Kakulas B - Search Results

1

Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.

Kwok JB, Taddei K, Hallupp M, Fisher C, Brooks WS, Broe GA, Hardy J, Fulham MJ, Nicholson GA, Stell R, St George Hyslop PH, Fraser PE, Kakulas B, Clarnette R, Relkin N, Gandy SE, Schofield PR, Martins RN. Kwok JB, et al. Among authors: kakulas b. Neuroreport. 1997 Apr 14;8(6):1537-42. doi: 10.1097/00001756-199704140-00043. Neuroreport. 1997. PMID: 9172170

2

Protein markers for Alzheimer disease in the frontal cortex and cerebellum.

Verdile G, Gnjec A, Miklossy J, Fonte J, Veurink G, Bates K, Kakulas B, Mehta PD, Milward EA, Tan N, Lareu R, Lim D, Dharmarajan A, Martins RN. Verdile G, et al. Among authors: kakulas b. Neurology. 2004 Oct 26;63(8):1385-92. doi: 10.1212/01.wnl.0000141848.45315.a6. Neurology. 2004. PMID: 15505153

3

Age-related congophilic inclusions in the brains of apolipoprotein E-deficient mice.

Robertson TA, Dutton NS, Martins RN, Roses AD, Kakulas BA, Papadimitriou JM. Robertson TA, et al. Among authors: kakulas ba. Neuroscience. 1998 Jan;82(1):171-80. doi: 10.1016/s0306-4522(97)00284-4. Neuroscience. 1998. PMID: 9483513

4

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. Mastaglia FL, et al. Among authors: kakulas ba. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):174-9. doi: 10.1136/jnnp.67.2.174. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406984 Free PMC article.

5

Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient mice.

Robertson TA, Dutton NS, Martins RN, Roses AD, Kakulas BA, Papadimitriou JM. Robertson TA, et al. Among authors: kakulas ba. Am J Pathol. 1997 Feb;150(2):417-27. Am J Pathol. 1997. PMID: 9033257 Free PMC article.

6

Butyrycholinesterase K variant and Alzheimer's disease.

Panegyres PK, Mamotte CD, Vasikaran SD, Wilton S, Fabian V, Kakulas BA. Panegyres PK, et al. Among authors: kakulas ba. J Neurol. 1999 May;246(5):369-70. doi: 10.1007/s004150050365. J Neurol. 1999. PMID: 10399868

7

Two distinct mutations in a single dystrophin gene: chance occurrence or premutation?

Laing NG, Layton MG, Johnsen RD, Chandler DC, Mears ME, Goldblatt J, Kakulas BA. Laing NG, et al. Among authors: kakulas ba. Am J Med Genet. 1992 Mar 1;42(5):688-92. doi: 10.1002/ajmg.1320420512. Am J Med Genet. 1992. PMID: 1632439

8

Deposition of Alzheimer's disease amyloid (A4) protein in the cerebral cortex in Parkinson's disease.

Mastaglia FL, Masters CL, Beyreuther K, Kakulas BA. Mastaglia FL, et al. Among authors: kakulas ba. Prog Clin Biol Res. 1989;317:475-84. Prog Clin Biol Res. 1989. PMID: 2690109

9

Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion.

Nowak KJ, Walsh P, Jacob RL, Johnsen RD, Peverall J, McNally EM, Wilton SD, Kakulas BA, Laing NG. Nowak KJ, et al. Among authors: kakulas ba. Neuromuscul Disord. 2000 Feb;10(2):100-7. doi: 10.1016/s0960-8966(99)00063-2. Neuromuscul Disord. 2000. PMID: 10714584

10

The neuropathology of progressive autonomic failure of central origin (the Shy-Drager syndrome).

Kakulas BA, Tan N, Ojeda VJ. Kakulas BA, et al. Clin Exp Neurol. 1986;22:103-11. Clin Exp Neurol. 1986. PMID: 3581499

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