Published in Acta Paediatr Scand on March 01, 1983
Outcome for congenital hypothyroidism. Arch Dis Child (1984) 1.51
The elimination of indigenous measles, mumps, and rubella from Finland by a 12-year, two-dose vaccination program. N Engl J Med (1994) 4.41
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis. Nature (1995) 3.78
Prevention of Hemophilus influenzae type b bacteremic infections with the capsular polysaccharide vaccine. N Engl J Med (1984) 3.37
Job strain in relation to body mass index: pooled analysis of 160 000 adults from 13 cohort studies. J Intern Med (2011) 3.14
Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med (1990) 2.96
Hereditary diseases in Finland; rare flora in rare soul. Ann Clin Res (1973) 2.75
Rapid effect on endemic measles, mumps, and rubella of nationwide vaccination programme in Finland. Lancet (1986) 2.21
Workplace bullying and the risk of cardiovascular disease and depression. Occup Environ Med (2003) 2.19
West syndrome: individualized ACTH therapy. Brain Dev (1997) 2.07
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease. Neurology (2001) 1.97
Sandwich hybridization as a convenient method for the detection of nucleic acids in crude samples. Gene (1983) 1.89
Mutations in the AIRE gene: effects on subcellular location and transactivation function of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy protein. Am J Hum Genet (2000) 1.87
Measles history and atopic diseases: a population-based cross-sectional study. JAMA (2000) 1.81
Fructose-induced hyperuricaemia. Lancet (1967) 1.80
Identification of tryptophan hydroxylase as an intestinal autoantigen. Lancet (1998) 1.77
Effects of supplemental alpha-tocopherol and beta-carotene on colorectal cancer: results from a controlled trial (Finland) Cancer Causes Control (2000) 1.75
Novel test for rapid viral diagnosis: detection of adenovirus in nasopharyngeal mucus aspirates by means of nucleic-acid sandwich hybridisation. Lancet (1983) 1.70
Fatal inhalation injury caused by airway fire during tracheostomy. Acta Anaesthesiol Scand (2007) 1.66
Preoperative levosimendan infusion in combined aortic valve and coronary bypass surgery. Br J Anaesth (2011) 1.65
Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism. Nat Genet (2000) 1.63
Low-level air pollution and upper respiratory infections in children. Am J Public Health (1991) 1.63
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis. Nat Genet (1998) 1.58
Ibuprofen or acetaminophen for the acute treatment of migraine in children: a double-blind, randomized, placebo-controlled, crossover study. Neurology (1997) 1.55
An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21. Nat Genet (1994) 1.53
Diet and risk of colorectal cancer in a cohort of Finnish men. Cancer Causes Control (1999) 1.50
Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism. Lancet (1965) 1.50
Low-level air pollution and hospital admissions for cardiac and cerebrovascular diseases in Helsinki. Am J Public Health (1996) 1.49
Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I. J Intern Med (2009) 1.45
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up study. Brain Dev (1995) 1.44
Randomized trial comparing natural and synthetic surfactant: increased infection rate after natural surfactant? Acta Paediatr (2000) 1.43
Chronic bronchitis, emphysema, and low-level air pollution in Helsinki, 1987-1989. Environ Res (1994) 1.43
Prolonged exclusive breast feeding and heredity as determinants in infantile atopy. Arch Dis Child (1987) 1.42
The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population. Am J Hum Genet (1996) 1.41
Infantile type of so-called neuronal ceroid-lipofuscinosis. Dev Med Child Neurol (1974) 1.39
Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18. Arch Dis Child (1973) 1.38
Insulin administration via a subcutaneous catheter. Effects on absorption. Diabetes Care (1993) 1.38
Congenital chloride diarrhoea. Clinical analysis of 21 Finnish patients. Arch Dis Child (1977) 1.37
Variation of growth in height and weight of children. II. After infancy. Acta Paediatr Scand (1990) 1.37
Gender, socioeconomic status and family status as determinants of food behaviour. Soc Sci Med (1998) 1.35
Randomized, placebo-controlled double blind study on the efficacy of influenza immunization on absenteeism of health care workers. Pediatr Infect Dis J (1999) 1.34
Exclusive breast-feeding for 9 months: risk of iron deficiency. J Pediatr (1984) 1.34
Job strain as a predictor of disability pension: the Finnish Public Sector Study. J Epidemiol Community Health (2008) 1.34
Cytomegalovirus in urine: detection of viral DNA by sandwich hybridization. J Clin Microbiol (1984) 1.33
Estimating the distribution of usual dietary intake by short-term measurements. Eur J Clin Nutr (2002) 1.32
Association of postmedication hypocortisolism with early first relapse of idiopathic nephrotic syndrome. Lancet (1977) 1.30
Work stress and health in primary health care physicians and hospital physicians. Occup Environ Med (2007) 1.29
Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies. J Neurol Sci (1973) 1.28
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes. Am J Hum Genet (1995) 1.27
Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies. Acta Neuropathol (1973) 1.27
Association between organizational inequity and incidence of psychiatric disorders in female employees. Psychol Med (2003) 1.25
A rapid fluorogenic palmitoyl-protein thioesterase assay: pre- and postnatal diagnosis of INCL. Mol Genet Metab (1999) 1.24
Congenital hypothyroidism. Aetiological and clinical aspects. Arch Dis Child (1972) 1.24
Mulibrey nanism: clinical features and diagnostic criteria. J Med Genet (2004) 1.23
Exclusively breast-fed healthy infants grow slower than reference infants. Pediatr Res (1985) 1.23
Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics (1991) 1.23
A novel format for a growth chart. Acta Paediatr Scand (1984) 1.22
Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients. J Neurol Sci (1973) 1.22
A national short-term follow-Up study of extremely low birth weight infants born in Finland in 1996-1997. Pediatrics (2001) 1.21
Asthma and ambient air pollution in Helsinki. J Epidemiol Community Health (1996) 1.21
Perinatal cytomegalovirus infection in man. Arch Dis Child (1977) 1.19
Randomised prospective study of short-term and long-term initial stay in hospital by children with diabetes mellitus. Lancet (1991) 1.17
Pharmacokinetics of quercetin from quercetin aglycone and rutin in healthy volunteers. Eur J Clin Pharmacol (2000) 1.16
Epidermal growth factor is a constant component of normal human tear fluid. Graefes Arch Clin Exp Ophthalmol (1989) 1.14
ss-cell autoantibodies, human leukocyte antigen II alleles, and type 1 diabetes in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. J Clin Endocrinol Metab (2000) 1.14
Effects of different progestogens on lipoproteins during postmenopausal replacement therapy. N Engl J Med (1981) 1.14
Antibodies to glutamic acid decarboxylase and insulin-dependent diabetes in patients with autoimmune polyendocrine syndrome type I. J Clin Endocrinol Metab (1996) 1.13
Growth in Turner's syndrome: spontaneous and fluoxymesterone stimulated. Acta Paediatr Scand Suppl (1979) 1.13
Muscle-eye-brain disease: a neuropathological study. Ann Neurol (1997) 1.12
Lysinuric protein intolerance. Am J Med (1975) 1.11
Explosive school-based measles outbreak: intense exposure may have resulted in high risk, even among revaccinees. Am J Epidemiol (1998) 1.10
Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses. Am J Hum Genet (1994) 1.10
Growth evaluation: parent and child specific height standards. Arch Dis Child (1989) 1.09
Glutamate decarboxylase-reactive peripheral blood lymphocytes from patients with IDDM express gut-specific homing receptor alpha4beta7-integrin. Diabetes (1997) 1.08
Intake of flavonols and flavones and risk of coronary heart disease in male smokers. Epidemiology (2001) 1.08
Rapid diagnosis of respiratory adenovirus infections in young adult men. J Clin Microbiol (1986) 1.08
Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease. J Neurol Sci (1994) 1.07
Nutrient intake and use of beverages and the risk of kidney stones among male smokers. Am J Epidemiol (1999) 1.07
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritance. Birth Defects Orig Artic Ser (1974) 1.07
Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction. Lancet (1973) 1.05
Neonatal Candida parapsilosis outbreak with a high case fatality rate. Pediatr Infect Dis J (1995) 1.05
Pituitary function in prolactinoma. Effect of surgery and postoperative bromocriptine therapy. Clin Endocrinol (Oxf) (1981) 1.04
The expression of autoimmune polyglandular disease type I appears associated with several HLA-A antigens but not with HLA-DR. J Clin Endocrinol Metab (1988) 1.04
Basolateral-membrane transport defect for lysine in lysinuric protein intolerance. Lancet (1980) 1.04
Congenital Na+ diarrhea: a new type of secretory diarrhea. J Pediatr (1985) 1.03
Expression of xenobiotic-metabolizing cytochrome P450 forms in human adult and fetal liver. Biochem Pharmacol (1994) 1.03
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis. Neurology (1999) 1.03
Reproducibility and validity of a food frequency questionnaire in a case-control study on breast cancer. J Clin Epidemiol (1996) 1.03
The transcription factors SOX9 and SOX10 are vitiligo autoantigens in autoimmune polyendocrine syndrome type I. J Biol Chem (2001) 1.03
Congenital chloride diarrhea, an autosomal recessive disease. Genetic study of 14 Finnish and 12 other families. Clin Genet (1971) 1.02
Caries and saliva in 12-18-year-old diabetics and controls. Scand J Dent Res (1992) 1.02
Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients. Acta Paediatr Scand (1967) 1.02
Serum cholesterol and lipoprotein concentrations in mothers during and after prolonged exclusive lactation. Metabolism (1992) 1.02
Decreased striatal dopamine transporter density in JNCL patients with parkinsonian symptoms. Neurology (2000) 1.01
Cellular and humoral immmunity in cartilage-hair hypoplasia. Pediatr Res (1978) 1.01
A variant of Jansky-Bielschowsky disease. Neuropediatrics (1982) 1.01
Identification of tyrosine hydroxylase as an autoantigen in autoimmune polyendocrine syndrome type I. Biochem Biophys Res Commun (2000) 1.01
Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease. J Clin Endocrinol Metab (1994) 1.01
The renal lesion in congenital chloride diarrhea. J Pediatr (1977) 1.01
Ophthalmological findings in a new syndrome with muscle, eye and brain involvement. Acta Ophthalmol (Copenh) (1978) 1.00