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Journal articles on the topic 'Physiologic'

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1

Levine, Samara, and Ozgul Muneyyirci-Delale. "Stress-Induced Hyperprolactinemia: Pathophysiology and Clinical Approach." Obstetrics and Gynecology International 2018 (December 3, 2018): 1–6. http://dx.doi.org/10.1155/2018/9253083.

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While prolactin is most well known for its role in lactation and suppression of reproduction, its physiological functions are quite diverse. There are many etiologies of hyperprolactinemia, including physiologic as well as pathologic causes. Physiologic causes include pregnancy, lactation, sleep-associated, nipple stimulation and sexual orgasm, chest wall stimulation, or trauma. Stress is also an important physiologic cause of hyperprolactinemia, and its clinical significance is still being explored. This review will provide an overview of prolactin physiology, the role of stress in prolactin secretion, as well as the general clinical approach to hyperprolactinemia.
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2

Etter, Nicole M. "What Have We Learned From Physiological Approaches to Characterizing Dysarthria and Other Speech Production Disorders?" Perspectives on Speech Science and Orofacial Disorders 20, no. 2 (October 2010): 37–46. http://dx.doi.org/10.1044/ssod20.2.37.

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Traditionally, speech-language pathologists (SLP) have been trained to develop interventions based on a select number of perceptual characteristics of speech without or through minimal use of objective instrumental and physiologic assessment measures of the underlying articulatory subsystems. While indirect physiological assumptions can be made from perceptual assessment measures, the validity and reliability of those assumptions are tenuous at best. Considering that neurological damage will result in various degrees of aberrant speech physiology, the need for physiologic assessments appears highly warranted. In this context, do existing physiological measures found in the research literature have sufficient diagnostic resolution to provide distinct and differential data within and between etiological classifications of speech disorders and versus healthy controls? The goals of this paper are (a) to describe various physiological and movement-related techniques available to objectively study various dysarthrias and speech production disorders and (b) to develop an appreciation for the need for increased systematic research to better define physiologic features of dysarthria and speech production disorders and their relation to know perceptual characteristics.
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3

Buchman, Timothy G. "Physiologic Stability and Physiologic State." Journal of Trauma: Injury, Infection, and Critical Care 41, no. 4 (October 1996): 599–605. http://dx.doi.org/10.1097/00005373-199610000-00002.

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4

Miller, Margaret, and Amanpreet Kaur. "General Management Principles of the Pregnant Woman." Seminars in Respiratory and Critical Care Medicine 38, no. 02 (April 2017): 123–34. http://dx.doi.org/10.1055/s-0037-1602167.

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AbstractPregnancy is a dynamic process that consists of profound physiological changes mediated by hormonal, mechanical, and circulatory pathways. Understanding of changes in physiology is essential for distinguishing abnormal and normal signs and symptoms in a pregnant patient. These physiological changes also have important pharmacotherapeutic considerations for a pregnant patient. Although there are limited data to guide decisions regarding medications and diagnostic procedures in pregnancy, a careful review of risks should be balanced with review of risk of withholding a medication or procedure. Interventional pulmonary procedures can be safely performed in pregnant women while keeping in mind the maternal anatomic and physiologic changes. Furthermore, management of a maternal cardiopulmonary arrest requires important modifications in patient positioning and intravenous access to ensure adequate efficacy of chest compressions, circulation, and airway management. This review will provide an overview of maternal physiologic changes with a focus on cardiopulmonary physiology, pharmacotherapeutic considerations, diagnostic and interventional pulmonary procedures during pregnancy, and cardiopulmonary resuscitation in pregnancy.
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5

Curtis, J. A. "Physiologic Anemia." Pediatrics in Review 16, no. 9 (September 1, 1995): 356–57. http://dx.doi.org/10.1542/pir.16-9-356.

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6

Curtis, Jane A. "Physiologic Anemia." Pediatrics In Review 16, no. 9 (September 1, 1995): 356–57. http://dx.doi.org/10.1542/pir.16.9.356.

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The changes in levels of hemoglobin and hematocrit in the first weeks of life are dramatic. O'Brien and Pearson, in a classic article, demonstrated that these levels drop from an average hemoglobin of 17 g/dL and a hematocrit of 52% in cord blood to a hemoglobin of 11.4 g/dL and a hematocrit of 33% at 75 days of age. The reasons for this drop and the physiologic mechanisms involved in causing it have fascinated a number of researchers. When considering the results of blood values, the first step is to be sure of the validity of the measurements. Early researchers in this area, such as Oettinger and Mills, noted a wide range of quoted normal values for hemoglobin and hematocrit of the newborn.
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7

Osguthorpe, Susan. "Physiologic Monitoring." AACN Advanced Critical Care 4, no. 1 (February 1, 1993): 9–10. http://dx.doi.org/10.4037/15597768-1993-1001.

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8

Laity, J. H., J. M. Slade, J. K. Petrella, T. A. Miszko, S. K. Agrawal, and M. E. Cress. "PHYSIOLOGIC RESERVE." Medicine & Science in Sports & Exercise 33, no. 5 (May 2001): S124. http://dx.doi.org/10.1097/00005768-200105001-00704.

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9

O'Grady, Stephen E., and Derek A. Poupard. "Physiologic horseshoeing." Journal of Equine Veterinary Science 23, no. 3 (March 2003): 123–24. http://dx.doi.org/10.1053/jevs.2003.36.

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10

Bunt, TJ. "Physiologic Amputation." AORN Journal 54, no. 6 (December 1991): 1220–24. http://dx.doi.org/10.1016/s0001-2092(07)66867-7.

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11

McDunn, Jonathan E., T. Philip Chung, Jason M. Laramie, R. Reid Townsend, and J. Perren Cobb. "Physiologic genomics." Surgery 139, no. 2 (February 2006): 133–39. http://dx.doi.org/10.1016/j.surg.2005.02.005.

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12

Tatum, William O., and Andrew Spector. "Physiologic Pseudoseizures." Journal of Clinical Neurophysiology 28, no. 3 (June 2011): 308–10. http://dx.doi.org/10.1097/wnp.0b013e31821c3dce.

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13

Cosner, Karen R., and Esther dejong. "Physiologic Second." MCN, The American Journal of Maternal/Child Nursing 18, no. 1 (January 1993): 38???43. http://dx.doi.org/10.1097/00005721-199301000-00011.

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14

Chmielewska, Ewa, and Paweł Kafarski. "Physiologic Activity of Bisphosphonates – Recent Advances." Open Pharmaceutical Sciences Journal 3, no. 1 (May 30, 2016): 56–78. http://dx.doi.org/10.2174/1874844901603010056.

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Background: Bisphosphonates are drugs commonly used for the medication and prevention of diseases caused by decreased mineral density. Despite such important medicinal use, they display a variety of physiologic activities, which make them promising anti-cancer, anti-protozoal, antibacterial and antiviral agents. Objective: To review physiological activity of bisphosphonates with special emphasis on their ongoing and potential applications in medicine and agriculture. Method: Critical review of recent literature data. Results: Comprehensive review of activities revealed by bisphosphonates. Conclusion: although bisphosphonates are mostly recognized by their profound effects on bone physiology their medicinal potential has not been fully evaluated yet. Literature data considering enzyme inhibition suggest possibilities of far more wide application of these compounds. These applications are, however, limited by their low bioavailability and therefore intensive search for new chemical entities overcoming this shortage are carried out.
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15

Rosenberg, Michael L. "Physiologic Anisocoria: A Manifestation of a Physiologic Sympathetic Asymmetry." Neuro-Ophthalmology 32, no. 3 (January 2008): 147–49. http://dx.doi.org/10.1080/01658100802115254.

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16

H M, Cheng. "A PHYSIOLOGIC JOURNEY." Journal of Health and Translational Medicine 15, no. 1 (June 25, 2012): 16–18. http://dx.doi.org/10.22452/jummec.vol15no1.4.

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17

McCARTHY, JAMES A., and MACHELLE M. SEIBEL. "Physiologic Hair Growth." Clinical Obstetrics and Gynecology 34, no. 4 (December 1991): 799–804. http://dx.doi.org/10.1097/00003081-199112000-00017.

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18

Alpert, Susan. "Physiologic monitoring devices." Critical Care Medicine 23, no. 10 (October 1995): 1626–27. http://dx.doi.org/10.1097/00003246-199510000-00005.

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19

Gomez-Builes, J. Carolina, Sergio A. Acuna, Bartolomeu Nascimento, Fabiana Madotto, and Sandro B. Rizoli. "Harmful or Physiologic." Anesthesia & Analgesia 127, no. 4 (October 2018): 840–49. http://dx.doi.org/10.1213/ane.0000000000003341.

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20

Siegel, Amber, and Kathryn Kreider. "Physiologic Steroid Tapering." Journal for Nurse Practitioners 15, no. 6 (June 2019): 463–64. http://dx.doi.org/10.1016/j.nurpra.2019.03.024.

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21

Spahn, Donat R., and Caveh Madjdpour. "Physiologic Transfusion Triggers." Anesthesiology 104, no. 5 (May 1, 2006): 905–6. http://dx.doi.org/10.1097/00000542-200605000-00002.

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22

Booth, Frank V. McL. "COMPUTERIZED PHYSIOLOGIC MONITORING." Critical Care Clinics 15, no. 3 (July 1999): 547–62. http://dx.doi.org/10.1016/s0749-0704(05)70070-1.

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23

Rogers, Anne T., and David A. Stump. "Cerebral Physiologic Monitoring." Critical Care Clinics 5, no. 4 (October 1989): 845–61. http://dx.doi.org/10.1016/s0749-0704(18)30411-1.

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24

O'Grady, Stephen E., and Derek A. Poupard. "Proper physiologic horseshoeing." Veterinary Clinics of North America: Equine Practice 19, no. 2 (August 2003): 333–51. http://dx.doi.org/10.1016/s0749-0739(03)00020-8.

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25

Maisels, M. Jeffrey, and Kathleen Gifford. "779 PHYSIOLOGIC JAUNDICE." Pediatric Research 19, no. 4 (April 1985): 240A. http://dx.doi.org/10.1203/00006450-198504000-00809.

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26

Vallet, Benoit, Sébastien Adamczyk, Olivier Barreau, and Gilles Lebuffe. "Physiologic transfusion triggers." Best Practice & Research Clinical Anaesthesiology 21, no. 2 (June 2007): 173–81. http://dx.doi.org/10.1016/j.bpa.2007.02.003.

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27

Costa, M., A. L. Goldberger, and C. K. Peng. "Modeling physiologic variability." Journal of Critical Care 20, no. 4 (December 2005): 386–97. http://dx.doi.org/10.1016/j.jcrc.2005.09.029.

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28

Colburn, Wayne A. "Physiologic Pharmacokinetic Modeling." Journal of Clinical Pharmacology 28, no. 8 (August 1988): 673–77. http://dx.doi.org/10.1002/j.1552-4604.1988.tb03199.x.

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29

Govindan, Srini. "0081 Physiologic anatomy, use of Infra-Red Thermography in Hypersomnia." Sleep 45, Supplement_1 (May 25, 2022): A37. http://dx.doi.org/10.1093/sleep/zsac079.079.

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Abstract Introduction In the words of Michel Salmon, " Between anatomy and physiology there is room for a functional anatomy and for a physiologic anatomy “. This concept was applied to analyze our (1) Sleep Research 21, 1992,341 (2) Sleep Research 22, 1993, 363, and (3) SLEEP 31, 2008, A219 publications on patients with Hypersomnia who had intracranial and extracranial blood flow evaluations. Methods For “Functional Anatomy”, Intracranial cerebral blood flow was done with Xenon 133 inhalation. For “Physiologic Anatomy”, Extracranial facial blood flow Imaging, Infra-Red thermography was done. 1992,3 and 2008 data was classified: Groups I, II and III. Group I had Intracranial and Extracranial blood flow study, 5% CO2 inhalation. Groups II had Extracranial flow study with 5 % CO2 and 100 % Oxygen inhalation. Groups III had Extracranial flow study 100 % Oxygen inhalation. Response interpretation: Normal response to 5% CO2, vasodilation. For 100% Oxygen / hyperoxia, vasoconstriction. Response is considered as normal or abnormal, if response is absent or paradoxical. Results Group I: All three patients 5% CO2 inhalation, intracranial Functional anatomy vasomotor response normal. Physiological Anatomy response abnormal. Group II, Physiological Anatomy study. 8 patients. CO2 response, 7/8 vasoconstriction, abnormal response. 100% Oxygen challenge, 4/8 had no vasoconstriction, abnormal response. Group III: Physiological anatomy. 7 patients tested with 100% Oxygen challenge. 6/7 abnormal response, (1 vasoconstriction, 4 no response, 2 vasodilation). Total of 18 patients in all groups, physiological anatomy/ Extracranial flow vasomotor response was abnormal in 16/18, (Group I = 3, Group II = 7, and Group III = 6) Conclusion In hypersomnia patients vasomotor testing, Functional Anatomy, intracranial flow vasomotion normal in 3/3 for hypercarbia inhalation. For Physiologic Anatomy, using Infra-Red Thermography to image extracranial facial blood flow (not coupled with metabolism) vasomotion was abnormal in 16/18 patients. 5% CO2 and 100% Oxygen inhalation used as contrast agents is well tolerated and facilitates imaging vasomotor dysfunction in the facial blood flow, trigeminal angiosomes, which can be correlated with hypersomnia. Association between trigeminal system and the hypocretin receptor 1 gene HCRTR1 gene has been reported. Support (If Any) None.
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30

Manga, Sharanya, Neha Muthavarapu, Renisha Redij, Bhavana Baraskar, Avneet Kaur, Sunil Gaddam, Keerthy Gopalakrishnan, et al. "Estimation of Physiologic Pressures: Invasive and Non-Invasive Techniques, AI Models, and Future Perspectives." Sensors 23, no. 12 (June 20, 2023): 5744. http://dx.doi.org/10.3390/s23125744.

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The measurement of physiologic pressure helps diagnose and prevent associated health complications. From typical conventional methods to more complicated modalities, such as the estimation of intracranial pressures, numerous invasive and noninvasive tools that provide us with insight into daily physiology and aid in understanding pathology are within our grasp. Currently, our standards for estimating vital pressures, including continuous BP measurements, pulmonary capillary wedge pressures, and hepatic portal gradients, involve the use of invasive modalities. As an emerging field in medical technology, artificial intelligence (AI) has been incorporated into analyzing and predicting patterns of physiologic pressures. AI has been used to construct models that have clinical applicability both in hospital settings and at-home settings for ease of use for patients. Studies applying AI to each of these compartmental pressures were searched and shortlisted for thorough assessment and review. There are several AI-based innovations in noninvasive blood pressure estimation based on imaging, auscultation, oscillometry and wearable technology employing biosignals. The purpose of this review is to provide an in-depth assessment of the involved physiologies, prevailing methodologies and emerging technologies incorporating AI in clinical practice for each type of compartmental pressure measurement. We also bring to the forefront AI-based noninvasive estimation techniques for physiologic pressure based on microwave systems that have promising potential for clinical practice.
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31

TYERS, G. FRANK O., MIN GAO, ROBERT I. HAYDEN, RICHARD LEATHER, THOMAS ASHTON, and MICHAEL KIELY. "Use of Physiologic Pacing After the Canadian Trial of Physiologic Pacing." Pacing and Clinical Electrophysiology 28, s1 (January 2005): S68—S69. http://dx.doi.org/10.1111/j.1540-8159.2005.00044.x.

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32

Simko, F. "Physiologic and pathologic myocardial hypertrophy – physiologic and pathologic regression of hypertrophy?" Medical Hypotheses 58, no. 1 (January 2002): 11–14. http://dx.doi.org/10.1054/mehy.2001.1399.

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33

Sica, Domenic A. "Angiotensin‐Converting Enzyme Inhibitors' Side Effects—Physiologic and Non‐Physiologic Considerations." Journal of Clinical Hypertension 7, s8 (August 2005): 17–23. http://dx.doi.org/10.1111/j.1524-6175.2005.04556.x.

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34

Esquivel, Jose J. Herrera, Juan Octavio Alonso-Larraga, García R. Luis Eduardo, Ignacio Guerrero-Hernández, and Martha Fernandez Rosales. "S1899 Physiologic Acid Reflux and Positive Symptom-Index, Is It Physiologic?" Gastroenterology 136, no. 5 (May 2009): A—288. http://dx.doi.org/10.1016/s0016-5085(09)61314-7.

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35

Weiss, Jeffrey P. "Urologic Issues During Pregnancy." Scientific World JOURNAL 4 (2004): 364–76. http://dx.doi.org/10.1100/tsw.2004.92.

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Pregnancy induces a variety of physiologic changes in the urinary tract. When such changes become accentuated the physiologic becomes the pathologic and symptoms arise, at times of significance enough to threaten the well being of mother and/or fetus. This article intends to describe the basis for urinary physiology and its pathologic counterparts during pregnancy. Such a background may then facilitate a rational management protocol for various urologic problems in the gravid state.
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36

Steinberg, E. L., M. Nissan, K. Bar-Ilan, A. Menahem, R. Arbel, and E. Luger. "PHYSIOLOGICAL CONSIDERATIONS IN FUNCTIONAL 3-D LUMBAR DIAGNOSIS: NON-PHYSIOLOGICAL TESTS." Journal of Musculoskeletal Research 07, no. 01 (March 2003): 25–38. http://dx.doi.org/10.1142/s0218957703000934.

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Lumbar spine function may be clinically assessed by subjective physician findings or by a more sophisticated mean such as 3-D dynamometric system. This system was developed to differentiate objectively between physiologic and non-physiological behavior of LBP patients. The same system is used, concurrently, to categorize the physiologic tests according to functional limitation. The four major parameters used for assessing spinal disability are: range of motion, maximal isometric torque, maximal velocity and maximal torque in the secondary axis. Six other independent parameters were used in order to assess non-cooperative or non-physiologic behavior. For the study, 108 non-symptomatic subjects and 595 LBP patients were tested. All patients had a physical examination before being tested on the dynamometric device (the IsoStation B-200). One hundred and ten patients were classified as non-physiological and 91 were classified in the gray zone. The results support the use of 3-D dynamometry to objectively classify the patient's performance reliability. The measured parameters are objective and reliable indicators of the patient's physical condition and credibility that should influence both the patient's assessment and treatment.
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37

Bader, Jackie E., and Jeffrey C. Rathmell. "Physiologic Media Alters Macrophage Phenotype and Activation State." Journal of Immunology 204, no. 1_Supplement (May 1, 2020): 226.8. http://dx.doi.org/10.4049/jimmunol.204.supp.226.8.

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Abstract Traditional cell culture media such as RPMI is consistently used in in-vitro studies in order to inform in-vivo translation. However traditional media poorly simulates physiological conditions which can lead to inaccurate interpretations of data and failed in-vivo applications. The recent development of human plasma like media (HPLM) mirrors physiologic conditions with more realistic levels of glucose, amino acids and other nutrients. We investigated bone marrow derived macrophage phenotype and activation in either RPMI or HPLM to better understand the effects of physiologic conditions on macrophages behavior. Classically activated M1 (100ng/mL LPS + 10ng/mL IFNγ) or alternatively activated M2 (20ng/mL IL-4) were investigated for metabolic activity and behavior. Macrophages cultured in HPLM exhibit a unique phenotype compared to RPMI with increased iNOS expression in response to LPS treatment and reduced CD206 after treatment with IL-4. These data suggest physiologic media can alter the behavior and function of macrophages in-vitro. Following more investigation, these unique activation states in physiologic conditions may uncover differential metabolic requirements and behavior not previously seen in traditional culture media.
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38

RT Lakey, Jonathan, Zach Villaverde, Tori Tucker, Michael Alexander, and Scott A. Hepford. "Improved Kidney Function Following Physiologic Insulin Resensitization Treatment Modality." Endocrinology and Disorders 5, no. 4 (August 18, 2021): 01–04. http://dx.doi.org/10.31579/2640-1045/080.

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Diabetes affects millions of people worldwide and is a leading cause of amputation, blindness, neuropathy, and chronic kidney disease. Chronic kidney disease results in the prolonged impairment of kidney function. Common medications and lifestyle modifications do not eliminate the long-term complications of diabetes, because they lack the ability to restore the periodic cycle of insulin that exists in healthy physiology. Our study used a precise administration of exogenous insulin, mimicking the physiologic profile of insulin secretion, which is more effective at stabilizing cellular blood glucose uptake and reducing diabetic complications than current drug and lifestyle modifications alone. In this case study report, we evaluated three diabetic or pre-diabetic patients who showed improvements in kidney function after beginning this treatment modality. We monitored their chronic kidney disease symptoms before and after the physiological insulin resensitization (PIR) process. We showed that the patients improved in kidney function after several months based on their laboratory metrics and CKD stage classification.
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39

Vijayaraman, Pugazhendhi, and Daniel Gellan. "Pursuit of physiologic pacing." Journal of Thoracic Disease 10, no. 10 (October 2018): E766—E767. http://dx.doi.org/10.21037/jtd.2018.09.123.

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40

Kovács, Enikő, Zsigmond Jenei, Anikó Horváth, László Gellér, Szabolcs Szilágyi, Ákos Király, Levente Molnár, Péter Sótonyi jr., Béla Merkely, and Endre Zima. "Physiologic effects of hypothermia." Orvosi Hetilap 152, no. 5 (January 2011): 171–81. http://dx.doi.org/10.1556/oh.2011.29006.

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Therapeutic use of hypothermia has come to the frontline in the past decade again in the prevention and in mitigation of neurologic impairment. The application of hypothermia is considered as a successful therapeutic measure not just in neuro- or cardiac surgery, but also in states causing brain injury or damage. According to our present knowledge this is the only proven therapeutic tool, which improves the neurologic outcome after cardiac arrest, decreasing the oxygen demand of the brain. Besides influencing the nervous system, hypothermia influences the function of the whole organ system. Beside its beneficial effects, it has many side-effects, which may be harmful to the patient. Before using it for a therapeutic purpose, it is very important to be familiar with the physiology and complications of hypothermia, to know, how to prevent and treat its side-effects. The purpose of this article is to summarize the physiologic and pathophysiologic effects of hypothermia. Orv. Hetil., 2011, 152, 171–181.
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41

Batirel, Hasan Fevzi. "Physiologic consequences of pneumonectomy." Shanghai Chest 5 (April 2021): 19. http://dx.doi.org/10.21037/shc-2019-rpts-24.

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42

Thakur, Ranjan K., and Andrea Natale. "Advances in Physiologic Pacing." Cardiac Electrophysiology Clinics 14, no. 2 (June 2022): xiii—xiv. http://dx.doi.org/10.1016/j.ccep.2022.04.001.

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43

Ellenbogen, Kenneth A., Pugazhendhi Vijayaraman, and Santosh Padala. "Advances in Physiologic Pacing." Cardiac Electrophysiology Clinics 14, no. 2 (June 2022): i. http://dx.doi.org/10.1016/s1877-9182(22)00039-9.

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44

Casaburi, Richard. "PHYSIOLOGIC RESPONSES TO TRAINING." Clinics in Chest Medicine 15, no. 2 (June 1994): 215–27. http://dx.doi.org/10.1016/s0272-5231(21)01069-8.

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45

Rudolf Hoehn-Saric. "Physiologic Responses in Anxiety." Current Psychiatry Reviews 3, no. 3 (August 1, 2007): 196–204. http://dx.doi.org/10.2174/157340007781369667.

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46

Gardner, Reed M., and Marianne Hujcs. "Fundamentals of Physiologic Monitoring." AACN Advanced Critical Care 4, no. 1 (February 1, 1993): 11–24. http://dx.doi.org/10.4037/15597768-1993-1002.

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For centuries, medical practitioners had no electronic medical instruments and had to rely on their senses of sight, hearing, smell, taste, and touch to obtain physiologic measurements. Although it is possible to estimate blood pressure by palpating the pulse at the radial or brachial artery, such estimates are not accurate. Determining arterial oxygen saturation of hemoglobin is more complex: how “blue” a patient appears depends on skin coloration, lighting, and the examiner’s sense of color. Finally, using radiographic images to validate pulmonary edema when clinicians suspect that there is an elevated left atrial or pulmonary artery wedge pressure also challenges human senses. However, today’s medical instruments use transducers and signal processors to convert patient information into a form that clinicians can easily perceive and understand. This article defines terms used with biomedical instrumentation and discusses the components of ideal physiologic patient monitoring systems
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47

Harris, G. D. "Physiologic management of DKA." Archives of Disease in Childhood 87, no. 5 (November 1, 2002): 451–52. http://dx.doi.org/10.1136/adc.87.5.451.

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48

Hammer, Claus, and E. Thein. "Determining Significant Physiologic Incompatibilities." Graft 4, no. 2 (March 2001): 108–10. http://dx.doi.org/10.1177/152216280100400206.

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49

GARDNER, REED M., and MARIANNE HUJCS. "Fundamentals of Physiologic Monitoring." AACN Clinical Issues: Advanced Practice in Acute and Critical Care 4, no. 1 (February 1993): 11–24. http://dx.doi.org/10.1097/00044067-199302000-00002.

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50

MacMahon, Edward B., David V. Carmines, and Roshen N. Irani. "Physiologic Bowing in Children." Journal of Pediatric Orthopaedics B 4, no. 1 (1995): 100–105. http://dx.doi.org/10.1097/01202412-199504010-00017.

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