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May 2, 2013
α1-Antitrypsin phenotypes and associated serum protein concentrations in a large clinical population
Joshua A Bornhorst, Dina N Greene, Edward R Ashwood, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 19, 2008
Evaluation of a fecal pancreatic elastase-1 enzyme-linked immunosorbent assay: Assessment versus an established assay and implication in classifying pancreatic function
J Alan Erickson, William E Aldeen, David G Grenache, et al.
American Journal of Clinical Pathology
|
August 21, 2016
A Library of Rare α1-Antitrypsin (AAT) Variant Phenotypes to Aid in the Diagnosis of AAT Deficiency
Neval Akbas, Graciela Gonzalez, Gregory J Buffone, et al.
Clinical Biochemistry
|
September 30, 2010
Performance characteristics of an automated assay for the quantitation of CYFRA 21-1 in human serum
Jay L Patel, J Alan Erickson, William L Roberts, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 31, 2010
Clinical and laboratory trends in fetal lung maturity testing
David G Grenache, Andrew R Wilson, Gilad A Gross, et al.
Clinical Biochemistry
|
June 19, 2016
Endogenous alkaline phosphatase interference in cardiac troponin I and other sensitive chemiluminescence immunoassays that use alkaline phosphatase activity for signal amplification
Daniel S Herman, Pratistha Ranjitkar, Diane Yamaguchi, et al.
American Journal of Clinical Pathology
|
January 29, 2013
Facilitating the laboratory diagnosis of α1-antitrypsin deficiency
Dina N Greene, M C Elliott-Jelf, Joely A Straseski, et al.
American Journal of Clinical Pathology
|
January 14, 2011
Concordance of butyrylcholinesterase phenotype with genotype: implications for biochemical reporting
M Laura Parnas, Melinda Procter, Monica A Schwarz, et al.
The American Journal of Pathology
|
July 11, 2002
The alpha(2) integrin subunit-deficient mouse: a multifaceted phenotype including defects of branching morphogenesis and hemostasis
Jianchun Chen, Thomas G Diacovo, David G Grenache, et al.
Chest
|
January 5, 2012
α1-antitrypsin deficiency in fraternal twins born with familial spontaneous pneumothorax
Dina N Greene, Melinda Procter, Patti Krautscheid, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 72) with videos related to
Sort By:
Page
of 8
Chest
|
May 2, 2013
α1-Antitrypsin phenotypes and associated serum protein concentrations in a large clinical population
Joshua A Bornhorst, Dina N Greene, Edward R Ashwood, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 19, 2008
Evaluation of a fecal pancreatic elastase-1 enzyme-linked immunosorbent assay: Assessment versus an established assay and implication in classifying pancreatic function
J Alan Erickson, William E Aldeen, David G Grenache, et al.
American Journal of Clinical Pathology
|
August 21, 2016
A Library of Rare α1-Antitrypsin (AAT) Variant Phenotypes to Aid in the Diagnosis of AAT Deficiency
Neval Akbas, Graciela Gonzalez, Gregory J Buffone, et al.
Clinical Biochemistry
|
September 30, 2010
Performance characteristics of an automated assay for the quantitation of CYFRA 21-1 in human serum
Jay L Patel, J Alan Erickson, William L Roberts, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 31, 2010
Clinical and laboratory trends in fetal lung maturity testing
David G Grenache, Andrew R Wilson, Gilad A Gross, et al.
Clinical Biochemistry
|
June 19, 2016
Endogenous alkaline phosphatase interference in cardiac troponin I and other sensitive chemiluminescence immunoassays that use alkaline phosphatase activity for signal amplification
Daniel S Herman, Pratistha Ranjitkar, Diane Yamaguchi, et al.
American Journal of Clinical Pathology
|
January 29, 2013
Facilitating the laboratory diagnosis of α1-antitrypsin deficiency
Dina N Greene, M C Elliott-Jelf, Joely A Straseski, et al.
American Journal of Clinical Pathology
|
January 14, 2011
Concordance of butyrylcholinesterase phenotype with genotype: implications for biochemical reporting
M Laura Parnas, Melinda Procter, Monica A Schwarz, et al.
The American Journal of Pathology
|
July 11, 2002
The alpha(2) integrin subunit-deficient mouse: a multifaceted phenotype including defects of branching morphogenesis and hemostasis
Jianchun Chen, Thomas G Diacovo, David G Grenache, et al.
Chest
|
January 5, 2012
α1-antitrypsin deficiency in fraternal twins born with familial spontaneous pneumothorax
Dina N Greene, Melinda Procter, Patti Krautscheid, et al.
Page
of 8