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Physiological Measurement|August 20, 2019
Advanced automatic detection of fetal body movements from multichannel magnetocardiographic signalsA Schmidt, R Witte, L Swiderski, et al.Biological Research in Pregnancy and Perinatology|January 1, 1986
Vascular resistance, metabolism and EEG within cerebral grey and white matter during hypoxia in neonatal pigletsU Zwiener, R Bauer, W Buchenau, et al.British Journal of Haematology|December 21, 2004
Peripheral blood CD34 count in myelofibrosis with myeloid metaplasia: a prospective evaluation of prognostic value in 94 patientsBrijesh Arora, Shireen Sirhan, James D Hoyer, et al.Pediatrics|August 3, 2004
Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonatesMichael Kaplan, Marguerite Herschel, Cathy Hammerman, et al.Conference Proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference|February 3, 2007
Evaluation of different rhythms by hidden Markov models in heart rate variability of hypertrophic cardiomyopathy patientsM Vallverdú, M Palacios, D Hoyer, et al.Pneumologie (Stuttgart, Germany)|April 1, 1997
[Deterministic-chaotic and spectral-functional analysis of heart rate and respiratory movements]U Zwiener, D Hoyer, R Bauer, et al.Hemoglobin|July 3, 2014
β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20Michelle L Kluge, James D Hoyer, Kenneth C Swanson, et al.Journal of Neurochemistry|April 2, 1998
Distinct changes in peptide YY binding to, and mRNA levels of, Y1 and Y2 receptors in the rat hippocampus associated with kindling epileptogenesisM Gobbi, M Gariboldi, C Piwko, et al.Neuroscience Letters|May 16, 1988
Visualization of a novel serotonin recognition site (5-HT1D) in the human brain by autoradiographyC Waeber, M M Dietl, D Hoyer, et al.British Journal of Haematology|August 25, 1999
Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical courseR F McClure, G W Dewald, J D Hoyer, et al.Pageof 37