Published in Neuropediatrics on June 01, 1996
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Recombinant human granulocyte-macrophage colony-stimulating factor in the treatment of febrile neutropenia: a double blind placebo-controlled study in children. Pediatr Infect Dis J (1994) 1.44
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Fasting hypoglycemia is common during maintenance therapy for childhood acute lymphoblastic leukemia. J Pediatr (2001) 1.43
Human parvovirus B19-induced epidemic acute red cell aplasia in patients with hereditary hemolytic anemia. Blood (1986) 1.42
Characteristics and outcome of acute infection with hepatitis B virus in children with cancer. Pediatr Infect Dis J (1991) 1.41
Myocardial function and postmortem myocardial histology in children given anthracycline therapy for cancer. Pediatr Hematol Oncol (1994) 1.41
Prospective evaluation of Candida antigen and antibody assays for detection of Candida infections in children with malignant disease. Acta Paediatr (1995) 1.41
Reduced mortality in dermatitis herpetiformis: a population-based study of 476 patients. Br J Dermatol (2012) 1.40
Prolonged breast feeding as prophylaxis for recurrent otitis media. Acta Paediatr Scand (1982) 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
The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probands. J Med Genet (1987) 1.38
Measles vaccination after exposure to natural measles. J Pediatr (1978) 1.37
Serum alpha-fetoprotein: diagnostic significance in liver disease. Br Med J (1974) 1.37
Need for iron supplementation in infants on prolonged breast feeding. J Pediatr (1978) 1.34
Gene deletions in X-linked muscular dystrophy. Am J Hum Genet (1989) 1.29
White matter changes on MRI during treatment in children with acute lymphoblastic leukemia: correlation with neuropsychological findings. Med Pediatr Oncol (2000) 1.23
The role of parvovirus B19 in aplastic crisis and erythema infectiosum (fifth disease). J Infect Dis (1986) 1.20
Developmental changes in serum iron, total iron-binding capacity, and transferrin saturation in infancy. J Pediatr (1977) 1.19
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies. Hum Mutat (1998) 1.18
Cerebroretinal microangiopathy with calcifications and cysts. Neurology (2006) 1.16
Muscle-eye-brain disease: a neuropathological study. Ann Neurol (1997) 1.12
Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription. Hum Mol Genet (1993) 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
Time of appearance of immunoglobulin-containing cells in the mucosa of the neonatal intestine. Pediatr Res (1980) 1.10
Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker. Am J Pathol (1997) 1.10
Eradication of neuroblastoma cells in vitro by monoclonal antibody and human complement: method for purging autologous bone marrow. Cancer Res (1985) 1.10
Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease. J Neurol Sci (1994) 1.07
Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy. Ophthalmology (1998) 1.07
Molecular changes in second primary lung and breast cancers after therapy for Hodgkin's disease. Cancer Epidemiol Biomarkers Prev (2000) 1.05
Respiratory virus infections during anticancer treatment in children. Pediatr Infect Dis J (1995) 1.05
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Am J Obstet Gynecol (1998) 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
Neuroradiologic findings in children with mitochondrial disorders. AJNR Am J Neuroradiol (1998) 1.04
Overrepresentation of 1q21-23 and 12q13-21 in lipoma-like liposarcomas but not in benign lipomas: a comparative genomic hybridization study. Cancer Genet Cytogenet (1997) 1.03
Deletion of the Ink4-locus (the p16ink4a, p14ARF and p15ink4b genes) predicts relapse in children with ALL treated according to the Nordic protocols NOPHO-86 and NOPHO-92. Leukemia (2002) 1.03
Acute thrombocytopenic purpura following measles, mumps and rubella vaccination. A report on 23 patients. Acta Paediatr (1993) 1.03
Complement activation in circulation and central nervous system after rituximab (anti-CD20) treatment of B-cell lymphoma. Leuk Lymphoma (2001) 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
Serum immunoglobulin E in atopic and non-atopic children aged 6 months to 5 years. A follow-up study. Acta Paediatr Scand (1982) 1.01
Five new cases of a recently described leukoencephalopathy with high brain lactate. Neurology (2004) 1.01
Carcinoembryonic antigen and alpha fetoprotein in malignant tumors of the female genital tract. Cancer (1975) 0.99
Fat composition of the infant diet does not influence subsequent serum lipid levels in man. Atherosclerosis (1983) 0.99
Second malignant neoplasms in patients treated for childhood leukemia. A population-based cohort study from the Nordic countries. The Nordic Society of Pediatric Oncology and Hematology (NOPHO). Acta Paediatr Scand (1991) 0.98
Morphometric and immunohistochemical study of jejunal biopsies from children with intestinal soy allergy. Eur J Pediatr (1981) 0.98
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Acta Paediatr (1999) 0.98
Iron absorption from infant milk formula and the optimal level of iron supplementation. Acta Paediatr Scand (1977) 0.97
Clinical significance of urinary and serum hydroxyproline determination in sarcoidosis. Clin Chim Acta (1971) 0.97
Gains and losses of DNA sequences in liposarcomas evaluated by comparative genomic hybridization. Genes Chromosomes Cancer (1996) 0.97
Autologous stem cell transplantation in adult patients with peripheral T-cell lymphoma: a nation-wide survey. Bone Marrow Transplant (2004) 0.97
Congenital myasthenic syndrome associated with episodic apnea and sudden infant death. Neuromuscul Disord (2002) 0.97
Studies of carcino-fetal proteins. II. Biochemical comparison of -fetoprotein from human fetuses and patients with hepatocellular cancer. Int J Cancer (1971) 0.97
Disc degeneration in young gymnasts. A magnetic resonance imaging study. Am J Sports Med (1990) 0.96
Osteonecrosis during the treatment of childhood acute lymphoblastic leukemia: a prospective MRI study. Med Pediatr Oncol (1999) 0.96
DTP and DTP-inactivated polio vaccines: comparison of adverse reactions and IGG, IGM and IGA antibody responses to DTP. Acta Paediatr Scand (1980) 0.96
Flavobacterium psychrophilum, invasion into and shedding by rainbow trout Oncorhynchus mykiss. Dis Aquat Organ (2000) 0.96
High level of alpha-fetoprotein in sera of adult mice. Int J Cancer (1973) 0.95
Muscle-eye-brain disease and Walker-Warburg syndrome. Am J Med Genet (1990) 0.95
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping. Am J Hum Genet (1999) 0.94
[Acidocillin concentration in middle ear exudate]. Antibiotiki (1976) 0.94
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis. J Med Genet (2009) 0.94
Inevitable and avoidable deaths in childhood ALL. Acta Paediatr Scand (1986) 0.93
White matter changes in children treated for acute lymphoblastic leukemia. Cancer (1992) 0.93
Inhibin gene expression in a large cell calcifying Sertoli cell tumour and serum inhibin and activin levels. APMIS (1998) 0.92
Prophylaxis of atopic disease by six months' total solid food elimination. Evaluation of 135 exclusively breast-fed infants of atopic families. Acta Paediatr Scand (1983) 0.92
Prospective controlled survey of viral infections in children with acute lymphoblastic leukemia during chemotherapy. Cancer (1995) 0.92
Late cranial MRI after cranial irradiation in survivors of childhood cancer. Neuroradiology (1994) 0.92
Transfer of latent atopy by bone marrow transplantation? A case report. J Allergy Clin Immunol (1984) 0.91
POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease. J Med Genet (2004) 0.91
Prophylaxis for atopic disease: role of infant feeding. Clin Rev Allergy (1984) 0.91
Cell-surface ganglioside GD2 in the immunohistochemical detection and differential diagnosis of neuroblastoma. Am J Clin Pathol (1991) 0.90