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Year Number of Results
2014 2
2015 1
2016 2
2017 1
2018 1
2020 1
2021 2
2023 1
2024 0

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Page 1
Novel homozygous mutation of plasminogen in ligneous conjunctivitis: a case report and literature review.
Xu L, Sun Y, Yang K, Zhao D, Wang Y, Ren S. Xu L, et al. Ophthalmic Genet. 2021 Apr;42(2):105-109. doi: 10.1080/13816810.2020.1867753. Epub 2021 Jan 11. Ophthalmic Genet. 2021. PMID: 33427557 Review.
Sanger sequencing was performed to screen the mutation site for the disease. In silico analysis was applied to predict the pathogenesis of the identified mutation. In addition, we reviewed the literatures on PLG mutations of LC. ...
Sanger sequencing was performed to screen the mutation site for the disease. In silico analysis was applied to predict the pathogenes …
Anterior Segment Surgeries Under Topical Fresh Frozen Plasma Treatment in Ligneous Conjunctivitis.
Ozbek-Uzman S, Yalniz-Akkaya Z, Nurozler Tabakci B, Singar E, Burcu A. Ozbek-Uzman S, et al. Cornea. 2021 Mar 1;40(3):299-302. doi: 10.1097/ICO.0000000000002573. Cornea. 2021. PMID: 33290319
PURPOSE: To evaluate the efficacy of topical fresh frozen plasma (FFP) therapy on clinical symptoms, findings, and prognosis after anterior segment surgeries in patients with ligneous conjunctivitis (LC). ...
PURPOSE: To evaluate the efficacy of topical fresh frozen plasma (FFP) therapy on clinical symptoms, findings, and prognosis after an …
Functional Fibrinolysis Assays Reveal Different Mechanisms underlying Plasminogen Dysfunction in Ligneous Conjunctivitis.
Bourrienne MC, Loyau S, Faille D, de Raucourt E, de Mazancourt P, Ho-Tin-Noé B, Gabison E, Ajzenberg N. Bourrienne MC, et al. Thromb Haemost. 2020 May;120(5):758-767. doi: 10.1055/s-0040-1709526. Epub 2020 May 5. Thromb Haemost. 2020. PMID: 32369847
The cell-based ECLT and plasminogen activation assay demonstrated that urokinase-mediated fibrinolysis was not impaired in patients with homozygous K19E mutation compared with the other mutants. CONCLUSION: We confirm that plasminogen levels fail to predict LC occurrence. …
The cell-based ECLT and plasminogen activation assay demonstrated that urokinase-mediated fibrinolysis was not impaired in patients with hom …
Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis.
Osaki T, Souri M, Song YS, Izumi N, Law R, Ichinose A. Osaki T, et al. J Thromb Thrombolysis. 2016 Aug;42(2):218-24. doi: 10.1007/s11239-016-1375-y. J Thromb Thrombolysis. 2016. PMID: 27193180
These two mutations were confirmed to be novel. Molecular modeling and splice site strength calculation predicted conformational disorder(s) for the Glu266 mutant and a drastic decrease in splicing efficiency for intron 12, respectively. ...
These two mutations were confirmed to be novel. Molecular modeling and splice site strength calculation predicted conformational diso …
Co-existing ligneous conjunctivitis and IgG4-related disease.
Chiang WY, Liu TT, Huang WT, Kuo MT. Chiang WY, et al. Indian J Ophthalmol. 2016 Jul;64(7):532-4. doi: 10.4103/0301-4738.190154. Indian J Ophthalmol. 2016. PMID: 27609168 Free PMC article.
To the best of our knowledge, IgG4-RD has never been reported with LC. By reporting the clinical course and literature review, we should pay attention to the association between these two diseases....
To the best of our knowledge, IgG4-RD has never been reported with LC. By reporting the clinical course and literature review, we sho …
Root dentin anomaly and a PLG mutation.
Tananuvat N, Charoenkwan P, Ohazama A, Ketuda Cairns JR, Kaewgahya M, Kantaputra PN. Tananuvat N, et al. Eur J Med Genet. 2014 Nov-Dec;57(11-12):630-5. doi: 10.1016/j.ejmg.2014.09.006. Epub 2014 Sep 30. Eur J Med Genet. 2014. PMID: 25281489
The parents were heterozygous for c.1193G>A mutation. The c.1193G>A mutation is novel and predicted to cause amino acid substitution p.Cys398Tyr. Thin root dentin in the patient who was affected with PLG mutation and immunolocalization of Plg during early root develo …
The parents were heterozygous for c.1193G>A mutation. The c.1193G>A mutation is novel and predicted to cause amino acid substit …
The prevalence and clinical manifestation of hereditary thrombophilia in Korean patients with unprovoked venous thromboembolisms.
Lee SY, Kim EK, Kim MS, Shin SH, Chang H, Jang SY, Kim HJ, Kim DK. Lee SY, et al. PLoS One. 2017 Oct 17;12(10):e0185785. doi: 10.1371/journal.pone.0185785. eCollection 2017. PLoS One. 2017. PMID: 29040284 Free PMC article.

Age <45 years and a family history of VTE were independent predictors for unprovoked VTE with HT (odds ratio, 9.435 [2.45-36.35]; P = 0.001 and 92.667 [14.95-574.29]; P < 0.001). ...A positive family history of VTE and age <45 years were independent predictors

Age <45 years and a family history of VTE were independent predictors for unprovoked VTE with HT (odds ratio, 9.435 [2.45-36.35]; …
Long-term follow-up in a pediatric patient with Ligneous Conjunctivitis due to PLG gene mutation in topical plasminogen treatment after successful use of ocular prosthesis for aesthetic rehabilitation: a case report.
Panfili FM, Valente P, Ficari A, Cortellessa F, Vecchio D, Gonfiantini MV, Buonuomo PS, Colafati GS, Agolini E, Bartuli M, Modugno AC, Macchiaiolo M. Panfili FM, et al. Ital J Pediatr. 2023 Aug 23;49(1):101. doi: 10.1186/s13052-023-01503-x. Ital J Pediatr. 2023. PMID: 37612758 Free PMC article.
11 results