Publications by authors named "R Apel"

Achalasia is a disorder of esophageal motility characterized by absent relaxation of the lower esophageal sphincter and abnormal peristalsis of the esophagus during swallowing. The etiology is divided into primary idiopathic achalasia and secondary achalasia and classified into 3 subtypes based on manometric evaluation, according to the Chicago 4.0 classification.

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Article Synopsis
  • * Researchers analyzed various data from IPF patients, finding elevated levels of the chemokine CXCL6, which correlates with poorer patient survival.
  • * The study suggests that CXCL6, produced by abnormal airway epithelial cells, enhances collagen production in lung fibroblasts, contributing to the pathology of IPF and highlighting a potential target for treatment.
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Objectives: The individual course of disease in idiopathic pulmonary fibrosis (IPF) is highly variable. Assessment of disease activity and prospective estimation of disease progression might have the potential to improve therapy management and indicate the onset of treatment at an earlier stage. The aim of this study was to evaluate whether regional ventilation, lung perfusion, and late enhancement can serve as early imaging markers for disease progression in patients with IPF.

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Glutamate (Glu) is the main mammalian brain neurotransmitter. Concerning the glutamatergic neurotransmission, excessive levels of glutamate in the synaptic cleft are extremally harmful. This phenomenon, named as excitotoxicity is involved in various acute and chronic brain diseases.

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