Published in Clin Orthop Relat Res on March 01, 1984
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell (2001) 11.99
Articular mobility in an African population. Ann Rheum Dis (1973) 7.01
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science (1997) 6.66
Tendon Lesions in Rheumatoid Arthritis. Ann Rheum Dis (1950) 5.52
Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. Am J Hum Genet (2001) 4.97
Genetic evidence for a switching and energy-transducing complex in the flagellar motor of Salmonella typhimurium. J Bacteriol (1986) 4.61
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene. Science (1997) 4.55
Lactic acidosis complicating the acquired immunodeficiency syndrome. Ann Intern Med (1993) 4.08
Purification and characterization of the flagellar hook-basal body complex of Salmonella typhimurium. J Bacteriol (1985) 4.04
Enthesopathy of rheumatoid and ankylosing spondylitis. Ann Rheum Dis (1971) 3.58
Undergraduate research. Genomics Education Partnership. Science (2008) 3.45
Randomized controlled trial of an oral CGRP receptor antagonist, MK-0974, in acute treatment of migraine. Neurology (2007) 3.43
Orthopaedic aspects of the Ehlers-Danlos syndrome. J Bone Joint Surg Br (1969) 3.30
Quantitative observations on mineralised and unmineralised bone in chronic renal azotaemia and intestinal malabsorption syndrome. J Pathol Bacteriol (1966) 2.73
Evidence for helper independent murine sarcoma virus. I. Segregation of replication-defective and transformation-defective viruses. Virology (1973) 2.67
Destructive lesions of vertebral bodies in ankylosing spondylitis. Ann Rheum Dis (1972) 2.59
Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfecta. EMBO J (1985) 2.52
Comparative cohort study of the outcomes of deep lamellar keratoplasty and penetrating keratoplasty for keratoconus. Eye (Lond) (2006) 2.43
Telomerase prevents the accelerated cell ageing of Werner syndrome fibroblasts. Nat Genet (2000) 2.26
Germinal centers without T cells. J Exp Med (2000) 2.25
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2. Am J Hum Genet (1990) 2.11
Radial ray defects and associated anomalies. Clin Genet (1989) 2.06
Development of a compact fast CCD camera and resonant soft x-ray scattering endstation for time-resolved pump-probe experiments. Rev Sci Instrum (2011) 2.05
Rheumatoid arthritis in a rural South African Negro population. Ann Rheum Dis (1975) 2.03
Help! Unusual X-ray appearances of a congenital bone disease of unknown aetiology. Pediatr Radiol (2001) 2.01
Early complications of permanent pacemaker implantation: no difference between dual and single chamber systems. Br Heart J (1995) 1.99
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27. Am J Hum Genet (2000) 1.98
Forward and backward running waves in the arteries: analysis using the method of characteristics. J Biomech Eng (1990) 1.96
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium. Am J Hum Genet (1992) 1.94
latheo encodes a subunit of the origin recognition complex and disrupts neuronal proliferation and adult olfactory memory when mutant. Neuron (1999) 1.94
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Am J Hum Genet (1996) 1.89
Changes in vascular endothelium related to lymphocyte collections in diseased synovia. Arthritis Rheum (1983) 1.88
Hypnosis or cognitive behavioral training for the reduction of pain and nausea during cancer treatment: a controlled clinical trial. Pain (1992) 1.88
Detection and distribution of aluminium in bone. J Clin Pathol (1984) 1.85
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. Am J Hum Genet (2001) 1.81
Sequential dermal microvascular and perivascular changes in the development of scleroderma. J Pathol (1992) 1.81
Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA. EMBO J (1991) 1.80
Osteoglophonic dwarfism. Pediatr Radiol (1980) 1.76
Flow-mediated dilatation following wrist and upper arm occlusion in humans: the contribution of nitric oxide. Clin Sci (Lond) (2001) 1.76
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa. Hum Mol Genet (1998) 1.75
Recovery after allogeneic marrow transplantation: prospective study of predictors of long-term physical and psychosocial functioning. Bone Marrow Transplant (1993) 1.72
Surgical aspects of the Ehlers-Danlos syndrome. A survey of 100 cases. Br J Surg (1969) 1.72
Hyperinsulinaemia and microvascular angina ("syndrome X") Lancet (1991) 1.69
The clinical features of sclerosteosis. A review of the manifestations in twenty-five affected individuals. Ann Intern Med (1976) 1.63
Vertebral end-plate lesions (Schmorl's nodes) in the dorsolumbar spine. Ann Rheum Dis (1976) 1.61
Efficacy of neonatal ocular prophylaxis for the prevention of chlamydial and gonococcal conjunctivitis. N Engl J Med (1989) 1.59
Variants of the Ehlers-Danlos syndrome. Clinical, biochemical, haematological, and chromosomal features of 100 patients. Ann Rheum Dis (1969) 1.59
The syndromic status of sclerosteosis and van Buchem disease. Clin Genet (1984) 1.58
The natural history of sclerosteosis. Clin Genet (2003) 1.58
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nat Genet (2000) 1.58
Rheumatic disorders in the South African Negro. Part II. Osteo-arthrosis. S Afr Med J (1975) 1.57
Endothelial control of arterial distensibility is impaired in chronic heart failure. Circulation (1995) 1.57
A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17. Hum Mol Genet (1994) 1.56
Survey of nationally registered emergency medical services providers: pediatric education. Ann Emerg Med (2000) 1.56
Identification of proteins of the outer (L and P) rings of the flagellar basal body of Escherichia coli. J Bacteriol (1987) 1.54
Are teamwork and professional autonomy compatible, and do they result in improved hospital care? Qual Health Care (2001) 1.54
A review of the osteopetroses. Postgrad Med J (1977) 1.53
Vestibular dysfunction in hereditary ataxia. Brain (1975) 1.53
Characterization of the fliE genes of Escherichia coli and Salmonella typhimurium and identification of the FliE protein as a component of the flagellar hook-basal body complex. J Bacteriol (1992) 1.52
Reversal of neuromuscular blockade: dose determination studies with atropine and glycopyrrolate given before or in a mixture with neostigmine. Anesth Analg (1981) 1.52
Refining the Amsterdam Criteria and Bethesda Guidelines: testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic. J Clin Oncol (2004) 1.51
Sclerosteosis - an autosomal recessive disorder. Clin Genet (1977) 1.50
Comparison of enzyme immunoassay and culture for diagnosis of chlamydial conjunctivitis and respiratory infections in infants. J Clin Microbiol (1987) 1.49
The dominant and recessive forms of cutis laxa. J Med Genet (1972) 1.48
The physiological load imposed on basketball players during competition. J Sports Sci (1995) 1.48
Spatial analysis of the distribution of Ixodes dammini (Acari: Ixodidae) on white-tailed deer in Ogle County, Illinois. J Med Entomol (1992) 1.47
DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesions. Proc Natl Acad Sci U S A (1993) 1.46
Posttranslational modifications of p53 in replicative senescence overlapping but distinct from those induced by DNA damage. Mol Cell Biol (2000) 1.46
Extracorporeal photopheresis (ECP) in the treatment of chronic graft-versus-host disease (GVHD) Bone Marrow Transplant (1999) 1.42
Dietary supplementation with marine omega-3 fatty acids improve systemic large artery endothelial function in subjects with hypercholesterolemia. J Am Coll Cardiol (2000) 1.42
Three years of experience with prospective randomized effectiveness studies. Control Clin Trials (1998) 1.42
Blood-pressure and its correlates in urban and tribal Africa. Lancet (1980) 1.40
Rheumatoid arthritis in a subtropical population. Ann Rheum Dis (1966) 1.40
Side effects of phenobarbital in toddlers; behavioral and cognitive aspects. J Pediatr (1979) 1.39
Lethal complications of the Ehlers-Danlos syndrome. Br Med J (1968) 1.39
Congenital hypertrichosis lanuginosa. Arch Dermatol (1970) 1.39
Epithelial development and differentiation in the mammary gland is not dependent on alpha 3 or alpha 6 integrin subunits. Dev Biol (2001) 1.38
Medical emergencies: atrial fibrillation and myocardial infarction. Anaesthesia (2013) 1.38
Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta? J Med Genet (1981) 1.38
Schizophrenia as an anomaly of development of cerebral asymmetry. A postmortem study and a proposal concerning the genetic basis of the disease. Arch Gen Psychiatry (1989) 1.38
Physical properties of the skin in the Ehlers-Danlos syndrome. Ann Rheum Dis (1969) 1.36
Endothelium and inelastic arteries: an early marker of vascular dysfunction in non-insulin dependent diabetes. BMJ (1996) 1.35
Rheumatoid arthritis in a tribal Xhosa population in the Transkei, Southern Africa. Ann Rheum Dis (1977) 1.34
Detection of immunoglobulin M (IgM), IgA, and IgG Norwalk virus-specific antibodies by indirect enzyme-linked immunosorbent assay with baculovirus-expressed Norwalk virus capsid antigen in adult volunteers challenged with Norwalk virus. J Clin Microbiol (1994) 1.33
Detection of covalent DNA-protein complexes: the adenovirus DNA-terminal protein complex and HeLa DNA-protein complexes. Cold Spring Harb Symp Quant Biol (1979) 1.32
Is telomere length in peripheral blood lymphocytes correlated with cancer susceptibility or radiosensitivity? Br J Cancer (2007) 1.32
Pomegranate extract inhibits Staphylococcus aureus growth and subsequent enterotoxin production. J Ethnopharmacol (2005) 1.32
Proteins tightly bound to HeLa cell DNA at nuclear matrix attachment sites. Mol Cell Biol (1983) 1.31
Crouzonodermoskeletal syndrome. J Clin Pediatr Dent (2004) 1.30
Isolation and ultrastructural analysis of microfibrillar structures from foetal bovine elastic tissues. Relative abundance and supramolecular architecture of type VI collagen assemblies and fibrillin. J Cell Sci (1991) 1.30
Rheumatoid arthritis of the cervical spine. Mod Trends Rheumatol (1971) 1.30
Osteoarthrosis in a rural South African Negro population. Ann Rheum Dis (1976) 1.29
Effects of training on the visual recognition of consonants. J Speech Hear Res (1977) 1.29
Sclerosteosis in South Africa. S Afr Med J (1979) 1.29
Comparison of two rapid microscopic methods and culture for detection of Chlamydia trachomatis in ocular and nasopharyngeal specimens from infants. J Clin Microbiol (1989) 1.28
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome. Clin Genet (1985) 1.27
Proteus syndrome in southern Africa: natural history and clinical manifestations in six individuals. Am J Med Genet (1987) 1.27
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats. Am J Hum Genet (1999) 1.26
Prevalence of anti-Rift-Valley-fever IgM antibody in abattoir workers in the Nile delta during the 1993 outbreak in Egypt. Bull World Health Organ (1996) 1.25