Crook R - Search Results

1

Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke.

Meschia JF, Brott TG, Brown RD Jr, Crook R, Worrall BB, Kissela B, Brown WM, Rich SS, Case LD, Evans EW, Hague S, Singleton A, Hardy J; SWISS Study Group; ISGS Study Group; MSGD Study Group. Meschia JF, et al. Among authors: crook r. Ann Neurol. 2005 Sep;58(3):351-61. doi: 10.1002/ana.20585. Ann Neurol. 2005. PMID: 16130105 Free PMC article.

2

The Ischemic Stroke Genetics Study (ISGS) Protocol.

Meschia JF, Brott TG, Brown RD Jr, Crook RJ, Frankel M, Hardy J, Merino JG, Rich SS, Silliman S, Worrall BB; Ischemic Stroke Genetics Study. Meschia JF, et al. BMC Neurol. 2003 Jul 8;3:4. doi: 10.1186/1471-2377-3-4. Epub 2003 Jul 8. BMC Neurol. 2003. PMID: 12848902 Free PMC article. Clinical Trial.

3

Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population.

Myllykangas L, Polvikoski T, Sulkava R, Verkkoniemi A, Crook R, Tienari PJ, Pusa AK, Niinistö L, O'Brien P, Kontula K, Hardy J, Haltia M, Pérez-Tur J. Myllykangas L, et al. Among authors: crook r. Ann Neurol. 1999 Sep;46(3):382-90. Ann Neurol. 1999. PMID: 10482269

4

A kindred with Parkinson's disease not showing genetic linkage to established loci.

Gwinn-Hardy KA, Crook R, Lincoln S, Adler CH, Caviness JN, Hardy J, Farrer M. Gwinn-Hardy KA, et al. Among authors: crook r. Neurology. 2000 Jan 25;54(2):504-7. doi: 10.1212/wnl.54.2.504. Neurology. 2000. PMID: 10668726

5

Presenilin mutations line up along transmembrane alpha-helices.

Hardy J, Crook R. Hardy J, et al. Among authors: crook r. Neurosci Lett. 2001 Jun 29;306(3):203-5. doi: 10.1016/s0304-3940(01)01910-3. Neurosci Lett. 2001. PMID: 11406330

6

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Farrer M, et al. Among authors: crook r. Ann Neurol. 1998 Mar;43(3):394-7. doi: 10.1002/ana.410430320. Ann Neurol. 1998. PMID: 9506559

7

Cotton wool plaques in non-familial late-onset Alzheimer disease.

Le TV, Crook R, Hardy J, Dickson DW. Le TV, et al. Among authors: crook r. J Neuropathol Exp Neurol. 2001 Nov;60(11):1051-61. doi: 10.1093/jnen/60.11.1051. J Neuropathol Exp Neurol. 2001. PMID: 11706935

8

Genetic analysis of synphilin-1 in familial Parkinson's disease.

Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Among authors: crook r. Neurobiol Dis. 2001 Apr;8(2):317-23. doi: 10.1006/nbdi.2000.0326. Neurobiol Dis. 2001. PMID: 11300726

9

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Baker M, et al. Among authors: crook r. Ann Neurol. 1997 Nov;42(5):794-8. doi: 10.1002/ana.410420516. Ann Neurol. 1997. PMID: 9392579

10

Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia.

Rippon GA, Crook R, Baker M, Halvorsen E, Chin S, Hutton M, Houlden H, Hardy J, Lynch T. Rippon GA, et al. Among authors: crook r. Arch Neurol. 2003 Jun;60(6):884-8. doi: 10.1001/archneur.60.6.884. Arch Neurol. 2003. PMID: 12810495

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