HuGE Literature Finder
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Mutational spectrum and novel candidate genes in Chinese children with sporadic steroid-resistant nephrotic syndrome. Pediatric research 2019 Feb . Li Jianguo, Wang Lijun, Wan Ling, Lin Tiantian, Zhao Wentao, Cui Hang, Li Huarong, Cao Li, Wu Jianxin, Zhang Ti |
Haptoglobin levels, but not Hp1-Hp2 polymorphism, are associated with polycystic ovary syndrome. Journal of assisted reproduction and genetics 2017 Sep . Carvalho Laura M L, Ferreira Cláudia N, de Oliveira Daisy K D, Rodrigues Kathryna F, Duarte Rita C F, Teixeira Márcia F A, Xavier Luana B, Candido Ana Lúcia, Reis Fernando M, Silva Ieda F O, Campos Fernanda M F, Gomes Karina |
Haptoglobin polymorphism in relation to coronary plaque characteristics on radiofrequency intravascular ultrasound and near-infrared spectroscopy in patients with coronary artery disease. International journal of cardiology 2016 Oct 221 682-7. Buljubasic Nermina, Oemrawsingh Rohit M, Smeets Mirjam B, Cheng Jin M, Regar Evelyn, van Geuns Robert-Jan M, Serruys Patrick W J C, Boersma Eric, Akkerhuis K Martijn, Kardys Isabella, Arslan Fat |
[Correlation Study on Chinese Medical Syndrome Types of Chronic Atrophic Gastritis Patients, Hp, and IL-1ß Polymorphism]. Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine / Zhongguo Zhong xi yi jie he xue hui, Zhongguo Zhong yi yan jiu yuan zhu ban 2015 Dec 35 (12): 1433-6. Zhang Jian-zhi, Feng Quan-lin, Hu Yi-lu, Yang Ti, Zhang Yi |
Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients. Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference 2015 Aug 2015 294-7. Bari Vlasta, Girardengo Giulia, Marchi Andrea, De Maria Beatrice, Brink Paul A, Crotti Lia, Schwartz Peter J, Porta Alber |
Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics. The American journal of surgical pathology 2012 Jun 36 (6): 876-82. Rosty Christophe, Buchanan Daniel D, Walsh Michael D, Pearson Sally-Ann, Pavluk Erika, Walters Rhiannon J, Clendenning Mark, Spring Kevin J, Jenkins Mark A, Win Aung K, Hopper John L, Sweet Kevin, Frankel Wendy L, Aronson Melyssa, Gallinger Steve, Goldblatt Jack, Woodall Sonja, Arnold Julie, Walker Neal I, Jass Jeremy R, Parry Susan, Young Joanne |
Cardiovascular manifestations in men and women carrying a FBN1 mutation. European heart journal 2010 Sep 31 (18): 2223-9. Détaint Delphine, Faivre Laurence, Collod-Beroud Gwenaelle, Child Anne H, Loeys Bart L, Binquet Christine, Gautier Elodie, Arbustini Eloisa, Mayer Karin, Arslan-Kirchner Mine, Stheneur Chantal, Halliday Dorothy, Beroud Christophe, Bonithon-Kopp Claire, Claustres Mireille, Plauchu Henri, Robinson Peter N, Kiotsekoglou Anatoli, De Backer Julie, Adès Lesley, Francke Uta, De Paepe Anne, Boileau Catherine, Jondeau Guillau |
Role of haptoglobin in polycystic ovary syndrome (PCOS), obesity and disorders of glucose tolerance in premenopausal women. PloS one 2009 4 (5): e5606. Alvarez-Blasco Francisco, Martínez-García Ma Angeles, Luque-Ramírez Manuel, Parraza Naiara, San Millán José L, Escobar-Morreale Héctor |
Helicobacter pylori infection and autoimmune thyroid disease in young patients: the disadvantage of carrying the human leukocyte antigen-DRB1*0301 allele. The Journal of clinical endocrinology and metabolism 2006 Jan 91 (1): 176-9. Larizza Daniela, Calcaterra Valeria, Martinetti Miryam, Negrini Riccardo, De Silvestri Annalisa, Cisternino Mariangela, Iannone A M, Solcia Enri |
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