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Results: 1-11 |
Results: 11
A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease
Authors: Panegyres, PK Toufexis, K Kakulas, BA Cernevakova, L Brown, P Ghetti, B Piccardo, P Dlouhy, SR
Citation: Pk. Panegyres et al., A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease, ARCH NEUROL, 58(11), 2001, pp. 1899-1902
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion
Authors: Nowak, KJ Walsh, P Jacob, RL Johnsen, RD Peverall, J McNally, EM Wilton, SD Kakulas, BA Laing, NG
Citation: Kj. Nowak et al., Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion, NEUROMUSC D, 10(2), 2000, pp. 100-107
Amyloid precursor protein gene isoforms in Alzheimer's disease and other neurodegenerative disorders
Authors: Panegyres, PK Zafiris-Toufexis, K Kakulas, BA
Citation: Pk. Panegyres et al., Amyloid precursor protein gene isoforms in Alzheimer's disease and other neurodegenerative disorders, J NEUR SCI, 173(2), 2000, pp. 81-92
The applied neuropathology of human spinal cord injury - In reply to Professor Dietz
Authors: Kakulas, BA
Citation: Ba. Kakulas, The applied neuropathology of human spinal cord injury - In reply to Professor Dietz, SPINAL CORD, 37(8), 1999, pp. 595-595
The applied neuropathology of human spinal cord injury
Authors: Kakulas, BA
Citation: Ba. Kakulas, The applied neuropathology of human spinal cord injury, SPINAL CORD, 37(2), 1999, pp. 79-88
Butyrylcholinesterase K variant and Alzheimer's disease
Authors: Panegyres, PK Mamotte, CDS Vasikaran, SD Wilton, S Fabian, V Kakulas, BA
Citation: Pk. Panegyres et al., Butyrylcholinesterase K variant and Alzheimer's disease, J NEUROL, 246(5), 1999, pp. 369-370
The contribution of molecular genetics in the diagnosis and management of neuromuscular disorders
Authors: Kakulas, BA Laing, NG Johnsen, RD
Citation: Ba. Kakulas et al., The contribution of molecular genetics in the diagnosis and management of neuromuscular disorders, SC J RE MED, 1999, pp. 5-22
Problems and solutions in the rehabilitation of patients with progressive muscular dystrophy
Authors: Kakulas, BA
Citation: Ba. Kakulas, Problems and solutions in the rehabilitation of patients with progressive muscular dystrophy, SC J RE MED, 1999, pp. 23-37
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy
Authors: Mastaglia, FL Nowak, KJ Stell, R Phillips, BA Edmondston, JE Dorosz, SM Wilton, SD Hallmayer, J Kakulas, BA Laing, NG
Citation: Fl. Mastaglia et al., Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy, J NE NE PSY, 67(2), 1999, pp. 174-179
Arthrogryposis multiplex congenita in Western Australia
Authors: Silberstein, EP Kakulas, BA
Citation: Ep. Silberstein et Ba. Kakulas, Arthrogryposis multiplex congenita in Western Australia, J PAEDIAT C, 34(6), 1998, pp. 518-523
White matter changes in human spinal cord injury
Authors: Kakulas, BA Lorimer, RL Gubbay, AD
Citation: Ba. Kakulas et al., White matter changes in human spinal cord injury, SPINAL CORD MONITORING, 1998, pp. 395-407
Risultati: 1-11 |