PubMed (cited) for id: 207750

Year	Number of Results
1978	2
1979	1
1980	1
1981	1
1984	3
1986	1
1987	1
1988	2
1989	2
2003	1
2011	1
2012	1
2024	0

1

Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia.

Johansen CT, Wang J, McIntyre AD, Martins RA, Ban MR, Lanktree MB, Huff MW, Péterfy M, Mehrabian M, Lusis AJ, Kathiresan S, Anand SS, Yusuf S, Lee AH, Glimcher LH, Cao H, Hegele RA. Johansen CT, et al. Circ Cardiovasc Genet. 2012 Feb 1;5(1):66-72. doi: 10.1161/CIRCGENETICS.111.960864. Epub 2011 Dec 1. Circ Cardiovasc Genet. 2012. PMID: 22135386 Free PMC article.

2

Apolipoprotein C-II deficiency presenting as a lipid encephalopathy in infancy.

Wilson CJ, Priore Oliva C, Maggi F, Catapano AL, Calandra S. Wilson CJ, et al. Ann Neurol. 2003 Jun;53(6):807-10. doi: 10.1002/ana.10598. Ann Neurol. 2003. PMID: 12783430

3

Combined deficiency of apolipoprotein C-II and lipoprotein lipase in familial hyperchylomicronemia.

Stalenhoef AF, Casparie AF, Demacker PN, Stouten JT, Lutterman JA, van 't Laar A. Stalenhoef AF, et al. Metabolism. 1981 Sep;30(9):919-26. doi: 10.1016/0026-0495(81)90072-x. Metabolism. 1981. PMID: 7266379

4

Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families.

Humphries SE, Williams L, Myklebost O, Stalenhoef AF, Demacker PN, Baggio G, Crepaldi G, Galton DJ, Williamson R. Humphries SE, et al. Hum Genet. 1984;67(2):151-5. doi: 10.1007/BF00272990. Hum Genet. 1984. PMID: 6547689

5

C-II anapolipoproteinemia and severe hypertriglyceridemia. Report of a rare case with absence of C-II apolipoprotein isoforms and review of the literature.

Saku K, Cedres C, McDonald B, Hynd BA, Liu BW, Srivastava LS, Kashyap ML. Saku K, et al. Am J Med. 1984 Sep;77(3):457-62. doi: 10.1016/0002-9343(84)90102-5. Am J Med. 1984. PMID: 6475985

6

Apolipoprotein C-II deficiency associated with nonfunctional mutant forms of apolipoprotein C-II.

Maguire GF, Little JA, Kakis G, Breckenridge WC. Maguire GF, et al. Can J Biochem Cell Biol. 1984 Sep;62(9):847-52. doi: 10.1139/o84-108. Can J Biochem Cell Biol. 1984. PMID: 6388756

7

New case of apoprotein C-II deficiency.

Capurso A, Pace L, Bonomo L, Catapano A, Schilirò G, La Rosa M, Assmann G. Capurso A, et al. Lancet. 1980 Feb 2;1(8162):268. doi: 10.1016/s0140-6736(80)90768-0. Lancet. 1980. PMID: 6101731 No abstract available.

8

Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients.

Baggio G, Manzato E, Gabelli C, Fellin R, Martini S, Enzi GB, Verlato F, Baiocchi MR, Sprecher DL, Kashyap ML, et al. Baggio G, et al. J Clin Invest. 1986 Feb;77(2):520-7. doi: 10.1172/JCI112332. J Clin Invest. 1986. PMID: 3944267 Free PMC article.

9

Structure of apolipoprotein C-IIToronto, a nonfunctional human apolipoprotein.

Connelly PW, Maguire GF, Hofmann T, Little JA. Connelly PW, et al. Proc Natl Acad Sci U S A. 1987 Jan;84(1):270-3. doi: 10.1073/pnas.84.1.270. Proc Natl Acad Sci U S A. 1987. PMID: 3467353 Free PMC article.

10

A deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto).

Cox DW, Wills DE, Quan F, Ray PN. Cox DW, et al. J Med Genet. 1988 Oct;25(10):649-52. doi: 10.1136/jmg.25.10.649. J Med Genet. 1988. PMID: 3225819 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

16 results

Results by year