Lewis P. Rowland - Publications

Affiliations: 
Columbia University College of Physicians and Surgeons, New York, NY, United States 
Area:
neuromuscular disease, scientist's role

43 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Williams L, Olszewska DA, Fearon C, Magennis B, McCarthy A, Rowland LP, Mayeux R, Page R, Fahn S, Beausang A, Lynch T. Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants. Movement Disorders Clinical Practice. 8: 954-958. PMID 34405105 DOI: 10.1002/mdc3.13265  0.641
2015 McCarthy A, Lonergan R, Olszewska DA, O'Dowd S, Cummins G, Magennis B, Fallon EM, Pender N, Huey ED, Cosentino S, O'Rourke K, Kelly BD, O'Connell M, Delon I, Farrell M, ... ... Rowland LP, et al. Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology. PMID 26297556 DOI: 10.1093/Brain/Awv234  0.599
2011 Hirano M, Quinzii CM, Mitsumoto H, Hays AP, Roberts JK, Richard P, Rowland LP. 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. PMID 21190393 DOI: 10.3109/17482968.2010.545952  0.304
2011 Traub R, Mitsumoto H, Rowland LP. Research advances in amyotrophic lateral sclerosis, 2009 to 2010. Current Neurology and Neuroscience Reports. 11: 67-77. PMID 21080240 DOI: 10.1007/s11910-010-0160-0  0.304
2010 Gilbert RM, Fahn S, Mitsumoto H, Rowland LP. Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 1868-75. PMID 20669307 DOI: 10.1002/mds.23200  0.585
2008 Rowland LP, Bird TD. Silver syndrome: The complexity of complicated hereditary spastic paraplegia. Neurology. 70: 1948-9. PMID 18490616 DOI: 10.1212/01.Wnl.0000312519.62351.5B  0.303
2008 Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, et al. 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. PMID 18179901 DOI: 10.1016/J.Ajhg.2007.09.013  0.301
2003 Rosenberg RN, Pedley TA, Baringer JR, Fahn S, Lisak RP, Mayeux RP, Olson SF, Ringel SP, Rowland LP, Selzer ME. At jeopardy: the NIH as we know it. Neurorehabilitation and Neural Repair. 17: 203-5. PMID 14677215 DOI: 10.1177/0888439003259700  0.678
2003 Rosenberg RN, Pedley TA, Baringer JR, Fahn S, Lisak RP, Mayeux RP, Olson SF, Ringel SP, Rowland LP, Selzer ME. At jeopardy: the NIH as we know it. Archives of Neurology. 60: 1191-2. PMID 12975281 DOI: 10.1001/archneur.60.9.1191  0.678
2001 Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994. Neurology. 57: S39-45. PMID 11775599  0.634
2001 Dabby R, Lange DJ, Trojaborg W, Hays AP, Lovelace RE, Brannagan TH, Rowland LP. Inclusion body myositis mimicking motor neuron disease. Archives of Neurology. 58: 1253-6. PMID 11493165 DOI: 10.1001/Archneur.58.8.1253  0.32
2000 Worrall BB, Rowland LP, Chin SS, Mastrianni JA. Amyotrophy in prion diseases. Archives of Neurology. 57: 33-8. PMID 10634430 DOI: 10.1001/Archneur.57.1.33  0.336
1999 Worrall BB, Rowland LP, Del Bene M, Leung D, Chin SS. Mother with amyotrophic lateral sclerosis and daughter with Creutzfeldt-Jakob disease. Archives of Neurology. 56: 1502-4. PMID 10593306 DOI: 10.1001/Archneur.56.12.1502  0.345
1996 Earnest MP, Norris JM, Eberhardt MS, Sands GH, Adams D, Brust JC, Garver CM, Helgason CM, Marotta JT, Messing RO, Rowland LP, Sanchez-Ramos JR, Sands G, Snodgrass SR, Ziegler DK, et al. Report of the AAN Task Force on access to health care: The effect of no personal health insurance on health care for people with neurologic disorders Neurology. 46: 1471-1480. PMID 8628506 DOI: 10.1212/Wnl.46.5.1471  0.466
1996 Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39: 507-20. PMID 8619529 DOI: 10.1002/Ana.410390413  0.462
1994 Fahn S, Mayeux R, Rowland LP. A new eponym: Wilhelmsen-Lynch disease. Neurology. 44: 1980. PMID 7936262 DOI: 10.1212/WNL.44.10.1980  0.61
1992 Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, Martinuzzi A, Mosewich R, Servidei S, Zammarchi E, Bonilla E, ... ... Rowland LP, et al. MELAS: Clinical features, biochemistry, and molecular genetics Annals of Neurology. 31: 391-398. PMID 1586140 DOI: 10.1002/Ana.410310408  0.555
1992 Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP. Melas: an original case and clinical criteria for diagnosis. Neuromuscular Disorders : Nmd. 2: 125-35. PMID 1422200 DOI: 10.1016/0960-8966(92)90045-8  0.559
1992 Rowland LP. Amyotrophic lateral sclerosis and autoimmunity. The New England Journal of Medicine. 327: 1752-3. PMID 1331792 DOI: 10.1056/NEJM199212103272411  0.3
1991 Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Clinical syndromes associated with ragged red fibers. Revue Neurologique. 147: 467-73. PMID 1962052  0.567
1989 Rowland LP. Life before MEDLINE: myasthenia gravis, muscular dystrophy, and myasthenic myopathy. Archives of Neurology. 46: 1047-8. PMID 2679505 DOI: 10.1001/archneur.1989.00520460021006  0.315
1988 Younger DS, Hays AP, Brust JC, Rowland LP. Granulomatous angiitis of the brain. An inflammatory reaction of diverse etiology. Archives of Neurology. 45: 514-8. PMID 3358703 DOI: 10.1001/Archneur.1988.00520290042012  0.544
1985 Pedley TA, Emerson RG, Warner CL, Rowland LP, Salen G. Treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid. Annals of Neurology. 18: 517-8. PMID 4073846 DOI: 10.1002/ana.410180418  0.489
1984 Rowland LP. Looking for the cause of amyotrophic lateral sclerosis. The New England Journal of Medicine. 311: 979-81. PMID 6472424 DOI: 10.1056/NEJM198410113111509  0.327
1983 Kety SS, Rowland LP, Sidman RL, Matthysse SW, Hicks SP. Genetics of Neurological and Psychiatric Disorders. Association for Research in Nervous and Mental Diseases, Volume 60 Journal of Neuropathology and Experimental Neurology. 42: 721. DOI: 10.1097/00005072-198311000-00011  0.522
1980 Rowland LP. 'Ophthalmoplegia plus' or Kearns-Sayre syndrome? Archives of Neurology. 37: 256. PMID 7362499 DOI: 10.1001/Archneur.1980.00500530094031  0.321
1979 Miranda A, DiMauro S, Eastwood A, Hays A, Johnson WG, Olarte M, Whitlock R, Mayeux R, Rowland LP. Lipid storage myopathy, ichthyosis, and steatorrhea. Muscle & Nerve. 2: 1-13. PMID 545139 DOI: 10.1002/Mus.880020102  0.319
1974 Rowland LP, Berenberg RA. Letter: Diagnosis of Leigh's disease questioned, defended. Neurology. 24: 598-9. PMID 4857555 DOI: 10.1212/WNL.24.6.598  0.304
1974 Boothby JA, DeJesus PV, Rowland LP. Reversible forms of motor neuron disease. Lead "neuritis". Archives of Neurology. 31: 18-23. PMID 4834538 DOI: 10.1001/Archneur.1974.00490370044005  0.307
1974 Earnest MP, Fahn S, Karp JH, Rowland LP. Normal pressure hydrocephalus and hypertensive cerebrovascular disease. Archives of Neurology. 31: 262-6. PMID 4414845 DOI: 10.1001/Archneur.1974.00490400076009  0.564
1968 Rowland LP, Layzer RB, Kagen LJ. Lack of some muscle proteins in serum of patients with Duchenne dystrophy. Archives of Neurology. 18: 272-6. PMID 4230622 DOI: 10.1001/Archneur.1968.00470330062006  0.3
1968 Rosenberg RN, Schotland DL, Lovelace RE, Rowland LP. Progressive ophthalmoplegia. Report of cases. Archives of Neurology. 19: 362-76. PMID 4175668 DOI: 10.1001/archneur.1968.00480040028002  0.336
1967 Rowland LP. Current Concepts of Myopathies. Archives of Neurology. 16: 337-338. DOI: 10.1001/ARCHNEUR.1967.00470210113014  0.312
1966 Rowland LP. Treatment of Neuromuscular Disorders Jama Neurology. 15: 112-112. DOI: 10.1001/Archneur.1966.00470130116021  0.302
1965 Schotland DL, Spiro D, Rowland LP, Carmel P. Ultrastructural studies of muscle in McArdle's disease. Journal of Neuropathology and Experimental Neurology. 24: 629-44. PMID 5213729 DOI: 10.1097/00005072-196510000-00006  0.317
1965 Rowland LP. Ciba Foundation Symposium: Control of Glycogen Metabolism. Archives of Neurology. 13: 332-332. DOI: 10.1001/archneur.1965.00470030112014  0.325
1964 ROWLAND LP, FAHN S, HIRSCHBERG E, HARTER DH. MYOGLOBINURIA. Archives of Neurology. 10: 537-62. PMID 14130414  0.476
1964 SCHOTLAND DL, ROWLAND LP. MUSCULAR DYSTROPHY. FEATURES OF OCULAR MYOPATHY, DISTAL MYOPATHY, AND MYOTONIC DYSTROPHY. Archives of Neurology. 10: 433-45. PMID 14120634 DOI: 10.1001/archneur.1964.00460170003001  0.327
1963 FAHN S, SCHOTLAND DL, ROWLAND LP. MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. Transactions of the American Neurological Association. 88: 145-7. PMID 14272202  0.536
1963 ROWLAND LP, FAHN S, SCHOTLAND DL. MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. Archives of Neurology. 9: 325-42. PMID 14055781 DOI: 10.1001/archneur.1963.00460100013001  0.592
1963 Rowland LP. Muscular Dystrophy in Man and Animals. Archives of Neurology. 9: 445-446. DOI: 10.1001/archneur.1963.00460100133018  0.34
1963 Schwartz JF, Rowland LP, Eder H, Marks PA, Osserman EF, Hirschberg E, Anderson H. Bassen-Kornzweig Syndrome: Deficiency of Serum β-Lipoprotein: A Neuromuscular Disorder Resembling Friedreich's Ataxia, Associated with Steatorrhea, Acanthocytosis, Retinitis Pigmentosa, and a Disorder of Lipid Metabolism Archives of Neurology. 8: 438-454. DOI: 10.1001/archneur.1963.00460040108010  0.303
1956 ROWLAND LP, HOEFER PF, ARANOW H, MERRITT HH. Fatalities in myasthenia gravis; a review of 39 cases with 26 autopsies. Neurology. 6: 307-26. PMID 13309613 DOI: 10.1212/Wnl.6.5.307  0.513
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