Published in Nature on November 25, 1967
Nature and extent of penicillin side-reactions, with particular reference to fatalities from anaphylactic shock. Bull World Health Organ (1968) 2.79
Lymphocytes in congenital immunological deficiency diseases. Clin Exp Immunol (1968) 1.87
The relationship between lymphocyte transformation and immune responses. II. Correlations between transformation and humoral and cellular immune responses. Clin Exp Immunol (1969) 1.41
Lymphocyte transformation with thyroglobulin in thyroid diseases. Clin Exp Immunol (1972) 0.83
Hapten-specific T-cell unresponsiveness induced bybenzylpenicilloyl autologous gamma globulin conjugates in human lymphocyes in vitro. J Clin Invest (1980) 0.77
[Penicillin induced lymphocyte transformation-penicillin hypersensitivity?]. Arch Dermatol Forsch (1972) 0.75
CLINICAL USES OF 2,3-DIMERCAPTOPROPANOL (BAL). III. STUDIES ON THE TOXICITY OF BAL ON PERCUTANEOUS AND PARENTERAL ADMINISTRATION. J Clin Invest (1946) 5.31
Antigen-bearing langerhans cells in skin, dermal lymphatics and in lymph nodes. Cell Immunol (1976) 4.52
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
Langerhans cells: role in contact hypersensitivity and relationship to lymphoid dendritic cells and to macrophages. Immunol Rev (1980) 2.10
CLINICAL USES OF 2,3-DIMERCAPTOPROPANOL (BAL). V. SKIN SENSITIZATION TO BAL. J Clin Invest (1946) 1.99
The role of Langerhans cells in allergic contact hypersensitivity. A review of findings in man and guinea pigs. J Invest Dermatol (1976) 1.93
NEW PENETRATING VEHICLES AND SOLVENTS. Science (1942) 1.86
The response of lymphocytes from non-immunized humans to antigen-antibody complexes. Clin Exp Immunol (1968) 1.79
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
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
Reduced Langerhans' cell Ia antigen and ATPase activity in patients with the acquired immunodeficiency syndrome. N Engl J Med (1984) 1.60
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
Trisomy 22: a clinical entity. J Pediatr (1971) 1.55
Penicillin allergy and the heterogenous immune responses of man to benzylpenicillin. J Clin Invest (1966) 1.54
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
Langerhans cells: a review of their nature with emphasis on their immunologic functions. Prog Allergy (1978) 1.37
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
Dermal and intravascular Langerhans cells at sites of passively induced allergic contact sensitivity. Cell Immunol (1975) 1.30
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
Types of cutaneous reactions to drugs. Importance in recognition of adverse reactions. JAMA (1967) 1.29
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
Benzylpenicilloyl specific serum antibodies to penicillin in man. I. Development of a sensitive hemagglutination assay method and haptenic specificities of antibodies. J Immunol (1966) 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
Occurrence of bullous pemphigoid after furosemide therapy. Arch Dermatol (1976) 1.21
DEMONSTRATING THE PRESENCE OF SULFONAMIDES IN THE TISSUES. Science (1943) 1.20
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. J Clin Invest (1978) 1.19
The role of langerhans cells in contact allergy. I. An ultrastructural study in actively induced contact dermatitis in guinea pigs. Acta Derm Venereol (1974) 1.18
Present-day incidence of superficially infecting pathogenic fungi. Species identified in a diagnostic laboratory of mycology between 1964 and 1966. Arch Dermatol (1967) 1.17
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
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
Immunologic studies in patients with serum sickness-like reactions following penicillin therapy. J Invest Dermatol (1967) 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
The most common contact allergens 1968-1970. Arch Dermatol (1973) 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
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenat Diagn (1992) 1.09
Polymorphism of human alpha fucosidase. Am J Hum Genet (1975) 1.09
A partial long arm deletion of chromosome 7:46,XY,del(7)(q32). J Med Genet (1977) 1.09
The biology of fungous infections of the feet. JAMA (1966) 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
XXXXY boy. A 15-month-old child with normal intellectual development. Am J Dis Child (1970) 1.06
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
Effect of glucocorticosteroids on epidermal Langerhans cells. J Exp Med (1982) 1.06
The response of cultured lymphocytes from patients with systemic lupus erythematosus to DNA. Arthritis Rheum (1967) 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
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
Improvement of muscle function in acid maltase deficiency by high-protein therapy. Neurology (1983) 1.00
Genetic heterogeneity in acid alpha-glucosidase deficiency. Am J Hum Genet (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
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
Langerhans cells: target cells in immune complex reactions. Cell Immunol (1977) 0.96
Congenital unilateral benign papillomatosis of the mouth. Arch Dermatol (1975) 0.95
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
Contact photosensitivity patterns to halogenated salicylanilides in man and guinea pigs. Arch Dermatol (1967) 0.95
Experiments on the biology of fungous infections of the feet. J Invest Dermatol (1966) 0.95
Morbilliform eruptions caused by penicillin. A study by electron microscopy and immunologic tests. J Invest Dermatol (1970) 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
Kniest syndrome with dominant inheritance and mucopolysacchariduria. Am J Hum Genet (1975) 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
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes". Am J Med Genet (1995) 0.92
Elevated lactate dehydrogenase values in patients with Pneumocystis carinii pneumonia. Chest (1988) 0.92
Agammaglobulinemia: some current concepts. Med Clin North Am (1965) 0.92
Structural features of photoallergy to salicylanilides and related compounds. J Invest Dermatol (1966) 0.92
Ciliary-dyskinesia factor in immunological and pulmonary disease. Lancet (1973) 0.91