McMonagle P - Search Results

1

Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities.

O'Riordan S, McMonagle P, Janssen JC, Fox NC, Farrell M, Collinge J, Rossor MN, Hutchinson M. O'Riordan S, et al. Among authors: mcmonagle p. Neurology. 2002 Oct 8;59(7):1108-10. doi: 10.1212/wnl.59.7.1108. Neurology. 2002. PMID: 12370477

2

Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.

Byrne PC, Mc Monagle P, Webb S, Fitzgerald B, Parfrey NA, Hutchinson M. Byrne PC, et al. Neurology. 2000 Apr 11;54(7):1510-7. doi: 10.1212/wnl.54.7.1510. Neurology. 2000. PMID: 10751268

3

Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.

McMonagle P, Byrne PC, Fitzgerald B, Webb S, Parfrey NA, Hutchinson M. McMonagle P, et al. Neurology. 2000 Dec 26;55(12):1794-800. doi: 10.1212/wnl.55.12.1794. Neurology. 2000. PMID: 11134375

4

The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.

McMonagle P, Webb S, Hutchinson M. McMonagle P, et al. J Neurol Neurosurg Psychiatry. 2002 Jan;72(1):43-6. doi: 10.1136/jnnp.72.1.43. J Neurol Neurosurg Psychiatry. 2002. PMID: 11784824 Free PMC article.

5

Hereditary spastic paraparesis and psychosis.

McMonagle P, Hutchinson M, Lawlor B. McMonagle P, et al. Eur J Neurol. 2006 Aug;13(8):874-9. doi: 10.1111/j.1468-1331.2006.01379.x. Eur J Neurol. 2006. PMID: 16879299

6

Dementia in SPG4 hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence.

Murphy S, Gorman G, Beetz C, Byrne P, Dytko M, McMonagle P, Kinsella K, Farrell M, Hutchinson M. Murphy S, et al. Among authors: mcmonagle p. Neurology. 2009 Aug 4;73(5):378-84. doi: 10.1212/WNL.0b013e3181b04c6c. Neurology. 2009. PMID: 19652142

7

Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.

Mc Monagle P, Byrne P, Burke T, Parfrey N, Hutchinson M. Mc Monagle P, et al. Neurology. 2001 Jan 9;56(1):139. doi: 10.1212/wnl.56.1.139. Neurology. 2001. PMID: 11148263 No abstract available.

8

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.

Hughes CA, Byrne PC, Webb S, McMonagle P, Patterson V, Hutchinson M, Parfrey NA. Hughes CA, et al. Among authors: mcmonagle p. Neurology. 2001 May 8;56(9):1230-3. doi: 10.1212/wnl.56.9.1230. Neurology. 2001. PMID: 11342696

9

Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.

McMonagle P, Byrne P, Hutchinson M. McMonagle P, et al. Neurology. 2004 Feb 10;62(3):407-10. doi: 10.1212/01.wnl.0000108629.04434.05. Neurology. 2004. PMID: 14872021

10

Clinical and genetic characterization of leukoencephalopathies in adults.

Lynch DS, Rodrigues Brandão de Paiva A, Zhang WJ, Bugiardini E, Freua F, Tavares Lucato L, Macedo-Souza LI, Lakshmanan R, Kinsella JA, Merwick A, Rossor AM, Bajaj N, Herron B, McMonagle P, Morrison PJ, Hughes D, Pittman A, Laurà M, Reilly MM, Warren JD, Mummery CJ, Schott JM, Adams M, Fox NC, Murphy E, Davagnanam I, Kok F, Chataway J, Houlden H. Lynch DS, et al. Among authors: mcmonagle p. Brain. 2017 May 1;140(5):1204-1211. doi: 10.1093/brain/awx045. Brain. 2017. PMID: 28334938 Free PMC article.

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