Search Results - "Bitting, Casey"

Repeat Coronary Artery Dissection in Pregnancy: A Case Report and Review of the Literature by Bitting, Casey P., Zumwalt, Ross E.

“…Non‐atherosclerotic spontaneous coronary artery dissection (NA‐SCAD) is a rare cause of morbidity and mortality with a propensity for young, healthy, and often…”
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The Determination of Insulin Overdose in Postmortem Investigations by Labay, Laura M., Bitting, Casey P., Legg, Kevin M., Logan, Barry K.

“…The analysis of biological specimens for the presence of exogenous insulin is of special interest in select postmortem investigations. Insulin analogues are…”
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Upregulation of P2Y2R, Active uPA, and PAI-1 Are Essential Components of Hantavirus Cardiopulmonary Syndrome by Bondu, Virginie, Bitting, Casey, Poland, Valerie L., Hanson, Joshua A., Harkins, Michelle S., Lathrop, Sarah, Nolte, Kurt B., Lawrence, Daniel A., Buranda, Tione

“…Sin Nombre virus (SNV) causes hantavirus cardiopulmonary pulmonary syndrome (HCPS) with the loss of pulmonary vascular endothelial integrity, and pulmonary…”
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Evaluation of a 2-Pyridone, KRQ-10018, against Mycobacterium tuberculosis In Vitro and In Vivo by LENAERTS, Anne J, BITTING, Casey, WOOLHISER, Lisa, GRUPPO, Veronica, MARIETTA, Karen S, JOHNSON, Christine M, ORME, Ian M

“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Upregulation of P2Y 2 R, Active uPA, and PAI-1 Are Essential Components of Hantavirus Cardiopulmonary Syndrome by Bondu, Virginie, Bitting, Casey, Poland, Valerie L, Hanson, Joshua A, Harkins, Michelle S, Lathrop, Sarah, Nolte, Kurt B, Lawrence, Daniel A, Buranda, Tione

“…Sin Nombre virus (SNV) causes hantavirus cardiopulmonary pulmonary syndrome (HCPS) with the loss of pulmonary vascular endothelial integrity, and pulmonary…”
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Navajo Neurohepatopathy : A Case Report and Literature Review Emphasizing Clinicopathologic Diagnosis by Bitting, C P, Hanson, J A

“…Navajo Neurohepatopathy (NNH) is a rare hepatocerebral mitochondrial DNA (mtDNA) depletion syndrome (MDS) with nonspecific clinical or pathologic features…”
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