Published in Ann Intern Med on May 01, 1967
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IgG4-related sclerosing disease. World J Gastroenterol (2008) 3.84
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Rethinking Ormond's disease: "idiopathic" retroperitoneal fibrosis in the era of IgG4-related disease. Medicine (Baltimore) (2013) 1.08
Current concept and diagnosis of IgG4-related disease in the hepato-bilio-pancreatic system. J Gastroenterol (2013) 1.04
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Orbital involvement in multifocal fibrosclerosis. Br J Ophthalmol (1995) 0.99
Aortic disease in idiopathic retroperitoneal and mediastinal fibrosis. J Clin Pathol (1972) 0.97
Retroperitoneal fibrosis in three siblings with the sickle cell trait. Can Med Assoc J (1973) 0.96
Riedel's thyroiditis masquerading as anaplastic thyroid carcinoma: a case report. J Med Case Rep (2010) 0.94
Recent advances in the concept and pathogenesis of IgG4-related disease in the hepato-bilio-pancreatic system. Gut Liver (2014) 0.92
Retroperitoneal fibrosis and scleroderma. Postgrad Med J (1980) 0.87
Idiopathic fibrosis of mediastinum: a discussion of three cases and review of the literature. J Clin Pathol (1978) 0.86
Bowlby's disease? Br Med J (1971) 0.86
Suspected idiopathic sclerosing orbital inflammation presenting as immunoglobulin G4-related disease: a case report. J Med Case Rep (2011) 0.83
A case of IgG4-related sclerosing disease complicated by sclerosing cholangitis, retroperitoneal fibrosis and orbital pseudotumour. BMJ Case Rep (2009) 0.82
Retroperitoneal fibrosis as a cause of fever of undetermined origin. West J Med (1981) 0.81
IgG4-Related Autoimmune Prostatitis: Is It an Unusual or Underdiagnosed Manifestation of IgG4-Related Disease? Case Rep Urol (2013) 0.81
IgG₄-related sclerosing disease: a novel mimic of inflammatory bowel disease. Dig Dis Sci (2010) 0.81
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Multifocal fibrosclerosis associated with suprasellar and macular lesions. Br J Ophthalmol (1983) 0.79
Riedel's thyroiditis with multiple organ fibrosis. Thorax (1984) 0.78
Bilateral recurrent orbital inflammation associated with retroperitoneal fibrosclerosis. Br J Ophthalmol (1985) 0.78
Multifocal fibrosclerosis and renal amyloidosis. Postgrad Med J (1983) 0.77
Increased lymphangiogenesis in Riedel thyroiditis (Immunoglobulin G4-related thyroid disease). Virchows Arch (2014) 0.76
Clinical Update in Aspects of the Management of Autoimmune Thyroid Diseases. Endocrinol Metab (Seoul) (2016) 0.76
Idiopathic retroperitoneal fibrosis. Br Med J (Clin Res Ed) (1981) 0.75
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Riedel's Thyroiditis in an Elderly Male Patient: A Rare Entity. J Clin Diagn Res (2014) 0.75
[Idiopathic mediastinal fibrosis]. Can Med Assoc J (1971) 0.75
Mediastinal and hilar fibrosis. Br Med J (1971) 0.75
Primary sclerosing cholangitis. A report of two cases. Can Med Assoc J (1969) 0.75
Immunoglobulin G4-Related Thyroid Diseases. Eur Thyroid J (2016) 0.75
Immunoglobulin G4-Related Retroperitoneal Fibrosis Treated with Hochuekkito, a Kampo Medicine, following Steroid Treatment. Case Rep Gastroenterol (2014) 0.75
Retroperitoneal fibrosis. Can Med Assoc J (1973) 0.75
Coexisting retroperitoneal and mediastinal fibrosis. Postgrad Med J (1983) 0.75
Proteomic approach used in the diagnosis of Riedel's thyroiditis: a case report. J Med Case Rep (2012) 0.75
An unusual cholangitis. Br Med J (1976) 0.75
[Histopathology of IgG4-related disease]. Z Rheumatol (2016) 0.75
[Hypophysitis : Types and differential diagnosis]. Pathologe (2016) 0.75
A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. JAMA (1995) 11.45
Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine (Baltimore) (1966) 6.15
Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. J Clin Invest (1973) 5.87
Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene. Lancet (1993) 2.91
The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes. Am J Hum Genet (1988) 2.85
Reward deficiency syndrome: a biogenetic model for the diagnosis and treatment of impulsive, addictive, and compulsive behaviors. J Psychoactive Drugs (2000) 2.82
Frequency of sickling disorders in U.S. blacks. N Engl J Med (1973) 2.74
Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarction. J Clin Invest (1973) 2.65
Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. Proc Natl Acad Sci U S A (1984) 2.64
Linkage studies in a large kindred with familial hypercholesterolemia. Am J Hum Genet (1974) 2.49
Hazards of indiscriminate screening for sickling. N Engl J Med (1971) 2.38
Public health and long-term genetic implications of intrauterine diagnosis and selective abortion. Birth Defects Orig Artic Ser (1971) 2.28
A general theory of carcinogenesis. Proc Natl Acad Sci U S A (1973) 2.28
The D2 dopamine receptor gene as a determinant of reward deficiency syndrome. J R Soc Med (1996) 1.98
The rationale for an ordered arrangement of chromatin in the interphase nucleus. Am J Hum Genet (1968) 1.95
Familial hypercholesterolemia in a large indred. Evidence for a monogenic mechanism. Ann Intern Med (1972) 1.90
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. Proc Natl Acad Sci U S A (1983) 1.89
Association of the dopamine transporter gene (DAT1) with poor methylphenidate response. J Am Acad Child Adolesc Psychiatry (1999) 1.88
Arrangement of chromatin in the nucleus. Hum Genet (1980) 1.82
Nuclear proteins. III. The fibrillar nature of the nuclear matrix. Exp Cell Res (1976) 1.77
Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study. Circulation (2000) 1.76
A partial cDNA clone for human apolipoprotein B. Proc Natl Acad Sci U S A (1985) 1.76
The structure and function of chromatin. Adv Hum Genet (1972) 1.74
Hereditary hemochromatosis: gene discovery and its implications for population-based screening. JAMA (1998) 1.73
Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria. Am J Hum Genet (1966) 1.72
Holocentric chromosomes in Oncopeltus: kinetochore plates are present in mitosis but absent in meiosis. Chromosoma (1972) 1.70
Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man. Science (1967) 1.68
Jewish diseases and origins. Nat Genet (1995) 1.65
Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarction. J Clin Invest (1973) 1.64
Initiation of deoxyribonucleic acid replication at the nuclear membrane in human cells. J Mol Biol (1968) 1.63
Pc 1 Duarte, a common polymorphism of a human brain protein, and its relationship to depressive disease and multiple sclerosis. Nature (1979) 1.61
Mechanisms of chromosome banding and implications for chromosome structure. Annu Rev Genet (1978) 1.57
Brave new world? Science (1974) 1.56
Screening for genetic diseases. N Engl J Med (1997) 1.55
Detection of major gene for Gilles de la Tourette syndrome. Am J Hum Genet (1984) 1.54
A pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activity. Am J Hum Genet (1969) 1.51
Association of chromatin fibers with the annuli of the nuclear membrane. Exp Cell Res (1970) 1.49
Nonrandom patterns of codon usage and of nucleotide substitutions in human alpha- and beta-globin genes: an evolutionary strategy reducing the rate of mutations with drastic effects? Proc Natl Acad Sci U S A (1981) 1.45
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. Am J Hum Genet (1987) 1.43
Partial albinism. JAMA (1966) 1.42
Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase. Anal Biochem (1989) 1.42
Electron microscopy of human fibroblasts in tissue culture during logarithmic and confluent stages of growth. Exp Cell Res (1970) 1.41
Population genetic studies in the Congo. 3. Blood groups (ABO, MNSs, Rh, Jsa). Am J Hum Genet (1966) 1.40
Mechanisms of chromosome banding. VIII. Hoechst 33258-DNA interaction. Chromosoma (1975) 1.40
Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon. Am J Hum Genet (1988) 1.38
The mechanism of C- and G-banding of chromosomes. Exp Cell Res (1973) 1.38
Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid. Am J Hum Genet (1996) 1.37
The advent of the "unpatients'. Nat Med (1996) 1.36
Dopamine D2 receptor gene variants: association and linkage studies in impulsive-addictive-compulsive behaviour. Pharmacogenetics (1995) 1.35
Genetics of hyperlipidemia in coronary heart disease. Trans Assoc Am Physicians (1972) 1.34
Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies. Am J Hum Genet (1992) 1.34
Analbuminemia in an American Indian girl. Clin Genet (1976) 1.33
Serum paraoxonase and its influence on paraoxon and chlorpyrifos-oxon toxicity in rats. Toxicol Appl Pharmacol (1990) 1.32
Hereditary dysplasia of bone with kyphoscoliosis, contractures, and abnormally shaped ears. J Pediatr (1968) 1.30
Molecular patterns of X chromosome-linked color vision genes among 134 men of European ancestry. Proc Natl Acad Sci U S A (1989) 1.30
Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families. Arterioscler Thromb Vasc Biol (1999) 1.27
Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studies. Am J Hum Genet (1983) 1.27
Evidence for ancient tetraploidy and conservation of linkage groups in mammalian chromosomes. Nature (1972) 1.26
Genetics of protan and deutan color-vision anomalies: an instructive family. Am J Hum Genet (1969) 1.25
Predictive genetic diagnosis. Am J Hum Genet (1994) 1.25
Restricted variation in the glycolytic enzymes of human brain and erythrocytes. Nat New Biol (1973) 1.25
A search for protein cores in chromosomes: is the scaffold an artifact? Am J Hum Genet (1980) 1.24
Current concepts in genetics. The genetic hyperlipidemias. N Engl J Med (1976) 1.23
Partial deletion of chromosome 6p: delineation of the syndrome. Am J Med Genet (1991) 1.22
Fine structure of kinetochore in Indian muntjac. Exp Cell Res (1971) 1.22
Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype. Nat Genet (1999) 1.22
The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis. JAMA (1965) 1.22
Myocardial infarction in the familial forms of hypertriglyceridemia. Metabolism (1976) 1.21
Impact of genetic manipulation on society and medicine. Science (1983) 1.19
The glutathione S-transferase mu polymorphism as a marker for susceptibility to lung carcinoma. Cancer Res (1993) 1.19
Paraoxon hydrolysis in human serum mediated by a genetically variable arylesterase and albumin. Am J Hum Genet (1984) 1.17
Optical Studies of the interaction of 4'-6'-diamidino-2-phenylindole with DNA and metaphase chromosomes. Chromosoma (1977) 1.16
Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3. Am J Hum Genet (1996) 1.16
Selective expression of human X chromosome-linked green opsin genes. Proc Natl Acad Sci U S A (1992) 1.15
Dopamine receptor genes are associated with age at first sexual intercourse. J Biosoc Sci (1999) 1.14
Increased frequency of thyroid autoantibodies in mothers of patients with Down's syndrome. Lancet (1965) 1.14
Mutation nomenclature: nicknames, systematic names, and unique identifiers. Hum Mutat (1996) 1.14
Nuclear proteins. I. Electrophoretic comparison of mouse nucleoli, heterochromatin, euchromatin and contractile proteins. Exp Cell Res (1975) 1.13
Mental retardation in methemoglobinemia due to diaphorase deficiency. N Engl J Med (1965) 1.13
Molecular basis of abnormal red-green color vision: a family with three types of color vision defects. Am J Hum Genet (1988) 1.13
Tourette syndrome: clinical and psychological aspects of 250 cases. Am J Hum Genet (1985) 1.13
Familial aggregation of coronary heart disease and its relation to known genetic risk factors. Am J Cardiol (1982) 1.12
Hemolysis in glucose-6-phosphate dehydrogenase deficiency. Fed Proc (1972) 1.12
Inconsistencies in genetic counseling and screening for consanguineous couples and their offspring: the need for practice guidelines. Genet Med (2001) 1.12
Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognition. Mol Psychiatry (2003) 1.11
Defective colour vision associated with a missense mutation in the human green visual pigment gene. Nat Genet (1992) 1.11
Higher order structure of chromosomes. Chromosoma (1979) 1.10
Nuclear proteins. IV. Deficiency of non-histone proteins in condensed chromatin of Drosophila virilis and mouse. Exp Cell Res (1977) 1.10
Human glucose-6-phosphate dehydrogenase variants. Bull World Health Organ (1971) 1.10
Variants of red cell glucose-6-phosphate dehydrogenase among Asiatic Indians. Ann Hum Genet (1968) 1.10
A common C-1018G polymorphism in the human 5-HT1A receptor gene. Psychiatr Genet (1999) 1.09
Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency. Am J Hum Genet (1992) 1.06
Non-histone proteins. The effect of nuclear washes and comparison of metaphase and interphase chromatin. Exp Cell Res (1973) 1.06
Polymorphism in red photopigment underlies variation in colour matching. Nature (1992) 1.05
Nuclear proteins. II. Similarity of nonhistone proteins in nuclear sap and chromatin, and essential absence of contractile proteins from mouse liver nuclei. J Cell Biol (1976) 1.04
Preventing coronary heart disease: B vitamins and homocysteine. Circulation (1998) 1.04
Determination of subfractions of amniotic fluid alpha-fetoprotein in diagnosing spina bifida and congenital nephrosis. Br Med J (1979) 1.04
The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece. Am J Hum Genet (1966) 1.04
Medical and human genetics 1977: trends and directions. Am J Hum Genet (1978) 1.03
Atypical cholinesterase gene E1a: rarity in Negroes and most Orientals. Science (1968) 1.03