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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2023. (Total: 223516Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Sarcoma and SOD1[original query]
The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 May 17 (5): 754-6.
Damme P Van, Goris A, Race V, Hersmus N, Dubois B, Bosch L Van Den, Matthijs G, Robberecht
Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis.
Muscle & nerve 2010 Aug 42 (2): 170-6.
Rademakers Rosa, Stewart Heather, Dejesus-Hernandez Mariely, Krieger Charles, Graff-Radford Neill, Fabros Marife, Briemberg Hannah, Cashman Neil, Eisen Andrew, Mackenzie Ian R
Genetic overlap between apparently sporadic motor neuron diseases.
PloS one 2012 7 (11): 11.
van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH
De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
Neurobiology of aging 2015 Aug .
Hübers Annemarie, Just Walter, Rosenbohm Angela, Müller Kathrin, Marroquin Nicolai, Goebel Ingrid, Högel Josef, Thiele Holger, Altmüller Janine, Nürnberg Peter, Weishaupt Jochen H, Kubisch Christian, Ludolph Albert C, Volk Alexander
Somatosensory pathway dysfunction in patients with amyotrophic lateral sclerosis in a completely locked-in state.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2023 10 .
Toshio Shimizu, Yuki Nakayama, Kentaro Hayashi, Yoko Mochizuki, Chiharu Matsuda, Michiko Haraguchi, Kota Bokuda, Takashi Komori, Kazushi Takahas
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