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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1956 1
1959 2
1964 1
1965 1
1967 3
1968 2
1969 2
1970 3
1971 1
1972 5
1973 3
1974 3
1975 3
1976 3
1977 7
1978 19
1979 14
1980 9
1981 8
1982 18
1983 18
1984 17
1985 18
1986 13
1987 14
1988 15
1989 10
1990 16
1991 13
1992 5
1993 14
1994 10
1995 11
1996 9
1997 8
1998 16
1999 22
2000 47
2001 54
2002 40
2003 37
2004 41
2005 27
2006 19
2007 15
2008 13
2009 16
2010 17
2011 12
2012 18
2013 10
2014 14
2015 17
2016 16
2017 19
2018 18
2019 15
2020 12
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776 results
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Page 1
Accelerated Atherogenicity in Tangier Disease.
Muratsu J, Koseki M, Masuda D, Yasuga Y, Tomoyama S, Ataka K, Yagi Y, Nakagawa A, Hamada H, Fujita S, Hattori H, Ohama T, Nishida M, Hiraoka H, Matsuzawa Y, Yamashita S. Muratsu J, et al. J Atheroscler Thromb. 2018 Oct 1;25(10):1076-1085. doi: 10.5551/jat.43257. Epub 2018 Mar 20. J Atheroscler Thromb. 2018. PMID: 29563393 Free PMC article.
We report a case of Tangier disease with Leriche syndrome and bleeding tendency. In this male patient, nasal hemorrhage had been observed frequently throughout childhood. ...In Tangier disease, HDL-C is markedly decreased because of ABCA1 deficiency. H …
We report a case of Tangier disease with Leriche syndrome and bleeding tendency. In this male patient, nasal hemorrhage had be …
Peripheral neuropathy in Tangier disease: A literature review and assessment.
Mercan M, Yayla V, Altinay S, Seyhan S. Mercan M, et al. J Peripher Nerv Syst. 2018 Jun;23(2):88-98. doi: 10.1111/jns.12265. Epub 2018 May 8. J Peripher Nerv Syst. 2018. PMID: 29582519 Review.
Tangier disease (TD) (OMIM#205400) is a rare cause of inherited metabolic neuropathies characterized by marked deficiency of high-density lipoproteins and accumulation of cholesterol esters in various tissue resulting from reverse cholesterol transport deficiency. .
Tangier disease (TD) (OMIM#205400) is a rare cause of inherited metabolic neuropathies characterized by marked deficiency of h
A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family.
Maranghi M, Truglio G, Gallo A, Grieco E, Verrienti A, Montali A, Gallo P, Alesini F, Arca M, Lucarelli M. Maranghi M, et al. Biochem Biophys Res Commun. 2019 Jan 8;508(2):487-493. doi: 10.1016/j.bbrc.2018.11.064. Epub 2018 Nov 30. Biochem Biophys Res Commun. 2019. PMID: 30503498 Free article.
Tangier disease is a rare disorder of lipoprotein metabolism that presents with extremely low levels of HDL cholesterol and apoprotein A-I. ...Clinical heterogeneity and mutational pattern of Tangier disease are poorly characterized. Moreover, also fam
Tangier disease is a rare disorder of lipoprotein metabolism that presents with extremely low levels of HDL cholesterol and ap
Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.
El Khoury P, Couvert P, Elbitar S, Ghaleb Y, Abou-Khalil Y, Azar Y, Ayoub C, Superville A, Guérin M, Rabès JP, Varret M, Boileau C, Jambart S, Giral P, Carrié A, Le Goff W, Abifadel M. El Khoury P, et al. J Clin Lipidol. 2018 Nov-Dec;12(6):1374-1382. doi: 10.1016/j.jacl.2018.08.013. Epub 2018 Sep 1. J Clin Lipidol. 2018. PMID: 30361172
RESULTS: We identified the first Lebanese pathogenic variant in ABCA1 gene causing Tangier disease in a consanguineous family. ...CONCLUSIONS: It is the first case of Tangier disease reported in Lebanon harboring a novel pathogenic variant in ABCA1. Fu …
RESULTS: We identified the first Lebanese pathogenic variant in ABCA1 gene causing Tangier disease in a consanguineous family. …
[Tangier disease].
Saku K, Jimi S, Ohta T, Arakawa K. Saku K, et al. Nihon Rinsho. 1994 Dec;52(12):3236-40. Nihon Rinsho. 1994. PMID: 7853716 Review. Japanese.
Tangier disease, a familial HDL-deficiency syndrome, was first reported by Fredrickson et al. in 1961. Since then, a great deal research on the mechanism of HDL-deficiency in this disease has been done from the prospective of lipoprotein compositions, in vivo
Tangier disease, a familial HDL-deficiency syndrome, was first reported by Fredrickson et al. in 1961. Since then, a great dea
Clinical utility gene card for: Tangier disease.
Hooper AJ, McCormick SPA, Hegele RA, Burnett JR. Hooper AJ, et al. Eur J Hum Genet. 2017 Jun;25(7). doi: 10.1038/ejhg.2017.72. Epub 2017 May 24. Eur J Hum Genet. 2017. PMID: 28537273 Free article. No abstract available.
Tangier disease may cause early onset of atherosclerotic cerebral infarction: A case report.
Liang Z, Li W, Yang S, Liu Z, Sun X, Gao X, Yu G. Liang Z, et al. Medicine (Baltimore). 2018 Sep;97(39):e12472. doi: 10.1097/MD.0000000000012472. Medicine (Baltimore). 2018. PMID: 30278532 Free PMC article.
The relevant literature on the clinical manifestations, laboratory examinations, and treatment of Tangier disease was reviewed. ...Child and Juvenile stroke patients with low HDL should not be excluded from the possibility of Tangier disease....
The relevant literature on the clinical manifestations, laboratory examinations, and treatment of Tangier disease was reviewed …
The iPSC Awakens ANGPTL3 in Tangier Disease.
Lee MKS, Murphy AJ. Lee MKS, et al. EBioMedicine. 2017 Apr;18:15-16. doi: 10.1016/j.ebiom.2017.04.004. Epub 2017 Apr 4. EBioMedicine. 2017. PMID: 28392245 Free PMC article. No abstract available.
Tangier disease: epidemiology, pathophysiology, and management.
Puntoni M, Sbrana F, Bigazzi F, Sampietro T. Puntoni M, et al. Am J Cardiovasc Drugs. 2012 Oct 1;12(5):303-11. doi: 10.2165/11634140-000000000-00000. Am J Cardiovasc Drugs. 2012. PMID: 22913675
Nearly all the children affected by Tangier disease were identified on the basis of large, yellow-orange tonsils, while half of the adult patients affected by Tangier disease came to medical attention because of symptoms of neuropathy. ...To date there …
Nearly all the children affected by Tangier disease were identified on the basis of large, yellow-orange tonsils, while half o …
Unusual yellow scaly colonic mucosal appearance: Tangier disease.
Struyve M, Ferrante M, van Overbeke L, Meersseman W, Cassiman D, Mortier L. Struyve M, et al. Gastrointest Endosc. 2018 Jul;88(1):193-195. doi: 10.1016/j.gie.2018.01.011. Epub 2018 Jan 17. Gastrointest Endosc. 2018. PMID: 29352969 No abstract available.
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