Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Sclerosis and HFE[original query] |
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Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences. Journal of the neurological sciences 2004 Dec 227 (1): 27-33. Wang Xin-Sheng, Lee Sang, Simmons Zachary, Boyer Philip, Scott Kevin, Liu Wenlei, Connor Jam |
Mutations in the hemochromatosis gene (HFE) and multiple sclerosis. Neuroscience letters 2005 Aug 383 (3): 301-4. Risti? Smiljana, Lovreci? Luca, Brajenovi?-Mili? Bojana, Starcevi?-Cizmarevi? Nada, Jazbec Sasa Sega, Sepci? Juraj, Kapovi? Miljenko, Peterlin Bor |
HFE H63D polymorphism is increased in patients with amyotrophic lateral sclerosis of Italian origin. Journal of neurology, neurosurgery, and psychiatry 2007 Mar 78 (3): 327. Restagno G, Lombardo F, Ghiglione P, Calvo A, Cocco E, Sbaiz L, Mutani R, Chiò |
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy. Genes and immunity 2008 Jan 9 (1): 7-15. D'Alfonso S, Bolognesi E, Guerini F R, Barizzone N, Bocca S, Ferrante D, Castelli L, Bergamaschi L, Agliardi C, Ferrante P, Naldi P, Leone M, Caputo D, Ballerini C, Salvetti M, Galimberti D, Massacesi L, Trojano M, Momigliano-Richiardi |
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population. Archives of neurology 2007 Jan 64 (1): 63-7. Sutedja Nadia A, Sinke Richard J, Van Vught Paul W J, Van der Linden Michiel W, Wokke John H J, Van Duijn Cornelia M, Njajou Omer T, Van der Schouw Yvonne T, Veldink Jan H, Van den Berg Leonard |
Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis. Journal of neuroimmunology 2008 Oct 203 (1): 104-7. Ramagopalan Sreeram V, Cukjati Marko, Cernilec Maja, DeLuca Gabriele C, Dyment David A, Degenhardt Alexandra, Sadovnick A Dessa, Serbec Vladka Curin, Ebers George C, Duquette Pier |
HFE gene mutations in a population of Italian Parkinson's disease patients. Parkinsonism & related disorders 2008 14 (5): 426-30. Biasiotto Giorgio, Goldwurm Stefano, Finazzi Dario, Tunesi Sara, Zecchinelli Anna, Sironi Francesca, Pezzoli Gianni, Arosio Pao |
H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China. European journal of neurology : the official journal of the European Federation of Neurological Societies 2011 Feb 18 (2): 359-61. He X, Lu X, Hu J, Xi J, Zhou D, Shang H, Liu L, Zhou H, Yan B, Yu L, Hu F, Liu Z, He L, Yao X, Xu |
HFE gene polymorphisms and severity in Portuguese patients with multiple sclerosis. European journal of neurology : the official journal of the European Federation of Neurological Societies 2011 Apr 18 (4): 663-6. Bettencourt A, Silva A M, Santos E, Gomes S, Mendonça D, Costa P P, Faustino P, Silva B |
Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis. BMC medical genetics 2012 13 (1): 70. Gemmati Donato, Zeri Giulia, Orioli Elisa, De Gaetano Francesca E, Salvi Fabrizio, Bartolomei Ilaria, D'Alfonso Sandra, Dall'osso Claudia, Leone Maurizio A, Singh Ajay V, Asselta Rosanna, Zamboni Pao |
Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis. Journal of the neurological sciences 2012 Jun 317 (1-2): 58-61. Praline Julien, Blasco Hélène, Vourc'h Patrick, Rat Valérian, Gendrot Chantal, Camu William, Andres Christian R, |
Molecular genetic studies of multiple sclerosis in the portuguese population. Acta médica portuguesa 2012 Jul 25 (4): 4. Bettencourt A, Martins da Silva A, Pinho E Costa P, Martins Silva B |
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis. Neurobiology of aging 2013 May 34 (5): 1517.e5-7. van Rheenen Wouter, Diekstra Frank P, van Doormaal Perry T C, Seelen Meinie, Kenna Kevin, McLaughlin Russell, Shatunov Aleksey, Czell David, van Es Michael A, van Vught Paul W J, van Damme Philip, Smith Bradley N, Waibel Stefan, Schelhaas H Jurgen, van der Kooi Anneke J, de Visser Marianne, Weber Markus, Robberecht Wim, Hardiman Orla, Shaw Pamela J, Shaw Christopher E, Morrison Karen E, Al-Chalabi Ammar, Andersen Peter M, Ludolph Albert C, Veldink Jan H, van den Berg Leonard |
HFE p.H63D polymorphism does not influence ALS phenotype and survival. Neurobiology of aging 2015 Oct 36 (10): 2906.e7-2906.e11. Chiò Adriano, Mora Gabriele, Sabatelli Mario, Caponnetto Claudia, Lunetta Christian, Traynor Bryan J, Johnson Janel O, Nalls Mike A, Calvo Andrea, Moglia Cristina, Borghero Giuseppe, Monsurrò Maria Rosaria, La Bella Vincenzo, Volanti Paolo, Simone Isabella, Salvi Fabrizio, Logullo Francesco O, Nilo Riva, Giannini Fabio, Mandrioli Jessica, Tanel Raffaella, Murru Maria Rita, Mandich Paola, Zollino Marcella, Conforti Francesca L, Penco Silvana, , , Brunetti Maura, Barberis Marco, Restagno Gabriel |
Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway? Neuro-degenerative diseases 2015 Nov . Gazzina Stefano, Premi Enrico, Zanella Isabella, Biasiotto Giorgio, Archetti Silvana, Cosseddu Maura, Scarpini Elio, Galimberti Daniela, Serpente Maria, Gasparotti Roberto, Padovani Alessandro, Borroni Barba |
Iron-related gene variants and brain iron in multiple sclerosis and healthy individuals. NeuroImage. Clinical 2018 17 530-540. Hagemeier Jesper, Ramanathan Murali, Schweser Ferdinand, Dwyer Michael G, Lin Fuchun, Bergsland Niels, Weinstock-Guttman Bianca, Zivadinov Robe |
H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population. Journal of integrative neuroscience 2020 10 19 (3): 495-499. Zhang Qing-Qing, Jiang Hong, Li Chun-Yan, Liu Ya-Ling, Tian Xin-Yi |
Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis. Biomedical reports 2022 1 16 (2): 12. Star?evi? ?izmarevi? Nada, ?urko-Cofek Božena, Barac-Latas Vesna, Peterlin Borut, Risti? Smilja |
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