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Anderson's disease 相关文献:
Acanthocytosis in Anderson's disease.
Lesesve JF, Perrin J, Georges A, Morali A.
Br J Haematol. 2009 Apr;145(1):1. doi: 10.1111/j.1365-2141.2008.07422.x. Epub 2008 Oct 25.
PMID:19016739
Guidance for the diagnosis and treatment of hypolipidemia disorders.
Bredefeld C, Hussain MM, Averna M, Black DD, Brin MF, Burnett JR, Charrière S, Cuerq C, Davidson NO, Deckelbaum RJ, Goldberg IJ, Granot E, Hegele RA, Ishibashi S, Karmally W, Levy E, Moulin P, Okazaki H, Poinsot P, Rader DJ, Takahashi M, Tarugi P, Traber MG, Di Filippo M, Peretti N.
J Clin Lipidol. 2022 Nov-Dec;16(6):797-812. doi: 10.1016/j.jacl.2022.08.009. Epub 2022 Sep 29.
PMID:36243606
Chylomicron Retention Disease.
Burnett JR, Hooper AJ, Hegele RA.
2022 Mar 24. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:35344313
[Anderson's disease/chylomicron retention disease].
Ohashi K.
Nihon Rinsho. 2001 Mar;59 Suppl 3:261-5.
PMID:11347073
[Anderson disease/chylomicron retention disease].
Miyahara A, Sugie H.
Nihon Rinsho. 2007 Jul 28;65 Suppl 7:597-9.
PMID:17824094
[Anderson's disease].
Polonovski C, Navarro J, Fontaine JL, de Gouyon F, Saudubray JM, Cathelineau L.
Ann Pediatr (Paris). 1970 May 2;17(5):342-54.
PMID:5421321
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease.
Berriot-Varoqueaux N, Dannoura AH, Moreau A, Verthier N, Sassolas A, Cadiot G, Lachaux A, Munck A, Schmitz J, Aggerbeck LP, Samson-Bouma ME.
Gastroenterology. 2001 Nov;121(5):1101-8. doi: 10.1053/gast.2001.29331.
PMID:11677202
[Fabry-Anderson's disease].
Andratschke C.
Fortschr Med. 1975 Dec 4;93(34):1697-702.
PMID:811519
Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families.
Pessah M, Benlian P, Beucler I, Loux N, Schmitz J, Junien C, Infante R.
J Clin Invest. 1991 Jan;87(1):367-70. doi: 10.1172/JCI114996.
PMID:1985110
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities.
Silvain M, Bligny D, Aparicio T, Laforêt P, Grodet A, Peretti N, Ménard D, Djouadi F, Jardel C, Bégué JM, Walker F, Schmitz J, Lachaux A, Aggerbeck LP, Samson-Bouma ME.
Clin Genet. 2008 Dec;74(6):546-52. doi: 10.1111/j.1399-0004.2008.01069.x. Epub 2008 Sep 11.
PMID:18786134
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