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Hypokalemic Periodic Paralysis Induced by Thymic Hyperplasia and Relieved by Thymectomy
Yang, Renrong et al. (2013)
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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation
Fan, Chunxiang et al. (2013)
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Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals
Charles, G. et al. (2013)
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Engulfment adaptor phosphotyrosine-binding-domain-containing 1 (GULP1) is a nucleocytoplasmic shuttling protein and is transactivationally active together with low-density lipoprotein receptor-related protein 1 (LRP1)
Wahler, Anke et al. (2013)
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ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation
Sarkozy, Anna et al. (2013)
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Diffusion Tensor Magnetic Resonance Imaging of the Brain in APP Transgenic Mice: A Cohort Study
Mueller, Hans-Peter et al. (2013)
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A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Weishaupt, Jochen H. et al. (2013)
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Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia
Nagel, Gabriele et al. (2013)
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The Nedd4-binding protein 3 (N4BP3) is crucial for axonal and dendritic branching in developing neurons
Schmeisser, Michael J. et al. (2013)
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Developmental and Functional Nature of Human iPSC Derived Motoneurons
Stockmann, Marianne et al. (2013)
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