Kwok JB - Search Results

1

Genetics of hand grip strength in mid to late life.

Chan JP, Thalamuthu A, Oldmeadow C, Armstrong NJ, Holliday EG, McEvoy M, Kwok JB, Assareh AA, Peel R, Hancock SJ, Reppermund S, Menant J, Trollor JN, Brodaty H, Schofield PR, Attia JR, Sachdev PS, Scott RJ, Mather KA. Chan JP, et al. Among authors: kwok jb. Age (Dordr). 2015 Feb;37(1):9745. doi: 10.1007/s11357-015-9745-5. Epub 2015 Feb 1. Age (Dordr). 2015. PMID: 25637336 Free PMC article.

2

A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's disease.

Brooks WS, Martins RN, De Voecht J, Nicholson GA, Schofield PR, Kwok JB, Fisher C, Yeung LU, Van Broeckhoven C. Brooks WS, et al. Among authors: kwok jb. Neurosci Lett. 1995 Oct 27;199(3):183-6. doi: 10.1016/0304-3940(95)12046-7. Neurosci Lett. 1995. PMID: 8577393

3

Exclusion of linkage between bipolar affective disorder and chromosome 16 in 12 Australian pedigrees.

Adams LJ, Salmon JA, Kwok JB, Vivero C, Donald JA, Mitchell PB, Schofield PR. Adams LJ, et al. Among authors: kwok jb. Am J Med Genet. 1997 May 31;74(3):304-10. doi: 10.1002/(sici)1096-8628(19970531)74:3<304::aid-ajmg12>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9184315

4

Nonparametric simulation-based statistical analyses for bipolar affective disorder locus on chromosome 21q22.3.

Kwok JB, Adams LJ, Salmon JA, Donald JA, Mitchell PB, Schofield PR. Kwok JB, et al. Am J Med Genet. 1999 Feb 5;88(1):99-102. doi: 10.1002/(sici)1096-8628(19990205)88:1<99::aid-ajmg18>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10050976

5

Novel Leu723Pro amyloid precursor protein mutation increases amyloid beta42(43) peptide levels and induces apoptosis.

Kwok JB, Li QX, Hallupp M, Whyte S, Ames D, Beyreuther K, Masters CL, Schofield PR. Kwok JB, et al. Ann Neurol. 2000 Feb;47(2):249-53. doi: 10.1002/1531-8249(200002)47:2<249::aid-ana18>3.0.co;2-8. Ann Neurol. 2000. PMID: 10665499

6

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

Stanford PM, Halliday GM, Brooks WS, Kwok JB, Storey CE, Creasey H, Morris JG, Fulham MJ, Schofield PR. Stanford PM, et al. Among authors: kwok jb. Brain. 2000 May;123 ( Pt 5):880-93. doi: 10.1093/brain/123.5.880. Brain. 2000. PMID: 10775534

7

Variable phenotype of Alzheimer's disease with spastic paraparesis.

Smith MJ, Kwok JB, McLean CA, Kril JJ, Broe GA, Nicholson GA, Cappai R, Hallupp M, Cotton RG, Masters CL, Schofield PR, Brooks WS. Smith MJ, et al. Among authors: kwok jb. Ann Neurol. 2001 Jan;49(1):125-9. doi: 10.1002/1531-8249(200101)49:1<125::aid-ana21>3.0.co;2-1. Ann Neurol. 2001. PMID: 11198283

8

Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation.

Brooks WS, Kwok JB, Halliday GM, Godbolt AK, Rossor MN, Creasey H, Jones AO, Schofield PR. Brooks WS, et al. Among authors: kwok jb. Neurology. 2004 Nov 9;63(9):1613-7. doi: 10.1212/01.wnl.0000142965.10778.c7. Neurology. 2004. PMID: 15534244

9

Similar early clinical presentations in familial and non-familial frontotemporal dementia.

Piguet O, Brooks WS, Halliday GM, Schofield PR, Stanford PM, Kwok JB, Spillantini MG, Yancopoulou D, Nestor PJ, Broe GA, Hodges JR. Piguet O, et al. Among authors: kwok jb. J Neurol Neurosurg Psychiatry. 2004 Dec;75(12):1743-5. doi: 10.1136/jnnp.2003.031948. J Neurol Neurosurg Psychiatry. 2004. PMID: 15548495 Free PMC article.

10

Pick bodies in a family with presenilin-1 Alzheimer's disease.

Halliday GM, Song YJ, Lepar G, Brooks WS, Kwok JB, Kersaitis C, Gregory G, Shepherd CE, Rahimi F, Schofield PR, Kril JJ. Halliday GM, et al. Among authors: kwok jb. Ann Neurol. 2005 Jan;57(1):139-43. doi: 10.1002/ana.20366. Ann Neurol. 2005. PMID: 15622541

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