Published in Lancet on October 15, 1977
Chronic cutaneous graft-versus-host disease in man. Am J Pathol (1978) 1.21
Cutaneous graft versus host disease. Br Med J (Clin Res Ed) (1987) 1.17
Rheumatic disorders and primary biliary cirrhosis: an appraisal of 170 Italian patients. Ann Rheum Dis (2001) 0.99
Influence of prior pregnancies on disease course and cause of death in systemic sclerosis. Ann Rheum Dis (2002) 0.92
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis. Nature (1995) 3.78
Roles of yeast DNA polymerases delta and zeta and of Rev1 in the bypass of abasic sites. Genes Dev (2001) 3.59
Longer delays in tuberculosis diagnosis among women in Vietnam. Int J Tuberc Lung Dis (1999) 3.30
Percentile curves for hemoglobin and red cell volume in infancy and childhood. J Pediatr (1979) 3.04
Ferritin in serum: diagnosis of iron deficiency and iron overload in infants and children. Blood (1974) 2.79
Prolonged breast-feeding as prophylaxis for atopic disease. Lancet (1979) 2.30
Health-related quality of life of adults surviving malignancies in childhood. Eur J Cancer (1996) 2.27
Fear and social isolation as consequences of tuberculosis in VietNam: a gender analysis. Health Policy (2001) 2.12
Muscle-eye-brain disease (MEB) Brain Dev (1989) 2.00
Central nervous system disease in childhood acute lymphoblastic leukemia: prognostic factors and results of treatment. Pediatr Hematol Oncol (1992) 1.99
Response of the jejunal mucosa to cow's milk in the malabsorption syndrome with cow's milk intolerance. A light- and electron-microscopic study. Acta Paediatr Scand (1973) 1.98
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology. Am J Med Genet (1998) 1.85
Iron deficiency in infancy and childhood. Am J Clin Nutr (1980) 1.82
Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein. Lancet (1976) 1.82
Regression of warts. An immunological study. Lancet (1975) 1.78
At what age does iron supplementation become necessary in low-birth-weight infants? J Pediatr (1977) 1.74
Efficacy and safety of lovastatin in adolescent males with heterozygous familial hypercholesterolemia: a randomized controlled trial. JAMA (1999) 1.70
Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients. Kidney Int (2000) 1.65
Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria. Lancet (1998) 1.63
Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment. Am J Med Genet (1984) 1.61
Peripheral blood cell counts in infants with Down's syndrome. Clin Genet (1996) 1.61
Osteitis caused by bacille Calmette-Guérin vaccination: a retrospective analysis of 222 cases. J Infect Dis (1995) 1.61
The glycosaminoglycan content of renal basement membranes in the congenital nephrotic syndrome of the Finnish type. Pediatr Nephrol (1992) 1.55
Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence. J Biol Chem (2001) 1.50
Prevalence of black-pigmented bacteroides species in root canal infections. J Endod (1989) 1.49
Differentiation of kidney mesenchyme in an experimental model system. Adv Morphog (1968) 1.44
Scientific rigour in qualitative research--examples from a study of women's health in family practice. Fam Pract (1994) 1.44
Isolated proteinuria: analysis of a school-age population. J Pediatr (1982) 1.43
Different tuberculosis in men and women: beliefs from focus groups in Vietnam. Soc Sci Med (1999) 1.43
Circinate erosive balanitis and HL-A 27. Acta Derm Venereol (1975) 1.42
Antibiotic treatment of symptomatic Mycoplasma genitalium infection in Scandinavia: a controlled clinical trial. Sex Transm Infect (2007) 1.42
Prolonged exclusive breast feeding and heredity as determinants in infantile atopy. Arch Dis Child (1987) 1.42
Functional interaction between the Werner Syndrome protein and DNA polymerase delta. Proc Natl Acad Sci U S A (2000) 1.42
Erythropoiesis of very low-birth-weight infants dependent on prenatal growth rate and protein status. Acta Paediatr (1994) 1.41
Characteristics and outcome of acute infection with hepatitis B virus in children with cancer. Pediatr Infect Dis J (1991) 1.41
"Salla disease": a new lysosomal storage disorder. Arch Neurol (1979) 1.40
Infantile type of so-called neuronal ceroid-lipofuscinosis. Dev Med Child Neurol (1974) 1.39
Four pairs of siblings with acute leukemia during 1966-1985 in the Nordic countries: indication of an elevated familial risk? Pediatr Hematol Oncol (1990) 1.39
Molecular epidemiological typing within the European Gonococcal Antimicrobial Resistance Surveillance Programme reveals predominance of a multidrug-resistant clone. Euro Surveill (2013) 1.39
Progressive unilateral hypertrophic myopathy: a case study. Muscle Nerve (1993) 1.39
Iron absorption in infants: high bioavailability of breast milk iron as indicated by the extrinsic tag method of iron absorption and by the concentration of serum ferritin. J Pediatr (1977) 1.39
Two new male contraceptives exert their effects by depleting germ cells prematurely from the testis. Biol Reprod (2001) 1.34
Exclusive breast-feeding for 9 months: risk of iron deficiency. J Pediatr (1984) 1.34
Microscopic hematuria in school children: epidemiology and clinicopathologic evaluation. J Pediatr (1979) 1.31
Association of postmedication hypocortisolism with early first relapse of idiopathic nephrotic syndrome. Lancet (1977) 1.30
Gene deletions in X-linked muscular dystrophy. Am J Hum Genet (1989) 1.29
Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies. J Neurol Sci (1973) 1.28
Long-term outcome of primary nephrotic syndrome. Arch Dis Child (1982) 1.28
Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies. Acta Neuropathol (1973) 1.27
Demonstration of laminin, a basement membrane glycoprotein, in routinely processed formalin-fixed human tissues. Histochemistry (1982) 1.27
Gonorrhea, genital chlamydial infection, and nonspecific urethritis in male partners of women hospitalized and treated for acute pelvic inflammatory disease. Sex Transm Dis (1993) 1.24
Exclusively breast-fed healthy infants grow slower than reference infants. Pediatr Res (1985) 1.23
Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients. J Neurol Sci (1973) 1.22
Cellular expression of xanthine oxidoreductase protein in normal human tissues. Lab Invest (1999) 1.20
Developmental changes in serum iron, total iron-binding capacity, and transferrin saturation in infancy. J Pediatr (1977) 1.19
Congenital nephrotic syndrome. Nephron (1973) 1.19
Long-term results in children with AML: NOPHO-AML Study Group--report of three consecutive trials. Leukemia (2005) 1.18
Immunohistochemical and electron microscopic characterization of the cellular infiltrate in alopecia (areata, totalis, and universalis). J Invest Dermatol (1984) 1.17
Prenatal diagnosis of Batten's disease. Lancet (1996) 1.17
Gyrate atrophy of the choroid and retina with hyperornithinemia: tubular aggregates and type 2 fiber atrophy in muscle. Neurology (1979) 1.16
Missing cruciate ligament in congenital short femur. J Bone Joint Surg Am (1983) 1.14
Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization. Br J Cancer (1997) 1.14
P fimbriae-dependent, lipopolysaccharide-independent activation of epithelial cytokine responses. Mol Microbiol (1999) 1.14
Bactericidal effect of pooled human serum on Bacteroides melaninogenicus, Bacteroides asaccharolyticus and Actinobacillus actinomycetemcomitans. Scand J Dent Res (1982) 1.14
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism. Neurology (1983) 1.13
Prenatal diagnosis of congenital nephrosis in 23 high-risk families. Am J Dis Child (1978) 1.13
Community perceptions of tuberculosis: A qualitative exploration from a gender perspective. Public Health (2011) 1.12
Lysinuric protein intolerance. Am J Med (1975) 1.11
Cytoplasmic inclusions in the vermiform appendix and skeletal muscle in two types of so-called neuronal ceroid-lipofuscinosis. Brain (1973) 1.11
Iron absorption from breast milk, cow's milk, and iron-supplemented formula: an opportunistic use of changes in total body iron determined by hemoglobin, ferritin, and body weight in 132 infants. Pediatr Res (1979) 1.11
A new class of symmetric bisbenzimidazole-based DNA minor groove-binding agents showing antitumor activity. J Med Chem (2001) 1.10
Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy. Neuromuscul Disord (1995) 1.10
Mannosidosis: clinical, fine-structural and biochemical findings in three cases. Acta Paediatr Scand (1973) 1.10
Prevention of anemia and iron deficiency in very low-birth-weight infants. J Pediatr (1982) 1.09
Tumor necrosis factor in children with malignancies. Cancer Res (1990) 1.09
Effects of progesterone on uterine leiomyoma growth and apoptosis. Steroids (2000) 1.09
Henoch-Schönlein nephritis: long-term prognosis of unselected patients. Arch Dis Child (1981) 1.08
Classification of fungi by means of pyrolysis-gas chromatography-pattern recognition. J Chromatogr (1979) 1.08
C-reactive protein compared with white blood cell count and erythrocyte sedimentation rate in the diagnosis of acute appendicitis in children. Acta Chir Scand (1986) 1.06
Changes in lactate dehydrogenase and esterase-specific activities, isozymic patterns, and cellular distribution during the growth cycle of PK cells in vitro. Exp Cell Res (1970) 1.06
Breast milk iron--a declining concentration during the course of lactation. Acta Paediatr Scand (1979) 1.05
Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome. Pediatr Res (1995) 1.04
Transforming growth factor-β decreases the cancer-initiating cell population within diffuse-type gastric carcinoma cells. Oncogene (2010) 1.04
Phagocytosis of Bacteroides melaninogenicus and Bacteroides gingivalis in vitro by human neutrophils. J Periodontal Res (1982) 1.03
Supplementary creatine as a treatment for gyrate atrophy of the choroid and retina. N Engl J Med (1981) 1.03
Outcome after first relapse in children with acute lymphoblastic leukemia: a population-based study of 315 patients from the Nordic Society of Pediatric Hematology and Oncology (NOPHO). Med Pediatr Oncol (1995) 1.03
Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1). Kidney Int (2006) 1.03
Three-dimensional structure of a mammalian purple acid phosphatase at 2.2 A resolution with a mu-(hydr)oxo bridged di-iron center. J Mol Biol (1999) 1.02
Developmental changes in red blood cell counts and indices of infants after exclusion of iron deficiency by laboratory criteria and continuous iron supplementation. J Pediatr (1978) 1.02
Chronic osteomyelitislike disease with negative bacterial cultures. Am J Dis Child (1988) 1.02
Serum cholesterol and lipoprotein concentrations in mothers during and after prolonged exclusive lactation. Metabolism (1992) 1.02
A variant of Jansky-Bielschowsky disease. Neuropediatrics (1982) 1.01
Reproduction following treatment for childhood leukemia: a population-based prospective cohort study of fertility and offspring. Med Pediatr Oncol (1991) 1.00
Pathology of congenital nemaline myopathy. A follow-up study. J Neurol Sci (1988) 1.00
Extracellular matrix and epithelial differentiation of Wilms' tumor. Am J Pathol (1985) 0.99
Fat composition of the infant diet does not influence subsequent serum lipid levels in man. Atherosclerosis (1983) 0.99
Brain iron: persistent deficiency following short-term iron deprivation in the young rat. Br J Haematol (1975) 0.98
Risk factors associated with asthma and rhinoconjunctivitis among Swedish farmers. Allergy (1999) 0.98
Ferritinemia as an indicator of systemic disease activity in children with systemic juvenile rheumatoid arthritis. Acta Paediatr Scand (1986) 0.98
Renal involvement in Schölein-Henoch purpura. Acta Paediatr Scand (1974) 0.98