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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2024. (Total: 233962Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Amyotrophic Lateral Sclerosis and CHGB[original query]
Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
Proceedings of the National Academy of Sciences of the United States of America 2009 Dec 106 (51): 21777-82.
Gros-Louis Francois, Andersen Peter M, Dupre Nicolas, Urushitani Makoto, Dion Patrick, Souchon Frederique, D'Amour Monique, Camu William, Meininger Vincent, Bouchard Jean-Pierre, Rouleau Guy A, Julien Jean-Pier
The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2011 May 12 (3): 210-4.
Blasco Hélène, Corcia Philippe, Veyrat-Durebex Charlotte, Coutadeur Cathleen, Fournier Clémentine, Camu William, Gordon Paul, Praline Julien, Andres Christian R, Vourc'h Patrick,
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort.
Gene 2015 Sep 568 (2): 186-9.
Claudia Ricci, Stefania Battistini, Francesca Avemaria, Michele Benigni, Claudia Tarlarini, Fabio Giannini, Massimo Corbo, Christian Lunetta, Silvana Pen
Genetic Modifiers of ALS: The Impact of Chromogranin B P413L in a Bulgarian ALS Cohort.
Genes 2024 9 15 (9): .
Ivan Tourtourikov, Tihomir Todorov, Teodor Angelov, Teodora Chamova, Ivailo Tournev, Vanyo Mitev, Albena Todoro
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