Lewis P. Rowland
Affiliations: | Columbia University College of Physicians and Surgeons, New York, NY, United States |
Area:
neuromuscular disease, scientist's roleGoogle:
"Lewis Rowland"Bio:
Mean distance: 13.48 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentor| Seymour S. Kety | post-doc | NIMH | |
| H. Houston Merritt | post-doc | Columbia University Medical School |
Children
Sign in to add trainee| A M. Barrett | grad student | 1992-1995 | Columbia University Medical School |
| Christopher Todd Anderson | grad student | 2003-2006 | Columbia University Medical School |
| Michael M. Segal | post-doc | 1984-1985 | Columbia University Medical School |
| Tim Lynch | post-doc | 1990 | Columbia University Medical School |
Collaborators
Sign in to add collaborator| Stanley Fahn | collaborator | Columbia University Medical School |
BETA: Related publications
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Publications
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| Williams L, Olszewska DA, Fearon C, et al. (2021) Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants. Movement Disorders Clinical Practice. 8: 954-958 |
| McCarthy A, Lonergan R, Olszewska DA, et al. (2015) Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology |
| Hirano M, Quinzii CM, Mitsumoto H, et al. (2011) Senataxin mutations and amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 12: 223-7 |
| Traub R, Mitsumoto H, Rowland LP. (2011) Research advances in amyotrophic lateral sclerosis, 2009 to 2010. Current Neurology and Neuroscience Reports. 11: 67-77 |
| Gilbert RM, Fahn S, Mitsumoto H, et al. (2010) Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 1868-75 |
| Rowland LP, Bird TD. (2008) Silver syndrome: The complexity of complicated hereditary spastic paraplegia. Neurology. 70: 1948-9 |
| Quinzii CM, Vu TH, Min KC, et al. (2008) X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American Journal of Human Genetics. 82: 208-13 |
| Rosenberg RN, Pedley TA, Baringer JR, et al. (2003) At jeopardy: the NIH as we know it. Neurorehabilitation and Neural Repair. 17: 203-5 |
| Rosenberg RN, Pedley TA, Baringer JR, et al. (2003) At jeopardy: the NIH as we know it. Archives of Neurology. 60: 1191-2 |
| Lynch T, Sano M, Marder KS, et al. (2001) Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994. Neurology. 57: S39-45 |