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2. Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients. Tefs K, Gueorguieva M, Klammt J, Allen CM, Aktas D, Anlar FY, Aydogdu SD, Brown D, Ciftci E, Contarini P, Dempfle CE, Dostalek M, Eisert S, Gökbuget A, Günhan O, Hidayat AA, Hügle B, Isikoglu M, Irkec M, Joss SK, Klebe S, Kneppo C, Kurtulus I, Mehta RP, Ornek K, Schneppenheim R, Seregard S, Sweeney E, Turtschi S, Veres G, Zeitler P, Ziegler M, Schuster V. Blood; 2006 Nov 01; 108(9):3021-6. PubMed ID: 16849641 [Abstract] [Full Text] [Related]
3. Ligneous conjunctivitis associated with type I plasminogen deficiency: A rare case. Dimopoulos D, Zacharioudakis A, Kazamias G, Danilatou V, Katerini D, Nodarakis M, Koutentaki ME, Koutentakis P. Eur J Ophthalmol; 2022 Sep 01; 32(5):NP1-NP4. PubMed ID: 34308677 [Abstract] [Full Text] [Related]
4. Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresis. Tefs K, Georgieva M, Seregard S, Tait CR, Luchtman-Jones L, Ziegler M, Hügle B, Schuster V. Thromb Haemost; 2004 Aug 01; 92(2):352-7. PubMed ID: 15269832 [Abstract] [Full Text] [Related]
6. Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity. Klammt J, Kobelt L, Aktas D, Durak I, Gokbuget A, Hughes Q, Irkec M, Kurtulus I, Lapi E, Mechoulam H, Mendoza-Londono R, Palumbo JS, Steitzer H, Tabbara KF, Ozbek Z, Pucci N, Sotomayor T, Sturm M, Drogies T, Ziegler M, Schuster V. Thromb Haemost; 2011 Mar 01; 105(3):454-60. PubMed ID: 21174000 [Abstract] [Full Text] [Related]
7. Homozygous type I plasminogen deficiency. Mingers AM, Heimburger N, Zeitler P, Kreth HW, Schuster V. Semin Thromb Hemost; 1997 Mar 01; 23(3):259-69. PubMed ID: 9255907 [Abstract] [Full Text] [Related]
8. Plasminogen Tochigi mice exhibit phenotypes similar to wild-type mice under experimental thrombotic conditions. Tashima Y, Banno F, Kita T, Matsuda Y, Yanamoto H, Miyata T. PLoS One; 2017 Mar 01; 12(7):e0180981. PubMed ID: 28686706 [Abstract] [Full Text] [Related]
9. 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. Thromb Haemost; 2020 May 01; 120(5):758-767. PubMed ID: 32369847 [Abstract] [Full Text] [Related]
10. Ligneous conjunctivitis. Schuster V, Seregard S. Surv Ophthalmol; 2003 May 01; 48(4):369-88. PubMed ID: 12850227 [Abstract] [Full Text] [Related]
11. Ligneous conjunctivitis: a local manifestation of a systemic disorder? Chen S, Wishart M, Hiscott P. J AAPOS; 2000 Oct 01; 4(5):313-5. PubMed ID: 11040483 [Abstract] [Full Text] [Related]
12. Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis. Schuster V, Zeitler P, Seregard S, Ozcelik U, Anadol D, Luchtman-Jones L, Meire F, Mingers AM, Schambeck C, Kreth HW. Thromb Haemost; 2001 Jun 01; 85(6):1004-10. PubMed ID: 11434676 [Abstract] [Full Text] [Related]
13. Management of ligneous conjunctivitis in a child with plasminogen deficiency. Pergantou H, Likaki D, Fotopoulou M, Katsarou O, Xafaki P, Platokouki H. Eur J Pediatr; 2011 Oct 01; 170(10):1333-6. PubMed ID: 21625933 [Abstract] [Full Text] [Related]
14. [Colonic pseudotumoral involvement as an expression of severe plasminogen deficiency]. Ceresetto JM, López RA, Humphreys AR, Duboscq C, Rabinovich OM, Emery NC, Rausch A, Zapata Tapia L, Dezanzo P, Young P. Medicina (B Aires); 2023 Oct 01; 83(6):1003-1006. PubMed ID: 38117723 [Abstract] [Full Text] [Related]
15. Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis. Schuster V, Mingers AM, Seidenspinner S, Nüssgens Z, Pukrop T, Kreth HW. Blood; 1997 Aug 01; 90(3):958-66. PubMed ID: 9242524 [Abstract] [Full Text] [Related]
16. Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiency. Çiftçi E, Ince E, Akar N, Dogru Ü, Tefs K, Schuster V. Eur J Pediatr; 2003 Jul 01; 162(7-8):462-465. PubMed ID: 12719968 [Abstract] [Full Text] [Related]
17. Clinical, histopathological, and genetic aspects in one case of ligneous conjunctivitis. Raimann R, Moya R, Anguita R, Kobus R, Pérez M, Gonzalez P. Ophthalmic Genet; 2018 Oct 01; 39(5):642-644. PubMed ID: 30058940 [Abstract] [Full Text] [Related]
18. Difficulties in mutation screening of the plasminogen (PLG) gene in patients with ligneous conjunctivitis and severe hypoplasminogenemia. Tefs K, Kobelt L, Ziegler M, Hügle B, Schuster V. Arch Ophthalmol; 2007 Sep 01; 125(9):1303; author reply 1303. PubMed ID: 17846386 [No Abstract] [Full Text] [Related]
19. Prenatal diagnosis in a family with severe type I plasminogen deficiency, ligneous conjunctivitis and congenital hydrocephalus. Schuster V, Seidenspinner S, Müller C, Rempen A. Prenat Diagn; 1999 May 01; 19(5):483-7. PubMed ID: 10360521 [Abstract] [Full Text] [Related]
20. Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI). Tefs K, Ott-Gueorguieva M, Kobelt L, Ziegler M, Hintze C, Hügle B, Schuster V. Blood Coagul Fibrinolysis; 2011 Sep 01; 22(6):499-505. PubMed ID: 21537161 [Abstract] [Full Text] [Related] Page: [Next] [New Search]