Published in Am J Ophthalmol on January 01, 1972
The fifth Frederick H. Verhoeff Lecture. The role of the lymphocyte (cell-mediated) immunity in ocular disease. Trans Am Ophthalmol Soc (1973) 0.75
THE BLOOD FLOW, VASCULAR RESISTANCE, AND OXYGEN CONSUMPTION OF THE BRAIN IN ESSENTIAL HYPERTENSION. J Clin Invest (1948) 3.95
In vivo and in vitro chromosomal damage induced by LSD-25. N Engl J Med (1967) 2.39
Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion. Humangenetik (1965) 2.37
The response of lymphocytes from non-immunized humans to antigen-antibody complexes. Clin Exp Immunol (1968) 1.79
The covalent structure of a human gamma G-immunoglobulin. II. Isolation and characterization of the cyanogen bromide fragments. Biochemistry (1968) 1.77
A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region. Hum Mol Genet (1997) 1.71
Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues. Ann Intern Med (1966) 1.67
Production and characterization of migration inhibitory factor(s) (MIF) of established lymphoid and non-lymphoid cell lines. J Immunol (1972) 1.65
Paternal trisomy 21 mosaicism and Down's syndrome. Am J Hum Genet (1971) 1.65
Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. Cytogenetics (1966) 1.62
Studies on lysosomes. XII. Redistribution of acid hydrolases in human lymphocytes stimulated by phytohemagglutinin. J Cell Biol (1968) 1.58
Criminality in XYY and XXY men. Science (1976) 1.57
Interpretation of tear film breakup. Arch Ophthalmol (1977) 1.56
Trisomy 22: a clinical entity. J Pediatr (1971) 1.55
Stability of HL-A and appearance of other antigens (LIVA) at the surface of lymphoblasts grown in vitro. Haematologica (1969) 1.53
The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern. Clin Genet (1972) 1.42
Location of the genes for human heavy chain immunoglobulin to chromosome 6. Proc Natl Acad Sci U S A (1978) 1.35
Appearance of hydrolase rich granules in human lymphocytes induced by phytohemagglutinin and antigens. Blood (1967) 1.35
Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. J Med Genet (1977) 1.30
Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome. J Med Genet (1974) 1.29
Vinyl chloride exposure and human chromosome aberrations. Mutat Res (1975) 1.28
Confirmation of the regional localization of the genes for human acid alpha-glucosidase (GAA) and adenosine deaminase (ADA) by somatic cell hybridization. Ann Hum Genet (1984) 1.28
Precise identification of various chromosomal abnormalities. Ann Hum Genet (1973) 1.27
Chromosomal localization of human haemoglobin structural genes. Nature (1972) 1.26
Stimulation of human tonsillar lymphocytes in vitro. Clin Exp Immunol (1966) 1.23
64Cu metabolism in Menkes and normal cultured skin fibroblasts. Pediatr Res (1978) 1.21
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. J Clin Invest (1978) 1.19
Neonatal hepatitis and biliary atresia associated with trisomy 17-18 syndrome. N Engl J Med (1969) 1.17
L-asparaginase and blastogenesis. Lancet (1969) 1.16
Partial thyroxine-binding globulin deficiency in a family. Pediatrics (1969) 1.15
Visual fields in diabetic retinopathy. Br J Ophthalmol (1971) 1.15
The production of immunoglobulins by human peripheral blood lymphocytes in vitro. Clin Exp Immunol (1967) 1.14
Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification. Pediatr Res (1975) 1.13
Letter: Genetic heterogeneity in fucosidosis. Lancet (1973) 1.13
Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies. Blood (1970) 1.12
Double Beta-Lipoprotein: A New Genetic Variant in Man. Science (1965) 1.12
Paternal uniparental disomy for chromosome 14: a case report and review. Am J Med Genet (1997) 1.10
Products of lymphoid cells in continuous culture. Am J Pathol (1970) 1.10
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenat Diagn (1992) 1.09
Familial de Lange syndrome. Report of three cases in a sibship. Clin Genet (1971) 1.09
Isozymes of human alpha-L-fucosidase detectable by starch gel electrophoresis. Clin Chim Acta (1974) 1.09
Polymorphism of human alpha fucosidase. Am J Hum Genet (1975) 1.09
Clinical experience with nucleosides in herpes simplex eye infections in man and animals. Ann N Y Acad Sci (1965) 1.09
A partial long arm deletion of chromosome 7:46,XY,del(7)(q32). J Med Genet (1977) 1.09
Familial x/x translocation: t(x;x)(p22;q13) Cytogenet Cell Genet (1974) 1.08
Trisomy 12 mosaicism detected by mid-trimester amniocentesis. Prenat Diagn (1990) 1.07
Studies on ciliary dyskinesia factor in cystic fibrosis. IV. Its possible identification as anaphylatoxin (C3a)-IgG complex. Life Sci (1974) 1.07
Studies on ciliary dyskinesia factor in cystic fibrosis. I. Bioassay and heterozygote detection in serum. Pediatr Res (1973) 1.06
Patient care, resident stress, and government regulation. Am J Dis Child (1989) 1.06
XXXXY boy. A 15-month-old child with normal intellectual development. Am J Dis Child (1970) 1.06
Histocompatibility (HL-A) antigens and primary open-angle glaucoma. Tissue Antigens (1976) 1.05
The response of cultured lymphocytes from patients with systemic lupus erythematosus to DNA. Arthritis Rheum (1967) 1.05
Intraocular penetration of cephaloridine in humans. Am J Ophthalmol (1968) 1.05
In situ hybridization of chromosome loci. Fed Proc (1975) 1.04
Letter: Complement components in cystic fibrosis. Lancet (1973) 1.04
Molecular cytogenetic analysis of uterine leiomyoma and leiomyosarcoma by comparative genomic hybridization. Cancer Genet Cytogenet (2000) 1.04
Serratia marcescens, an ocular pathogen; new considerations. Arch Ophthalmol (1971) 1.04
The incidence of uveitis in multiple sclerosis. Am J Ophthalmol (1966) 1.04
Cell-specific differences in membrane beta-glucosidase from normal and Gaucher cells. Biochim Biophys Acta (1977) 1.01
Observations on cell lines derived from a patient with Hodgkin's disease. Cancer Res (1978) 1.01
Marginal (ring) corneal ulcer as presenting manifestation of Wegener's granuloma. A clinicopathologic study. Trans Am Acad Ophthalmol Otolaryngol (1971) 1.01
Tissue and species specificity of BCP 54, the major soluble protein of bovine cornea. Exp Eye Res (1981) 1.01
The role of lymphocyte (cell-mediated) immunity in ocular disease. The fifth Frederick H. Verhoeff lecture. Am J Ophthalmol (1973) 1.01
Genetic heterogeneity in acid alpha-glucosidase deficiency. Am J Hum Genet (1983) 1.00
Ocular pigmentation and pressure and outflow responses to pilocarpine and epinephrine. Am J Ophthalmol (1971) 1.00
Improvement of muscle function in acid maltase deficiency by high-protein therapy. Neurology (1983) 1.00
The frequency of chromosome aberrations in tall men with special reference to 47, XYY and 47, XXY. Am J Hum Genet (1976) 0.99
Response of lymphocytes to penicillin: comparison with skin tests and circulating antibodies in man. Nature (1967) 0.98
Genetic and clinical considerations of long-arm deletion of the X chromosome. Pediatrics (1970) 0.97
Duplication of 16q and deletion of 15q. Am J Med Genet (1989) 0.97
A clinical evaluation of the effects of topically applied levobunolol and timolol on increased intraocular pressure. Am J Ophthalmol (1982) 0.96
Confirmation of the assignment of genes of human immunoglobulin heavy chains to chromosome 14 by analysis of Ig synthesis by man-mouse hybridomas. Eur J Immunol (1981) 0.95
Isolation and characterization of BCP 54, the major soluble protein of bovine cornea. Exp Eye Res (1981) 0.95
The potential use of quinolones in future ocular antimicrobial therapy. Am J Ophthalmol (1988) 0.95
Fucosidosis type 2. Pediatrics (1976) 0.94
Further regional localization of the genes for human acid alpha glucosidase (GAA), peptidase D (PEPD), and alpha mannosidase B (MANB) by somatic cell hybridization. Hum Genet (1985) 0.94
Human-mosquito somatic cell hybrids induced by ultraviolet-inactivated Sendai virus. Nat New Biol (1971) 0.93
Recurrent abortions and chromosome abnormalities. J Obstet Gynaecol Br Commonw (1972) 0.93
Cytogenetics of fetal wastage. N Engl J Med (1975) 0.93
Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism. J Med Genet (1978) 0.93
Properties of beta-glucosidase in cultured skin fibroblasts from controls and patients with Gaucher disease. Am J Hum Genet (1978) 0.93
Fetal wastage and maternal mosaicism. Obstet Gynecol (1972) 0.93
Assignment of the gene locus for human alpha-L-fucosidase to chromosome 1 by analysis of somatic cell hybrids. Somatic Cell Genet (1978) 0.93
Agammaglobulinemia: some current concepts. Med Clin North Am (1965) 0.92
Oral isosorbide and intraocular pressure. Am J Ophthalmol (1970) 0.92
Acid alpha-glucosidase: kinetic and immunologic properties of enzyme variants in health and disease. Isozymes Curr Top Biol Med Res (1983) 0.92
Kniest syndrome with dominant inheritance and mucopolysacchariduria. Am J Hum Genet (1975) 0.92
Inhibition of leucocyte migration by corneal antigen in chronic viral keratitis. Nat New Biol (1971) 0.92
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes". Am J Med Genet (1995) 0.92
Ciliary-dyskinesia factor in immunological and pulmonary disease. Lancet (1973) 0.91
Pompe's disease: detection of heterozygotes by lymphocyte stimulation. Science (1969) 0.91
An isozyme of acid alpha-glucosidase with reduced catalytic activity for glycogen. Am J Hum Genet (1980) 0.91
Clinical evaluation of the Humphrey automatic refractor. Arch Ophthalmol (1984) 0.91
In situ hybridization for gene mapping. Cytogenet Cell Genet (1975) 0.91
Lymphocyte stimulation by allogeneic and autochthonous cultured lymphoid cells. Cell Immunol (1970) 0.91
Increased copper metallothionein in Menkes cultured skin fibroblasts. Pediatr Res (1981) 0.90
Topical hetrazan in the treatment of ocular onchocerciasis. Am J Ophthalmol (1970) 0.90
Clinical applications of comparative genomic hybridization. Genet Med (2001) 0.90