Mc Monagle P - Search Results

1

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.

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. Among authors: mc monagle p. Neurology. 2000 Apr 11;54(7):1510-7. doi: 10.1212/wnl.54.7.1510. Neurology. 2000. PMID: 10751268

3

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

4

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. Neurology. 2009 Aug 4;73(5):378-84. doi: 10.1212/WNL.0b013e3181b04c6c. Neurology. 2009. PMID: 19652142

5

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

6

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

7

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. Neurology. 2001 May 8;56(9):1230-3. doi: 10.1212/wnl.56.9.1230. Neurology. 2001. PMID: 11342696

8

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.

9

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. Neurology. 2002 Oct 8;59(7):1108-10. doi: 10.1212/wnl.59.7.1108. Neurology. 2002. PMID: 12370477

10

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

Fonknechten N, Mavel D, Byrne P, Davoine CS, Cruaud C, Bönsch D, Samson D, Coutinho P, Hutchinson M, McMonagle P, Burgunder JM, Tartaglione A, Heinzlef O, Feki I, Deufel T, Parfrey N, Brice A, Fontaine B, Prud'homme JF, Weissenbach J, Dürr A, Hazan J. Fonknechten N, et al. Hum Mol Genet. 2000 Mar 1;9(4):637-44. doi: 10.1093/hmg/9.4.637. Hum Mol Genet. 2000. PMID: 10699187

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