Relevant bibliographies by topics / Pulmonary imaging

Academic literature on the topic 'Pulmonary imaging'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Pulmonary imaging"

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van Beek, E. J. R. "Pulmonary Imaging." Imaging Decisions MRI 13, no. 1 (March 2009): 1. http://dx.doi.org/10.1111/j.1617-0830.2009.01129.x.

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JONES, M. R., and J. H. REID. "Thoracic vascular imaging: thoracic aortic disease and pulmonary embolism." Imaging 22, no. 1 (May 2013): 20100064. http://dx.doi.org/10.1259/imaging.20100064.

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Jones, M. R., and J. H. Reid. "Emergency chest radiology: thoracic aortic disease and pulmonary embolism." Imaging 18, no. 3 (September 2006): 122–38. http://dx.doi.org/10.1259/imaging/81369175.

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Scherer, P. M., and D. L. Chen. "Imaging Pulmonary Inflammation." Journal of Nuclear Medicine 57, no. 11 (September 1, 2016): 1764–70. http://dx.doi.org/10.2967/jnumed.115.157438.

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Hansell, D. M., and C. D. R. Flower. "Imaging pulmonary embolism." BMJ 316, no. 7130 (February 14, 1998): 490–91. http://dx.doi.org/10.1136/bmj.316.7130.490.

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Alton, H. "Pulmonary vascular imaging." Paediatric Respiratory Reviews 2, no. 3 (September 2001): 227–37. http://dx.doi.org/10.1053/prrv.2001.0145.

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Emmett, M., and J. M. Rothstein. "Pulmonary embolism imaging." Cleveland Clinic Journal of Medicine 72, no. 11 (November 1, 2005): 1059. http://dx.doi.org/10.3949/ccjm.72.11.1059.

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Frechen, Dirk, Stefan Krüger, Ingo Paetsch, Sebastian Kozerke, Bernhard Schnackenburg, Michael Frick, Nikolaus Marx, and Cosima Jahnke. "Pulmonary Perfusion Imaging." Journal of the American College of Cardiology 60, no. 22 (December 2012): 2335–37. http://dx.doi.org/10.1016/j.jacc.2012.07.063.

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Hatabu, Hiroto. "Functional Pulmonary Imaging." Academic Radiology 18, no. 4 (April 2011): 401. http://dx.doi.org/10.1016/j.acra.2011.01.017.

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Fedullo, Peter F., and Deborah Shure. "Pulmonary Vascular Imaging." Clinics in Chest Medicine 8, no. 1 (March 1987): 53–64. http://dx.doi.org/10.1016/s0272-5231(21)00466-4.

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Dissertations / Theses on the topic "Pulmonary imaging"

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Yoshimaru, Eriko Suzanne. "Magnetic Resonance Imaging Techniques for Rodent Pulmonary Imaging." Diss., The University of Arizona, 2013. http://hdl.handle.net/10150/293388.

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Magnetic Resonance Imaging (MRI) is a safe and widely used diagnostic imaging method that allows in vivo observation of anatomy and characterization of tissues. MRI provides a method to monitor patients without invasive measures, making it suitable for both diagnostics and longitudinal monitoring of various pathologies. A notable example of this is the work carried out by the Alzheimer's Disease Neuroimaging Initiative (ADNI), which utilizes imaging, including multiple MRI techniques, to monitor disease progression in AD patients and evaluates treatment responses and prevention strategies. Similarly, MRI has been extensively used in evaluating diseases in a variety of animal models. In order to detect subtle anatomical changes over time, small differences in MR images must be accurately extracted. Furthermore, to ensure that the extracted differences are due to anatomical changes rather than equipment variance, it becomes essential to monitor and to assess the MRI system stability. In the first chapter of the dissertation, a method for monitoring pre-clinical MRI system performance is discussed. The technique developed during the study provides a fast and simple method to monitor pre-clinical MRI systems but also has applications for all areas of MRI. The second chapter describes the development of a 3D UTE MRI method for pulmonary imaging in freely breathing mice. The development of the 3D UTE sequence for pulmonary MRI has demonstrated its ability to collect images without noticeable motion artifacts and with appreciable signal from the lung parenchyma. Furthermore, images at two distinct respiratory phases were reconstructed from a single data set, providing functional information of the rodents' lungs. Finally, in the third chapter, 3D ¹⁹F UTE MRI is evaluated for imaging in vivo distributions of perfluorocarbon (PFC) nanoemulsions for measuring pulmonary inflammation. Building upon the development of pulmonary imaging, fluorinated contrast agents made from PFCs were used to target immune cells in response to pulmonary pathology. Both 3D ¹H and ¹⁹F UTE MRI were used to acquire pulmonary images of mouse models documented to have pulmonary pathology. Even though the mice had confirmed elevation in alveolar macrophage counts, no visible ¹⁹F signal accumulation within the pulmonary tissue was observed with MRI.
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Saba, Tarek Sami. "The assessment of pulmonary haemodynamics with magnetic resonance imaging in pulmonary hypertension." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/29346.

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In this thesis we set out to investigate whether anatomical and blood flow measurements made with MRI can detect and quantify raised pulmonary artery pressure at cardiac catheterisation. We then looked to see whether MRI has any advantages over Doppler echocardiography, the current gold standard non-invasive investigation. We enrolled twenty-eight subjects who were undergoing cardiac catheterisation and Doppler echocardiography for investigation of suspected pulmonary hypertension at the Scottish Pulmonary Vascular Unit between September 1999 and March 2001. We used MRI to measure right and left ventricular mass, volume, and wall thickness, and aortic and pulmonary artery diameter. We calculated a novel ventricular mass indeed by dividing right ventricular mass by left ventricular mass. We then performed a flow quantification in the right pulmonary artery to measure mean and peak velocity of blood flow, acceleration time and ejection time, and calculated the ratio of acceleration time over ejection time. Finally we attempted to study the changes in these variables following straight leg raising exercise. In summary, we have shown that anatomical measurements made in the cardiopulmonary circulation with MRI can be used to estimate pulmonary artery pressure with greater accuracy than doppler echocardiography. These estimates are likely to be more reliable than those provided by echocardiography, and may also give a measure of the recent burden of pulmonary vascular disease. An analogy may be made with the use of glycosylated haemoglobin instead of glucose in diabetes; pulmonary artery pressure fluctuates on a minute by minute basis whereas anatomical measurements reflect sustained changes in pulmonary haemodynamics. Furthermore, we have shown that MRI measurements of blood flow are sensitive and specific indicators of pulmonary hypertension, and can be used to study exercise-related changes in blood flow.
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Schuessler, Thomas Florian. "Advances in pulmonary monitoring and thoracic imaging." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=34444.

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The high incidence of pulmonary disease in critically ill patients necessitates new and improved techniques for pulmonary monitoring and thoracic imaging. To investigate pulmonary monitoring techniques using pressure and flow signals, I developed a comprehensive computational model of subjects breathing spontaneously or with the support of an assist-ventilator. The model was used to quantitatively assess measurement techniques for dynamic intrinsic positive end-expiratory pressure (PEEP$ rm sb{i})$ and inspiratory work of breathing. The results demonstrate that some means of correction for both expiratory muscle activity and cardiogenic oscillations on esophageal pressure is necessary if dynamic PEEP$ rm sb{i}$ and work of breathing are to be measured accurately on-line. I also conclude that the discrepancies between static and dynamic PEEP$ rm sb{i}$ are caused by heterogeneity of the expiratory flow limitation. An adaptive filter to reduce the cardiogenic oscillations on esophageal pressure was developed and validated in a computer simulation. In four intensive care patients, the adaptive filter markedly attenuated the apparent cardiogenic oscillations and reduced the standard deviation of the measured PEEP$ rm sb{i}$ by 57%. Investigation of the interactions between patients and a pressure support ventilator using the computer model confirmed our present understanding of patient-ventilator asynchrony and indicated that patient and ventilator form a highly nonlinear dynamic system, so that the optimal ventilator settings most likely vary between patients and with time. In the second part of this thesis, I investigated the importance of inaccuracies in conventional Finite Elements for thoracic Electrical Impedance Tomography (EIT) imaging. Augmenting the number of first-order Finite Elements did not efficiently reduce these inaccuracies. A computer simulation suggested that the accuracy of the forward solution needs to be improved by at least 30 dB before useful
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Schuessler, Thomas F. "Advances in pulmonary monitoring and thoracic imaging." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ30376.pdf.

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Van, Tassel Lora. "Imaging Evaluation of the Solitary Pulmonary Nodule." Thesis, The University of Arizona, 2012. http://hdl.handle.net/10150/221418.

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A Thesis submitted to The University of Arizona College of Medicine - Phoenix in partial fulfillment of the requirements for the Degree of Doctor of Medicine.
An estimated 150,000 solitary pulmonary nodules (SPNs) are identified at chest radiography each year, making it important for physicians to understand how to characterize them and evaluate patients for potential malignancy. We performed an extensive literature search to identify risk factors, characteristics of SPNs, and available technologies used to identify and evaluate these nodules through a comprehensive literature search. Additionally, we present evidence-based management schemes for incidentally identified nodules. CONCLUSIONS: A number of features visible at thoracic CT are useful for determining whether an SPN is benign or malignant. FDG PET/CT plays an important role in the diagnosis and management of lung cancer and is an increasingly valuable tool for the characterization and management of SPNs. Unlike CT and MRI imaging, PET provides metabolic activity of a nodule. The information provided by PET/CT imaging allows for both morphological and anatomical characteristics as well as physiological data in the form of metabolism within the nodule itself. The information gained from PET is extremely useful for directing patient management and may obviate the need for invasive diagnostic procedures.
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Johns, Christopher. "Improving the diagnostic pathway of pulmonary hypertension using cardio-pulmonary magnetic resonance imaging." Thesis, University of Sheffield, 2018. http://etheses.whiterose.ac.uk/20207/.

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Whilst pulmonary hypertension is a relatively uncommon condition, it is associated with a poor quality of life and poor survival. It is therefore important that we correctly identify patients who suffer from pulmonary hypertension, assess the underlying cause (an essential step for treatment) and seek those who are at risk of death. Current guidelines centre on right heart catheterisation as the recommended tool to answer these important clinical questions. Since it was first described in the mid-1950s, there have been significant improvements in the survival of patients with pulmonary hypertension, mainly due to the introduction of vasodilator therapies and surgical procedures. There have been parallel improvements in imaging technologies, the most tangible of which is cardiac MRI, allowing time resolved assessment of cardiac structure and function. Despite these improvements in non-invasive methodologies, there remains heavy reliance upon invasively measured pressures and flow for the diagnosis, phenotyping and assessment of risk in patients with pulmonary hypertension. The aim of this PhD thesis is to evaluate, and hopefully increase, the role of cardio pulmonary vascular MRI in the non-invasive assessment of pulmonary hypertension. I show that cardiac MRI metrics, particularly when combined in a regression model, are able to predict mean pulmonary arterial pressure. Such models are able to identify with reasonable accuracy the presence of pulmonary hypertension in patients referred to a tertiary referral centre. The role of cardio-pulmonary MRI in the assessment of the underlying group of pulmonary hypertension, such as chronic thrombo-embolic pulmonary hypertension and PH-left heart disease, is then explored as identification of patients who may respond to PH specific therapy is an important step. Finally, the role of MRI in the assessment of prognosis, concentrating specifically on patients with PH left heart disease and PH in patients with chronic obstructive pulmonary disease is assessed.
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McLeod, Karen A. "Intravascular ultrasound and magnetic resonance imaging of the pulmonary arteries in pulmonary hypertension." Thesis, University of Edinburgh, 1997. http://hdl.handle.net/1842/28597.

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The main aim of this thesis is to describe the changes which are detectable on intravascular ultrasound and magnetic resonance imaging in patients with pulmonary hypertension and to determine whether these imaging modalities could be of use for the clinical assessment of the condition. Intravascular ultrasound was performed in 10 young adults with Eisenmenger's Syndrome and 4 infants with pulmonary hypertension secondary to a left to right shunt. Vasodilator studies were performed in 5 of the patients with Eisenmenger's. The vessel wall appeared as a single echogenic layer in all patients making it difficult to define or measure medial thickness with certainty. Morphological changes of intimal hypertrophy and atherosclerosis were evident in patients with Eisenmenger's whereas in the infants the intima appeared thin and smooth, typical of normal artery. The technique gave excellent definition of the vessel lumen allowing continuous measurement of changes in luminal dimensions in response to vasodilators. MRI of the pulmonary arteries was performed in 11 patients with Eisenmenger's and 6 normal controls. In patients with pulmonary hypertension the pulmonary arteries were found to be dilated with reduced distensibility when compared with normals. Calculations of Qp:Qs by MRI in patients with systemic to pulmonary shunts and pulmonary hypertension did not correlate well with values from cardiac catheterisation in all patients. In conclusion, magnetic resonance imaging was found to have limited role in the assessment of pulmonary hypertension but with new technical developments could become a non-invasive method of studying pulmonary hypertension in the future. The morphological changes detectable by intravascular ultrasound tend to be in severe disease only but the technique provides a unique method of studying pulmonary vascular reactivity in life.
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Wang, Lei. "FDG-PET imaging of pulmonary vascular remodelling in PAH." Thesis, Imperial College London, 2016. http://hdl.handle.net/10044/1/58197.

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Pulmonary artery hypertension (PAH) is a disease of progressive pulmonary vascular remodelling characterised by dysregulated proliferation and inflammation. With increasing acceptance that glucose metabolism is perturbed in proliferating and inflammatory cells in PAH, the present thesis took interest in the application of molecular 18F-2-fluoro-2-deoxyglucose positron emission tomography (FDG-PET) imaging, widely used in the oncology clinic, in the assessment of PAH patients. Our hypothesis is that FDG-PET imaging can be used as a potential tool for the in vivo assessment of pulmonary vascular remodelling and evaluation of anti-remodelling therapies in PAH. In the first part of the thesis, a clinical applicable dynamic FDG-PET acquisition protocol with kinetic Patlak analysis was assessed in idiopathic PAH (IPAH) patients and PAH associated with systemic lupus erythematosus (SLE-PAH) patients for detection and quantification of lung FDG uptake. Mean lung FDG uptake was increased in both IPAH and SLE-PAH patients compared to that in healthy controls. There was heterogeneity of lung FDG uptake within PAH population, which aligns with our current understanding of the complex and regional pathology in PAH. Lung FDG uptake of SLE-PAH patients significantly correlated with SLE disease activity markers. In the following in vivo FDG-PET study, treatments with liraglutide and tacrolimus significantly attenuated the increased pulmonary artery pressure and right heart hypertrophy, as well as pulmonary vascular muscularisation and inflammatory cell infiltration in monocrotaline-induced PAH rat models, accompanied by a decreased lung FDG uptake. These data support further evaluation of the use of FDG-PET as a potential tool for evaluating these therapies in clinical trials. We learnt that FDG-PET imaging lacks specificity to differentiate proliferation from inflammation as an underlying disease process. Future development of other PET tracer may help to identify a marker that interrogates the pulmonary pathology of interest.
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Walvick, Ronn P. "Magnetic Resonance Imaging of Neural and Pulmonary Vascular Function." Digital WPI, 2010. https://digitalcommons.wpi.edu/etd-dissertations/372.

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"Magnetic resonance imaging (MRI) has emerged as the imaging modality of choice in a wide variety experimental and clinical applications. In this dissertation, I will describe novel MRI techniques for the characterization of neural and pulmonary vascular function in preclinical models of disease. In the first part of this dissertation, experimental results will be presented comparing the identification of ischemic lesions in experimental stroke using dynamic susceptibility contrast (DSC) and a well validated arterial spin labeling (ASL). We show that DSC measurements of an index of cerebral blood flow are sensitive to ischemia, treatment, and stroke subregions. Further, we derived a threshold of cerebral blood flow for ischemia as measured by DSC. Finally, we show that ischemic lesion volumes as defined by DSC are comparable to those defined by ASL. In the second part of this dissertation, a methodology of visualizing clots in experimental animal models of stroke is presented. Clots were rendered visible by MRI through the addition of a gadolinium based contrast agent during formation. Modified clots were used to induce an experimental embolic middle cerebral artery occlusion. Clots in the cerebral vasculature were visualized in vivo using MRI. Further, the efficacy of recombinant tissue plasminogen activator (r-tPA) and the combination of r-tPA and recombinant annexin-2 (rA2) was characterized by clot visualization during lysis. In the third part of this dissertation, we present results of the application of hyperpolarized helium (HP-He) in the characterization of new model of experimental pulmonary ischemia. The longitudinal relaxation time of HP-He is sensitive to the presence of paramagnetic oxygen. During ischemia, oxygen exchange from the airspaces of the lungs to the capillaries is hindered resulting in increased alveolar oxygen content which resulted in the shortening of the HP-He longitudinal relaxation time. Results of measurements of the HP-He relaxation time in both normal and ischemic animals are presented. In the final part of this dissertation, I will present results of a new method to measure pulmonary blood volume (PBV) using proton based MRI. A T1 weighted, inversion recovery spin echo sequence with cardiac and respiratory gating was developed to measure the changes in signal intensity of lung parenchyma before and after the injection of a long acting intravascular contrast agent. PBV is related to the signal change in the lung parenchyma and blood before and after contrast agent. We validate our method using a model of hypoxic pulmonary vasoconstriction in rats."
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Miele, Amy Caroline. "Comparative pulmonary fibrosis : imaging fibroproliferation in donkey and man." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/17885.

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Pulmonary fibrosis is a chronic and debilitating condition that proposes several challenges to both veterinary and medical clinicians. Despite considerable research, many fibrotic lung diseases remain elusive in terms of aetiology, pathogenesis and treatment. Furthermore, progress is hindered by the lack of a translatable animal model with durable and persistent fibrosis. Asinine Pulmonary Fibrosis (APF) is a spontaneous syndrome of aged donkeys with high prevalence (35%). No previous detailed characterisation of APF has been performed and disease diagnosis remains a challenge. APF was studied with regard to clinical, pathological and molecular features and the suitability of this condition as a model for a rare fibrotic lung disease in humans known as pleuroparenchymal fibroelastosis (PPFE) was assessed. In addition, target activatable optical imaging reagents for the real time detection of two key molecular markers of fibrosis: matrix metalloproteinases (MMPs) and lysyl oxidases (LOXF) were evaluated in spontaneous ex vivo models of fibrosis. Such reagents may be used alongside fibred confocal fluorescence microscopy (FCFM), a relatively noninvasive and cutting edge diagnostic tool, to detect and monitor fibroproliferation in animals and man. Whole lungs were collected from 32 aged donkeys at routine necropsy. Gross examination revealed pulmonary fibrosis in 19 donkeys (APF cases), while 13 (controls) had grossly normal lungs. HRCT images and histology sections were reviewed independently and blindly for each of the lungs. Ten of 19 APF lungs were categorised as being ‘consistent with’ PPFE according to previously defined histological and imaging criteria. All 10 PPFE-like lungs had marked pleural and subpleural fibrosis, predominantly within the upper lung zone, with accompanying intra-alveolar fibrosis and elastosis. An activatable Smartprobe for the detection of LOXF, TWB-219, was synthesised by The Bradley Group, Department of Chemistry (UoEDC). The probe was based on a tandem amine oxidation and β-elimination mechanism, resulting in signal amplification detected at the 488nm wavelength. The probe showed increased fluorescence in the presence of diamine oxidase as well as on incubation with aged human lung tissue cell-free homogenate as determined by a fluorescent plate reader. This signal amplification could be inhibited by β-aminopropionitrile, a recognised LOX inhibitor as well as by an in-house inhibitor specific to LOX. An evolutionary family of MMP probes with varying cleavage sequences and structures, synthesised by the UoEDC, was evaluated at each stage of progression with regard to signal to noise ratio, sensitivity and specificity. Probes were tested against recombinant enzymes from the MMP family as well as neutrophil elastase and plasmin. Signal amplification was also assessed on incubation with human and ovine ex vivo lung tissue. The final ‘lead’ MMP probe, SVC-186, was cleaved by MMP-2, -9 and -13. Signal amplification was also seen following incubation with both human and ovine tissue with significant inhibition in the presence of the pan- MMP inhibitor, marimastat. In conclusion, APF is an emerging condition of aged donkeys that shares key pathological and imaging features with human PPFE. Diagnosis of APF and other fibrotic lung conditions across species remains a challenge to veterinary and medical professionals. As such, optical imaging tools may provide dynamic, real time information on the presence and progression of fibroproliferation in the lung. TWB- 219 and SVC-186 produce a detectable increase in fluorescent signal at the 488nm wavelength when activated by LOXF and MMPs respectively. These probes have been shown to function in human ex vivo tissue as assessed by FCFM.
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Books on the topic "Pulmonary imaging"

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Ohno, Yoshiharu, Hiroto Hatabu, and Hans-Ulrich Kauczor, eds. Pulmonary Functional Imaging. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-43539-4.

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Kanne, Jeffrey P. Clinically Oriented Pulmonary Imaging. Totowa, NJ: Humana Press, 2012.

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Kanne, Jeffrey P., ed. Clinically Oriented Pulmonary Imaging. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-542-8.

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Atlas of pulmonary vascular imaging. New York: Thieme, 2010.

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B, Higgins Charles, ed. Thoracic imaging: Pulmonary and cardiovascular radiology. 2nd ed. Philadelphia: Wolters Kluwer/Lippincott Williams & Wilkins Health, 2011.

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McGuinness, Francis E. Clinical Imaging in Non-Pulmonary Tuberculosis. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59635-3.

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Ghosh, Subha. Handbook of Imaging in Pulmonary Disease. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68165-4.

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E, Heffner John, ed. Pulmonary pearls. Philadelphia: Hanley & Belfus, 1988.

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Ahuja, Anil T. Imaging in SARS. London: GMM, 2004.

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Ellis, Stephen M. The WHO manual of diagnostic imaging: Radiographic anatomy and interpretation of the chest and the pulmonary system. Edited by Flower Christopher, Ostensen Harald, Pettersson Holger 1942-, International Society of Radiology, and World Health Organization. Geneva: Published by the World Health Organization in collaboration with the International Society of Radiology, 2006.

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Book chapters on the topic "Pulmonary imaging"

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Wilson, A. G. "Imaging." In Chronic Obstructive Pulmonary Disease, 351–72. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4525-9_14.

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Yaddanapudi, Kavitha. "Pulmonary Sarcoidosis." In PET/MR Imaging, 63–64. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65106-4_26.

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Yaddanapudi, Kavitha. "Pulmonary Infarct." In PET/MR Imaging, 71–72. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65106-4_30.

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Bayona, Jorge Carrillo, Liliana Arias Álvarez, and Paulina Ojeda León. "Pulmonary Interstitium." In Learning Chest Imaging, 197–219. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34147-2_9.

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Jayasekera, Geeshath, and Andrew J. Peacock. "Advanced Imaging in Pulmonary Hypertension." In Pulmonary Hypertension, 199–217. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23594-3_12.

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Lee, Edward Y., and Gulraiz Chaudry. "Pulmonary Hypertension." In Imaging in Pediatric Pulmonology, 253–67. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-23979-4_12.

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Carraway, Thomas, Anne C. Coates, and Charles K. Grimes. "Pulmonary Incidentaloma." In Imaging in Pediatric Pulmonology, 423–25. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-23979-4_22.

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Coates, Anne Cameron, and Robert G. Zwerdling. "Pulmonary Incidentalomas." In Imaging in Pediatric Pulmonology, 373–76. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-5872-3_19.

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Chawla, Ashish. "Imaging of Pulmonary Artery." In Thoracic Imaging, 235–67. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-2544-1_9.

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Chawla, Ashish. "Imaging of Pulmonary Nodules." In Thoracic Imaging, 85–100. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-2544-1_4.

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Conference papers on the topic "Pulmonary imaging"

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Gil, Daniel A., Joe T. Sharick, Ute A. Gamm, Michael A. Choma, and Melissa C. Skala. "Functional optical imaging of tracheal health (Conference Presentation)." In Optical Techniques in Pulmonary Medicine IV, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2017. http://dx.doi.org/10.1117/12.2252226.

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Pahlevaninezhad, Hamid, Anthony Lee, Geoffrey Hohert, Carley Schwartz, Tawimas Shaipanich, Alexander J. Ritchie, Wei Zhang, Calum E. MacAulay, Stephen Lam, and Pierre M. Lane. "In vivo imaging of pulmonary nodule and vasculature using endoscopic co-registered optical coherence tomography and autofluorescence imaging (Conference Presentation)." In Optical Techniques in Pulmonary Medicine III, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2016. http://dx.doi.org/10.1117/12.2209686.

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Leung, Hui Min, Lael M. Yonker, Hongmei Mou, Avira Som, Bryan P. Hurley, and Guillermo J. Tearney. "In vivo OCT imaging of the airways (Conference Presentation)." In Optical Techniques in Pulmonary Medicine IV, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2017. http://dx.doi.org/10.1117/12.2252160.

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Hariri, Lida P., Matthew J. Niederst, Hillary Mulvey, David C. Adams, Haichuan Hu, Isabel Chico-Calero, Margit V. Szabari, et al. "Multimodal imaging of lung cancer and its microenvironment (Conference Presentation)." In Optical Techniques in Pulmonary Medicine III, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2016. http://dx.doi.org/10.1117/12.2214658.

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Cui, Dongyao, Kengyeh K. Chu, Timothy N. Ford, Daryl Chulho Hyun, Hui Min Leung, Biwei Yin, Susan E. Birket, George M. Solomon, Steven M. Rowe, and Guillermo J. Tearney. "Imaging demonstration of a flexible micro-OCT endobronchial probe (Conference Presentation)." In Optical Techniques in Pulmonary Medicine IV, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2017. http://dx.doi.org/10.1117/12.2251449.

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Linguraru, Marius George, Nisha Mukherjee, Robert L. Van Uitert, Ronald M. Summers, Mark T. Gladwin, Roberto F. Machado, and Bradford J. Wood. "Pulmonary artery segmentation and quantification in sickle cell associated pulmonary hypertension." In Medical Imaging, edited by Xiaoping P. Hu and Anne V. Clough. SPIE, 2008. http://dx.doi.org/10.1117/12.770485.

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Szabari, Margit V., Vanessa J. Kelly, Matthew B. Applegate, Chunmin Chee, Khay M. Tan, Lida P. Hariri, R. Scott Harris, Tilo Winkler, and Melissa J. Suter. "Using optical coherence tomography (OCT) imaging in the evaluation of airway dynamics (Conference Presentation)." In Optical Techniques in Pulmonary Medicine III, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2016. http://dx.doi.org/10.1117/12.2216306.

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Zhou, Chuan, Heang-Ping Chan, Lubomir M. Hadjiiski, Smita Patel, Philip N. Cascade, Berkman Sahiner, Jun Wei, Jun Ge, and Ella A. Kazerooni. "Automatic pulmonary vessel segmentation in 3D computed tomographic pulmonary angiographic (CTPA) images." In Medical Imaging, edited by Joseph M. Reinhardt and Josien P. W. Pluim. SPIE, 2006. http://dx.doi.org/10.1117/12.655343.

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Kiraly, Atilla P., David P. Naidich, and Carol L. Novak. "Cartwheel projections of segmented pulmonary vasculature for the detection of pulmonary embolism." In Medical Imaging, edited by Robert L. Galloway, Jr. and Kevin R. Cleary. SPIE, 2005. http://dx.doi.org/10.1117/12.595858.

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Pieper, Mario, Hinnerk Schulz-Hildebrandt, Gereon Hüttmann, and Peter König. "Imaging of mucus clearance in the airways of living spontaneously breathing mice by optical coherence microscopy (Conference Presentation)." In Optical Techniques in Pulmonary Medicine III, edited by Melissa J. Suter, Stephen Lam, and Matthew Brenner. SPIE, 2016. http://dx.doi.org/10.1117/12.2209054.

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