Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 30 (of 43 Records) |
| Query Trace: Hellp Syndrome[original query] |
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| No association of polymorphisms in the glutathione S-transferase genes with pre-eclampsia, eclampsia and HELLP syndrome in a Turkish population. The journal of obstetrics and gynaecology research 2005 Jun 31 (3): 236-41. Cetin Meral, Pinarbasi Ergun, Percin Ferda E, Akgün Egemen, Percin Sibel, Pinarbasi Hatice, Gurlek Fatma, Cetin A |
| Fas (TNFRSF6) gene polymorphism in pregnant women with hemolysis, elevated liver enzymes, and low platelets and in their neonates. Obstetrics and gynecology 2006 Mar 107 (3): 582-7. Sziller István, Hupuczi Petronella, Normand Neil, Halmos Amrita, Papp Zoltán, Witkin Steven |
| Susceptibility to pre-eclampsia is associated with multiple genetic polymorphisms in maternal biotransformation enzymes. Gynecologic and obstetric investigation 2007 63 (4): 209-13. Zusterzeel Petra L M, Peters Wilbert H M, Burton Graham J, Visser Willy, Roelofs Hennie M J, Steegers Eric A |
| High frequency of methylenetetrahydrofolate reductase 677TT genotype in Hungarian HELLP syndrome patients determined by quantitative real-time PCR. Journal of human hypertension 2007 Feb 21 (2): 154-8. Nagy B, Hupuczi P, Papp |
| Neither maternal nor fetal mutation (E474Q) in the alpha-subunit of the trifunctional protein is frequent in pregnancies complicated by HELLP syndrome. Journal of perinatal medicine 2007 35 (1): 76-8. Mütze Sabine, Ahillen Ines, Rudnik-Schoeneborn Sabine, Eggermann Thomas, Leeners Brigitte, Neumaier-Wagner Peruka M, Kuse Sabine, Rath Werner, Zerres Kla |
| Mannose-binding lectin (MBL) codon 54 gene polymorphism protects against development of pre-eclampsia, HELLP syndrome and pre-eclampsia-associated intrauterine growth restriction. Molecular human reproduction 2007 Apr 13 (4): 281-5. Sziller I, Babula O, Hupuczi P, Nagy B, Rigó B, Szabó G, Papp Z, Linhares I M, Witkin S |
| The 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene is not associated with HELLP syndrome. Journal of thrombosis and thrombolysis 2009 Feb 27 (2): 141-5. Muetze Sabine, Eggermann Thomas, Leeners Brigitte, Birke Cornelia, Kuse Sabine, Ortlepp Jan Rudolf, Rudnik-Schoeneborn Sabine, Zerres Klaus, Rath Wern |
| Ser128Arg E-selectin and Thr715Pro P-selectin polymorphisms and severe preeclampsia. The Journal of reproductive medicine 2007 Sep 52 (9): 815-8. Derzbach László, Balogh Adám, Bokodi Géza, Vásárhelyi Barna, Rigó Ján |
| [Screening for G1528C mutation in mitochondrial trifunctional protein gene in pregnant women with severe preeclampsia and new born infant]. Zhonghua fu chan ke za zhi 2006 Oct 41 (10): 672-5. Wang R, Yang Z, Zhu JM, Wang JL, Yang HX, Wang Q, Zhai GR, Li Z, Yu M |
| Maternal factor V Leiden mutation is associated with HELLP syndrome in Caucasian women. Acta obstetricia et gynecologica Scandinavica 2008 87 (6): 635-42. Muetze Sabine, Leeners Brigitte, Ortlepp Jan R, Kuse Sabine, Tag Carmen G, Weiskirchen Ralf, Gressner Axel M, Rudnik-Schoeneborn Sabine, Zerres Klaus, Rath Wern |
| Association between tumor necrosis factor (TNF)-alpha G-308A gene polymorphism and preeclampsia complicated by severe fetal growth restriction. Clinica chimica acta; international journal of clinical chemistry 2008 Jun 392 (1-2): 52-7. Molvarec Attila, Jermendy Agnes, Nagy Bálint, Kovács Margit, Várkonyi Tibor, Hupuczi Petronella, Prohászka Zoltán, Rigó Ján |
| Maternal TLR4 and NOD2 gene variants, pro-inflammatory phenotype and susceptibility to early-onset preeclampsia and HELLP syndrome. PloS one 2008 3 (4): e1865. van Rijn Bas B, Franx Arie, Steegers Eric A P, de Groot Christianne J M, Bertina Rogier M, Pasterkamp Gerard, Voorbij Hieronymus A M, Bruinse Hein W, Roest Ma |
| Vascular endothelial growth factor (VEGF) polymorphisms in HELLP syndrome patients determined by quantitative real-time PCR and melting curve analyses. Clinica chimica acta; international journal of clinical chemistry 2008 Mar 389 (1-2): 126-31. Nagy Bálint, Savli Hakan, Molvarec Attila, Várkonyi Tibor, Rigó Barbara, Hupuczi Petronella, Rigó Ján |
| Leptin gene (TTTC)(n) microsatellite polymorphism in pre-eclampsia and HELLP syndrome. Clinical chemistry and laboratory medicine : CCLM / FESCC 2009 47 (9): 1033-7. Nagy Balint, Varkonyi Tibor, Molvarec Attila, Lazar Levente, Hupuczi Petronella, Than Nandor Gabor, Rigo Jan |
| Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome. Clinica chimica acta; international journal of clinical chemistry 2009 Jul 405 (1-2): 148-52. Bertalan Rita, Patocs Attila, Nagy Balint, Derzsy Zoltan, Gullai Nora, Szappanos Agnes, Rigo Janos, Racz Karo |
| Leptin receptor (LEPR) SNP polymorphisms in HELLP syndrome patients determined by quantitative real-time PCR and melting curve analysis. BMC medical genetics 2010 11 (1): 25. Várkonyi Tibor, Lázár Levente, Molvarec Attila, Than Nándor Gábor, Rigó János, Nagy Báli |
| Frequency of hereditary thrombophilia, anticoagulant activity, and homocysteine levels in patients with hemolysis, elevated liver functions and low thrombocyte count (HELLP) syndrome. The journal of obstetrics and gynaecology research 2011 Jun 37 (6): 527-33. Dogan Ovgu Ozkan, Simsek Yavuz, Celen Sevki, Danisman Nu |
| Low-molecular-weight heparin added to aspirin in the prevention of recurrent early-onset pre-eclampsia in women with inheritable thrombophilia: the FRUIT-RCT. Journal of thrombosis and haemostasis : JTH 2011 Nov . de Vries JI, van Pampus MG, Hague WM, Bezemer PD, Joosten JH |
| eNOSI4 and EPHX1 polymorphisms affect maternal susceptibility to preeclampsia: analysis of five polymorphisms predisposing to cardiovascular disease in 279 Caucasian and 241 African women. Archives of gynecology and obstetrics 2014 Mar 289 (3): 581-93. Groten T, Schleussner E, Lehmann T, Reister F, Holzer B, Danso K A, Zeillinger |
| Association of plasminogen activator inhibitor-type 1 (-675 4G/5G) polymorphism with pre-eclampsia: systematic review. PloS one 2013 8 (2): e56907. Morgan Jessie A, Bombell Sarah, McGuire Willi |
| Association between ACVR2A and early-onset preeclampsia: replication study in a Northeastern Brazilian population. Placenta 2015 Feb 36 (2): 186-90. Ferreira L C, Gomes C E M, Araújo A C P, Bezerra P F, Duggal P, Jeronimo S M |
| Association of Nitric Oxide Synthase and Matrix Metalloprotease Single Nucleotide Polymorphisms with Preeclampsia and Its Complications. PloS one 2015 10 (8): e0136693. Leonardo Daniela P, Albuquerque Dulcinéia M, Lanaro Carolina, Baptista Letícia C, Cecatti José G, Surita Fernanda G, Parpinelli Mary A, Costa Fernando F, Franco-Penteado Carla F, Fertrin Kleber Y, Costa Maria Lau |
| The maternal 14 bp Ins/Del polymorphism in HLA-G is not associated with preeclampsia risk. International journal of immunogenetics 2017 Nov . Ferreira L C, Lopes T P B, Guimarães T B, Gomes C E M, Jeronimo S M |
| FAS A-670G and Fas ligand IVS2nt A 124G polymorphisms are significantly increased in women with pre-eclampsia and may contribute to HELLP syndrome: a case-controlled study. BJOG : an international journal of obstetrics and gynaecology 2018 Aug . Raguema N, Zitouni H, Ben Ali Gannoun M, Benletaifa D, Almawi W Y, Mahjoub T, Lavoie J |
| Germline mutations in the alternative pathway of complement predispose to HELLP syndrome. JCI insight 2018 Mar 3 (6): . Vaught Arthur J, Braunstein Evan M, Jasem Jagar, Yuan Xuan, Makhlin Igor, Eloundou Solange, Baines Andrea C, Merrill Samuel A, Chaturvedi Shruti, Blakemore Karin, Sperati C John, Brodsky Robert |
| PHLDA2 gene polymorphisms and risk of HELLP syndrome and severe preeclampsia. Pregnancy hypertension 2020 Jan 19 190-194. Ding Li, Blitz Matthew J, Wing Deborah A, Epstein Aaron J, Gjessing Håkon K, Wilson Melissa |
| Genetic association of ERAP1 and ERAP2 with eclampsia and preeclampsia in northeastern Brazilian women. Scientific reports 2021 Mar 11 (1): 6764. Ferreira Leonardo Capistrano, Gomes Carlos Eduardo Maia, Duggal Priya, De Paula Holanda Ingrid, de Lima Amanda Samara, do Nascimento Paulo Ricardo Porfírio, Jeronimo Selma Maria Bezer |
| Quantitative Alterations in Complement Alternative Pathway and Related Genetic Analysis in Severe Phenotype Preeclampsia. Kidney360 2022 4 2 (9): 1463-1472. Alrahmani Layan, Gonzalez Suarez Maria L, Cousin Margot A, Moyer Ann M, Willrich Maria Alice V, White Wendy M, Wick Myra J, Tostrud Linda J, Narang Kavita, Garovic Vesna |
| STOX1 promotor region -922 T?>?C polymorphism is associated with Early-Onset preeclampsia. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology 2022 11 1-7. Akin Seyda, Pinarbasi Ergun, Bildirici Aslihan Esra, Cekin Nilg |
| Increased Complement Activation and Decreased ADAMTS13 Activity Are Associated with Genetic Susceptibility in Patients with Preeclampsia/HELLP Syndrome Compared to Healthy Pregnancies: An Observational Case-Controlled Study. Journal of personalized medicine 2024 4 14 (4): . Theodora-Maria Venou, Evangelia Vetsiou, Christos Varelas, Angelos Daniilidis, Kyriakos Psarras, Evaggelia-Evdoxia Koravou, Maria Koutra, Tasoula Touloumenidou, Vasilis Tsolakidis, Apostolia Papalexandri, Fani Minti, Evdokia Mandala, Konstantinos Dinas, Efthymia Vlachaki, Eleni Gavriila |
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