Lachmann, Robin H.
University College Hospital
5 papers on CoChatORCID 0000-0002-2618-2581
Most cited papers
- Verified
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson’s disease
Neumann, J., Bras, J., Deas, E., O'Sullivan, S. S., Parkkinen, L., Lachmann, R. H., Li, A., Holton, J., Guerreiro, R., Paudel, R., et al. (2009) · Brain
Lysosomal Storage Disorders ResearchParkinson's Disease Mechanisms and Treatments
Cited by 696
- Verified
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy
Engelen, M., van Ballegoij, W. J. C., Mallack, E. J., Van Haren, K. P., Köhler, W., Salsano, E., van Trotsenburg, A. S. P., Mochel, F., Sevin, C., Regelmann, M. O., et al. (2022) · Neurology
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 156
- Verified
Herpes simplex virus‐based vectors
Lachmann, R. (2004) · International Journal of Experimental Pathology
Virus-based gene therapy researchHerpesvirus Infections and Treatments
Cited by 76
- Verified
Safety and efficacy of leriglitazone for preventing disease progression in men with adrenomyeloneuropathy (ADVANCE): A randomised, double-blind, multi-centre, placebo-controlled phase 2-3 trial
Köhler, W., Engelen, M., Eichler, F., Lachmann, R., Fatemi, A., Sampson, J., Salsano, E., Gamez, J., Molnar, M. J., Pascual, S., et al. (2023) · The Lancet Neurology
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 48
- Verified
Bladder and Bowel Dysfunction Is Common in Both Men and Women with Mutation of the ABCD1 Gene for X-Linked Adrenoleukodystrophy
Hofereiter, J., Smith, M. D., Seth, J., Tudor, K. I., Fox, Z., Emmanuel, A., Murphy, E., Lachmann, R. H., & Panicker, J. (2015) · JIMD Reports
Urinary Bladder and Prostate ResearchMetabolism and Genetic Disorders
Cited by 18
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