Bertold Schrank
Publications by Year
Research Areas
Neurogenetic and Muscular Disorders Research, Amyotrophic Lateral Sclerosis Research, Muscle Physiology and Disorders, RNA modifications and cancer, Hereditary Neurological Disorders
Most-Cited Works
- → Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism(1992)717 cited
- → Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos(1997)657 cited
- → A genetic mapping system in Caenorhabditis elegans based on polymorphic sequence-tagged sites.(1992)500 cited
- → Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome(2009)306 cited
- → High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study(2004)188 cited
- → Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease(1997)173 cited
- → Effect of High‐Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis(2019)160 cited
- → Interaction Between a Putative Mechanosensory Membrane Channel and a Collagen(1996)148 cited
- → A Randomized, Double Blind, Placebo-Controlled Trial of Pioglitazone in Combination with Riluzole in Amyotrophic Lateral Sclerosis(2012)146 cited
- → Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial(2013)102 cited