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Anderson's disease 相关文献:
Chimeric antigen receptor T-cell therapy - assessment and management of toxicities.
Neelapu SS, Tummala S, Kebriaei P, Wierda W, Gutierrez C, Locke FL, Komanduri KV, Lin Y, Jain N, Daver N, Westin J, Gulbis AM, Loghin ME, de Groot JF, Adkins S, Davis SE, Rezvani K, Hwu P, Shpall EJ.
Nat Rev Clin Oncol. 2018 Jan;15(1):47-62. doi: 10.1038/nrclinonc.2017.148. Epub 2017 Sep 19.
PMID:28925994
[Anderson's disease/chylomicron retention disease].
Ohashi K.
Nihon Rinsho. 2001 Mar;59 Suppl 3:261-5.
PMID:11347073
Chronic Inflammatory Placental Disorders Associated With Recurrent Adverse Pregnancy Outcome.
Cornish EF, McDonnell T, Williams DJ.
Front Immunol. 2022 Apr 22;13:825075. doi: 10.3389/fimmu.2022.825075. eCollection 2022.
PMID:35529853
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
[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
Growing teratoma syndrome.
Nitecki R, Hameed N, Bhosale P, Shafer A.
Int J Gynecol Cancer. 2023 Feb 6;33(2):299-303. doi: 10.1136/ijgc-2022-004265.
PMID:36746506
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
[Fabry-Anderson's disease].
Andratschke C.
Fortschr Med. 1975 Dec 4;93(34):1697-702.
PMID:811519
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms.
Jansen S, van der Werf IM, Innes AM, Afenjar A, Agrawal PB, Anderson IJ, Atwal PS, van Binsbergen E, van den Boogaard MJ, Castiglia L, Coban-Akdemir ZH, van Dijck A, Doummar D, van Eerde AM, van Essen AJ, van Gassen KL, Guillen Sacoto MJ, van Haelst MM, Iossifov I, Jackson JL, Judd E, Kaiwar C, Keren B, Klee EW, Klein Wassink-Ruiter JS, Meuwissen ME, Monaghan KG, de Munnik SA, Nava C, Ockeloen CW, Pettinato R, Racher H, Rinne T, Romano C, Sanders VR, Schnur RE, Smeets EJ, Stegmann APA, Stray-Pedersen A, Sweetser DA, Terhal PA, Tveten K, VanNoy GE, de Vries PF, Waxler JL, Willing M, Pfundt R, Veltman JA, Kooy RF, Vissers LELM, de Vries BBA.
Eur J Hum Genet. 2019 May;27(5):738-746. doi: 10.1038/s41431-018-0292-2. Epub 2019 Jan 24.
PMID:30679813
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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