Published in Duodecim on January 01, 1977
Tinzaparin in acute ischaemic stroke (TAIST): a randomised aspirin-controlled trial. Lancet (2001) 3.69
Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein. N Engl J Med (1995) 3.54
Neurologic manifestations of infective endocarditis: a 17-year experience in a teaching hospital in Finland. Arch Intern Med (2000) 2.37
CNS manifestations of Nasu-Hakola disease: a frontal dementia with bone cysts. Neurology (2001) 2.27
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nat Med (1998) 2.20
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol (1995) 2.10
Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study. Neurology (2001) 1.98
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases) Brain Pathol (1995) 1.86
Human rabies of bat origin in Europe. Lancet (1986) 1.85
Atypical and anaplastic meningiomas: radiology, surgery, radiotherapy, and outcome. Surg Neurol (1986) 1.83
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration. EMBO J (2000) 1.79
Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet (1992) 1.79
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease). Am J Med Genet (1992) 1.78
Prevalence of severe dementia in Finland. Neurology (1985) 1.62
Expression of endothelial cell-specific receptor tyrosine kinases and growth factors in human brain tumors. Am J Pathol (1995) 1.60
Abundant expression of HIV Nef and Rev proteins in brain astrocytes in vivo is associated with dementia. AIDS (1995) 1.59
Accuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findings. J Neurol Neurosurg Psychiatry (1983) 1.59
Genomewide scan of multiple sclerosis in Finnish multiplex families. Am J Hum Genet (1997) 1.57
Multiple sclerosis: in situ evidence for antibody- and complement-mediated demyelination. Ann Neurol (1998) 1.56
Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med (1990) 1.50
Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II. N Engl J Med (1991) 1.48
Raised plasma endothelin during acute migraine attack. Cephalalgia (1992) 1.45
Infantile type of so-called neuronal ceroid-lipofuscinosis. Dev Med Child Neurol (1974) 1.39
More about: cell and molecular biology of simian virus 40: implications for human infections and disease. J Natl Cancer Inst (2000) 1.39
An autosomal locus predisposing to deletions of mitochondrial DNA. Nat Genet (1995) 1.36
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43). Ann Neurol (1996) 1.32
Progressive myoclonus epilepsy. A clinical and histopathological study. Acta Neurol Scand (1974) 1.32
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils. Proc Natl Acad Sci U S A (1993) 1.31
Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. J Clin Invest (1992) 1.30
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
Intracranial hemangiopericytoma: radiology, surgery, radiotherapy, and outcome in 21 patients. Surg Neurol (1985) 1.29
Glial fibrillary acidic protein and intermediate filaments in human glioma cells. Acta Neuropathol (1979) 1.29
Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies. J Neurol Sci (1973) 1.28
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
Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies. Acta Neuropathol (1973) 1.27
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
Vascular growth factors and receptors in capillary hemangioblastomas and hemangiopericytomas. Am J Pathol (1996) 1.25
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein. Biochem Biophys Res Commun (1990) 1.25
Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis. FEBS Lett (1993) 1.24
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease. Neurology (1997) 1.23
Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients. J Neurol Sci (1973) 1.22
Significant variation in mortality and functional outcome after acute ischaemic stroke between Western countries: data from the tinzaparin in acute ischaemic stroke trial (TAIST). J Neurol Neurosurg Psychiatry (2005) 1.21
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome). Clin Genet (1991) 1.21
Accuracy of the clinical diagnosis of vascular dementia: a prospective clinical and post-mortem neuropathological study. J Neurol Neurosurg Psychiatry (1988) 1.19
The growth rate of intracranial meningiomas and its relation to histology. An analysis of 43 patients. Surg Neurol (1985) 1.19
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Am J Pathol (1990) 1.16
Contribution of APOE promoter polymorphisms to Alzheimer's disease risk. Neurology (2002) 1.14
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred. Lancet (1991) 1.13
The normal population distribution of PRNP codon 129 polymorphism. Acta Neurol Scand (2003) 1.13
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. Ann Neurol (2000) 1.12
Diphenyl poisoning in fruit paper production: a new health hazard. Arch Environ Health (1973) 1.12
Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population. Am J Hum Genet (2000) 1.11
Cytoplasmic inclusions in the vermiform appendix and skeletal muscle in two types of so-called neuronal ceroid-lipofuscinosis. Brain (1973) 1.11
Distribution of a major connective tissue protein, fibronectin, in normal and neoplastic human nervous tissue. Acta Neuropathol (1980) 1.11
Regional and temporal variation in the incidence of multiple sclerosis in Finland 1979-1993. Neuroepidemiology (2000) 1.08
Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype. J Neuropathol Exp Neurol (2001) 1.08
Mutually exclusive expression of fibronectin and glial fibrillary acidic protein in cultured brain cells. Exp Cell Res (1980) 1.07
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritance. Birth Defects Orig Artic Ser (1974) 1.07
Variant Alzheimer's disease with spastic paraparesis: clinical characterization. Neurology (2000) 1.06
Surfactant proteins A and B as interactive genetic determinants of neonatal respiratory distress syndrome. Hum Mol Genet (2000) 1.05
'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
Familial Creutzfeldt-Jakob disease. J Neurol Sci (1979) 1.04
Immunocytochemical studies of Alzheimer neuronal perikarya with intermediate filament antisera. J Neurol Sci (1983) 1.04
Histochemical and electron microscopic observations on the myoneural junctions of rats with carbon disulfide induced polyneuropathy. Scand J Work Environ Health (1977) 1.04
End of life decisions: attitudes of Finnish physicians. J Med Ethics (2004) 1.04
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin. Ann Neurol (1992) 1.04
Two-locus linkage analysis in multiple sclerosis (MS). Genomics (1994) 1.03
Diffuse vacuolization (spongiosis) and arteriolosclerosis in the frontal white matter occurs in vascular dementia. Arch Neurol (1996) 1.02
Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome. Invest Ophthalmol Vis Sci (1994) 1.02
Changing incidence and outcome of infants with respiratory distress syndrome in the 1990s: a population-based survey. Acta Paediatr (2004) 1.01
Biochemical and fine structural studies on brain and liver biopsies in aspartylglucosaminuria. Neurology (1971) 1.01
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type. Biochem J (1990) 1.01
Isolation of human immunodeficiency virus (HIV) at autopsy one to six days postmortem. Am J Clin Pathol (1990) 1.01
Expression of growth factors and growth factor receptors in capillary hemangioblastoma. J Neuropathol Exp Neurol (1996) 1.00
Low prevalence of Huntington's disease in Finland. Lancet (1987) 0.99
Distribution of endothelial and basement membrane markers in angiogenic tumors of the nervous system. Acta Neuropathol (1983) 0.99
Two patients with a 46,XX,Er chromosome constitution. Acta Paediatr Scand (1968) 0.99
Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population. Ann Neurol (1999) 0.99
Tie endothelial cell-specific receptor tyrosine kinase is upregulated in the vasculature of arteriovenous malformations. J Neuropathol Exp Neurol (1996) 0.98
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation. Ann Neurol (1992) 0.96
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
Ezrin expression in stromal cells of capillary hemangioblastoma. An immunohistochemical survey of brain tumors. Am J Pathol (1996) 0.96
Muscle-eye-brain disease and Walker-Warburg syndrome. Am J Med Genet (1990) 0.95
Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: two new cases. J Neurol Sci (1988) 0.95
Eleven new cases of aspartylglucosaminuria. J Ment Defic Res (1970) 0.95
MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type. Neuroradiology (1997) 0.95
Cutis laxa in hereditary gelsolin amyloidosis. Br J Dermatol (2005) 0.93
Neuropsychological differentiation between normal aging, Alzheimer's disease and vascular dementia. Acta Neurol Scand (1986) 0.93
Neuropathological studies in three Scandinavian cases of progressive myoclonus epilepsy. Acta Neurol Scand (1969) 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
Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry. J Neuropathol Exp Neurol (1997) 0.92
High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence. J Neurochem (1983) 0.92