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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
169 related items for PubMed ID: 32205061
1. Successful management of acute pancreatitis due to apolipoprotein C-II deficiency in a 37-day-old infant. Yıldız Y, Uysal Yazıcı M, Çınar HG, Özbay Hoşnut F, Kurt Çolak F, Kılıç M. Pancreatology; 2020 Jun; 20(4):644-646. PubMed ID: 32205061 [Abstract] [Full Text] [Related]
3. Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation. Kose E, Armagan C, Teke Kısa P, Onay H, Arslan N. J Pediatr Endocrinol Metab; 2018 Nov 27; 31(11):1289-1293. PubMed ID: 30307897 [Abstract] [Full Text] [Related]
7. Molecular and functional characterization of familial chylomicronemia syndrome. Teramoto R, Tada H, Kawashiri MA, Nohara A, Nakahashi T, Konno T, Inazu A, Mabuchi H, Yamagishi M, Hayashi K. Atherosclerosis; 2018 Feb 27; 269():272-278. PubMed ID: 29153744 [Abstract] [Full Text] [Related]
8. Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1. Ahmad Z, Wilson DP. J Clin Lipidol; 2014 Feb 27; 8(6):635-639. PubMed ID: 25499947 [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 27; 120(3):e123-e127. PubMed ID: 35533124 [Abstract] [Full Text] [Related]
20. Apolipoprotein C-II deficiency with no rare variant in the APOC2 gene. Takase S, Osuga J, Fujita H, Hara K, Sekiya M, Igarashi M, Takanashi M, Takeuchi Y, Izumida Y, Ohta K, Kumagai M, Nishi M, Kubota M, Masuda Y, Taira Y, Okazaki S, Iizuka Y, Yahagi N, Ohashi K, Yoshida H, Yanai H, Tada N, Gotoda T, Ishibashi S, Kadowaki T, Okazaki H. J Atheroscler Thromb; 2013 Jun 27; 20(5):481-93. PubMed ID: 23470567 [Abstract] [Full Text] [Related] Page: [Next] [New Search]