Marion Stoll
The University of Sydney(AU)Concord Repatriation General Hospital(AU)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, Genetic Neurodegenerative Diseases, Endoplasmic Reticulum Stress and Disease
Most-Cited Works
- → Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia(2015)103 cited
- → Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation inC19orf12(2013)92 cited
- → Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasia(2016)42 cited
- → RFC1 expansions can mimic hereditary sensory neuropathy with cough and Sjögren syndrome(2020)31 cited
- → The REVLIRIT CLL5 AGMT Study - a Phase I/II Trial Combining Fludarabine/Rituximab with Escalating Doses of Lenalidomide Followed by Rituximab/Lenalidomide in Untreated Chronic Lymphocytic Leukemia (CLL): Results of a Planned Interim Analysis.(2009)24 cited
- → Re‐evaluation of phytohormone‐independent division of tobacco protoplast‐derived cells(1999)21 cited
- → Spatial heterogeneity of myocardial perfusion predicts local potassium channel expression and action potential duration(2007)19 cited
- → Seasonal changes in blood cells of Arctic char (Salvelinus alpinus L.) from a high mountain lake(2000)19 cited
- → Bone health in facioscapulohumeral muscular dystrophy: A cross‐sectional study(2017)16 cited
- → Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy(2021)11 cited