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Archives of Pathology & Laboratory Medicine
|
November 8, 2002
Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders
Richard D Press, Kenneth A Bauer, Jody L Kujovich, et al.
Diagnostic Cytopathology
|
June 4, 2004
Identification of cytomegalovirus in a liquid-based gynecologic sample using morphology, immunohistochemistry, and DNA real-time PCR detection
Harmanjatinder S Sekhon, Richard D Press, Waldemar A Schmidt, et al.
The Journal of Molecular Diagnostics : JMD
|
August 9, 2008
ABL kinase domain pseudoexon insertion is not uncommon in BCR-ABL transcripts
Neil B Quigley, Donald C Henley, Roger A Hubbard, et al.
The Journal of Molecular Diagnostics : JMD
|
February 16, 2008
An intron-derived insertion/truncation mutation in the BCR-ABL kinase domain in chronic myeloid leukemia patients undergoing kinase inhibitor therapy
Jennifer Laudadio, Michael W N Deininger, Michael J Mauro, et al.
The Journal of Molecular Diagnostics : JMD
|
February 20, 2009
Multi-Site PCR-based CMV viral load assessment-assays demonstrate linearity and precision, but lack numeric standardization: a report of the association for molecular pathology
Daynna J Wolff, Denise Lamarche Heaney, Paul D Neuwald, et al.
Blood
|
July 24, 2009
Determining the rise in BCR-ABL RNA that optimally predicts a kinase domain mutation in patients with chronic myeloid leukemia on imatinib
Richard D Press, Stephanie G Willis, Jennifer Laudadio, et al.
Leukemia
|
December 18, 2019
Insights on mechanisms of clonal evolution in chronic neutrophilic leukemia on ruxolitinib therapy
Ryan C Stoner, Richard D Press, Julia E Maxson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
Highly accurate molecular genetic testing for HFE hereditary hemochromatosis: results from 10 years of blinded proficiency surveys by the College of American Pathologists
Richard D Press, Garrett Eickelberg, Thomas J McDonald, et al.
American Journal of Hematology
|
September 30, 2009
HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants
James C Barton, Susie A Lafreniere, Catherine Leiendecker-Foster, et al.
International Journal of Molecular Sciences
|
September 9, 2023
Cytogenetically Cryptic Acute Promyelocytic Leukemia: A Diagnostic Challenge
Maedeh Mohebnasab, Peng Li, Bo Hong, et al.
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of 6
Search research articles
Search
Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Archives of Pathology & Laboratory Medicine
|
November 8, 2002
Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders
Richard D Press, Kenneth A Bauer, Jody L Kujovich, et al.
Diagnostic Cytopathology
|
June 4, 2004
Identification of cytomegalovirus in a liquid-based gynecologic sample using morphology, immunohistochemistry, and DNA real-time PCR detection
Harmanjatinder S Sekhon, Richard D Press, Waldemar A Schmidt, et al.
The Journal of Molecular Diagnostics : JMD
|
August 9, 2008
ABL kinase domain pseudoexon insertion is not uncommon in BCR-ABL transcripts
Neil B Quigley, Donald C Henley, Roger A Hubbard, et al.
The Journal of Molecular Diagnostics : JMD
|
February 16, 2008
An intron-derived insertion/truncation mutation in the BCR-ABL kinase domain in chronic myeloid leukemia patients undergoing kinase inhibitor therapy
Jennifer Laudadio, Michael W N Deininger, Michael J Mauro, et al.
The Journal of Molecular Diagnostics : JMD
|
February 20, 2009
Multi-Site PCR-based CMV viral load assessment-assays demonstrate linearity and precision, but lack numeric standardization: a report of the association for molecular pathology
Daynna J Wolff, Denise Lamarche Heaney, Paul D Neuwald, et al.
Blood
|
July 24, 2009
Determining the rise in BCR-ABL RNA that optimally predicts a kinase domain mutation in patients with chronic myeloid leukemia on imatinib
Richard D Press, Stephanie G Willis, Jennifer Laudadio, et al.
Leukemia
|
December 18, 2019
Insights on mechanisms of clonal evolution in chronic neutrophilic leukemia on ruxolitinib therapy
Ryan C Stoner, Richard D Press, Julia E Maxson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
Highly accurate molecular genetic testing for HFE hereditary hemochromatosis: results from 10 years of blinded proficiency surveys by the College of American Pathologists
Richard D Press, Garrett Eickelberg, Thomas J McDonald, et al.
American Journal of Hematology
|
September 30, 2009
HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants
James C Barton, Susie A Lafreniere, Catherine Leiendecker-Foster, et al.
International Journal of Molecular Sciences
|
September 9, 2023
Cytogenetically Cryptic Acute Promyelocytic Leukemia: A Diagnostic Challenge
Maedeh Mohebnasab, Peng Li, Bo Hong, et al.
Page
of 6