Further evidence for location of the spherocytosis gene on chromosome 8.

PubWeight™: 1.04‹?› | Rank: Top 15%

🔗 View Article (PMID 6881776)

Published in Ann Intern Med on August 01, 1983

Authors

E B Bass, S W Smith, R E Stevenson, W F Rosse

Articles by these authors

(truncated to the top 100)

Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med (1994) 15.82

p53 is required for radiation-induced apoptosis in mouse thymocytes. Nature (1993) 13.46

Pain in sickle cell disease. Rates and risk factors. N Engl J Med (1991) 9.75

Internists' attitudes about clinical practice guidelines. Ann Intern Med (1994) 6.55

More informative abstracts of articles describing clinical practice guidelines. Ann Intern Med (1993) 6.54

The VF-14. An index of functional impairment in patients with cataract. Arch Ophthalmol (1994) 6.00

The "battering syndrome": prevalence and clinical characteristics of domestic violence in primary care internal medicine practices. Ann Intern Med (1995) 5.77

The use of angioplasty, bypass surgery, and amputation in the management of peripheral vascular disease. N Engl J Med (1991) 4.41

Importance of hospital volume in the overall management of pancreatic cancer. Ann Surg (1998) 4.19

Users' guides to the medical literature. VIII. How to use clinical practice guidelines. A. Are the recommendations valid? The Evidence-Based Medicine Working Group. JAMA (1995) 4.14

Clinical characteristics of women with a history of childhood abuse: unhealed wounds. JAMA (1997) 4.13

Promotion criteria for clinician-educators in the United States and Canada. A survey of promotion committee chairpersons. JAMA (1997) 3.63

Surgical rates and operative mortality for open and laparoscopic cholecystectomy in Maryland. N Engl J Med (1994) 3.53

A phenomenology of scut. Ann Intern Med (1991) 3.46

The value of routine preoperative medical testing before cataract surgery. Study of Medical Testing for Cataract Surgery. N Engl J Med (2000) 3.45

Apoptotic signals delivered through the T-cell receptor of a T-cell hybrid require the immediate-early gene nur77. Nature (1994) 2.69

Knowledge and access to information on recruitment of underrepresented populations to cancer clinical trials. Evid Rep Technol Assess (Summ) (2005) 2.69

The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal haemoglobinuria. Nature (1988) 2.66

Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses. Lancet (1972) 2.65

Cytoplasmic free Ca2+ in human platelets: Ca2+ thresholds and Ca-independent activation for shape-change and secretion. FEBS Lett (1982) 2.60

Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody. J Clin Invest (1966) 2.58

Radiologists' review of radiographs interpreted confidently by emergency physicians infrequently leads to changes in patient management. Ann Emerg Med (1998) 2.43

Do all programmed cell deaths occur via apoptosis? Proc Natl Acad Sci U S A (1993) 2.35

Statewide regionalization of pancreaticoduodenectomy and its effect on in-hospital mortality. Ann Surg (1998) 2.32

Obstetrical and gynecological complications in fragile X carriers: a multicenter study. Am J Med Genet (1994) 2.31

Metabolic acidosis in restraint-associated cardiac arrest: a case series. Acad Emerg Med (1999) 2.30

Synthesis of the literature on the effectiveness of regional anesthesia for cataract surgery. Ophthalmology (2001) 2.30

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics. Am J Med Genet (1997) 2.19

Practice guidelines. What are internists looking for? J Gen Intern Med (1996) 2.17

Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet (1998) 2.16

Contrasting views of physicians and nurses about an inpatient computer-based provider order-entry system. J Am Med Inform Assoc (1999) 2.13

Privacy in clinical information systems in secondary care. BMJ (1999) 2.12

National study of cataract surgery outcomes. Variation in 4-month postoperative outcomes as reflected in multiple outcome measures. Ophthalmology (1994) 2.09

Relation between prepublication release of clinical trial results and the practice of carotid endarterectomy. JAMA (2000) 2.04

Inositol phosphorylceramide, a novel substance and the chief member of a major group of yeast sphingolipids containing a single inositol phosphate. J Biol Chem (1974) 1.99

Cataract surgical techniques. Preferences and underlying beliefs. Arch Ophthalmol (1995) 1.97

Reforming the core clerkship in internal medicine: the SGIM/CDIM Project. Society of General Internal Medicine/Clerkship Directors in Internal Medicine. Ann Intern Med (2001) 1.91

Intensive care unit nurse staffing and the risk for complications after abdominal aortic surgery. Eff Clin Pract (2001) 1.86

The cooperative study of sickle cell disease: review of study design and objectives. Am J Pediatr Hematol Oncol (1982) 1.85

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor. Cell (1994) 1.85

Epidemiological correlates of diabetic neuropathy. Report from Pittsburgh Epidemiology of Diabetes Complications Study. Diabetes (1989) 1.79

Reproducibility and responsiveness of the VF-14. An index of functional impairment in patients with cataracts. Arch Ophthalmol (1995) 1.74

Morphologic changes in the membranes of red blood cells undergoing hemolysis. Am J Med (1966) 1.70

High-speed ultrasound volumetric imaging system. II. Parallel processing and image display. IEEE Trans Ultrason Ferroelectr Freq Control (1991) 1.68

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet (1996) 1.68

US nephrologists' recommendation of dialysis modality: results of a national survey. Am J Kidney Dis (2000) 1.65

Phenotype and genotype in mucolipidoses II and III alpha/beta: a study of 61 probands. J Med Genet (2009) 1.64

Relation of low-severity violence to women's health. J Gen Intern Med (1998) 1.64

Complex gastrointestinal surgery: impact of provider experience on clinical and economic outcomes. J Am Coll Surg (1999) 1.64

Subjective assessment of fever by parents: comparison with measurement by noncontact tympanic thermometer and calibrated rectal glass mercury thermometer. Ann Emerg Med (1996) 1.61

Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissues. Pediatrics (1986) 1.60

Adverse intraoperative medical events and their association with anesthesia management strategies in cataract surgery. Ophthalmology (2001) 1.60

Menkes disease: a biochemical abnormality in cultured human fibroblasts. Proc Natl Acad Sci U S A (1976) 1.60

Successful use of propofol in refractory delirium tremens. Ann Emerg Med (1997) 1.60

Complications encountered in the treatment of pilon fractures. J Orthop Trauma (1992) 1.59

Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. 3. The membrane defects caused by complement lysis. J Exp Med (1966) 1.57

Adverse events, including death, associated with the use of 1,4-butanediol. N Engl J Med (2001) 1.57

Paroxysmal nocturnal haemoglobinuria. Clin Haematol (1985) 1.55

Users' guides to the Medical Literature. VIII. How to use clinical practice guidelines. B. what are the recommendations and will they help you in caring for your patients? The Evidence-Based Medicine Working Group. JAMA (1995) 1.54

Familial cold urticaria. A generalized reaction involving leukocytosis. Arch Intern Med (1969) 1.53

Patient preferences for anaesthesia management during cataract surgery. Br J Ophthalmol (2004) 1.51

Variation in ophthalmic testing before cataract surgery. Results of a national survey of ophthalmologists. Arch Ophthalmol (1994) 1.51

Explososcan: a parallel processing technique for high speed ultrasound imaging with linear phased arrays. J Acoust Soc Am (1984) 1.49

Phylogenetic relationships of chemoautotrophic bacterial symbionts of Solemya velum say (Mollusca: Bivalvia) determined by 16S rRNA gene sequence analysis. J Bacteriol (1992) 1.47

Strategies for improving minority healthcare quality. Evid Rep Technol Assess (Summ) (2004) 1.46

The content and cost of cataract surgery. Arch Ophthalmol (1993) 1.44

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am J Hum Genet (1990) 1.44

A quantitative approach to speckle reduction via frequency compounding. Ultrason Imaging (1986) 1.43

Hyperglycemia with hyperosmolal dehydration in nondiabetic infants. J Pediatr (1970) 1.42

Identification of the messenger RNAs coding for the gag and env gene products of the murine mammary tumor virus. Proc Natl Acad Sci U S A (1979) 1.42

Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel. Genomics (1999) 1.42

Multilayer piezoelectric ceramics for two-dimensional array transducers. IEEE Trans Ultrason Ferroelectr Freq Control (1994) 1.41

Post-myocardial infarction depression. Evid Rep Technol Assess (Summ) (2005) 1.40

Congenital malformations in offspring of phenylketonuric mothers. Pediatrics (1967) 1.40

Folic acid absorption in women with a history of pregnancy with neural tube defect. Am J Clin Nutr (1995) 1.39

The relative hydrophobicity of oncornaviral structural proteins. Virology (1978) 1.38

Quality control studies on fetal bovine serum used in tissue culture. In Vitro (1974) 1.37

Splenectomy for primary and recurrent immune thrombocytopenic purpura (ITP). Current criteria for patient selection and results. Ann Surg (1987) 1.37

The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria. Blood (1996) 1.34

Autism and macrocephaly. Lancet (1997) 1.33

X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27. J Med Genet (1999) 1.33

Increased enzymatic activity of the alternative pathway convertase when bound to the erythrocytes of paroxysmal nocturnal hemoglobinuria. J Clin Invest (1982) 1.32

Phase aberration correction in medical ultrasound using speckle brightness as a quality factor. J Acoust Soc Am (1989) 1.31

Acquired DNA mutations associated with in vivo hydroxyurea exposure. Blood (2000) 1.29

Mechanisms of immune lysis of red blood cells in vitro. I. Paroxysmal nocturnal hemoglobinuria cells. J Clin Invest (1973) 1.29

Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts. Clin Chim Acta (1975) 1.29

Platelet antibody in autoimmune thrombocytopenia. Br J Haematol (1975) 1.27

Speckle pattern correlation with lateral aperture translation: experimental results and implications for spatial compounding. IEEE Trans Ultrason Ferroelectr Freq Control (1986) 1.25

Variations in the red cells in paroxysmal nocturnal haemoglobinuria. Br J Haematol (1973) 1.24

Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria. J Clin Invest (1974) 1.24

Hazards of oral anticoagulants during pregnancy. JAMA (1980) 1.23

Fundamental correlation lengths of coherent speckle in medical ultrasonic images. IEEE Trans Ultrason Ferroelectr Freq Control (1988) 1.21

Comparison of binding characteristics of factors B and H to C3b on normal and paroxysmal nocturnal hemoglobinuria erythrocytes. J Immunol (1983) 1.20

Chlorpropamide-induced immune hemolytic anemia. N Engl J Med (1970) 1.20

Progress in two-dimensional arrays for real-time volumetric imaging. Ultrason Imaging (1998) 1.20

Risk factors for retinal detachment after cataract surgery. A population-based case-control study. Ophthalmology (1996) 1.19

Electrostatic micromachine scanning mirror for optical coherence tomography. Opt Lett (2003) 1.19

Variation in utilization of procedures for treatment of peripheral arterial disease. A look at patient characteristics. Arch Intern Med (1993) 1.19

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. J Med Genet (1995) 1.18

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene. Clin Genet (2002) 1.18