Search Results - "Andrews, Caroline M."

Plasma and synovial fluid pharmacokinetics of a single intravenous dose of meropenem in adult horses by Langston, Vernon C., Fontenot, Robin L., Byers, Julie A., Andrews, Caroline M., Mochal‐King, Cathleen A.

“…The objective of this study was to determine the pharmacokinetics of meropenem in horses after intravenous (IV) administration. A single IV dose of meropenem…”
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Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome by MacKinnon, Sarah, MSc, OC(C), Oystreck, Darren T., MMedSci, OC(C), Andrews, Caroline, MS, Chan, Wai-Man, MS, Hunter, David G., MD, PhD, Engle, Elizabeth C., MD

“…Objective To improve diagnostic assessment in Moebius syndrome by (1) creating more selective diagnostic subgroups and (2) conducting genetic evaluation in a…”
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Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: A New Syndrome by Irahara, Kaori, MD, Saito, Yoshiaki, MD PhD, Sugai, Kenji, MD PhD, Nakagawa, Eiji, MD,PhD, Saito, Takashi, MD PhD, Komaki, Hirofumi, MD PhD, Nakata, Yasuhiro, MD PhD, Sato, Noriko, MD PhD, Baba, Kazumi, MD, Yamamoto, Toshiyuki, MD PhD, Chan, Wai-Man, BS, Andrews, Caroline, MS, Engle, Elizabeth C., MD, Sasaki, Masayuki, MD PhD

“…Abstract Background Horizontal gaze palsy and progressive scoliosis is caused by mutations in the ROBO3 gene, which plays a role in axonal guidance during…”
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Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography by Thomas, Mervyn G., BSc, Kumar, Anil, MD, Mohammad, Sarim, BSc, Proudlock, Frank A., PhD, Engle, Elizabeth C., MD, Andrews, Caroline, MS, Chan, Wai-Man, BS, Thomas, Shery, PhD, Gottlob, Irene, MD

“…Purpose To characterize and grade the spectrum of foveal hypoplasia based on different stages of arrested development of the fovea. Grading was performed using…”
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HOXA1 mutations are not a common cause of Möbius syndrome by Rankin, Jessica K., MD, Andrews, Caroline, MS, Chan, Wai-Man, Engle, Elizabeth C., MD

“…The HOXA1 -related syndromes result from autosomal-recessive truncating mutations in the homeobox transcription factor, HOXA1 . Limited horizontal gaze and…”
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