Marion Stoll

Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia

Marie Coutelier, Cyril Goizet, Alexandra Dürr et al. · Brain · 2015 · 103 citations · Full text

Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in<i>C19orf12</i>

Guida Landouré, Peng-Peng Zhu, Charles Marques Lourenço et al. · Human Mutation · 2013 · 91 citations · Full text

Biology, Rare Diseases, Neurodegenerative Diseases +15

Novel motor phenotypes in patients with <i>VRK1</i> mutations without pontocerebellar hypoplasia

Marion Stoll, Hooi‐Ling Teoh, James Lee et al. · Neurology · 2016 · 41 citations · Full text

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.

Alexander Egle, Michael Steurer, Thomas Melchardt et al. · Blood · 2009 · 24 citations

Re‐evaluation of phytohormone‐independent division of tobacco protoplast‐derived cells

Jeff Schell, Ton Bisseling, Marion Dülz et al. · The Plant Journal · 1999 · 20 citations

Engineering, Botany, Genetics +17