Published in Nature on June 11, 1966
Aberrant muscle antigen exposure in mice is sufficient to cause myositis in a Treg cell-deficient milieu. Arthritis Rheum (2013) 1.49
Lymphocyte stimulation with muscle homogenate in polymyositis and other muscle-wasting disorders. J Neurol Neurosurg Psychiatry (1969) 1.49
Lymphotoxin formation by lymphocytes and muscle in polymyositis. J Clin Invest (1972) 1.26
A quantitative test to detect lymphocytes sensitized against the surface of muscle cells. Clin Exp Immunol (1976) 0.93
Fibrosing alveolitis and polymyositis. Thorax (1970) 0.90
Macrophage migration inhibition studies of lymphocytes taken from guinea-pigs suffering from experimental polymyositis. Clin Exp Immunol (1976) 0.81
Human muscle-derived, tissue specific, myocytotoxic T cell lines in dermatomyositis. Clin Exp Immunol (1987) 0.76
Degeneration of cardiac and skeletal muscle in radiation chimeras. Am J Pathol (1969) 0.75
Herpes zoster brachial plexus neuritis. Clin Neuropathol (1997) 1.54
Mental deficiency associated with muscular dystrophy. A neuropathological study. Brain (1966) 1.47
Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation. J Neurol Neurosurg Psychiatry (1998) 1.44
Retropulsion of intervertebral discs associated with traumatic hyperextension of the cervical spine and absence of vertebral fracture: an uncommon mechanism of spinal cord injury. Spinal Cord (2002) 1.41
Preclinical lesions and their progression in the experimental spongiform encephalopathies (kuru and Creutzfeldt-Jakob disease) in primates. J Neuropathol Exp Neurol (1977) 1.39
Further observations on the pathology of Kuru. (A study of the two cerebra in serial section). J Neuropathol Exp Neurol (1967) 1.28
Destruction of differentiated muscle cultures by sensitised lymphoid cells. J Pathol Bacteriol (1966) 1.24
Autosomal dominant distal myopathy: linkage to chromosome 14. Am J Hum Genet (1995) 1.22
Clinical and pathological aspects of a fatal case of mulga (Pseudechis australis) snakebite. Med J Aust (1969) 1.14
Regeneration of muscle in Duchenne muscular dystrophy: an electron microscope study. J Neurol Sci (1970) 1.12
Sequential loss of myelin proteins during Wallerian degeneration in the human spinal cord. Brain (2005) 1.09
Pathology of spinal injuries. Cent Nerv Syst Trauma (1984) 1.07
Myopathies associated with hypothyroidism: a review based upon 13 cases. Aust N Z J Med (1988) 1.06
Use of the dog model for Duchenne muscular dystrophy in gene therapy trials. Neuromuscul Disord (1997) 1.03
Experimental muscle diseases. Methods Achiev Exp Pathol (1975) 0.99
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry (1999) 0.99
A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease. Arch Neurol (2001) 0.99
Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family. Hum Mutat (1994) 0.97
High-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscle of dystrophic dogs: prolongation of expression with immunosuppression. Hum Gene Ther (1998) 0.96
Central pontine myelinolysis in a child with leukemia. Arch Neurol (1966) 0.95
TGF-beta1 and TGF-beta2 expression after traumatic human spinal cord injury. Spinal Cord (2007) 0.92
Apolipoprotein-E genotyping in diagnosis of Alzheimer's disease. Lancet (1996) 0.90
Ovine congenital progressive muscular dystrophy: clinical syndrome and distribution of lesions. Aust Vet J (1986) 0.89
Burst fractures in the thoracic and lumbar spine. A clinico-neuropathologic analysis. Spine (Phila Pa 1976) (1989) 0.89
Medullary haemorrhage: a report of two cases. J Neurol Neurosurg Psychiatry (1969) 0.89
A TaqI map of the dystrophin gene useful for deletion and carrier status analysis. J Med Genet (1992) 0.89
The clinical neuropathology of spinal cord injury. A guide to the future. Paraplegia (1987) 0.89
Thrombosis of the internal carotid artery after closed head injury. Proc Aust Assoc Neurol (1971) 0.88
Polymyositis presenting with respiratory failure. J Neurol Sci (1984) 0.87
Neuropathology of human spinal cord injury sustained in sports-related activities. J Neurotrauma (1997) 0.86
A calcium-citro-phosphate technique for the histochemical localization of myosin ATPase. Stain Technol (1972) 0.86
Comparative anatomy and histochemistry of human and canine latissimus dorsi muscle. J Heart Transplant (1990) 0.86
A modified histochemical technique for sarcoplasmic reticular ATPase. Histochemie (1972) 0.85
Muscular dystrophy in young girls. Proc Aust Assoc Neurol (1975) 0.85
Incubation film technique for the histochemical localization of creatine kinase. Histochemie (1971) 0.85
Central neural antigens: detection and diagnostic application. Crit Rev Clin Lab Sci (1986) 0.84
Vesicular changes in the myopathies of AIDS. Ultrastructural observations and their relationship to zidovudine treatment. J Neurol Neurosurg Psychiatry (1990) 0.84
In vitro destruction of human foetal muscle cultures by peripheral blood lymphocytes from patients with polymyositis and lupus erythematosus. Proc Aust Assoc Neurol (1971) 0.84
Encephalopathy and fatty degeneration of the viscera: an evaluation. Brain (1970) 0.83
Vertebral metastases and spinal cord compression. Clin Exp Neurol (1978) 0.83
The natural history of Duchenne muscular dystrophy--an ultrastructural study. Proc Aust Assoc Neurol (1969) 0.83
Two distinct mutations in a single dystrophin gene: chance occurrence or premutation? Am J Med Genet (1992) 0.82
The clinical significance of type 1 fiber predominance. Muscle Nerve (1993) 0.82
Regeneration in Duchenne muscular dystrophy: a histological and histochemical study. Brain (1969) 0.82
Limb girdle syndromes. Clinical, morphological and electrophysiological studies. J Neurol Sci (1990) 0.82
Regeneration in Duchenne muscular dystrophy. A histological electron-microscopic and histochemical study. Proc Aust Assoc Neurol (1969) 0.82
Butyrycholinesterase K variant and Alzheimer's disease. J Neurol (1999) 0.81
Multiple myeloma with bilateral orbital infiltration and polyneuropathy. Med J Aust (1980) 0.81
A new myopathy with type II muscle fibre hypoplasia. Proc Aust Assoc Neurol (1974) 0.81
Multifocal progressive neurological disorder caused by neoplastic angioendotheliosis. Med J Aust (1984) 0.81
The natural history of human muscle diseases studied by means of serial biopsy. Proc Aust Assoc Neurol (1968) 0.81
The neuropathology of the 17-18 trisomy syndrome. Proc Aust Assoc Neurol (1968) 0.81
A histological and histochemical study of skeletal muscle regeneration in polymyositis. J Neurol Sci (1970) 0.81
Differentiation of Becker muscular dystrophy from limb-girdle muscular dystrophy and Kugelberg-Welander disease using a cDNA probe. Med J Aust (1990) 0.80
Amyloid precursor protein gene isoforms in Alzheimer's disease and other neurodegenerative disorders. J Neurol Sci (2000) 0.80
Needle muscle biopsy: will it make open biopsy obsolete? Aust N Z J Med (1985) 0.80
Decontamination of formaldehyde-fixed cerebral tissues of Creutzfeldt-Jakob disease by autoclaving, without the loss of microscopic visual quality. J Neuropathol Exp Neurol (1985) 0.80
Restricted forms of muscular dystrophy: a study of 11 cases. Proc Aust Assoc Neurol (1969) 0.80
Age-related congophilic inclusions in the brains of apolipoprotein E-deficient mice. Neuroscience (1998) 0.80
The natural history of minicore-multicore myopathy. Muscle Nerve (1991) 0.80
A myopathy with cellular inclusions. Trans Am Neurol Assoc (1965) 0.79
Cerebral amyloid angiopathy and intracerebral hemorrhage with special reference to the pons. Clin Neuropathol (1994) 0.79
An investigation of possible transynaptic neuronal degeneration in human spinal cord injury. J Neurol Sci (1988) 0.79
Normal and abnormal human muscle in tissue culture. Proc Aust Assoc Neurol (1968) 0.79
The effect of temperature on the pH stability of myosin ATPase as demonstrated histochemically. Histochemie (1974) 0.79
Significance of the biopsy site of the latissimus dorsi muscle for fiber typing. J Heart Lung Transplant (1992) 0.79
On the specificity of the histochemical technique for sarcoplasmic reticular adenosine triphosphatase: a light and electron microscopic study. Histochemistry (1975) 0.78
Causes of organic dementia: a necropsy survey of 60 cases. Med J Aust (1986) 0.78
Experimental kuru in the gibbon and sooty mangabey and Creutzfeldt-Jakob disease in the pigtailed macaque. With a summary of the host range of the subacute spongiform virus encephalopathies. J Med Primatol (1976) 0.78
Palatal myoclonus and associated movements. Proc Aust Assoc Neurol (1974) 0.78
The mRNA of the NR1 subtype of glutamate receptor in Alzheimer's disease. J Neural Transm (Vienna) (2002) 0.78
Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map. Nucleic Acids Res (1990) 0.78
Skeletal muscle structure in endemic cretinism. Am J Pathol (1966) 0.78
Prevalence of cerebral vascular amyloid-beta deposition and stroke in an aging Australian population: a postmortem study. J Clin Neurosci (2003) 0.78
Direct dystrophin and reporter gene transfer into dog muscle in vivo. Muscle Nerve (1998) 0.78
Muscle lipids in Duchenne muscular dystrophy. Aust J Exp Biol Med Sci (1981) 0.78
Comparison of basic fibroblast growth factor in X-linked dystrophin-deficient myopathies of human, dog and mouse. Growth Factors (1993) 0.78
Angelman's syndrome: a neuropathological study. Acta Neuropathol (1992) 0.78
Intracranial thrombosis of the internal carotid artery after closed head injury. J Neurol Neurosurg Psychiatry (1969) 0.78
Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient mice. Am J Pathol (1997) 0.77
Spongiform leucoencephalopathy associated with congenital myoclonia syndrome in the dog. J Comp Pathol (1978) 0.77
Vertebral metastases and spinal cord compression. Paraplegia (1983) 0.77
Histochemical and contractile property changes during human muscle development. Muscle Nerve (1993) 0.77
Neck injuries. Lancet (1991) 0.77
Neuromuscular diseases: muscle. Curr Opin Neurol (1996) 0.76
Toxoplasmosis in the Rottnest quokka (Setonix brachyurus). Aust J Exp Biol Med Sci (1966) 0.76
A histochemical analysis of mammalian oxidative skeletal muscle fibres using the enzymes of energetic metabolism. Histochemie (1973) 0.76
Minicores and congential fibre type disproportion observed in a family. J Paediatr Child Health (1995) 0.76
Alzheimer's disease and apolipoprotein E genotype in Western Australia: an autopsy-verified series. Med J Aust (1996) 0.76
Creatine kinase, a histochemical study by the gelatin film-lead precipitation technique. Histochemie (1972) 0.76
Further histochemical properties of rabbit skeletal muscle fibres. Histochemie (1973) 0.76
Clinical and neuropathological observations in phenylketonuria. Proc Aust Assoc Neurol (1968) 0.75
Virus-like particles in proximity to myelin in a case of progressive multifocal leukoencephalopathy. Proc Aust Assoc Neurol (1966) 0.75
Arthrogryposis multiplex congenita in Western Australia. J Paediatr Child Health (1998) 0.75
Apolipoprotein E genotyping in the diagnosis of Alzheimer's disease: a cautionary view. Ann Neurol (1995) 0.75
A syndrome of myopathy and polycythaemia in a young man. Clin Exp Neurol (1977) 0.75
Gliomas: a review of an 11-year series. Aust N Z J Surg (1975) 0.75
Positive immunostaining of ovine congenital progressive muscular dystrophy with antibody against N- and C-terminal dystrophin. Aust Vet J (1990) 0.75
Genetic counselling in neuromuscular diseases in Western Australia. Proc Aust Assoc Neurol (1974) 0.75
The effect of EDTA on the histochemical myofibrillar ATPase reaction. Acta Histochem Suppl (1976) 0.75