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Neurocritical Care|January 6, 2021
Pterygopalatine Fossa Blockade as Novel, Narcotic-Sparing Treatment for Headache in Patients with Spontaneous Subarachnoid HemorrhageCameron R Smith, W Christopher Fox, Christopher P Robinson, et al.
Journal of Addiction Medicine|July 20, 2011
Open trial of injectable risperidone for methamphetamine dependenceCharles W Meredith, Craig Jaffe, Monique Cherrier, et al.
Human Reproduction (Oxford, England)|September 18, 2010
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy lossE Rajcan-Separovic, D Diego-Alvarez, W P Robinson, et al.
The Journal of the Acoustical Society of America|May 12, 2009
Absolute calibration of hydrophones immersed in sandy sedimentGary B N Robb, Stephen P Robinson, Pete D Theobald, et al.
Plos One|January 21, 2017
Multi-Channel Optical Coherence Elastography Using Relative and Absolute Shear-Wave Time of FlightEli Elyas, Alex Grimwood, Janine T Erler, et al.
American Journal of Human Genetics|April 1, 1997
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restrictionW P Robinson, I J Barrett, L Bernard, et al.
Developmental Cell|February 15, 2024
Single-cell assessment of primary and stem cell-derived human trophoblast organoids as placenta-modeling platformsMatthew J Shannon, Gina L McNeill, Burak Koksal, et al.
Neoplasia (New York, N.Y.)|June 22, 2005
Acute tumor response to ZD6126 assessed by intrinsic susceptibility magnetic resonance imagingSimon P Robinson, Tammy L Kalber, Franklyn A Howe, et al.
Scientific Reports|September 27, 2019
Dual-probe molecular MRI for the in vivo characterization of atherosclerosis in a mouse model: Simultaneous assessment of plaque inflammation and extracellular-matrix remodelingCarolin Reimann, Julia Brangsch, Jan O Kaufmann, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
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