Published in Duodecim on January 01, 1970
Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet (1992) 1.79
Prevalence of severe dementia in Finland. Neurology (1985) 1.62
Accuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findings. J Neurol Neurosurg Psychiatry (1983) 1.59
A double-blind study comparing oxcarbazepine and carbamazepine in patients with newly diagnosed, previously untreated epilepsy. Epilepsy Res (1989) 1.59
Chronic subdural hematoma in adults. Influence of patient's age on symptoms, signs, and thickness of hematoma. J Neurosurg (1975) 1.58
Genomewide scan of multiple sclerosis in Finnish multiplex families. Am J Hum Genet (1997) 1.57
Epidemiology of chronic subdural haematoma. Acta Neurochir (Wien) (1975) 1.55
Raised plasma endothelin during acute migraine attack. Cephalalgia (1992) 1.45
Quality of life 4 years after stroke. Stroke (1988) 1.42
Depression after stroke: results of the FINNSTROKE Study. Stroke (1998) 1.32
Studies on the clustering of multiple sclerosis in Finland I: Comparison between the domiciles and places of birth in selected subpopulations. Acta Neurol Scand (1975) 1.29
Demonstration of fibronectin in human cerebrospinal fluid. J Lab Clin Med (1978) 1.28
Diagnosis and management of brain death. Br Med J (1979) 1.28
Dementia among medical inpatients. Evaluation of 2000 consecutive admissions. Arch Intern Med (1986) 1.27
Classic amyotrophic lateral sclerosis with dementia. Arch Neurol (1982) 1.26
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein. Biochem Biophys Res Commun (1990) 1.25
Toxic effects of ergotamine used for migraine. Headache (1978) 1.21
Epilepsy after stroke. Epilepsia (1992) 1.20
Accuracy of the clinical diagnosis of vascular dementia: a prospective clinical and post-mortem neuropathological study. J Neurol Neurosurg Psychiatry (1988) 1.19
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Am J Pathol (1990) 1.16
The profile of recovery from stroke and factors influencing outcome. Stroke (1985) 1.13
Diphenyl poisoning in fruit paper production: a new health hazard. Arch Environ Health (1973) 1.12
Regional and temporal variation in the incidence of multiple sclerosis in Finland 1979-1993. Neuroepidemiology (2000) 1.08
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritance. Birth Defects Orig Artic Ser (1974) 1.07
'Iatrogenic' brain stem infarction. A complication of x-ray examination of the cervical spine and following posterior tamponation of the nose. Eur Neurol (1975) 1.05
Immunocytochemical studies of Alzheimer neuronal perikarya with intermediate filament antisera. J Neurol Sci (1983) 1.04
End of life decisions: attitudes of Finnish physicians. J Med Ethics (2004) 1.04
Two-locus linkage analysis in multiple sclerosis (MS). Genomics (1994) 1.03
Biochemical and fine structural studies on brain and liver biopsies in aspartylglucosaminuria. Neurology (1971) 1.01
An epidemic due to sulphonamide-resistant group A meningococci in the Helsinki area (Finland). Epidemiological and clinical observations. Scand J Infect Dis (1976) 1.00
Low prevalence of Huntington's disease in Finland. Lancet (1987) 0.99
Two patients with a 46,XX,Er chromosome constitution. Acta Paediatr Scand (1968) 0.99
Neuronal intranuclear inclusion disease in identical twins. Ann Neurol (1984) 0.96
Increasing prevalence of multiple sclerosis in Finland. Acta Neurol Scand (2001) 0.96
Eleven new cases of aspartylglucosaminuria. J Ment Defic Res (1970) 0.95
Neuropsychological differentiation between normal aging, Alzheimer's disease and vascular dementia. Acta Neurol Scand (1986) 0.93
Toward understanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitro expression reveals an abnormal gelsolin fragment. Hum Mol Genet (1994) 0.93
High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence. J Neurochem (1983) 0.92
Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between English and Finnish patients with special reference to storage materials. Clin Chim Acta (1973) 0.92
Two pericentric inversions of human chromosome 11. J Med Genet (1977) 0.92
The value of CT and very low field MRI in the etiological diagnosis of dizziness. Acta Neurol Scand (1988) 0.91
Letter: Amyotrophic lateral sclerosis and autonomic nervous system. Lancet (1976) 0.91
Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies. Acta Neuropathol (1975) 0.91
Studies on N-aspartyl-beta-glucosaminidase in aspartylglycosaminuria. Clin Chim Acta (1975) 0.90
Post-stroke depression and functional recovery in a population-based stroke register. The Finnstroke study. Eur J Neurol (1999) 0.90
CT in the differential diagnosis between Alzheimer's disease and vascular dementia. Acta Neurol Scand (1987) 0.89
Aortic dissection and paraparesis. Eur Neurol (1980) 0.89
Monoamine metabolite concentrations in lumbar cerebrospinal fluid of patients with histologically verified Alzheimer's dementia. J Neurol Neurosurg Psychiatry (1984) 0.89
Serum amyloid A protein, albumin and prealbumin in Alzheimer's disease and in demented patients with Down's syndrome. Acta Neurol Scand (1986) 0.89
Prognosis of patients with middle cerebral artery occlusion. Stroke (1976) 0.89
Neurofilament subunit--related proteins in neuronal intranuclear inclusions. Ann Neurol (1984) 0.88
Malignant diseases among patients with multiple sclerosis. J Neurol (1977) 0.88
Seizures associated with propofol anesthesia. Epilepsia (1993) 0.88
Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF). J Neurol Sci (1994) 0.88
An association between epileptic seizures and increased serum bacterial antibody levels. Epilepsia (1983) 0.88
CSF in Alzheimer's disease. Studies on blood-brain barrier function and intrathecal protein synthesis. J Neurol Sci (1985) 0.88
The incidence of Pku in Finland. Acta Paediatr Scand (1971) 0.87
Declining incidence and mortality rates of stroke in Finland from 1972 to 1991. Results of three population-based stroke registers. Stroke (1996) 0.87
Familial multiple sclerosis: MRI findings in clinically affected and unaffected siblings. J Neurol Neurosurg Psychiatry (1992) 0.87
The epidemiology of multiple sclerosis in Finland: increase of prevalence and stability of foci in high-risk areas. Acta Neurol Scand (1983) 0.87
Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families. Am J Hum Genet (1991) 0.87
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus. Am J Hum Genet (1990) 0.86
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan. Hum Mutat (1995) 0.86
Glucose tolerance in amyotrophic lateral sclerosis. Acta Neurol Scand (1984) 0.86
Prognosis of patients with unilateral extracranial occlusion of the internal carotid artery. Stroke (1976) 0.85
Aspartylglucosaminuria. I. Fine structural studies on liver, kidney and brain. Acta Neuropathol (1972) 0.85
Aspartylglucosaminuria. II. Biochemical studies on brain, liver, kidney and spleen. Acta Neuropathol (1972) 0.85
HLA antigens in Alzheimer's disease. Tissue Antigens (1980) 0.85
Combined dexamethasone and low-molecular-weight dextran in acute brain infarction: double-blind study. Br Med J (1976) 0.84
Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin-related amyloidosis. FEBS Lett (1997) 0.83
Suspected dementia: evaluation of 323 consecutive referrals. Acta Neurol Scand (1987) 0.83
Serum and cerebrospinal fluid proteins and the blood-brain barrier in Alzheimer's disease and multi-infarct dementia. Eur Neurol (1987) 0.83
Outcome of stroke in the Espoo--Kauniainen area, Finland. Ann Clin Res (1980) 0.82
The change in size of intracranial arteriovenous malformations. J Neurol Sci (1973) 0.82
Geographic and social distribution of patients with amyotrophic lateral sclerosis. Arch Neurol (1977) 0.82
Amyotrophic lateral sclerosis. Proteins of neuronal cell membranes, axons and myelin of the precentral gyrus and other cortical areas. Brain (1973) 0.82
Dolichols in brain and urinary sediment in neuronal ceroid lipofuscinosis. Neurology (1983) 0.82
Chronic bilateral subdural haematoma in adults. Acta Neurochir (Wien) (1979) 0.82
Herpes simplex virus encephalitis: new diagnostic and clinical features and results of therapy. Arch Neurol (1980) 0.82
Subacute sclerosing panencephalitis as a cause of chronic dementia and relapsing brain disorder. J Neurol Neurosurg Psychiatry (1972) 0.82
Glial filaments are a major brain fraction in infantile neuronal ceroid-lipofuscinosis. Acta Neuropathol (1985) 0.82
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmol (Copenh) (1986) 0.81
EEG in the differential diagnosis between Alzheimer's disease and vascular dementia. Acta Neurol Scand (1988) 0.81
Brain scanning in detection of intracranial arteriovenous malformations. Acta Neurol Scand (1973) 0.81
Dolichol and dolichyl phosphate in the neuronal ceroid-lipofuscinoses and other diseases. Am J Med Genet Suppl (1988) 0.81
Reappraisal of HLA in multiple sclerosis: close linkage in multiplex families. Eur J Hum Genet (1993) 0.81
Studies on the pathogenesis of multiple sclerosis. Basic proteins in the myelin and white matter of multiple sclerosis, subacute sclerosing panencephalitis and postvaccinal leucoencephalitis. Eur Neurol (1971) 0.81
Golli-MBP gene in multiple sclerosis susceptibility. J Neuroimmunol (1998) 0.81
Clinical neurological findings among car painters exposed to a mixture of organic solvents. Scand J Work Environ Health (1980) 0.81
Flight induced by infusion of bicuculline methiodide into periventricular structures. Brain Res (1984) 0.81
Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis. Genomics (1992) 0.80
Blood dolichol in lysosomal diseases. Biochem Cell Biol (1992) 0.80
Thin-layer chromatographic demonstration of aspartylglycosylamine and a novel acidic carbohydrate in human tissues. J Chromatogr (1972) 0.80
Hereditary recurrent brachial plexus neuropathy with dysmorphic features. Acta Neurol Scand (1985) 0.80
Selenium, vitamin E and copper in multiple sclerosis. Acta Neurol Scand (1976) 0.80
Flight induced by microinjection of D-tubocurarine or alpha-bungarotoxin into medial hypothalamus or periaqueductal gray matter: cholinergic or GABAergic mediation? Behav Brain Res (1986) 0.80
Prevalence of phenylketonuria and some other metabolic disorders among mentally retarded patients in Finland. Acta Neurol Scand (1967) 0.80
A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease. J Neurol Sci (1983) 0.80
Raised levels of cerebral cortex dolichols in Alzheimer's disease. Lancet (1982) 0.80