Rowland LP - Search Results

1

Closing the tau loop: the missing tau mutation.

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, Spillantini MG, Rowland LP, Fahn S, Craig P, Hutton M, Lynch T. McCarthy A, et al. Among authors: rowland lp. Brain. 2015 Oct;138(Pt 10):3100-9. doi: 10.1093/brain/awv234. Epub 2015 Aug 21. Brain. 2015. PMID: 26297556 Free PMC article.

2

Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants.

Williams L, Olszewska DA, Fearon C, Magennis B, McCarthy A, Rowland LP, Mayeux R, Page R, Fahn S, Beausang A, Lynch T. Williams L, et al. Among authors: rowland lp. Mov Disord Clin Pract. 2021 Jun 24;8(6):954-958. doi: 10.1002/mdc3.13265. eCollection 2021 Aug. Mov Disord Clin Pract. 2021. PMID: 34405105 Free PMC article.

3

A new eponym: Wilhelmsen-Lynch disease.

Fahn S, Mayeux R, Rowland LP. Fahn S, et al. Among authors: rowland lp. Neurology. 1994 Oct;44(10):1980. doi: 10.1212/wnl.44.10.1980. Neurology. 1994. PMID: 7936262 No abstract available.

4

Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes.

Gilbert RM, Fahn S, Mitsumoto H, Rowland LP. Gilbert RM, et al. Among authors: rowland lp. Mov Disord. 2010 Sep 15;25(12):1868-75. doi: 10.1002/mds.23200. Mov Disord. 2010. PMID: 20669307

5

MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.

ROWLAND LP, FAHN S, SCHOTLAND DL. ROWLAND LP, et al. Arch Neurol. 1963 Oct;9:325-42. doi: 10.1001/archneur.1963.00460100013001. Arch Neurol. 1963. PMID: 14055781 No abstract available.

6

Normal pressure hydrocephalus and hypertensive cerebrovascular disease.

Earnest MP, Fahn S, Karp JH, Rowland LP. Earnest MP, et al. Among authors: rowland lp. Arch Neurol. 1974 Oct;31(4):262-6. doi: 10.1001/archneur.1974.00490400076009. Arch Neurol. 1974. PMID: 4414845 No abstract available.

7

Premorbid weight, body mass, and varsity athletics in ALS.

Scarmeas N, Shih T, Stern Y, Ottman R, Rowland LP. Scarmeas N, et al. Among authors: rowland lp. Neurology. 2002 Sep 10;59(5):773-5. doi: 10.1212/wnl.59.5.773. Neurology. 2002. PMID: 12221178

8

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.

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. Wilhelmsen KC, et al. Among authors: rowland lp. Ann Neurol. 1996 Apr;39(4):507-20. doi: 10.1002/ana.410390413. Ann Neurol. 1996. PMID: 8619529 Review.

9

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.

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. Lynch T, et al. Among authors: rowland lp. Neurology. 2001 Nov;57(10 Suppl 3):S39-45. Neurology. 2001. PMID: 11775599 No abstract available.

10

Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility.

Majoor-Krakauer D, Ottman R, Johnson WG, Rowland LP. Majoor-Krakauer D, et al. Among authors: rowland lp. Neurology. 1994 Oct;44(10):1872-7. doi: 10.1212/wnl.44.10.1872. Neurology. 1994. PMID: 7936240

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