Cited by 141Liver Diseases and ImmunityPediatric Hepatobiliary Diseases and TreatmentsLiver Disease and Transplantation

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

Diminished survival in asymptomatic primary biliary cirrhosis

Open access

Balasubramaniam, Kumaravelu, Grambsch, Patricia M., Wiesner, Russell H., Lindor, Keith D., Dickson, E.Rolland·1990·Gastroenterology

DOI 10.1016/0016-5085(90)91091-j

Open this paper in CoChat — free account

Abstract

Data from 73 asymptomatic patients with primary biliary cirrhosis were analyzed to determine clinical course and long-term survival. Of these, 44 entered a D-penicillamine treatment trial; 29 qualified but chose not to participate. Median follow-up was 7.6 yr (range, 2.8-12.2 yr). Liver biopsy at the initial visit showed advanced disease (fibrosis, cirrhosis) in 61% of the patients. During prospective clinical follow-up, which was available for 37 of the 44 study patients, one or more symptoms of liver disease developed in 33 (89%); esophageal varices were found in 15 (41%), and histologic progression to cirrhosis was found in 20 (67%) of the 30 precirrhotic patients. Significant (p less than 0.01) biochemical progression was reflected by a decrease in mean serum albumin concentrations and an increase in mean serum bilirubin levels in 32 patients followed for 4-6 yr. Survival data were available for all 73 patients; 17 died (11 secondary to liver failure), and 1 underwent liver transplantation. These patients had a 4-fold increase in mortality rate (p less than 0.001) compared with the U.S. population matched for age, race, and sex.

Integrity signals

Registry

Crossref · 10.1016/0016-5085(90)91091-j

Cites

24 of 24 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Nonparametric Estimation from Incomplete Observations
Kaplan, E. L., & Meier, P. (1992) · Springer series in statistics · doi:10.1007/978-1-4612-4380-9_25 · Cited by 45,239
Nonparametric Estimation from Incomplete Observations
Kaplan, E. L., & Meier, P. (1958) · Journal of the American Statistical Association · doi:10.1080/01621459.1958.10501452 · Cited by 39,158
Nonparametrics: Statistical Methods Based on Ranks
Mergenthaler, M. J., & Lehmann, E. L. (1979) · Technometrics · doi:10.2307/1268531 · Cited by 3,353
Nonparametrics: Statistical Methods Based on Ranks.
Beaver, R. J., & Lehmann, E. L. (1976) · Biometrics · doi:10.2307/2529529 · Cited by 2,067
A Class of Rank Test Procedures for Censored Survival Data
Harrington, D. P., & Fleming, T. R. (1982) · Biometrika · doi:10.1093/biomet/69.3.553 · Cited by 1,194
Staging of chronic nonsuppurative destructive cholangitis (syndrome of primary biliary cirrhosis)
Ludwig, J., Dickson, E. R., & McDonald, G. S. A. (1978) · Virchows Archiv A Pathological Anatomy and Histology · doi:10.1007/bf00432479 · Cited by 753
Self-citation
[Primary biliary cirrhosis].
Celaya, F. B. (1989) · PubMed · Cited by 508
The presentation and diagnosis of 100 patients with primary biliary cirrhosis
Sherlock, S., & Scheuer, P. J. (1973) · New England Journal of Medicine · doi:10.1056/nejm197309272891306 · Cited by 504
The prognostic importance of clinical and histologic features in asymptomatic and symptomatic primary biliary cirrhosis
Roll, J., Boyer, J. L., Barry, D., & Klatskin, G. (1983) · New England Journal of Medicine · doi:10.1056/nejm198301063080101 · Cited by 417
Serum bilirubin: a prognostic factor in primary biliary cirrhosis
Shapiro, J. M., Smith, H., & Schaffner, F. (1979) · Gut · doi:10.1136/gut.20.2.137 · Cited by 319

Show all 24 references

Sorted by citations

Primary Biliary Cirrhosis
Schwab, M. (2011) · Springer eBooks · doi:10.1007/978-3-642-16483-5_4730 · Cited by 1,241
Primary Biliary Cirrhosis
Kaplan, M. M. (1996) · New England Journal of Medicine · doi:10.1056/nejm199611213352107 · Cited by 459
Natural history of early primary biliary cirrhosis
Metcalf, J. V., Mitchison, H. C., Palmer, J. M., Jones, D. E., Bassendine, M. F., & James, O. F. (1996) · The Lancet · doi:10.1016/s0140-6736(96)04410-8 · Cited by 421
Management of primary biliary cirrhosis
Heathcote, J. (2000) · Hepatology · doi:10.1053/he.2000.5984 · Cited by 412
The effect of ursodeoxycholic acid therapy on the natural course of primary biliary cirrhosis
Corpechot, C., Carrat, F., Bahr, A., Chrétien, Y., Poupon, R., & Poupon, R. Y. (2005) · Gastroenterology · doi:10.1053/j.gastro.2004.11.009 · Cited by 392
The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines
Hirschfield, G. M., Dyson, J. K., Alexander, G. J. M., Chapman, M. H., Collier, J., Hübscher, S., Patanwala, I., Pereira, S. P., Thain, C., Thorburn, D., et al. (2018) · Gut · doi:10.1136/gutjnl-2017-315259 · Cited by 362
Asymptomatic primary biliary cirrhosis: clinical features, prognosis, and symptom progression in a large population based cohort
Prince, M. I., Chetwynd, A., Craig, W. L., Metcalf, J. V., & James, O. F. W. (2004) · Gut · doi:10.1136/gut.2003.023937 · Cited by 261
Primary Biliary Cirrhosis
Hirschfield, G. M., & Heathcote, E. J. (2010) · Wiley eBooks · doi:10.1002/9781444314403.ch32 · Cited by 261
Primary biliary cirrhosis once rare, now common in the United Kingdom?
James, O. F., Bhopal, R., Howel, D., Gray, J., Burt, A. D., & Metcalf, J. V. (1999) · Hepatology · doi:10.1002/hep.510300213 · Cited by 213
Primary biliary cirrhosis
Hübscher, S. G., Elias, E., Buckels, J. A. C., Mayer, A. D., McMaster, P. D., & Neuberger, J. (1993) · Journal of Hepatology · doi:10.1016/s0168-8278(05)80244-2 · Cited by 180
Primary biliary cirrhosis
Kumagi, T., & Heathcote, E. J. (2008) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-3-1 · Cited by 182
Primary biliary cirrhosis: survival of a large cohort of symptomatic and asymptomatic patients followed for 24 years
Mahl, T. C., Shockcor, W., & Boyer, J. L. (1994) · Journal of Hepatology · doi:10.1016/s0168-8278(05)80139-4 · Cited by 163
Alkaline phosphatase normalization is associated with better prognosis in primary sclerosing cholangitis
Stanich, P. P., Björnsson, E., Gossard, A. A., Enders, F., Jorgensen, R. A., & Lindor, K. D. (2011) · Digestive and Liver Disease · doi:10.1016/j.dld.2010.12.008 · Cited by 164
Self-citation
Hypercholesterolemia and Atherosclerosis in Primary Biliary Cirrhosis: What Is the Risk?
Crippin, J. S., Lindor, K. D., Jorgensen, R., Kottke, B. A., Harrison, J. M., Murtaugh, P. A., & Dickson, R. E. (1992) · Hepatology · doi:10.1002/hep.1840150518 · Cited by 149
Self-citation
Four year follow up of fatigue in a geographically defined primary biliary cirrhosis patient cohort
Jones, D. E. J., Bhala, N., Burt, J., Goldblatt, J., Prince, M., & Newton, J. L. (2006) · Gut · doi:10.1136/gut.2005.080317 · Cited by 136
Asymptomatic primary biliary cirrhosis: a study of its natural history and prognosis
Springer, J., Cauch-Dudek, K., O'Rourke, K., Wanless, I. R., & Heathcote, E. J. (1999) · American Journal of Gastroenterology · doi:10.1111/j.1572-0241.1999.00770.x · Cited by 141
Molecular Mechanisms of Ursodeoxycholic Acid Toxicity & Side Effects: Ursodeoxycholic Acid Freezes Regeneration & Induces Hibernation Mode
Kotb, M. A. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13078882 · Cited by 117
A placebo-controlled trial of primary biliary cirrhosis treatment with colchicine and ursodeoxycholic acid
Vuoristo, M., Färkkilä, M. A., Karvonen, A., Leino, R., Lehtola, J., Mäkinen, J., Mattila, J. J., Friman, C., Seppälä, K., Tuominen, J., et al. (1995) · Gastroenterology · doi:10.1016/0016-5085(95)90696-7 · Cited by 111
Cholestatic Liver Disease: Current Treatment Strategies and New Therapeutic Agents
Hasegawa, S., Yoneda, M., Kurita, Y., Nogami, A., Honda, Y., Hosono, K., & Nakajima, A. (2021) · Drugs · doi:10.1007/s40265-021-01545-7 · Cited by 118
Primary biliary cirrhosis—presentation and diagnosis
Leuschner, U. (2003) · Clinics in Liver Disease · doi:10.1016/s1089-3261(03)00101-6 · Cited by 104
Prediction of prognosis of primary biliary cirrhosis in Japan
Inoue, K., Hirohara, J., Nakano, T., Seki, T., Sasaki, H., Higuchi, K., Ohta, Y., Onji, M., Muto, Y., & Moriwaki, H. (1995) · Liver International · doi:10.1111/j.1600-0676.1995.tb00110.x · Cited by 98
Primary sclerosing cholangitis
Silveira, M. G., & Lindor, K. D. (2008) · Canadian Journal of Gastroenterology · doi:10.1155/2008/824168 · Cited by 94
Self-citation
Pediatric-onset primary biliary cirrhosis
Dahlan, Y., Smith, L., Simmonds, D., Jewell, L. D., Wanless, I., Heathcote, E. J., & Bain, V. G. (2003) · Gastroenterology · doi:10.1016/j.gastro.2003.08.022 · Cited by 92
Natural history of primary biliary cirrhosis
Parés, A., & Rodés, J. (2003) · Clinics in Liver Disease · doi:10.1016/s1089-3261(03)00100-4 · Cited by 89
Ursodeoxycholic acid for primary biliary cirrhosis
Gluud, C. N., & Christensen, E. (2001) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd000551 · Cited by 85
Pruritus and fatigue in primary biliary cirrhosis
Bergasa, N. V., Mehlman, J. K., & Jones, E. A. (2000) · Best Practice & Research Clinical Gastroenterology · doi:10.1053/bega.2000.0109 · Cited by 83
Early biochemical response to ursodeoxycholic acid predicts symptom development in patients with asymptomatic primary biliary cirrhosis
Azemoto, N., Abe, M., Murata, Y., Hiasa, Y., Hamada, M., Matsuura, B., & Onji, M. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-009-0051-9 · Cited by 82
Accurate prediction of death by serial determination of galactose elimination capacity in primary biliary cirrhosis: A comparison with the mayo model
Reichen, J., Widmer, T., & Cotting, J. (1991) · Hepatology · doi:10.1002/hep.1840140316 · Cited by 62
Evaluation of Fatigue in U.S. Patients with Primary Biliary Cirrhosis
Stanca, C. M., Bach, N., Krause, C., Tandon, N., Freni, M. A., Gutierrez, J. A., Bodian, C., Lopez, J., Berk, P. D., Bodenheimer, H. C., et al. (2005) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2005.41315.x · Cited by 62
Diseases of the bile ducts
Nakanuma, Y., Zen, Y., & Portmann, B. C. (2012) · MacSween's Pathology of the Liver · doi:10.1016/b978-0-7020-3398-8.00010-6 · Cited by 56
Predicting outcome in primary biliary cirrhosis
Lammers, W. J., Kowdley, K. V., & van Buuren, H. R. (2014) · Annals of Hepatology · doi:10.1016/s1665-2681(19)30838-5 · Cited by 56
Methotrexate for primary biliary cirrhosis
Giljača, V., Poropat, G., Štimac, D., & Gluud, C. N. (2010) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004385.pub3 · Cited by 53
Ursodeoxycholic acid in chronic liver disease.
Caestecker, J. S. D., Jazrawi, R. P., Petroni, M. L., & Northfield, T. C. (1991) · Gut · doi:10.1136/gut.32.9.1061 · Cited by 53
Long-term prognosis of primary biliary cirrhosis (PBC) in Japan and analysis of the factors of stage progression in asymptomatic PBC (a-PBC)
Nakano, T. (2002) · Hepatology Research · doi:10.1016/s1386-6346(01)00148-6 · Cited by 49
Pruritus and fatigue in primary biliary cirrhosis
Bergasa, N. V. (2003) · Clinics in Liver Disease · doi:10.1016/s1089-3261(03)00105-3 · Cited by 48
Effects of ursodeoxycholic acid after 4 to 12 years of therapy in early and late stages of primary biliary cirrhosis
Leuschner, U., Güldütuna, S., Imhof, M., Hübner, K., Benjaminov, A., & Leuschner, M. (1994) · Journal of Hepatology · doi:10.1016/s0168-8278(94)80111-8 · Cited by 47
PRIMARY BILIARY CIRRHOSIS AND PRIMARY SCLEROSING CHOLANGITIS
Angulo, P., & Lindor, K. D. (1999) · Clinics in Liver Disease · doi:10.1016/s1089-3261(05)70084-2 · Cited by 46
Self-citation
Natural History of Primary Biliary Cirrhosis
Mayo, M. J. (2008) · Clinics in Liver Disease · doi:10.1016/j.cld.2008.02.012 · Cited by 45
Primary Biliary Cirrhosis
Czul, F., Peyton, A., & Levy, C. (2013) · Clinics in Liver Disease · doi:10.1016/j.cld.2012.12.003 · Cited by 37
Primary biliary cirrhosis: new perspectives in diagnosis and treatment
Prince, M. I., & Jones, D. E. J. (2000) · Postgraduate Medical Journal · doi:10.1136/pmj.76.894.199 · Cited by 37
Colchicine for primary biliary cirrhosis
Gong, Y., & Gluud, C. N. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004481.pub2 · Cited by 35
D-penicillamine for primary biliary cirrhosis
Gong, Y., Klingenberg, S. L., & Gluud, C. N. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004789.pub2 · Cited by 34
HLA class II markers and clinical heterogeneity in Swedish patients with primary biliary cirrhosis
Waßmuth, R., Depner, F., Danielsson, A., Hultcrantz, R., Lööf, L., Olson, R., Prytz, H., Sandberg–Gertzén, H., Wallerstedt, S. M., & Lindgren, S. C. (2002) · Tissue Antigens · doi:10.1034/j.1399-0039.2002.590504.x · Cited by 34
Azathioprine for primary biliary cirrhosis
Gong, Y., Christensen, E., & Gluud, C. N. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006000.pub2 · Cited by 33
Granulomatous liver disease and cholestasis
Matheus, T., & Muñoz, S. J. (2004) · Clinics in Liver Disease · doi:10.1016/s1089-3261(03)00137-5 · Cited by 33
Methotrexate therapy for the symptomatic treatment of primary biliary cirrhosis patients, who are biochemical incomplete responders to ursodeoxycholic acid therapy
Babatin, M. A., Sanai, F. M., & Swain, M. G. (2006) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2006.03048.x · Cited by 29
Update on New Drugs and Those in Development for the Treatment of Primary Biliary Cholangitis.
Bahar, R., Wong, K. A., Liu, C. H., & Bowlus, C. L. (2018) · Europe PMC (PubMed Central) · Cited by 29
Different response to ursodeoxycholic acid (UDCA) in primary biliary cirrhosis according to severity of disease
Floreani, A., Zappalà, F., Mazzetto, M. O., Naccarato, R., Plebani, M., & Chiaramonte, M. (1994) · Digestive Diseases and Sciences · doi:10.1007/bf02090053 · Cited by 26
The diagnosis and treatment of primary biliary cirrhosis
Kim, K., & Jeong, S. (2011) · The Korean Journal of Hepatology · doi:10.3350/kjhep.2011.17.3.173 · Cited by 25
Prevalence and associated factors with esophageal varices in early primary biliary cirrhosis
Ikeda, F., Okamoto, R., Baba, N., Fujioka, S., Shoji, B., Yabushita, K., Ando, M., Matsumura, S., Kubota, J., Yasunaka, T., et al. (2012) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.2012.07114.x · Cited by 24
Natural history of primary biliary cirrhosis
Abe, M., & Onji, M. (2008) · Hepatology Research · doi:10.1111/j.1872-034x.2008.00351.x · Cited by 25
Mortality rate of patients with asymptomatic primary biliary cirrhosis diagnosed at age 55 years or older is similar to that of the general population
Kubota, J., Ikeda, F., Terada, R., Kobashi, H., Fujioka, S.-I., Okamoto, R., Baba, S., Morimoto, Y., Ando, M., Makino, Y., et al. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-009-0090-2 · Cited by 23
Primary biliary cirrhosis: Report of a focus study group
Bergasa, N. V., Mason, A. L., Floreani, A., Heathcote, J., Swain, M. G., Jones, D. E. J., Lindor, K., Bassendine, M. F., & Worman, H. J. (2004) · Hepatology · doi:10.1002/hep.1840400434 · Cited by 23
Self-citation
Liver and Biliary Tract
Brown, W. R. (2005) · Elsevier eBooks · doi:10.1016/b978-012491543-5/50082-6 · Cited by 22
PRIMARY BILIARY CIRRHOSIS
Jones, D. E., James, O., & Bassendine, M. F. (1998) · Clinics in Liver Disease · doi:10.1016/s1089-3261(05)70007-6 · Cited by 22
A brief review on prognostic models of primary biliary cholangitis
Chen, S., Duan, W., You, H., & Jia, J. (2017) · Hepatology International · doi:10.1007/s12072-017-9819-9 · Cited by 20
Geoepidemiology and changing mortality in primary biliary cholangitis
Floreani, A., Tanaka, A., Bowlus, C. L., & Gershwin, M. E. (2017) · Journal of Gastroenterology · doi:10.1007/s00535-017-1333-2 · Cited by 20
Methotrexate for primary biliary cirrhosis
Gong, Y., & Gluud, C. N. (2005) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004385.pub2 · Cited by 20
Cyclosporin A for primary biliary cirrhosis
Gong, Y., Christensen, E., & Gluud, C. N. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd005526.pub2 · Cited by 19
Abnormalities of serum apo A1 containing lipoprotein particles in patients with primary biliary cirrhosis
O’Kane, M., Lynch, P. L. M., Callender, M. E., & Trimble, E. R. (1997) · Atherosclerosis · doi:10.1016/s0021-9150(97)06108-x · Cited by 19
Bile Duct Diseases
Zen, Y., Hübscher, S. G., & Nakanuma, Y. (2017) · Elsevier eBooks · doi:10.1016/b978-0-7020-6697-9.00009-1 · Cited by 16
Primary biliary cirrhosis: survival of a cohort followed for 10 years
Uddenfeldt, P., & Danielsson, A. (2000) · Journal of Internal Medicine · doi:10.1046/j.1365-2796.2000.00733.x · Cited by 15
Rationale for trials of long-term mycophenolate mofetil therapy for primary biliary cirrhosis
Jones, E. A. (2002) · Hepatology · doi:10.1053/jhep.2002.31607 · Cited by 16
Risk stratification and prognostic modelling in primary biliary cholangitis
Goet, J. C., Harms, M. H., Carbone, M., & Hansen, B. E. (2018) · Best Practice & Research Clinical Gastroenterology · doi:10.1016/j.bpg.2018.06.006 · Cited by 16
Current concepts in the pathogenesis of primary biliary cirrhosis
Charatcharoenwitthaya, P., & Lindor, K. D. (2005) · Annals of Hepatology · doi:10.1016/s1665-2681(19)32061-7 · Cited by 15
Self-citation
Early primary biliary cirrhosis: Just delayed or different?
Lindor, K. D. (1997) · Hepatology · doi:10.1002/hep.510260135 · Cited by 15
Self-citation
Reduction in serum levels of antimitochondrial (M2) antibodies following immunoglobulin therapy in severe combined immunodeficient (SCID) mice reconstituted with lymphocytes from patients with primary biliary cirrhosis (PBC)
Abedi, M. R., Hammarström, L. L. G., Broomé, U., Angelin, B., Smith, C. I. E., & Christensson, B. (1996) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.1996.d01-767.x · Cited by 15
Immunosupressive therapy for primary biliary cirrhosis
Beukers, R., & Schalm, S. W. (1992) · Journal of Hepatology · doi:10.1016/0168-8278(92)90123-7 · Cited by 15
Improving prognosis in primary biliary cholangitis – Therapeutic options and strategy
Harms, M. H., van Buuren, H. R., & van der Meer, A. J. (2018) · Best Practice & Research Clinical Gastroenterology · doi:10.1016/j.bpg.2018.06.004 · Cited by 14
Treatment of primary biliary cirrhosis
Szalay, F. (2001) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(01)00055-9 · Cited by 14
Ursodeoxycholic acid therapy for primary biliary cirrhosis. A 10-year British single-centre population-based audit of efficacy and survival
Bateson, M. C., & Gedling, P. (1998) · Postgraduate Medical Journal · doi:10.1136/pgmj.74.874.482 · Cited by 13
Liver and Biliary Tract
Brown, W. R., & Howell, C. D. (1994) · Elsevier eBooks · doi:10.1016/b978-0-12-524730-6.50047-6 · Cited by 12
Primary biliary cirrhosis in patients with breast cancer: studying the link
Bergasa, N. V. (1998) · Medical Hypotheses · doi:10.1016/s0306-9877(98)90263-8 · Cited by 12
Asymptomatic primary biliary cirrhosis.
Goodwin, L. (2004) · PubMed · Cited by 12
Current Treatment Options for Primary Biliary Cholangitis
Wong, K. A., Bahar, R., Liu, C. H., & Bowlus, C. L. (2018) · Clinics in Liver Disease · doi:10.1016/j.cld.2018.03.003 · Cited by 11
PREDICTIVE MODELS OF NATURAL HISTORY IN PRIMARY BILIARY CIRRHOSIS
Kim, W. R., & Dickson, E. R. (1998) · Clinics in Liver Disease · doi:10.1016/s1089-3261(05)70010-6 · Cited by 10
Self-citation
Azathioprine for primary biliary cirrhosis
Gong, Y., Christensen, E., & Gluud, C. N. (2006) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006000 · Cited by 10
Primary biliary cirrhosis: When and why does the disease develop?
Floreani, A., Ostuni, P. A., Ferrara, F., & Guido, M. (2006) · Digestive and Liver Disease · doi:10.1016/j.dld.2006.03.001 · Cited by 9
Primary biliary cirrhosis
Bar‐Dayan, Y., Gershwin, M. E., Levi, Y., Amital, H., & Shoenfeld, Y. (1998) · Immunologic Research · doi:10.1007/bf02788754 · Cited by 9
Primary Biliary Cirrhosis
Heathcote, J. (2004) · Wiley eBooks · doi:10.1002/9780470987025.ch28 · Cited by 9
HEPATOLOGY IN THE NEW MILLENNIUM
Ramrakhiani, S., & Bacon, B. R. (2000) · Medical Clinics of North America · doi:10.1016/s0025-7125(05)70277-7 · Cited by 8
Primary biliary cirrhosis clinical research single-topic conference
Lindor, K. D., Hoofnagle, J. H., Maddrey, W. C., Mackay, I. E., & Dickson, E. R. (1996) · Hepatology · doi:10.1002/hep.510230332 · Cited by 8
Self-citation
Management of primary biliary cholangitis prior to obeticholic acid availability
Durazzo, M., Bonetto, S., Fagoonee, S., Morgando, A., & Pellicano, R. (2018) · Minerva Medica · doi:10.23736/s0026-4806.18.05774-9 · Cited by 7
Management of Autoimmune and Cholestatic Liver Disorders
Krok, K. L., & Muñoz, S. J. (2009) · Clinics in Liver Disease · doi:10.1016/j.cld.2009.02.011 · Cited by 6
Cumulative risk of developing a new symptom in patients with primary biliary cholangitis and its impact on prognosis
Kimura, N., Setsu, T., Arao, Y., Sakai, N., Watanabe, Y., Abé, H., Kamimura, H., Sakamaki, A., Yokoo, T., Kamimura, K., et al. (2022) · JGH Open · doi:10.1002/jgh3.12789 · Cited by 6
Survival in asymptomatic primary biliary cirrhosis
Kaplan, M. M. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)91113-k · Cited by 6
The natural history of asymptomatic primary biliary cirrhosis
Kurtovic, J., Riordan, S. M., & Williams, R. L. (2005) · QJM · doi:10.1093/qjmed/hci058 · Cited by 5
Liver transplantation and primary biliary cirrhosis
Burroughs, A. K., Biagini, M. R., McCormick, P. A., & Rolles, K. (1989) · Postgraduate Medical Journal · doi:10.1136/pgmj.65.766.553 · Cited by 5
Immunointervention in primary biliary cirrhosis: an overview.
Bray, G., & Williams, R. (1992) · Journal of Autoimmunity · doi:10.1016/0896-8411(92)90047-t · Cited by 3
The timing of liver transplantation in primary biliary cirrhosis
Angulo, P., & Dickson, E. R. (2000) · Best Practice & Research Clinical Gastroenterology · doi:10.1053/bega.2000.0110 · Cited by 5
Self-citation
Primary Biliary Cirrhosis
Clark, V., & Levy, C. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-118-5_3 · Cited by 5
Historia natural de la cirrosis biliar primaria
Parés, A. R. (2008) · Gastroenterología y Hepatología · doi:10.1157/13127093 · Cited by 5
Clinical Course and Genetic Susceptibility of Primary Biliary Cirrhosis: Analysis of a Prospective Cohort
Almasio, P. L., Licata, A., Maida, M. F., Macaluso, F. S., Costantino, A., Alessi, N., Grimaudo, S., Accardi, G., Caruso, C., & Craxì, A. (2016) · Hepatitis Monthly · doi:10.5812/hepatmon.31681 · Cited by 5
Hospital prevalence of asymptomatic primary biliary cirrhosis: 4-year study based on analysis of 4468 consecutive in-patients.
Magrini, A., Nicodemo, S., & Puoti, C. (2008) · Liver · doi:10.1111/j.1600-0676.1996.tb00765.x · Cited by 4
Colchicine for primary biliary cirrhosis
Gong, Y., & Gluud, C. N. (2003) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004481 · Cited by 4
Methotrexate for primary biliary cirrhosis
Gong, Y., & Gluud, C. N. (2003) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004385 · Cited by 4
Clinical characteristics of primary biliary cirrhosis - idiopathic inflammatory myopathy overlap syndrome: A single center study
Wu, J., Yin, Y., Han, X., Di, H., Han, Y., Shen, M., Zhang, Y., & Zeng, X. (2024) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2024.08.005 · Cited by 3
Liver Diseases in the Elderly
Levinson, J. R., & Gordon, S. C. (1991) · Clinics in Geriatric Medicine · doi:10.1016/s0749-0690(18)30557-3 · Cited by 3
Primary Biliary Cholangitis
Bergasa, N. V. (2021) · Springer eBooks · doi:10.1007/978-1-4471-4715-2_3 · Cited by 3
The natural history of primary biliary cirrhosis.
Boyer, J. L., Shockcor, W. T., & Mahl, T. C. (1992) · Europe PMC (PubMed Central) · Cited by 3

Authors: Balasubramaniam, K., Grambsch, P. M., Wiesner, R. H., Lindor, K. D., & Dickson, E. R.
Affiliations: Mayo Clinic (US)
ORCID: Lindor, Keith D.
Venue: Gastroenterology
Publisher: Elsevier BV
Published: 1990-06
Volume: 98
Issue: 6
Pages: 1567-1571
ISSN: 0016-5085 (ISSN-L)
DOI: 10.1016/0016-5085(90)91091-j
OpenAlex: W140612521
Cited by: 141
References: 24
Citations by year: 2026: 1 · 2025: 2 · 2024: 2 · 2023: 1 · 2022: 1 · 2021: 2 · 2020: 1 · 2018: 7 · 2017: 5 · 2016: 1 · 2014: 1 · 2013: 1 · 2012: 3
FWCI: 4.06
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Gastroenterology (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Diabetes and Digestive and Kidney Diseases (DK34238 02, R01DK034238)
Topics: Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
Keywords: primary biliary cirrhosis, asymptomatic patients, long-term survival, mortality, D-penicillamine, disease progression, esophageal varices, liver failure, serum albumin, serum bilirubin, liver transplantation
MeSH terms: Adult, Aged, Bilirubin, Female, Follow-Up Studies, Humans, Liver, Liver Cirrhosis, Biliary, Male, Middle Aged, Penicillamine, Prospective Studies, Serum Albumin, Survival Rate

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Diminished survival in asymptomatic primary biliary cirrhosis

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks