May 29, 2011). Retrieved October 15, 2012. {{cite book}}: |work= ignored (help)

omim.org

Online Mendelian Inheritance in Man (OMIM): HYPERLIPOPROTEINEMIA, TYPE I - 238600, updated 03/18/2004. As of October 2012, mention of type Ia no longer appears in the OMIM record.

prnewswire.com

"Tryngolza (olezarsen) approved in U.S. as first-ever treatment for adults living with familial chylomicronemia syndrome as an adjunct to diet" (Press release). Ionis Pharmaceuticals. 19 December 2024. Retrieved 20 December 2024 – via PR Newswire.

technologyreview.com

Regalado, Antonio (May 4, 2016). "The World's Most Expensive Medicine Is a Bust". MIT Technology Review.

worldcat.org

search.worldcat.org

James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6. OCLC 62736861.
Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1. OCLC 212399895.