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Chest|January 1, 1995
Hemodynamic correlates of outcome in patients undergoing orthotopic liver transplantation. Evidence for early postoperative myocardial depressionS A Nasraway, R D Klein, T B Spanier, et al.
Pediatric Pulmonology|May 16, 2022
Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®Remi Z Welbel, Casey M Rand, Amy Zhou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 9, 2000
alpha-Melanocyte-stimulating hormone is contained in nerve terminals innervating thyrotropin-releasing hormone-synthesizing neurons in the hypothalamic paraventricular nucleus and prevents fasting-induced suppression of prothyrotropin-releasing hormone gene expressionC Fekete, G Légrádi, E Mihály, et al.
Critical Care Medicine|March 1, 1995
Multiple organ failure after liver transplantationT B Spanier, R D Klein, S A Nasraway, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|March 14, 2007
Growth deceleration and restoration after serious burn injuryKathy Prelack, Johanna Dwyer, Gerry E Dallal, et al.
Pediatric Pulmonology|May 8, 2009
Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicineDebra E Weese-Mayer, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A|January 24, 2019
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersYakov Sivan, Amy Zhou, Lawrence J Jennings, et al.
Molecular Ecology|May 5, 2016
In memoriam: Richard G. Harrison - his life and legacyDaniel J Howard, Richard K Grosberg, Mohamed A F Noor, et al.
Chemsuschem|March 19, 2015
Solvent-enabled nonenyzmatic sugar production from biomass for chemical and biological upgradingJeremy S Luterbacher, David Martin Alonso, Jacqueline M Rand, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 19, 2008
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B geneGabriela M Repetto, Raul J Corrales, Selim G Abara, et al.
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