Published in J Pediatr on November 01, 1993
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Regulation of cell fate decision of undifferentiated spermatogonia by GDNF. Science (2000) 5.44
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients. J Pediatr (1997) 2.12
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A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment. J Cell Biol (1992) 1.84
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Dependence of kidney morphogenesis on the expression of nerve growth factor receptor. Science (1991) 1.54
Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls. Arch Gen Psychiatry (1998) 1.50
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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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
Prolonged breast feeding as prophylaxis for recurrent otitis media. Acta Paediatr Scand (1982) 1.39
Allograft with unrelated donor accentuates the gastrointestinal toxicity associated with high-dose melphalan and total body irradiation preparative for bone marrow transplantation in children. Pediatr Transplant (2000) 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
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Need for iron supplementation in infants on prolonged breast feeding. J Pediatr (1978) 1.34
Neuronal ceroid lipofuscinoses in childhood. Neurol Sci (2000) 1.34
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
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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
Long-term results in children with AML: NOPHO-AML Study Group--report of three consecutive trials. Leukemia (2005) 1.18
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Gyrate atrophy of the choroid and retina with hyperornithinemia: tubular aggregates and type 2 fiber atrophy in muscle. Neurology (1979) 1.16
Cerebroretinal microangiopathy with calcifications and cysts. Neurology (2006) 1.16
BMP-4 affects the differentiation of metanephric mesenchyme and reveals an early anterior-posterior axis of the embryonic kidney. Dev Dyn (2000) 1.16
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism. Neurology (1983) 1.13
Initial differentiation of the metanephric mesenchyme is independent of WT1 and the ureteric bud. Dev Genet (1999) 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
Mismatch negativity indicates vowel discrimination in newborns. Hear Res (1995) 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
Colon interposition or gastric tube? Follow-up study of colon-esophagus and gastric tube-esophagus patients. J Pediatr Surg (1983) 1.10
Congenital varicella-zoster virus infection after maternal subclinical infection: clinical and neuropathological findings. J Perinatol (2001) 1.08
Primary structure and expression of a novel human laminin alpha 4 chain. FEBS Lett (1995) 1.07
Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease. J Neurol Sci (1994) 1.07
Door to thrombolysis: ER reorganization and reduced delays to acute stroke treatment. Neurology (2006) 1.07
Viral meningoencephalitis: a review of diagnostic methods and guidelines for management. Eur J Neurol (2010) 1.03
Acute disseminated encephalomyelitis following nephropathia epidemica. Acta Neurol Scand (2002) 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
A variant of Jansky-Bielschowsky disease. Neuropediatrics (1982) 1.01
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
The tip-top branching ureter. Curr Opin Cell Biol (1997) 0.99
Fat composition of the infant diet does not influence subsequent serum lipid levels in man. Atherosclerosis (1983) 0.99
CT angiographic analysis of carotid artery stenosis: comparison of manual assessment, semiautomatic vessel analysis, and digital subtraction angiography. AJNR Am J Neuroradiol (2007) 0.99
Long-term adverse effects on dentition in children with poor-risk neuroblastoma treated with high-dose chemotherapy and autologous stem cell transplantation with or without total body irradiation. Bone Marrow Transplant (2002) 0.98
EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis. Dev Med Child Neurol (1997) 0.98
Iron absorption from infant milk formula and the optimal level of iron supplementation. Acta Paediatr Scand (1977) 0.97
Experience over 17 years with antioxidant treatment in Spielmeyer-Sjögren disease. Am J Med Genet Suppl (1988) 0.96
Infantile neuronal ceroid-lipofuscinosis (INCL): diagnostic criteria. J Inherit Metab Dis (1993) 0.95
Muscle-eye-brain disease and Walker-Warburg syndrome. Am J Med Genet (1990) 0.95
The ontogenetically earliest discriminative response of the human brain. Psychophysiology (1996) 0.94
DC-EEG discloses prominent, very slow activity patterns during sleep in preterm infants. Clin Neurophysiol (2002) 0.94
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis. J Med Genet (2009) 0.94
Association between influenza during pregnancy and childhood leukaemia. Br Med J (1973) 0.94
Rat glomerular cells do not express podocytic markers when cultured in vitro. Lab Invest (1991) 0.94
Transient effect of L-tryptophan in progressive myoclonus epilepsy without Lafora bodies: clinical and electrophysiological study. Epilepsia (1980) 0.94
Inevitable and avoidable deaths in childhood ALL. Acta Paediatr Scand (1986) 0.93
Marchiafava-Bignami disease: two cases with favourable outcome. Eur J Neurol (2001) 0.93
Structure of the human laminin gamma 2 chain gene (LAMC2): alternative splicing with different tissue distribution of two transcripts. Genomics (1996) 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
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
Primary structure of mouse and rat nephrin cDNA and structure and expression of the mouse gene. J Am Soc Nephrol (2000) 0.90
Cell-surface ganglioside GD2 in the immunohistochemical detection and differential diagnosis of neuroblastoma. Am J Clin Pathol (1991) 0.90
Neurotrophin 3 rescues neuronal precursors from apoptosis and promotes neuronal differentiation in the embryonic metanephric kidney. Proc Natl Acad Sci U S A (1995) 0.90
Central auditory processing of durational changes in complex speech patterns by newborns: an event-related brain potential study. Dev Neuropsychol (2001) 0.89
The spectrum of Jansky-Bielschowsky disease. Neuropediatrics (1991) 0.89
Mild brain atrophy in early HIV infection: the lack of association with cognitive deficits and HIV-specific intrathecal immune response. J Neurol Sci (1990) 0.89
Exchange transfusion with fresh heparinized blood is a safe procedure. Experiences from 1 069 newborns. Acta Paediatr Scand (1985) 0.89
Localization of glial cell line-derived neurotrophic factor (GDNF) mRNA in embryonic rat by in situ hybridization. Eur J Neurosci (1996) 0.89
Serum immunoglobulin A in healthy infants: an accelerated postnatal increase in formula-fed compared to breast-fed infants. J Pediatr (1979) 0.88
POLG1 manifestations in childhood. Neurology (2011) 0.88
Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates. Neuroimage (2008) 0.88
Circulating dendritic cell subset levels after allogeneic stem cell transplantation in children correlate with time post transplant and severity of acute graft-versus-host disease. Bone Marrow Transplant (2005) 0.88
Evidence of riboflavin depletion in breast-fed newborns and its further acceleration during treatment of hyperbilirubinemia by phototherapy. Acta Paediatr Scand (1979) 0.88
Pneumatic tourniquet paralysis. Case report. J Bone Joint Surg Br (1983) 0.88
Opportunistic osteomyelitis in the jaws of children on immunosuppressive chemotherapy. J Pediatr Hematol Oncol (1996) 0.88
Slow disappearance of peripheral blast cells: an independent risk factor indicating poor prognosis in children with acute lymphoblastic leukemia. Blood (1988) 0.87
Birch pollen allergy in children. Role of milk feeding during the first birch season of life. Allergy (1982) 0.87
Familial multiple sclerosis: MRI findings in clinically affected and unaffected siblings. J Neurol Neurosurg Psychiatry (1992) 0.87
Pain medication during terminal care of children with cancer. J Pain Symptom Manage (1998) 0.86
C-reactive protein in rapid diagnosis and follow-up of bacterial septicemia in children with leukemia. Pediatr Infect Dis (1983) 0.85
The human laminin beta 2 chain (S-laminin): structure, expression in fetal tissues and chromosomal assignment of the LAMB2 gene. Matrix Biol (1995) 0.85
Serum IgE in healthy infants fed breast milk or cow's milk-based formulas. Clin Allergy (1979) 0.85