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You searched for: Author/Creator Alber, Michael

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1. ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. (June 2017)

4. Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany. (10th August 2021)

6. Influence of the slurry-stabilized tunnel face on shield TBM tool wear regarding the soil mechanical changes – Experimental evidence of changes in the tribological system. (April 2018)

8. KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect. Issue 5 (8th November 2018)

9. Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. Issue 6 (12th June 2012)