Collinge J - Search Results

1

Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.

Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: collinge j. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

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 protein immunocytochemistry helps to establish the true incidence of prion diseases.

Lantos PL, McGill IS, Janota I, Doey LJ, Collinge J, Bruce MT, Whatley SA, Anderton BH, Clinton J, Roberts GW, et al. Lantos PL, et al. Among authors: collinge j. Neurosci Lett. 1992 Nov 23;147(1):67-71. doi: 10.1016/0304-3940(92)90776-4. Neurosci Lett. 1992. PMID: 1480325

4

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

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

Prion dementia.

Collinge J, Palmer MS, Rossor MN, Janota I, Lantos PL. Collinge J, et al. Lancet. 1993 Mar 6;341(8845):627; author reply 627-8. Lancet. 1993. PMID: 8094847 No abstract available.

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