Lecithin cholesterol acyltransferase deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lecithin cholesterol acyltransferase deficiency" in English language version.

refsWebsite

Global rank English rank

11nih.gov

4^th place

6doi.org

2^nd place

2medscape.com

719^th place

636^th place

1jlr.org

low place

1ahajournals.org

3,608^th place

6,526^th place

1handle.net

102^nd place

76^th place

1worldcat.org

5^th place

1semanticscholar.org

11^th place

8^th place

ahajournals.org

atvb.ahajournals.org

Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frasc G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G (Sep 2005). "The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families". Arteriosclerosis, Thrombosis, and Vascular Biology. 25 (9): 1972–1978. doi:10.1161/01.ATV.0000175751.30616.13. hdl:11380/636978. ISSN 1079-5642. PMID 15994445.

doi.org

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J (February 1997). "The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes". J. Lipid Res. 38 (2): 191–205. doi:10.1016/S0022-2275(20)37433-2. PMID 9162740.
Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frasc G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G (Sep 2005). "The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families". Arteriosclerosis, Thrombosis, and Vascular Biology. 25 (9): 1972–1978. doi:10.1161/01.ATV.0000175751.30616.13. hdl:11380/636978. ISSN 1079-5642. PMID 15994445.
Koster, H; Savoldelli, M; Dumon, M. F.; Dubourg, L; Clerc, M; Pouliquen, Y (1992). "A fish-eye disease-like familial condition with massive corneal clouding and dyslipoproteinemia. Report of clinical, histologic, electron microscopic, and biochemical features". Cornea. 11 (5): 452–64. doi:10.1097/00003226-199209000-00016. PMID 1424675. S2CID 27089164.
Kuivenhoven, J. A.; Pritchard, H; Hill, J; Frohlich, J; Assmann, G; Kastelein, J (1997). "The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes". Journal of Lipid Research. 38 (2): 191–205. doi:10.1016/S0022-2275(20)37433-2. PMID 9162740.
Kuivenhoven, J. A.; van Voorst tot Voorst EJ; Wiebusch, H; Marcovina, S. M.; Funke, H; Assmann, G; Pritchard, P. H.; Kastelein, J. J. (1995). "A unique genetic and biochemical presentation of fish-eye disease". Journal of Clinical Investigation. 96 (6): 2783–91. doi:10.1172/JCI118348. PMC 185988. PMID 8675648.
Contacos, C; Sullivan, D. R.; Rye, K. A.; Funke, H; Assmann, G (1996). "A new molecular defect in the lecithin: Cholesterol acyltransferase (LCAT) gene associated with fish eye disease". Journal of Lipid Research. 37 (1): 35–44. doi:10.1016/S0022-2275(20)37633-1. PMID 8820100.

handle.net

hdl.handle.net

Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frasc G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G (Sep 2005). "The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families". Arteriosclerosis, Thrombosis, and Vascular Biology. 25 (9): 1972–1978. doi:10.1161/01.ATV.0000175751.30616.13. hdl:11380/636978. ISSN 1079-5642. PMID 15994445.

jlr.org

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J (February 1997). "The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes". J. Lipid Res. 38 (2): 191–205. doi:10.1016/S0022-2275(20)37433-2. PMID 9162740.

medscape.com

emedicine.medscape.com

"Lecithin-Cholesterol Acyltransferase Deficiency: Overview, Presentation, Differential Diagnosis". 2016-08-08. {{cite journal}}: Cite journal requires |journal= (help)
"Lecithin-Cholesterol Acyltransferase Deficiency: Overview, Presentation, Differential Diagnosis". 2016-08-08. {{cite journal}}: Cite journal requires |journal= (help)

nih.gov

pubmed.ncbi.nlm.nih.gov

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J (February 1997). "The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes". J. Lipid Res. 38 (2): 191–205. doi:10.1016/S0022-2275(20)37433-2. PMID 9162740.
Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frasc G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G (Sep 2005). "The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families". Arteriosclerosis, Thrombosis, and Vascular Biology. 25 (9): 1972–1978. doi:10.1161/01.ATV.0000175751.30616.13. hdl:11380/636978. ISSN 1079-5642. PMID 15994445.
Koster, H; Savoldelli, M; Dumon, M. F.; Dubourg, L; Clerc, M; Pouliquen, Y (1992). "A fish-eye disease-like familial condition with massive corneal clouding and dyslipoproteinemia. Report of clinical, histologic, electron microscopic, and biochemical features". Cornea. 11 (5): 452–64. doi:10.1097/00003226-199209000-00016. PMID 1424675. S2CID 27089164.
Kuivenhoven, J. A.; Pritchard, H; Hill, J; Frohlich, J; Assmann, G; Kastelein, J (1997). "The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes". Journal of Lipid Research. 38 (2): 191–205. doi:10.1016/S0022-2275(20)37433-2. PMID 9162740.
Kuivenhoven, J. A.; van Voorst tot Voorst EJ; Wiebusch, H; Marcovina, S. M.; Funke, H; Assmann, G; Pritchard, P. H.; Kastelein, J. J. (1995). "A unique genetic and biochemical presentation of fish-eye disease". Journal of Clinical Investigation. 96 (6): 2783–91. doi:10.1172/JCI118348. PMC 185988. PMID 8675648.
Contacos, C; Sullivan, D. R.; Rye, K. A.; Funke, H; Assmann, G (1996). "A new molecular defect in the lecithin: Cholesterol acyltransferase (LCAT) gene associated with fish eye disease". Journal of Lipid Research. 37 (1): 35–44. doi:10.1016/S0022-2275(20)37633-1. PMID 8820100.

ghr.nlm.nih.gov

Reference, Genetics Home. "complete LCAT deficiency". Genetics Home Reference. Retrieved 2016-12-11.
Reference, Genetics Home. "fish-eye disease". Genetics Home Reference. Retrieved 2016-12-11.

nlm.nih.gov

Kaneshiro, N.K. (2014). "Autosomal Recessive". National Institutes of Health, Medline Plus.

ncbi.nlm.nih.gov

Kuivenhoven, J. A.; van Voorst tot Voorst EJ; Wiebusch, H; Marcovina, S. M.; Funke, H; Assmann, G; Pritchard, P. H.; Kastelein, J. J. (1995). "A unique genetic and biochemical presentation of fish-eye disease". Journal of Clinical Investigation. 96 (6): 2783–91. doi:10.1172/JCI118348. PMC 185988. PMID 8675648.

rarediseases.info.nih.gov

"Fish-eye disease | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2018-04-17.

semanticscholar.org

api.semanticscholar.org

Koster, H; Savoldelli, M; Dumon, M. F.; Dubourg, L; Clerc, M; Pouliquen, Y (1992). "A fish-eye disease-like familial condition with massive corneal clouding and dyslipoproteinemia. Report of clinical, histologic, electron microscopic, and biochemical features". Cornea. 11 (5): 452–64. doi:10.1097/00003226-199209000-00016. PMID 1424675. S2CID 27089164.

worldcat.org

search.worldcat.org

Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frasc G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G (Sep 2005). "The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families". Arteriosclerosis, Thrombosis, and Vascular Biology. 25 (9): 1972–1978. doi:10.1161/01.ATV.0000175751.30616.13. hdl:11380/636978. ISSN 1079-5642. PMID 15994445.