Collinge J - Search Results

1

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Among authors: collinge j. Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29. Brain. 2008. PMID: 18234697 Free PMC article.

2

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R, et al. Collinge J, et al. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

3

Prion dementia without characteristic pathology.

Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL. Collinge J, et al. Lancet. 1990 Jul 7;336(8706):7-9. doi: 10.1016/0140-6736(90)91518-f. Lancet. 1990. PMID: 1973256

4

Sporadic Creutzfeldt-Jakob disease in a 16-year-old in the UK.

Britton TC, al-Sarraj S, Shaw C, Campbell T, Collinge J. Britton TC, et al. Among authors: collinge j. Lancet. 1995 Oct 28;346(8983):1155. doi: 10.1016/s0140-6736(95)91827-2. Lancet. 1995. PMID: 7475611 No abstract available.

5

Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease.

Houlden H, Crook R, Duff K, Hutton M, Collinge J, Roques P, Rossor M, Hardy J. Houlden H, et al. Among authors: collinge j. Neurosci Lett. 1995 Mar 31;188(3):202-4. doi: 10.1016/0304-3940(95)11422-s. Neurosci Lett. 1995. PMID: 7609909

6

Frontal lobe or 'nonspecific' dementias are genetically heterogeneous.

Ashworth A, Brown J, Gydesen S, Sorensen SA, Rossor MN, Hardy J, Collinge J. Ashworth A, et al. Among authors: collinge j. Neurology. 1995 Sep;45(9):1781. doi: 10.1212/wnl.45.9.1781. Neurology. 1995. PMID: 7675248 No abstract available.

7

G/T polymorphism in CRYA2 gene.

Ashworth A, Campbell T, Palmer M, Collinge J, Brown J. Ashworth A, et al. Among authors: collinge j. Hum Mol Genet. 1994 Sep;3(9):1712. doi: 10.1093/hmg/3.9.1712. Hum Mol Genet. 1994. PMID: 7833944 No abstract available.

8

Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus.

Houlden H, Crook R, Hardy J, Roques P, Collinge J, Rossor M. Houlden H, et al. Among authors: collinge j. Neurosci Lett. 1994 Jun 20;174(2):222-4. doi: 10.1016/0304-3940(94)90026-4. Neurosci Lett. 1994. PMID: 7970184

9

Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

Collinge J, Palmer MS, Sidle KC, Mahal SP, Campbell T, Brown J, Hardy J, Brun AE, Gustafson L, Bakker E, et al. Collinge J, et al. J Neurol Neurosurg Psychiatry. 1994 Jun;57(6):762. doi: 10.1136/jnnp.57.6.762. J Neurol Neurosurg Psychiatry. 1994. PMID: 8006666 Free PMC article. No abstract available.

10

Deletions in the prion protein gene are not associated with CJD.

Palmer MS, Mahal SP, Campbell TA, Hill AF, Sidle KC, Laplanche JL, Collinge J. Palmer MS, et al. Among authors: collinge j. Hum Mol Genet. 1993 May;2(5):541-4. doi: 10.1093/hmg/2.5.541. Hum Mol Genet. 1993. PMID: 8100163

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