Published in Clin Nephrol on March 01, 1978
A clinicopathologic study of enterocyte-adherent Escherichia coli: a cause of protracted diarrhea in infants. Gastroenterology (1982) 8.38
Serum C'3 lytic system in patients with glomerulonephritis. Science (1969) 4.44
Evidence for nuclear emissions during acoustic cavitation. Science (2002) 4.15
The influence of drug interval on the effect of methotrexate and fluorouracil in the treatment of advanced colorectal cancer. J Clin Oncol (1991) 3.36
An ultrastructural study of enteropathogenic Escherichia coli infection in human infants. Ultrastruct Pathol (1983) 2.36
Complete sequence of the bithorax complex of Drosophila. Proc Natl Acad Sci U S A (1995) 2.29
Nuclear emissions during self-nucleated acoustic cavitation. Phys Rev Lett (2006) 2.28
Characteristics of a non-complement-dependent C3-reactive complex formed form factors in nephritic and normal serum. J Exp Med (1970) 2.08
Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox. Science (1991) 2.01
Evidence for in vivo breakdown of beta-10-globulin in hypocomplementemic glomerulonephritis. J Clin Invest (1967) 1.90
Cloning and expression of a Streptococcus sanguis surface antigen that interacts with a human salivary agglutinin. Infect Immun (1988) 1.75
Clinical implementation of dynamic intensity-modulated radiotherapy: Dosimetric aspects and initial experience. J Med Phys (2008) 1.72
Paediatric sedation for CT scanning: the safety and efficacy of quinalbarbitone in a district general hospital setting. Br J Radiol (2000) 1.72
A serum factor in chronic hypocomplementemic hephritis distinct from immunoglobulins and activating the alternate pathway of complement. J Exp Med (1974) 1.63
Effect of diphenylhydantoin on the metabolism of dexamethasone. N Engl J Med (1970) 1.55
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids. Johns Hopkins Med J (1982) 1.39
Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder. J Clin Endocrinol Metab (1997) 1.39
Familial and nonfamilal benign hematuria. J Pediatr (1966) 1.36
Hypocomplementemia of membranoproliferative nephritis. Dependence of the nephritic factor reaction on properdin factor B. J Clin Invest (1973) 1.35
The nephroblastomatosis complex and its relationship to Wilms' tumor: a clinicopathologic treatise. Perspect Pediatr Pathol (1976) 1.35
The relationship of the spiral turns of the cochlea and the length of the basilar membrane to the range of audible frequencies in ground dwelling mammals. J Acoust Soc Am (1985) 1.33
The C3 nephritic factor and membranoproliferative nephritis: correlation of serum levels of the nephritic factor with C3 levels, with therapy, and with progression of the disease. J Pediatr (1972) 1.32
Continuing C3 breakdown after bilateral nephrectomy in patients with membrano-proliferative glomerulonephritis. J Clin Invest (1971) 1.31
Saliva-mediated aggregation of Enterococcus faecalis transformed with a Streptococcus sanguis gene encoding the SSP-5 surface antigen. Infect Immun (1989) 1.29
Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. J Clin Invest (1997) 1.23
Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levels. J Pediatr (1997) 1.22
The 1989 report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Nephrol (1990) 1.21
Comparison of the gastrointestinal syndrome after total-body or total-abdominal irradiation. Radiat Res (1989) 1.18
The hepatic lesion in Reye's syndrome. Gastroenterology (1975) 1.16
An unusual presentation of Wegener's granulomatosis mimicking inflammatory bowel disease. Gastroenterology (1984) 1.16
Composition of nephritic factor-generated glomerular deposits in membranoproliferative glomerulonephritis type 2. Am J Kidney Dis (2001) 1.15
Classical complement pathway activation in membranoproliferative glomerulonephritis. Kidney Int (1976) 1.15
Serum complement levels in infancy: age related changes. Pediatr Res (1979) 1.14
Homotransplantation of both kidneys from an anencephalic monster to a 17 pound boy with Eagle-Barret syndrome. Surgery (1969) 1.14
Partial properdin deficiency. J Lab Clin Med (1980) 1.14
Shunt nephritis: the nature of the serum cryoglobulins and their relation to the complement profile. J Pediatr (1976) 1.13
Salivary-agglutinin-mediated adherence of Streptococcus mutans to early plaque bacteria. Infect Immun (1991) 1.12
Transneuronal cell atrophy in the congenitally deaf white cat. J Comp Neurol (1973) 1.12
Hepatic cholesterol ester storage disease, a familial disorder. I. Clinical aspects. Am J Med (1968) 1.11
Transplantation of cadaver kidneys from anencephalic donors. J Pediatr (1978) 1.09
Patterns of complement activation in idiopathic membranoproliferative glomerulonephritis, types I, II, and III. Am J Kidney Dis (1990) 1.08
A gene family in Drosophila melanogaster coding for trypsin-like enzymes. Nucleic Acids Res (1985) 1.08
Serum immune complexes in membranoproliferative and other glomerulonephritides. Kidney Int (1977) 1.06
Effect of ageing of serum on consumption of antibody by beta-1C-globulin determinants; evidence for circulating breakdown products in glomerulonephritis. Clin Exp Immunol (1968) 1.06
Cardiovascular anomalies associated with tetralogy of Fallot. Am J Cardiol (1967) 1.05
Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane. Clin Nephrol (1977) 1.04
Gonadal function, testicular histology, and meiosis following cyclophosphamide therapy in patients with nephrotic syndrome. J Pediatr (1976) 1.04
Cushing's disease with cure by resection of a pituitary adenoma. Evidence against a primary hypothalamic defect. Am J Med (1974) 1.04
Inherited complement component deficiencies in membranoproliferative glomerulonephritis. Kidney Int (1983) 1.04
The antigenic and molecular alterations of C3 in the fluid phase during an immune reaction in normal human serum. Demonstration of a new conversion product, C3x. J Exp Med (1971) 1.03
Growth and development of children with renal transplants. Use of alternate-day steroid therapy. J Pediatr (1973) 1.03
A serum inhibitor of blastogenesis in idiopathic nephrotic syndrome transferred by lymphocytes. Clin Immunol Immunopathol (1979) 1.03
Composite ganglioneuroblastoma. An assessment of the significance of histological maturation in neuroblastoma diagnosed beyond infancy. Arch Pathol Lab Med (1981) 1.02
The chronic glomerulonephritides of childhood. Part I. J Pediatr (1978) 1.01
Liver ultrastructure in abetalipoproteinemia: Evolution of micronodular cirrhosis. Gastroenterology (1974) 1.01
Single-dose metyrapone test. Arch Intern Med (1970) 1.01
A "silent" phase of hypocomplementemic persistent nephritis detectable by reduced serum beta-1c-globulin levels. J Pediatr (1969) 1.01
Transitional cell carcinoma in a urachal cyst. J Urol (1999) 1.00
The renal lesion in syndromes of multiple congenital malformations. Cerebrohepatorenal syndrome; Jeune asphyxiating thoracic dystrophy; tuberous sclerosis; Meckel syndrome. Birth Defects Orig Artic Ser (1974) 0.99
Membranoproliferative hypocomplementemic glomerulonephritis. Nephron (1973) 0.99
Mechanisms of hypocomplementemia in glomerulonephritis. Kidney Int (1973) 0.99
Glycogen storage disease, types I to X: criteria for morphologic diagnosis. Hum Pathol (1974) 0.99
Brain ultrastructure in Reye's disease. II. Acute injury and recovery processes in three children. J Neuropathol Exp Neurol (1979) 0.99
Optimization of dose distribution with multi-leaf collimator using field-in-field technique for parallel opposing tangential beams of breast cancers. J Med Phys (2008) 0.98
Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys. J Pediatr (1967) 0.98
Comparison of intramuscular and intravenous recombinant alpha-2 interferon in melanoma and other cancers. Ann Intern Med (1985) 0.98
Intrauterine disseminated intravascular coagulation: a syndrome of multiple pregnancy with a dead twin fetus. J Pediatr (1969) 0.98
Complement profiles in acute post-streptococcal glomerulonephritis. Pediatr Nephrol (1988) 0.98
A sensitive radioimmunoassay for plasma ACTH levels. J Clin Endocrinol Metab (1966) 0.98
One layer or two layer colonic anastomoses? Am J Surg (1970) 0.97
An analgesiometry system for use in rabbits with some preliminary data on the effects of buprenorphine and lofentanil. Lab Anim (1988) 0.97
Renal homotransplantation in children. Arch Surg (1970) 0.96
An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis. Kidney Int (1983) 0.96
The effects of bone on proton NMR relaxation times of surrounding liquids. Invest Radiol (1986) 0.95
Differences between membranoproliferative glomerulonephritis types I and III in clinical presentation, glomerular morphology, and complement perturbation. Am J Kidney Dis (1987) 0.95
Renal allograft survival according to primary diagnosis: a report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Nephrol (1995) 0.95
Evaluation methods for detecting changes in beam output and energy in radiation beams from high-energy linear accelerators. J Med Phys (2007) 0.95
A serum thyroxine method: application in thyroid disease and iodine-treated patients. J Clin Endocrinol Metab (1965) 0.94
Antibody to a cryptic, solid phase C1Q antigen in membranoproliferative nephritis. Kidney Int (1989) 0.94
Hypocomplementemic glomerulonephritis in an infant and mother. Evidence for an abnormal form of C3. Am J Nephrol (1987) 0.94
First determination of the weak charge of the proton. Phys Rev Lett (2013) 0.94
Wrist pain syndrome in the gymnast. Pathogenetic, diagnostic, and therapeutic considerations. Am J Sports Med (1989) 0.94
Regression of membranoproliferative glomerulonephritis type II (dense deposit disease): observations in six children. Am J Kidney Dis (1988) 0.94
The liver in generalized glycogen storage disease. Light microscopic observations. Am J Pathol (1966) 0.94
Membranoproliferative glomerulonephritis characterized by focal, segmental proliferative lesions. Clin Nephrol (1982) 0.94
Extrapolation chamber mounted on perspex for calibration of high energy photon and electron beams from a clinical linear accelerator. J Med Phys (2009) 0.94
Mesangiocapillary glomerulonephritis: changes in glomerular morphology with long-term alternate-day prednisone therapy. J Pediatr (1975) 0.93
A simplified metyrapone test with determination of plasma ll-deoxycortisol (Metyrapone test with plasma S). J Clin Endocrinol Metab (1969) 0.93
The effect of null C4 alleles on complement function. Clin Immunol Immunopathol (1985) 0.93