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collagen HI glomerulopathy相关文献:
Novel Therapies for Alport Syndrome.
Chavez E, Rodriguez J, Drexler Y, Fornoni A.
Front Med (Lausanne). 2022 Apr 25;9:848389. doi: 10.3389/fmed.2022.848389. eCollection 2022.
PMID:35547199
Collagenofibrotic glomerulopathy.
Kurien AA, Larsen CP, Cossey LN.
Clin Kidney J. 2015 Oct;8(5):543-7. doi: 10.1093/ckj/sfv061. Epub 2015 Aug 7.
PMID:26413279
Collagen Type III Glomerulopathies.
Cohen AH.
Adv Chronic Kidney Dis. 2012 Mar;19(2):101-6. doi: 10.1053/j.ackd.2012.02.017.
PMID:22449347
[Collagen type III glomerulopathy: a morphologic study].
Li L, Zou WZ, Wang SX, Wang SL, Wang W, Han ZH, Du J, Bo L.
Zhonghua Bing Li Xue Za Zhi. 2005 Jul;34(7):385-8.
PMID:16251038
Complement factor H-deficient mice develop spontaneous hepatic tumors.
Laskowski J, Renner B, Pickering MC, Serkova NJ, Smith-Jones PM, Clambey ET, Nemenoff RA, Thurman JM.
J Clin Invest. 2020 Aug 3;130(8):4039-4054. doi: 10.1172/JCI135105.
PMID:32369457
Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a "new disease entity"?
Roy S, Nalwa A, Keith J, Weck K, Singh H, Nickeleit V.
Ultrastruct Pathol. 2019;43(4-5):209-215. doi: 10.1080/01913123.2019.1683666. Epub 2019 Nov 4.
PMID:31682783
Nail-patella glomerulopathy without associated constitutional abnormalities.
Zuppan CW, Weeks DA, Cutler D.
Ultrastruct Pathol. 2003 Sep-Oct;27(5):357-61.
PMID:14708727
Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children.
Christodoulaki V, Kosma K, Marinakis NM, Tilemis FN, Stergiou N, Kampouraki A, Kapogiannis C, Karava V, Mitsioni A, Mila M, Kanaka-Gantenbein C, Makrythanasis P, Tzetis M, Traeger-Synodinos J.
Genes (Basel). 2024 Aug 2;15(8):1016. doi: 10.3390/genes15081016.
PMID:39202375
Immune Complex Associated Glomerulonephritis in a Patient with Prefibrotic Primary Myelofibrosis: A Case Report.
Atlani M, Sharma T, Joshi D, Kumar A.
Indian J Nephrol. 2021 Jan-Feb;31(1):50-53. doi: 10.4103/ijn.IJN_222_19. Epub 2021 Jan 27.
PMID:33994688
Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities - Renal Asian Genetics Network (DRAGoN).
Lu L, Yap YC, Nguyen DQ, Chan YH, Ng JL, Zhang YC, Chan CY, Than M, Liu ID, Asim S, Moorani K, Naeem B, Ijaz I, Nguyen TMT, Lee ML, Eng C, Huque SS, Ng YH, Ganesan I, Chao SM, Chong SL, Tan PH, Loh A, Davila S, Kumar V, Ling JZ, Moorakonda RB, Tan KM, Ng AY, Poon KS, Schaefer F, Lipska-Zietkiewicz B, Yap HK, Ng KH; Deciphering Diversities: Renal Asian Genetics Network (DRAGoN).
Clin Genet. 2022 May;101(5-6):541-551. doi: 10.1111/cge.14116. Epub 2022 Feb 1.
PMID:35064937
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