Relevant bibliographies by topics / The metabolic syndrome

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'The metabolic syndrome'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "The metabolic syndrome"

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Karimova, Maksuda Ahmedjanovna, and Dilnoza Kakhramanovna Kurbanbaeva. "Problems Of Metabolic Syndrome." American Journal of Medical Sciences and Pharmaceutical Research 03, no. 06 (June 10, 2021): 52–55. http://dx.doi.org/10.37547/tajmspr/volume03issue06-08.

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At the beginning of the third millennium, for mankind, which overcame the epidemic of life-threatening infections during its centuries-old history, the problem of cardiovascular diseases (CVD) came to the fore in relevance among all causes of morbidity and mortality. A significant role in this was played by lifestyle modification associated with limiting physical activity, increasing the calorie content of food, and a steady increase in emotional stress. All of this potentiates the main risk factors for CVD, which are a “negative asset of progress,” namely increased blood pressure (BP), dyslipidemia, diabetes mellitus (DM) and obesity. Since 1988, after G. Reaven's Banting lecture, it is customary to designate the interconnected combination of these pathologies by the single term "metabolic syndrome X".
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Jeengar, Pooja, and Madhubala Chauhan. "Association of metabolic syndrome in polycystic ovarian syndrome." New Indian Journal of OBGYN 3, no. 2 (January 2017): 90–94. http://dx.doi.org/10.21276/obgyn.2017.3.2.5.

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Wikiera, Beata, Agnieszka Zubkiewicz-Kucharska, Julita Nocoń-Bohusz, and Anna Noczyńska. "Metabolic disorders in polycystic ovary syndrome." Pediatric Endocrinology Diabetes and Metabolism 23, no. 4 (2017): 204–8. http://dx.doi.org/10.18544/pedm-23.04.0094.

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STĂNESCU, Ana Maria Alexandra, Ana Maria GOANŢĂ, Roxana IGNĂTESCU, Ekua Asafoaba APPIAH, Ioana Veronica GRĂJDEANU, and Lucian IONIŢĂ. "COMPARISON BETWEEN HUMANS AND ANIMAL DIAGNOSED WITH METABOLIC SYNDROME AND OBESITY ASSOCIATED METABOLIC PROBLEMS." Romanian Journal of Medical Practice 12, no. 4 (December 31, 2017): 250–55. http://dx.doi.org/10.37897/rjmp.2017.4.14.

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Metabolic syndrome is an increasingly recognised problem worldwide. The diagnostic criteria may vary from country to country and between humans and animals. It is therefore essential to have a globally regulated diagnostic criteria for both animals and humans.
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Siddharth Bharatbhai, Rajpura, and Desai Archish Ishvarbhai. "Metabolic Syndrome among Polycystic Ovarian Syndrome: A Cross Sectional Study." Indian Journal of Obstetrics and Gynecology 7, no. 1 (2019): 65–71. http://dx.doi.org/10.21088/ijog.2321.1636.7119.12.

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Sohail, Sumbul, Shabnum Nadeem, and Fouzia Ali. "METABOLIC SYNDROME;." Professional Medical Journal 24, no. 09 (September 8, 2017): 1286–94. http://dx.doi.org/10.29309/tpmj/2017.24.09.812.

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Metabolic syndrome is a congregation of central obesity, dyslipidemia, raised bloodsugar levels, increasing the individual’s susceptibility to Type II Diabetes and cardiovasculardiseases. Objectives: (1) To determine the prevalence of metabolic syndrome in young, urban,female population. (2) To determine the risk factors in poor, urban, female population. StudyDesign: This was a descriptive cross sectional study. Setting: The department of Gynae/Obst Unit II KMDC/Abbasi Shaheed hospital. Period: One year starting from January 2016 toDecember 2016. Material and Method: Approval was taken from ESRC of KMDC. All healthyasymptomatic married/single women between 18-49 years of age were included while women<18 or >50 years of age, diabetic, hypertensive or having bleeding disorders were excludedfrom study. Laboratory data included blood sugar, triglycerides, HDL-cholesterol, collected byphlebotomist from the participants in fasting state through venipuncture. A Chi-square test wasapplied to evaluate the association of demographic group variables and metabolic syndrome.P-value <0.05 was considered as statistically significant. There was no conflict of interest. Result:A total of 343 participants were recruited. The socio and demographic data is summarized inTable-I. The prevalence of Metabolic syndrome was found to be high. 227(66.2%) of participantswere having Metabolic syndrome according to NCEP ATP III criteria. 63(18.4 %) had history ofPIH while 52(15.2%) had family history of hypertension and 126(36.7 %) had family historyof both Hypertension and Diabetes. 232 (67.6 %) of women had sedentary life style and only3(0.9%) practiced aerobic exercises. 287(83.7%) had their waist circumference of >80cm, themean systolic blood pressure was 127.5 +-23.76 while the mean diastolic blood pressure was86.99+-57.36. The mean of BMI was at higher level 30.97+-6.41. Obesity is the most commonrisk factor for Metabolic syndrome. The mean of fasting blood sugar was 105.08+-42.16which was on higher side. The mean of Triglycerides 142.43+-61.12 and HDL 39.04+-12.45were within normal limits. Increased prevalence was observed in women who had PIH duringpregnancy and childbirth 25.1% v 5.2%(p value=0.001). Conclusion: Prevention and treatmentof metabolic syndrome is a big challenge. Lifestyle interventions should begin from the earlychildhood to reduce weight and to prevent development of obesity and metabolic syndrome.
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Strashok, L. A., O. V. Buznytska, and О. М. Meshkova. "Indicators of lipid metabolism disorders in the blood serum of adolescents with metabolic syndrome." Ukrainian Biochemical Journal 92, no. 6 (December 24, 2020): 137–42. http://dx.doi.org/10.15407/ubj92.06.137.

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Bano, Fauzia, and Arvind K. Srivastava. "HERBS IN THERAPEUTIC MANAGEMENT OF METABOLIC SYNDROME." Era's Journal of Medical Research 7, no. 1 (June 2020): 99–106. http://dx.doi.org/10.24041/ejmr2020.17.

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BONDARENKO, O., and M. SOROCHKA. "Metabolic Syndrome – Modern overview of the Problem." Experimental and Clinical Physiology and Biochemistry 2016, no. 2 (June 15, 2016): 45–52. http://dx.doi.org/10.25040/ecpb2016.02.045.

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Gogia, Atul, and PK Agarwal. "Metabolic syndrome." Indian Journal of Medical Sciences 60, no. 2 (2006): 72. http://dx.doi.org/10.4103/0019-5359.19918.

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Dissertations / Theses on the topic "The metabolic syndrome"

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Bickerton, Alex Sam Thomas. "Fat metabolism and the metabolic syndrome." Thesis, University of Oxford, 2008. http://ora.ox.ac.uk/objects/uuid:9108a8ca-8b3e-4e45-98e2-4765c009774f.

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Background: The metabolic syndrome is associated with an increased risk of diabetes and vascular disease. In order to understand the pathophysiological processes underlying such risk, it is necessary to develop a better understanding of normal fat metabolism and abnormalities associated with the syndrome. The hypothesis tested in this thesis is that specific abnormalities in adipose tissue and muscle fat metabolism characterise the metabolic syndrome. Methods: Fasting biochemical parameters were measured in a cohort of overweight men with and without the metabolic syndrome. Stable-isotope labeling and arterio-venous difference measurements were conducted in 18 men to elucidate pathways of exogenous and endogenous fat metabolism under fasting and postprandial conditions in adipose tissue and skeletal muscle. In addition, a pilot study of the effects of heat and electrical stimulation on adipose tissue metabolism was undertaken. Results: Cohort study - The prevalence of the metabolic syndrome depended on the definition used. Total cholesterol and apoB were greater in those with the metabolic syndrome than in those without. There was no difference in fasting NEFAs. Metabolic investigation - There was significant postprandial uptake of NEFA from the circulating NEFA pool by adipose tissue. Chylomicrons were confirmed as the preferred substrate of LPL. There was preferential uptake of FAs derived from chylomicron hydrolysis. There was release of NEFA across muscle. In the metabolic syndrome, adipose tissue NEFA output is lower during fasting and falls less following a meal than in the healthy obese. Clearance of dietary-derived TG is lower across both adipose tissue and muscle in the metabolic syndrome. Pilot study – Heat increased measures of lipolysis whereas electrical stimulation had no effect. Conclusions: Fat metabolism in individuals with the metabolic syndrome is characterised by metabolic inflexibility but not insulin resistance.
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Tsai, I.-Jung. "Perturbations of arachidonic acid metabolism in the metabolic syndrome." University of Western Australia. School of Medicine and Pharmacology, 2009. http://theses.library.uwa.edu.au/adt-WU2010.0065.

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[Truncated abstract] Arachidonic acid is oxidised in vivo by non-enzymatic (free radical) or enzymatic pathways (cyclooxygenase, lipoxygenase, and cytochrome P450) to form a range of biologically active eicosanoids. Specifically, arachidonic acid is metabolised by cytochrome P450 -hydroxylase to produce vasoactive 20-hydroxyeicosatetraenoic acid (20-HETE), and by 5-lipoxygenase to produce proinflammatory leukotriene B4 (LTB4), which can further be metabolised by -hydroxylase to from 20-OH-LTB4 and 20-COOH-LTB4. F2-Isoprostanes (F2-IsoPs) are produced through free radical attack on arachidonic acid and have been recognised as the most reliable markers of lipid peroxidation in vivo. The metabolic syndrome (MetS) is characterised by abdominal obesity, hypertension, insulin resistance, glucose intolerance, and dyslipidemia. It is associated with low-grade inflammation and oxidative stress and an increased risk of developing cardiovascular diseases. Dietary weight loss is strongly recommended for the management of the MetS and can potentially minimise the risk of cardiovascular diseases and diabetes in individuals with the MetS. Little is known regarding the role of these arachidonic acid metabolites in the MetS and the effect of weight loss on their metabolism. Chapter three comprised of three in vitro studies aimed to examine 20-HETE synthesis in human blood cells. 20-HETE acts as a second messenger for vasoconstrictor actions of angiotensin II (Ang II) and endothelin-1 (ET-1) in renal and mesenteric beds. Human neutrophils and platelets are integral to the inflammatory process. ... Production of LTB4 and 20-OH-LTB4 was significantly lower compared with controls (P<0.005) and remained so after adjustment for neutrophil count (P<0.05).The weight loss intervention resulted in a 4.6kg reduction in body weight and a 6.6cm decrease in waist circumference and a significant increase in LTB4 and 20-OH- LTB4 in the weight loss group. Chapter Five continued to investigate the role of other arachidonic acid metabolites, 20-HETE and F2-IsoPs in the MetS and the effect of weight loss. In the case-control study (Human study 1), plasma and urinary 20-HETE and F2-IsoPs were significantly elevated in the MetS group, but no significant difference was found in stimulated-neutrophil 20-HETE. A significant gender x group interaction was observed in that women with the MetS had higher urinary 20-HETE and F2-IsoPs compared to controls (P<0.0001). In a randomised controlled trial (Human study 2), relative to the weight- maintenance group, a 4.6 kg loss in weight resulted in a 2 mmHg fall in blood pressure but did not alter the production of 20-HETE or F2-IsoPs. No significant differences were shown in 20-HETE released from stimulated-neutrophils before and after weight loss. 20-HETE and oxidative stress may be important mediators of cardiovascular disease risk in the MetS. Although a 4% reduction in body weight reduced BP, there were no changes in plasma or urinary 20-HETE or F2-IsoPs. In summary, in vitro studies show that human neutrophils and platelets can produce 20-HETE in response to Ang II and ET-1, and human studies demonstrate that the presence of MetS has a significant impact on arachidonic acid metabolism and effective weight loss can restore leukocyte synthesis of LTB4.
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Zibadi, Sherma. "Metabolic Syndrome-Induced Cardiac Fibrosis." Diss., The University of Arizona, 2009. http://hdl.handle.net/10150/195321.

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Recent studies support the association between metabolic syndrome (MetS), a cluster of cardiovascular risk factors, and diastolic dysfunction. Disproportionate collagen accumulation, particularly cross-linking of collagen, plays a key role in translating interstitial fibrosis into mechanical chamber stiffness and diastolic dysfunction. Characteristic changes in the expression and activity of myocardial lysyl oxidase (LOX), a matrix modifying enzyme that catalyzes cross-linked collagen, are unclear in MetS. We established a diet-induced MetS model to study diastolic dysfunction by treating male C57BL/6 mice a high-fat high-simple carbohydrate (HFHSC) diet for 6 months. Despite blunted gene expression of LOX isoforms, MetS mice demonstrated significant increase in the ratio of protein expression of mature to proenzyme LOX, enhanced LOX activity, and increased cardiac cross-linked collagen compared with controls. This fibrotic response coincided with marked increase in left ventricular end-diastolic pressure and stiffness and impaired diastolic filling pattern. Our data demonstrate that diet-induced MetS alters the remodeling enzyme LOX, thereby increasing the amount of crosslinking and inducing diastolic dysfunction.Furthermore we examined the role of T-lymphocytes in myocardial LOX regulation in diet-induced fibrotic hearts. Female SCID mice which are devoid of functional T-lymphocytes and C57BL/6 mice were treated with HFHSC diet for 12 months. Similar to male C67BL/6, female HFHSC-fed C57BL/6 mice demonstrated significant increase in maturation and catalytic activity of myocardial LOX, cross-linking, ventricular stiffness and diastolic dysfunction. Whereas induction of LOX protein was minimal in SCID mice compared with wild-type counterparts. Correspondingly fibrillar cross-linked collagen formation and diastolic dysfunction were less prominent in SCID mice. Our results suggest a potential role of T-lymphocytes in induction of myocardial stiffness and diastolic dysfunction through modulation of LOX-dependent collagen maturation.Moreover we studied the role of leptin, an adipokine over-produced in MetS with fibrotic effects in non-cardiac tissues, as a key mediator of profibrogenic responses in the heart by administrating leptin to C57BL/6 and leptin-deficient ob/ob mice. With exogenous leptin administration ob/ob mice displayed passive diastolic filling dysfunction that coincided with increase in myocardial collagen compared with ob/ob controls. Our findings suggest profibrotic effects of leptin in the heart, primarily through predominance of collagen synthesis over degradation.
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Tweedy, Maureen P. Guarnaccia Charles Anthony. "Metabolic syndrome and psychosocial factors." [Denton, Tex.] : University of North Texas, 2009. http://digital.library.unt.edu/permalink/meta-dc-11005.

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Gobin, Reeta Rukmini Devi. "Metabolic syndrome and cardiovascular disease." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610102.

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Hodge, Stephanie Jean. "Psychosocial underpinnings of metabolic syndrome." Thesis, Ulster University, 2018. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.737993.

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The rate of obesity throughout Europe has more than doubled over the past 20 years. It was hypothesised that certain patterns of adiposity and associated co-morbidity metabolic parameters were related to certain psychological traits and neurochemical markers. The study aim was to measure associations between adiposity, metabolic markers, psychological traits and the neurochemicals whole blood serotonin and salivary cortisol, in a single study. Participants were healthy (n=102), males (n=35) and females (n=67), aged 20-65 years (mean 39.7 years). The literature review found that some patterns of adiposity were associated with metabolic risk factors more strongly than were others. Gynoid fat may be a healthier state of adiposity in terms of cardiovascular health. Negative emotional traits, such as anxiety were associated with greater risk for metabolic syndrome/obesity, whilst positive measures such as optimism were linked with lower risk. Experimental findings showed optimism being linked with lower adiposity and life satisfaction associated with greater high density lipoprotein (HDL) cholesterol. Associations between whole blood (WB) serotonin and anthropometric measures found lower WB serotonin being associated with greater adiposity, and that this may be sex-linked. The theory that adiposity may be linked to salivary cortisol and certain psychological factors showed positive associations between gynoid fat, BMI and resilience. Higher salivary cortisol was also correlated with greater perceived stress, and with lower trait mood. These data imply a link between cortisol, adiposity and psychological factors. There are few studies in the literature linking these cross-disciplinary fields. Results suggest that serotonin could be an antecedent and/or a consequence of obesity. Data also suggest that psychometric and salivary cortisol factors, particularly resilience, may interplay together to contribute towards adiposity. This study also implies that the positive traits of optimism, resilience and life satisfaction are related to better metabolic health and more “healthy” patterns of fat deposition.
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Selig, Patricia Marie. "Factors Associated with Metabolic Syndrome." VCU Scholars Compass, 2003. https://scholarscompass.vcu.edu/etd/5960.

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The metabolic syndrome, a clinical condition linked to diabetes and cardiovascular disease is a powerful predictor for overall mortality, and is present in more than 20% of the US. population (Ford, Giles, & Dietz, 2002). This study examines gender differences as well as other factors associated with metabolic syndrome as defined by the Adult Treatment Panel III of the National Cholesterol Education Program. A sample of 10,134 adults between 20-64 years of age was selected from the Third National Health and Nutrition Survey. Metabolic syndrome was present in 19.6 % of this sample. An ecological model of health services was used to analyze metabolic syndrome. The four model domains include population characteristics, environmental factors, health behaviors, and utilization of health care services. The descriptive results showed statistically significant differences in individuals with metabolic syndrome and without metabolic syndrome. Those with metabolic syndrome were proportionately more older, reported a past medical history of cardiovascular disease and family history of diabetes, had lower levels of education and a lower annual household income. There were no differences between men and women in age, geographic residence, education or health insurance coverage. However, there were higher proportions of women with metabolic syndrome in all race categories when compared to men with metabolic syndrome with the exception of Caucasians. A family history of diabetes, a family history of cardiovascular disease, a past personal history of cardiovascular disease, level of income, habitual activity and having a usual source of health care were found to be statistically significant between men and women with metabolic syndrome. Results of the logistic regression analysis revealed that overall, women were 30% less likely to have metabolic syndrome, yet African American women and Hispanic American women were nearly twice as likely to have metabolic syndrome than Caucasian women. Further research on gender differences for shared medical conditions is needed.
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Tweedy, Maureen P. "Metabolic Syndrome and Psychosocial Factors." Thesis, University of North Texas, 2009. https://digital.library.unt.edu/ark:/67531/metadc11005/.

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Metabolic syndrome is a constellation of risk factors, including abdominal obesity, hypertriglyceridemia, low HDL cholesterol, high blood pressure, and high fasting glucose, that commonly cluster together and can result in cardiovascular disease. The prevalence of metabolic syndrome and the components that comprise the syndrome vary by age and by racial/ethnic group. In addition, previous research has indicated that the risk factors contributing to metabolic syndrome may be exacerbated by exposure to perceived stress. This study utilized data from the 2002, 2004, and 2006 Health and Retirement Study (HRS) and National Health and Nutrition Examination Survey (NHANES) data sets. It was hypothesized that depression and anxiety (conceptualized as stress in this study) increase the risk of presenting with metabolic syndrome while social support decreases the risk of metabolic syndrome. While results of cross-sectional analysis do not indicate a significant relationship between depression and metabolic syndrome (t = -.84, ns), longitudinal analysis does indicate a significant relationship between depression and metabolic syndrome over time (t = -5.20, p <.001). However, anxiety is not significantly related to metabolic syndrome when the relationship is examined through cross-sectional analysis (t = -1.51, ns) and longitudinal analysis (χ² = 13.83, ns). Similarly, social support is not significantly related to metabolic syndrome when examined in cross-sectional (χ² = .63, ns) and longitudinal (t = 1.53, ns) analysis. Although level of stress is not significantly related to metabolic syndrome as a whole, there is a significant relationship between stress and both triglyceride level (t = -2.94, p = .003) and blood glucose level (t = -3.26, p = .001).
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Bowman, Thomas A. "Hepatic CEACAM1 Protects Against Metabolic Abnormalities Associated with Metabolic Syndrome." University of Toledo Health Science Campus / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=mco1271358149.

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Yasmin, Ephia. "Metabolic aspects of polycystic ovary syndrome." Thesis, University of Leeds, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545722.

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Books on the topic "The metabolic syndrome"

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Ahima, Rexford S., ed. Metabolic Syndrome. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-12125-3.

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Farooqui, Akhlaq A. Metabolic Syndrome. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7318-3.

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Wang, Minghan, ed. Metabolic Syndrome. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.

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The metabolic syndrome. 2nd ed. Chichester, West Sussex: Wiley-Blackwell, 2011.

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Scott, Isaacs. Overcoming metabolic syndrome. Omaha, Neb: Addicus Books, 2006.

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Beck-Nielsen, Henning, ed. The Metabolic Syndrome. Vienna: Springer Vienna, 2013. http://dx.doi.org/10.1007/978-3-7091-1331-8.

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Lipshultz, Steven E., Sarah E. Messiah, and Tracie L. Miller, eds. Pediatric Metabolic Syndrome. London: Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-2366-8.

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Byrne, Christopher D., and Sarah H. Wild, eds. The Metabolic Syndrome. Oxford, UK: Wiley-Blackwell, 2011. http://dx.doi.org/10.1002/9781444347319.

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Byrne, Christopher D., and Sarah H. Wild, eds. The Metabolic Syndrome. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470025131.

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Hansen, Barbara Caleen, and George A. Bray, eds. The Metabolic Syndrome. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-116-5.

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Book chapters on the topic "The metabolic syndrome"

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Farooqui, Akhlaq A. "Essential Fatty Acid Metabolism in Metabolic Syndrome and Neurological Disorders." In Metabolic Syndrome, 67–101. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7318-3_3.

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Speakman, John R. "Evolution of Obesity." In Metabolic Syndrome, 1–23. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-12125-3_9-1.

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Wang, Minghan. "Gut as an Endocrine Organ: The Role of Nutrient Sensing in Energy Metabolism." In Metabolic Syndrome, 1–28. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch1.

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Wang, Minghan. "Current Antidiabetic Therapies and Mechanisms." In Metabolic Syndrome, 253–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch10.

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Burcelin, Remy, Cendrine Cabou, Christophe Magnan, and Pierre Gourdy. "GLP-1 Biology, Signaling Mechanisms, Physiology, and Clinical Studies." In Metabolic Syndrome, 279–325. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch11.

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McIntosh, C. H. S., S. J. Kim, R. A. Pederson, U. Heiser, and H. U. Demuth. "Dipeptidyl Peptidase IV Inhibitors for Treatment of Diabetes." In Metabolic Syndrome, 327–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch12.

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Ryan, Margaret, and Serge A. Jabbour. "Sodium Glucose Cotransporter 2 Inhibitors." In Metabolic Syndrome, 359–75. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch13.

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Micanovic, Radmila, James D. Dunbar, and Alexei Kharitonenkov. "Fibroblast Growth Factor 21 as a Novel Metabolic Regulator." In Metabolic Syndrome, 377–89. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch14.

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Tong, Qiang. "Sirtuins as Potential Drug Targets for Metabolic Diseases." In Metabolic Syndrome, 391–422. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch15.

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Hale, Clarence, and David J. St. Jean. "11β-Hydroxysteroid Dehydrogenase Type 1 as a Therapeutic Target for Type 2 Diabetes." In Metabolic Syndrome, 423–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470910016.ch16.

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Conference papers on the topic "The metabolic syndrome"

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Muñoz-Diosdado, A., L. Ramírez-Hernández, A. M. Aguilar-Molina, J. A. Zamora-Justo, R. A. Gutiérrez-Calleja, and C. D. Virgilio-González. "Holter registers and metabolic syndrome." In XIII MEXICAN SYMPOSIUM ON MEDICAL PHYSICS. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4901381.

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Cosmescu, Adriana, and Doina Felea. "P67 Metabolic syndrome: case report." In 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7–10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313273.155.

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Savira, Maya, Rusdiana, Sry Suryani Widjaja, and M. Syahputra. "Comparison Malondialdehyde (MDA) Level between Obesity Non Metabolic Syndrome and Obesity with Metabolic Syndrome Patients." In International Conference of Science, Technology, Engineering, Environmental and Ramification Researches. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0010081806440647.

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Ekici, Aydanur, Emel Bulcun, Mehmet Ekici, Pinar Yildiz, Tulay Karakoc, and Dilay Cimen. "Metabolic syndrome in interstitial lung diseases." In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa3823.

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Midori Shinzato, Marcia, Pamela Judith Silva, Franciely Bueno Wigeneske, and Elias Silva de Medeiros. "PAINFUL MUSCULOSKELETAL DISEASES IN METABOLIC SYNDROME." In Congresso Brasileiro de Reumatologia 2020. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2020.17344.

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Lobova, Tatyana Aleksandrovna. "Metabolic syndrome: pathogenetic aspects and prognostic value." In VIII International applied research conference. TSNS Interaktiv Plus, 2016. http://dx.doi.org/10.21661/r-111348.

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Zaibi, Haifa, Sarra Maazaoui, Jihen Ben Amar, Ines Laaouini, Saloua Azzebi, M. Ali Baccar, Besma Dhahri, and Hichem Aouina. "Metabolic syndrome in chronic obstructive pulmonary disease." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa719.

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Ali, W., UP Kushwaha, and W. Mohd. "Oxidized LDL as a biomarker in metabolic syndrome." In Late Breaking Abstracts: – Diabetes Kongress 2017 – 52. Jahrestagung der DDG. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1603549.

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Agrawal, Shaleka, Girish Ramlugun, Jesse Ashton, Gregory Sands, Manuel Zarzoso, Jichao Zhao, and Kevin JAMART. "Structural Basis of Atrial Arrhythmogenesis in Metabolic Syndrome." In 2019 Computing in Cardiology Conference. Computing in Cardiology, 2019. http://dx.doi.org/10.22489/cinc.2019.248.

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Dhiemitra Aulia Dewi, Agil, and Silvi Lailatul Mahfida. "A Cross Sectional Study: Metabolic Syndrome in Yogyakarta." In Proceedings of the 5th International Conference on Health Sciences (ICHS 2018). Paris, France: Atlantis Press, 2019. http://dx.doi.org/10.2991/ichs-18.2019.2.

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Reports on the topic "The metabolic syndrome"

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Hawksworth, Dorota, and Arthur Burnett II. Metabolic syndrome and men’s health. BJUI Knowledge, August 2019. http://dx.doi.org/10.18591/bjuik.0482.

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Kirby, Michael, and Jonny Coxon. The metabolic syndrome, erectile dysfunction and testosterone deficiency. BJUI Knowledge, September 2019. http://dx.doi.org/10.18591/bjuik.0484.

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Li, Mengdie, Yating Yang, Haixia Wang, and Tianhao Bao. Meta-analysis of risk factors for metabolic syndrome in schizophrenia. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2021. http://dx.doi.org/10.37766/inplasy2021.4.0023.

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Voicehovska, Julija, Mila Vlaskovska, Jana Janovska, Sergejs Babikovs, Vladimirs Voicehovskis, Andrejs Skesters, Alise Silova, et al. Oxidative Stress Markers Diagnostic Value in Metabolic Syndrome Dermal Manifestations: a Prospective Clinical Trial. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, February 2018. http://dx.doi.org/10.7546/crabs.2018.02.15.

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Voicehovska, Julija, Mila Vlaskovska, Jana Janovska, Sergejs Babikovs, Vladimirs Voicehovskis, Andrejs Skesters, Alise Silova, et al. Oxidative Stress Markers Diagnostic Value in Metabolic Syndrome Dermal Manifestations: a Prospective Clinical Trial. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, February 2018. http://dx.doi.org/10.7546/grabs2018.2.15.

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Gao, Hui, Cheng Zhang, and Fangbiao Tao. Association between prenatal phthalate exposure and gestational metabolic syndrome parameters: A systematic review of epidemiological study. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2020. http://dx.doi.org/10.37766/inplasy2020.12.0065.

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Cicero, Arrigo F. G. Effects of a combined nutraceutical on glucose and lipid metabolism in women with post-menopausal incident metabolic syndrome: a double-blind, placebocontrolled, randomized clinical trial. Science Repository, June 2019. http://dx.doi.org/10.31487/j.jfnm.2019.02.01.

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Zhang, Fangfang, Lili Liu, Tian Li, and Zubing Mei. Prognostic value of metabolic syndrome for risk of stroke recurrence and mortality: A comprehensive systematic review with meta-analysis. INPLASY - International Platform of Registered Systematic Review Protocols, April 2020. http://dx.doi.org/10.37766/inplasy2020.4.0183.

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Powell, Isaac, Jennifer Beebe-Dimmer, and Lance Heilbrun. The Influence of Metabolic Syndrome on Prostate Cancer Progression and Risk of Recurrence in African American and European American Men. Fort Belvoir, VA: Defense Technical Information Center, October 2012. http://dx.doi.org/10.21236/ada570389.

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Yu, Xiao-hong, Xi-wen Yu, Qi Zhang, Yu-ping Wang, and Guo-qiang Yu. Yangxin Decoction combined acupuncture on blood lipid metabolism in Qi Deficiency and Blood Stasis type of Chest Bi-Syndrome: A protocol of systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, July 2020. http://dx.doi.org/10.37766/inplasy2020.7.0047.

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You might also be interested in the extended bibliographies on the topic 'The metabolic syndrome' for particular source types:
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