Published in Br J Dermatol on October 01, 1994
Chronic urticaria. Br J Dermatol (1995) 1.05
The paucity of ethical analysis in allergology. Allergy Asthma Clin Immunol (2013) 0.75
High response rate to additive-free diet in chronic urticaria. Br J Dermatol (1996) 0.75
Perspectives on the basic reproductive ratio. J R Soc Interface (2005) 5.34
Value-based pathology: a cost-benefit analysis of the examination of routine and nonroutine tonsil and adenoid specimens. Am J Clin Pathol (1997) 4.51
Selective inhibition of receptor-coupled phospholipase C-dependent processes in human platelets and polymorphonuclear neutrophils. J Pharmacol Exp Ther (1990) 3.55
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet (2000) 3.48
The Alder Hey affair: implications for pathology practice. J Clin Pathol (2001) 3.38
Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet (1997) 2.82
The gut: a central organ after surgical stress. Surgery (1988) 2.76
Insulin receptor phosphorylation, insulin receptor substrate-1 phosphorylation, and phosphatidylinositol 3-kinase activity are decreased in intact skeletal muscle strips from obese subjects. J Clin Invest (1995) 2.66
Erosive pustular dermatosis of the scalp. Br J Dermatol (1979) 2.56
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA (1999) 2.56
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nat Genet (1998) 2.52
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum Mol Genet (2001) 2.48
Congenital cytomegalovirus infection. N Engl J Med (1977) 2.35
Broadband observations of the naked-eye gamma-ray burst GRB 080319B. Nature (2008) 2.16
A re-examination of risk estimates from the NIOSH Occupational Noise and Hearing Survey (ONHS) J Acoust Soc Am (1997) 2.09
Congenital cytomegalovirus infection: diagnostic and prognostic significance of the detection of specific immunoglobulin M antibodies in cord serum. Pediatrics (1982) 2.07
Venous stasis ulcers, stasis dermatitis and mothers' political ambitions for their offspring. Br J Dermatol (1989) 2.03
Biochemical characterization of a filtered synaptoneurosome preparation from guinea pig cerebral cortex: cyclic adenosine 3':5'-monophosphate-generating systems, receptors, and enzymes. J Neurosci (1985) 2.02
The new dermatology. J R Coll Physicians Lond (1990) 1.94
Pattern formation in the blue-green alga, Anabaena. I. Basic mechanisms. J Cell Sci (1973) 1.92
Metabolic imaging of malignant pleural mesothelioma with fluorodeoxyglucose positron emission tomography. Chest (1998) 1.91
Camptodactyly and simialr atraumatic flexion deformities of the proximal interphalangeal joints of the fingers. A study of thirty-one cases. J Bone Joint Surg Am (1968) 1.89
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nat Genet (1999) 1.82
Eye signs in craniopharyngioma. Br J Ophthalmol (1975) 1.80
Sustained endotoxemia leads to marked down-regulation of early steps in the insulin-signaling cascade. Crit Care Med (2001) 1.78
Pattern formation in the blue-green alga Anabaena. II. Controlled proheterocyst regression. J Cell Sci (1973) 1.78
Recurrent meningitis and Mondini dysplasia. Arch Otolaryngol Head Neck Surg (1990) 1.77
Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Hum Mutat (2001) 1.77
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa. Am J Hum Genet (2000) 1.76
Circulatory effects of heroin in patients with myocardial infarction. Lancet (1967) 1.75
The prevalence of acne vulgaris in adolescence. Br J Dermatol (1971) 1.72
Glutamine metabolism by the intestinal tract. JPEN J Parenter Enteral Nutr (1985) 1.71
Teratogenicity of 2-ethoxyethanol by dermal application. Drug Chem Toxicol (1982) 1.70
Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10. Hum Mol Genet (1996) 1.69
Biochemical changes in the collagen of the palmar fascia in patients with Dupuytren's disease. J Bone Joint Surg Am (1981) 1.69
Clinical and metabolic efficacy of glutamine-supplemented parenteral nutrition after bone marrow transplantation. A randomized, double-blind, controlled study. Ann Intern Med (1992) 1.68
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Hum Mol Genet (2001) 1.68
Treatment of rosacea by metronidazole. Lancet (1976) 1.68
Challenge test battery in chronic urticaria. Br J Dermatol (1976) 1.67
Localization of Usher syndrome type II to chromosome 1q. Genomics (1990) 1.67
Prognostic value of FDG PET imaging in malignant pleural mesothelioma. J Nucl Med (1999) 1.67
A single dose of endotoxin increases intestinal permeability in healthy humans. Arch Surg (1988) 1.66
Bioregulation of lysosomal enzyme secretion from human neutrophils: roles of guanosine 3':5'-monophosphate and calcium in stimulus-secretion coupling. Proc Natl Acad Sci U S A (1975) 1.65
Oral evening-primrose-seed oil improves atopic eczema. Lancet (1982) 1.64
Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nat Genet (1998) 1.63
Why retrobulbar anaesthesia? Br J Ophthalmol (1988) 1.63
Erosive pustular dermatosis of the scalp--a definition. Br J Dermatol (1988) 1.62
Mutants of Anabaena cylindrica altered in heterocyst spacing. Arch Microbiol (1975) 1.62
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. J Med Genet (2001) 1.61
Related cell-surface antigens expressed with positional specificity in Drosophila imaginal discs. Proc Natl Acad Sci U S A (1984) 1.60
Ten per cent polarized optical emission from GRB 090102. Nature (2009) 1.58
Highly polarized light from stable ordered magnetic fields in GRB 120308A. Nature (2013) 1.57
Performance of a whole-body PET scanner using curve-plate NaI(Tl) detectors. J Nucl Med (2001) 1.56
Giant-cell tumors of the bones of the hand. J Hand Surg Am (1980) 1.55
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. Hum Mol Genet (1999) 1.54
Increased intestinal permeability associated with infection in burn patients. Arch Surg (1988) 1.53
Abnormal movement of the arytenoid region during exercise presenting as exercise-induced asthma in an adolescent athlete. Chest (1994) 1.52
Effect of oral contraceptives on haemoglobin, packed-cell volume, serum-iron, and total iron-binding capacity in healthy women. Lancet (1967) 1.50
ROR gamma: the third member of ROR/RZR orphan receptor subfamily that is highly expressed in skeletal muscle. Biochem Biophys Res Commun (1994) 1.48
The Lang lecture 1986. The enigma of primary open-angle glaucoma. Trans Ophthalmol Soc U K (1986) 1.48
Allometric scaling in comparative biology: problems of concept and method. Am J Physiol (1984) 1.48
Successful demand management in histopathology: a model using sputum cytology. J Clin Pathol (2001) 1.47
[ The family physician's sentinel function studied with reference to referrals and referral cards]. Ned Tijdschr Geneeskd (1996) 1.47
Hypertrichosis due to minoxidil. Br J Dermatol (1979) 1.45
Pyrazoline bisphosphonate esters as novel antiinflammatory and antiarthritic agents. J Med Chem (1993) 1.45
Endobronchial tumors in children: an uncommon clinical entity. Ann Otol Rhinol Laryngol (2001) 1.45
Sneddon's syndrome (livedo reticularis and cerebral thrombosis) with livedo vasculitis and anticardiolipin antibodies. Br J Dermatol (1989) 1.44
Circulatory effects of pethidine in patients with acute myocardial infarction. Lancet (1967) 1.43
Urticaria and hepatitis C. Br J Dermatol (1997) 1.41
Management of congenital buccopharyngeal membrane. Cleft Palate Craniofac J (1997) 1.39
Study finds sleeping pills overprescribed. Science (1979) 1.39
Drug interactions with methotrexate. Br J Dermatol (1991) 1.37
Insulin-like growth factor-I receptor internalization regulates signaling via the Shc/mitogen-activated protein kinase pathway, but not the insulin receptor substrate-1 pathway. J Biol Chem (1998) 1.37
Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum Mol Genet (1995) 1.36
Prostaglandins and pruritus. Br J Dermatol (1976) 1.36
A position-specific cell surface antigen in the drosophila wing imaginal disc. Cell (1981) 1.35
Effect of schizophrenia on frontotemporal activity during word encoding and recognition: a PET cerebral blood flow study. Am J Psychiatry (2001) 1.35
Rethinking allometry. J Theor Biol (1980) 1.34
Distinct biologically active receptors for insulin, insulin-like growth factor I, and insulin-like growth factor II in cultured skeletal muscle cells. J Biol Chem (1985) 1.33
Two frequent missense mutations in Pendred syndrome. Hum Mol Genet (1998) 1.31
Phorbol myristate acetate-induced release of granule enzymes from human neutrophils: inhibition by the calcium antagonist, 8-(N,N-diethylamino)-octyl 3,4,5-trimethoxybenzoate hydrochloride. Biochem Biophys Res Commun (1979) 1.31
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4). Hum Mol Genet (2000) 1.30
Infection with cytomegalovirus during pregnancy: specific IgM antibodies as a marker of recent primary infection. J Infect Dis (1982) 1.30
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I. Am J Hum Genet (2000) 1.29
Refining the diagnosis of hydatidiform mole: image ploidy analysis and p57KIP2 immunohistochemistry. Histopathology (2003) 1.28
Dual time point fluorine-18 fluorodeoxyglucose positron emission tomography: a potential method to differentiate malignancy from inflammation and normal tissue in the head and neck. Eur J Nucl Med (1999) 1.28
Excretion of cytomegalovirus in mothers: observations after delivery of congenitally infected and normal infants. J Infect Dis (1982) 1.27
Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafness. Arch Otolaryngol Head Neck Surg (2001) 1.26
Laryngomalacia and its treatment. Laryngoscope (1999) 1.26
Use of isolated nuclei in the indirect fluorescent-antibody test for human cytomegalovirus infection: comparison with microneutralization, anticomplement, and conventional indirect fluorescent-antibody assays. J Clin Microbiol (1978) 1.25
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. Hum Mol Genet (1999) 1.25
Treatment of atopic eczema with evening primrose oil. Lancet (1981) 1.24
Effects of contractile activity on tyrosine phosphoproteins and PI 3-kinase activity in rat skeletal muscle. Am J Physiol (1995) 1.24
Neonatal screening for congenital cytomegalovirus infection by detection of virus in saliva. J Infect Dis (1993) 1.24
Maintenance of small bowel mucosa with glutamine-enriched parenteral nutrition. JPEN J Parenter Enteral Nutr (1990) 1.23
Mood effects on limbic blood flow correlate with emotional self-rating: a PET study with oxygen-15 labeled water. Psychiatry Res (1995) 1.21
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. Hum Mutat (1998) 1.21
Granuloma annulare, rheumatoid nodules and necrobiosis lipoidica. Br J Dermatol (1977) 1.21
Imported yellow fever in a United States citizen. Clin Infect Dis (1997) 1.20
Health and economic implications of a work-site smoking-cessation program: a simulation analysis. J Occup Environ Med (1996) 1.19