Publications by authors named "C Michael B Henderson"
Background: Psoriasiform dermatitis can be defined both clinically and histologically, but is not a traditionally recognized clinical or histologic diagnosis.
Objective: Analyze the final clinical diagnosis, demographics and clinical characteristics in patients with histologic psoriasiform dermatitis.
Methods: Retrospective cross-sectional analysis of patients with histologic psoriasiform dermatitis 2004-2017.
Interventions to Reduce Discrimination and Stigma: The State of the Art.
Focus (Am Psychiatr Publ)
January 2025
Background: There is a rich literature on the nature of mental health-related stigma and the processes by which it severely affects the life chances of people with mental health problems. However, applying this knowledge to deliver and evaluate interventions to reduce discrimination and stigma in a lasting way is a complex and long-term challenge.
Methods: We conducted a narrative synthesis of systematic reviews published since 2012, and supplemented this with papers published subsequently as examples of more recent work.
Article Synopsis
- The study investigates CP symmetry violation in the decay of D^{+} particles into K^{-}K^{+}π^{+} using data from proton-proton collisions at a high energy of 13 TeV.
- A unique model-independent method was employed to analyze the phase-space distributions of D^{+} and D^{-} particles, correcting for any instrumental biases using D_{s}^{+} decays.
- The findings indicate no significant evidence of CP violation, with a p value of 8.1%, and measure specific CP asymmetry observables, marking this study as the most sensitive search of its kind in multibody decays.
Spinal muscular atrophy (SMA) is caused by low levels of the survival motor neuron (SMN) protein. Even though SMN is ubiquitously expressed, the disease selectively affects motor neurons, leading to progressive muscle weakness. Even among motor neurons, certain motor units appear more clinically resistant to SMA.
View Article and Find Full Text PDFBoys With Duchenne Muscular Dystrophy Have Diastolic Dysfunction Based on CMR.
Circ Cardiovasc Imaging
December 2024
Article Synopsis
- Cardiomyopathy is a major cause of death in boys with Duchenne muscular dystrophy (DMD), and this study investigates cardiac function using cardiac magnetic resonance (CMR) imaging to compare DMD patients with healthy controls.
- The study involved 179 DMD patients and 96 healthy controls, focusing on measuring left ventricular (LV) function, with findings demonstrating significant differences in ventricular volumes and ejection rates, indicating compromised cardiac function in DMD patients.
- Results suggest that certain CMR filling and ejection indices correlate with increased mortality in DMD patients, highlighting the potential for these measures to serve as important prognostic tools.