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C2 deficiency相关文献:
[C2 deficiency].
Ohno T.
Ryoikibetsu Shokogun Shirizu. 2000;(32):193-5.
PMID:11212687
Overcoming C2 deficiency.
Miller EC, Atkinson JP.
Clin Immunol. 2012 Sep;144(3):269-71. doi: 10.1016/j.clim.2012.07.005. Epub 2012 Jul 20.
PMID:22863655
Gonococcal Arthritis and C2 Deficiency.
Benavent Núñez D, Tornero Marín C, Bonilla Hernán G, García Perea A, Balsa Criado A, Rico Nieto A.
Reumatol Clin (Engl Ed). 2019 Nov-Dec;15(6):e125-e127. doi: 10.1016/j.reuma.2017.08.010. Epub 2017 Nov 2.
PMID:29102589
Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies.
El Sissy C, Rosain J, Vieira-Martins P, Bordereau P, Gruber A, Devriese M, de Pontual L, Taha MK, Fieschi C, Picard C, Frémeaux-Bacchi V.
Front Immunol. 2019 Aug 8;10:1936. doi: 10.3389/fimmu.2019.01936. eCollection 2019.
PMID:31440263
Molecular heterogeneity in deficiency of complement protein C2 type I.
Wang X, Circolo A, Lokki ML, Shackelford PG, Wetsel RA, Colten HR.
Immunology. 1998 Feb;93(2):184-91. doi: 10.1046/j.1365-2567.1998.00392.x.
PMID:9616367
Complement deficiency states.
Agnello V.
Medicine (Baltimore). 1978 Jan;57(1):1-23. doi: 10.1097/00005792-197801000-00001.
PMID:337041
Homozygous C2 deficiency: association with defective alternative pathway function and immunoglobulin deficiency.
Sanal O, Yel L, Tezcan I, Ersoy F, Berkel AI.
Int Arch Allergy Immunol. 1996 Jun;110(2):195-8. doi: 10.1159/000237287.
PMID:8645999
Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.
Johnson CA, Densen P, Hurford RK Jr, Colten HR, Wetsel RA.
J Biol Chem. 1992 May 5;267(13):9347-53.
PMID:1577763
Genetic deficiency of C4, C2 or C1q and lupus syndromes. Association with anti-Ro (SS-A) antibodies.
Meyer O, Hauptmann G, Tappeiner G, Ochs HD, Mascart-Lemone F.
Clin Exp Immunol. 1985 Dec;62(3):678-84.
PMID:3878757
Hereditary complement (C2) deficiency with dermatomyositis.
Leddy JP, Griggs RC, Klemperer MR, Frank MM.
Am J Med. 1975 Jan;58(1):83-91. doi: 10.1016/0002-9343(75)90537-9.
PMID:1090155
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