Neutral lipid storage disease (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Neutral lipid storage disease" in English language version.

refsWebsite

Global rank English rank

16nih.gov

4^th place

10doi.org

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3worldcat.org

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1youtube.com

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1ghostarchive.org

32^nd place

21^st place

1semanticscholar.org

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doi.org

Lefèvre C, Jobard F, Caux F, et al. (November 2001). "Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome". Am. J. Hum. Genet. 69 (5): 1002–12. doi:10.1086/324121. PMC 1274347. PMID 11590543.
Yamaguchi, Tomohiro; Osumi, Takashi (2009). "Chanarin–Dorfman syndrome: Deficiency in CGI-58, a lipid droplet-bound coactivator of lipase". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1791 (6): 519–523. doi:10.1016/j.bbalip.2008.10.012. ISSN 1388-1981. PMID 19061969.
Schweiger, Martina; Eichmann, Thomas O.; Taschler, Ulrike; Zimmermann, Robert; Zechner, Rudolf; Lass, Achim (2014-01-01), "Chapter Ten - Measurement of Lipolysis", in MacDougald, Ormond A. (ed.), Methods of Adipose Tissue Biology, Part B, Methods in Enzymology, vol. 538, Academic Press, pp. 171–193, doi:10.1016/B978-0-12-800280-3.00010-4, ISBN 978-0-12-800280-3, PMC 4018506, PMID 24529439
Missaglia, Sara; Maggi, Lorenzo; Mora, Marina; Gibertini, Sara; Blasevich, Flavia; Agostoni, Piergiuseppe; Moro, Laura; Cassandrini, Denise; Santorelli, Filippo Maria; Gerevini, Simonetta; Tavian, Daniela (May 2017). "Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement". Neuromuscular Disorders. 27 (5): 481–486. doi:10.1016/j.nmd.2017.01.011. ISSN 0960-8966. PMC 5424884. PMID 28258942.
Korbelius, Melanie; Vujic, Nemanja; Sachdev, Vinay; Obrowsky, Sascha; Rainer, Silvia; Gottschalk, Benjamin; Graier, Wolfgang F.; Kratky, Dagmar (13 August 2019). "ATGL/CGI-58-Dependent Hydrolysis of a Lipid Storage Pool in Murine Enterocytes". Cell Reports. 28 (7): 1923–1934.e4. doi:10.1016/j.celrep.2019.07.030. ISSN 2211-1247. PMC 6713565. PMID 31412256.
Zhang W, Wen B, Lu J, Zhao Y, Hong D, Zhao Z, et al. (Oct 2019). "Neutral Lipid Storage Disease with Myopathy in China: A Large Multicentric Cohort Study". Orphanet Journal of Rare Diseases. 14 (1): 234. doi:10.1186/s13023-019-1209-z. PMC 6815004. PMID 31655616. 234.
Vasiljevski ER, Summers MA, Little DG, Schindeler A (October 2018). "Lipid storage myopathies: Current treatments and future directions". Progress in Lipid Research. 72: 1–17. doi:10.1016/j.plipres.2018.08.001. PMID 30099045. S2CID 51966990.
Missaglia S, Coleman RA, Mordente A, Tavian D (Feb 2019). "Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function". Cells. 8 (2): 187. doi:10.3390/cells8020187. PMC 6406896. PMID 30795549. 187.
Jordan GH (1953). "The Familial Occurrence of Fat Containing Vacuoles in the Leukocytes Diagnosed in two Brothers Suffering from Dystrophia Musculorum Progressiva (ERB)". Acta Medica Scandinavica. 145 (6): 419–423. doi:10.1111/j.0954-6820.1953.tb07038.x. PMID 13079655.
Winokur D, LiPera W (15 February 2018). "Jordans Anomaly". Blood. 131 (7): 837. doi:10.1182/blood-2017-10-812677. PMID 29449305.

ghostarchive.org

Viel, Alain (2 June 2017). "Harvard University, "Principles of Biochemistry."". YouTube. Archived from the original on 2021-12-15.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lefèvre C, Jobard F, Caux F, et al. (November 2001). "Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome". Am. J. Hum. Genet. 69 (5): 1002–12. doi:10.1086/324121. PMC 1274347. PMID 11590543.
Yamaguchi, Tomohiro; Osumi, Takashi (2009). "Chanarin–Dorfman syndrome: Deficiency in CGI-58, a lipid droplet-bound coactivator of lipase". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1791 (6): 519–523. doi:10.1016/j.bbalip.2008.10.012. ISSN 1388-1981. PMID 19061969.
Schweiger, Martina; Eichmann, Thomas O.; Taschler, Ulrike; Zimmermann, Robert; Zechner, Rudolf; Lass, Achim (2014-01-01), "Chapter Ten - Measurement of Lipolysis", in MacDougald, Ormond A. (ed.), Methods of Adipose Tissue Biology, Part B, Methods in Enzymology, vol. 538, Academic Press, pp. 171–193, doi:10.1016/B978-0-12-800280-3.00010-4, ISBN 978-0-12-800280-3, PMC 4018506, PMID 24529439
Missaglia, Sara; Maggi, Lorenzo; Mora, Marina; Gibertini, Sara; Blasevich, Flavia; Agostoni, Piergiuseppe; Moro, Laura; Cassandrini, Denise; Santorelli, Filippo Maria; Gerevini, Simonetta; Tavian, Daniela (May 2017). "Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement". Neuromuscular Disorders. 27 (5): 481–486. doi:10.1016/j.nmd.2017.01.011. ISSN 0960-8966. PMC 5424884. PMID 28258942.
Korbelius, Melanie; Vujic, Nemanja; Sachdev, Vinay; Obrowsky, Sascha; Rainer, Silvia; Gottschalk, Benjamin; Graier, Wolfgang F.; Kratky, Dagmar (13 August 2019). "ATGL/CGI-58-Dependent Hydrolysis of a Lipid Storage Pool in Murine Enterocytes". Cell Reports. 28 (7): 1923–1934.e4. doi:10.1016/j.celrep.2019.07.030. ISSN 2211-1247. PMC 6713565. PMID 31412256.
Zhang W, Wen B, Lu J, Zhao Y, Hong D, Zhao Z, et al. (Oct 2019). "Neutral Lipid Storage Disease with Myopathy in China: A Large Multicentric Cohort Study". Orphanet Journal of Rare Diseases. 14 (1): 234. doi:10.1186/s13023-019-1209-z. PMC 6815004. PMID 31655616. 234.
Vasiljevski ER, Summers MA, Little DG, Schindeler A (October 2018). "Lipid storage myopathies: Current treatments and future directions". Progress in Lipid Research. 72: 1–17. doi:10.1016/j.plipres.2018.08.001. PMID 30099045. S2CID 51966990.
Missaglia S, Coleman RA, Mordente A, Tavian D (Feb 2019). "Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function". Cells. 8 (2): 187. doi:10.3390/cells8020187. PMC 6406896. PMID 30795549. 187.
Jordan GH (1953). "The Familial Occurrence of Fat Containing Vacuoles in the Leukocytes Diagnosed in two Brothers Suffering from Dystrophia Musculorum Progressiva (ERB)". Acta Medica Scandinavica. 145 (6): 419–423. doi:10.1111/j.0954-6820.1953.tb07038.x. PMID 13079655.
Winokur D, LiPera W (15 February 2018). "Jordans Anomaly". Blood. 131 (7): 837. doi:10.1182/blood-2017-10-812677. PMID 29449305.

ncbi.nlm.nih.gov

Lefèvre C, Jobard F, Caux F, et al. (November 2001). "Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome". Am. J. Hum. Genet. 69 (5): 1002–12. doi:10.1086/324121. PMC 1274347. PMID 11590543.
Schweiger, Martina; Eichmann, Thomas O.; Taschler, Ulrike; Zimmermann, Robert; Zechner, Rudolf; Lass, Achim (2014-01-01), "Chapter Ten - Measurement of Lipolysis", in MacDougald, Ormond A. (ed.), Methods of Adipose Tissue Biology, Part B, Methods in Enzymology, vol. 538, Academic Press, pp. 171–193, doi:10.1016/B978-0-12-800280-3.00010-4, ISBN 978-0-12-800280-3, PMC 4018506, PMID 24529439
Missaglia, Sara; Maggi, Lorenzo; Mora, Marina; Gibertini, Sara; Blasevich, Flavia; Agostoni, Piergiuseppe; Moro, Laura; Cassandrini, Denise; Santorelli, Filippo Maria; Gerevini, Simonetta; Tavian, Daniela (May 2017). "Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement". Neuromuscular Disorders. 27 (5): 481–486. doi:10.1016/j.nmd.2017.01.011. ISSN 0960-8966. PMC 5424884. PMID 28258942.
Korbelius, Melanie; Vujic, Nemanja; Sachdev, Vinay; Obrowsky, Sascha; Rainer, Silvia; Gottschalk, Benjamin; Graier, Wolfgang F.; Kratky, Dagmar (13 August 2019). "ATGL/CGI-58-Dependent Hydrolysis of a Lipid Storage Pool in Murine Enterocytes". Cell Reports. 28 (7): 1923–1934.e4. doi:10.1016/j.celrep.2019.07.030. ISSN 2211-1247. PMC 6713565. PMID 31412256.
Zhang W, Wen B, Lu J, Zhao Y, Hong D, Zhao Z, et al. (Oct 2019). "Neutral Lipid Storage Disease with Myopathy in China: A Large Multicentric Cohort Study". Orphanet Journal of Rare Diseases. 14 (1): 234. doi:10.1186/s13023-019-1209-z. PMC 6815004. PMID 31655616. 234.
Missaglia S, Coleman RA, Mordente A, Tavian D (Feb 2019). "Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function". Cells. 8 (2): 187. doi:10.3390/cells8020187. PMC 6406896. PMID 30795549. 187.

semanticscholar.org

api.semanticscholar.org

Vasiljevski ER, Summers MA, Little DG, Schindeler A (October 2018). "Lipid storage myopathies: Current treatments and future directions". Progress in Lipid Research. 72: 1–17. doi:10.1016/j.plipres.2018.08.001. PMID 30099045. S2CID 51966990.

worldcat.org

search.worldcat.org

Yamaguchi, Tomohiro; Osumi, Takashi (2009). "Chanarin–Dorfman syndrome: Deficiency in CGI-58, a lipid droplet-bound coactivator of lipase". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1791 (6): 519–523. doi:10.1016/j.bbalip.2008.10.012. ISSN 1388-1981. PMID 19061969.
Missaglia, Sara; Maggi, Lorenzo; Mora, Marina; Gibertini, Sara; Blasevich, Flavia; Agostoni, Piergiuseppe; Moro, Laura; Cassandrini, Denise; Santorelli, Filippo Maria; Gerevini, Simonetta; Tavian, Daniela (May 2017). "Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement". Neuromuscular Disorders. 27 (5): 481–486. doi:10.1016/j.nmd.2017.01.011. ISSN 0960-8966. PMC 5424884. PMID 28258942.
Korbelius, Melanie; Vujic, Nemanja; Sachdev, Vinay; Obrowsky, Sascha; Rainer, Silvia; Gottschalk, Benjamin; Graier, Wolfgang F.; Kratky, Dagmar (13 August 2019). "ATGL/CGI-58-Dependent Hydrolysis of a Lipid Storage Pool in Murine Enterocytes". Cell Reports. 28 (7): 1923–1934.e4. doi:10.1016/j.celrep.2019.07.030. ISSN 2211-1247. PMC 6713565. PMID 31412256.

youtube.com

Viel, Alain (2 June 2017). "Harvard University, "Principles of Biochemistry."". YouTube. Archived from the original on 2021-12-15.