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Clinical Chemistry|June 1, 1991
Quantitative fluorometric screening test for fecal porphyrinsM R Pudek, W E Schreiber, A JamaniAmerican Journal of Clinical Pathology|November 1, 1989
Screening tests for porphobilinogen are insensitive. The problem and its solutionW E Schreiber, A Jamani, M R PudekClinical Chemistry|September 1, 1994
Molecular diagnosis of acute intermittent porphyria by analysis of DNA extracted from hair rootsW E Schreiber, F Fong, A JamaniClinical Biochemistry|June 1, 1990
Low concentration galactose determination in plasma adapted to the Cobas-BioM R Pudek, A Jamani, V Bernstein, et al.Human Genetics|May 1, 1994
Frameshift mutations in exons 9 and 10 of the porphobilinogen deaminase gene produce a crossreacting immunological material (CRIM)-negative form of acute intermittent porphyriaW E Schreiber, F Fong, A JamaniAmerican Journal of Clinical Pathology|June 1, 1995
Acute intermittent porphyria in a native North American family. Biochemical and molecular analysisW E Schreiber, A Jamani, J G ArmstrongHuman Mutation|January 1, 1997
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase geneW E Schreiber, X Zhang, J Senz, et al.Human Genetics|August 1, 1995
Heteroduplex analysis detects frameshift and point mutations in patients with acute intermittent porphyriaW E Schreiber, F Fong, B A Nassar, et al.Clinical Biochemistry|June 1, 1981
Triiodothyronine--binding immunoglobulin in a euthyroid patientM R Pudek, H W McIntoshCanadian Family Physician Medecin De Famille Canadien|February 2, 2011
Glycosylated hemoglobins: a reviewA A Nanji, M R PudekPageof 6