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Acta Medica Scandinavica|January 1, 1986
Familial alpha 1-antichymotrypsin deficiencyS Eriksson, B Lindmark, H LiljaBiochimica Et Biophysica Acta|July 27, 1989
The microheterogeneity of desialylated alpha 1-antichymotrypsin: the occurrence of two amino-terminal isoforms, one lacking a His-Pro dipeptideB Lindmark, H Lilja, R Alm, et al.Scandinavian Journal of Gastroenterology|May 1, 1991
Partial deficiency of alpha 1-antichymotrypsin is associated with chronic cryptogenic liver diseaseB Lindmark, S ErikssonActa Medica Scandinavica|January 1, 1985
Regional differences in the idiopathic hemochromatosis gene frequency in SwedenB Lindmark, S ErikssonAllergy|April 1, 1990
Heterozygous alpha 1-antichymotrypsin and PiZ alpha 1-antitrypsin deficiency. Prevalence and clinical spectrum in asthmatic childrenB Lindmark, E Svenonius, S ErikssonActa Medica Scandinavica|January 1, 1986
Lack of association between hemochromatosis and alpha-antitrypsin deficiencyS Eriksson, B Lindmark, S OlssonJournal of Hepatology|January 1, 1986
A Swedish family with alpha 1-antitrypsin deficiency, haemochromatosis, haemoglobinopathy D and early death in liver cirrhosisS Eriksson, B Lindmark, L HanikHistopathology|March 1, 1990
Hepatocyte inclusions of alpha 1-antichymotrypsin in a patient with partial deficiency of alpha 1-antichymotrypsin and chronic liver diseaseB Lindmark, H Millward-Sadler, F Callea, et al.Journal of Internal Medicine|July 1, 1992
Hepatitis C in chronic liver disease: an epidemiological study based on 566 consecutive patients undergoing liver biopsy during a 10-year periodH Verbaan, A Widell, S Lindgren, et al.Journal of Hepatology|July 1, 1993
The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung diseaseJ P Faber, W Poller, K Olek, et al.Pageof 94