| 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 |
0.639 |
|
| 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 |
0.598 |
|
| 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 |
0.305 |
|
| 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 |
0.584 |
|
| 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 |
0.677 |
|
| 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 |
0.677 |
|
| 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 |
0.632 |
|
| 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 |
0.461 |
|
| 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 |
0.608 |
|
| 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 |
0.328 |
|
| 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 |
0.315 |
|
| 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 |
0.301 |
|
| 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 |
0.475 |
|
| 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 |
0.591 |
|
| 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 |
0.474 |
|
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